Skip to main content
Download PDF
  • Original Paper
  • Open access
  • Published:

Vidarabine, an anti-herpes agent, prevents occlusal-disharmony-induced cardiac dysfunction in mice

The Journal of Physiological Sciences volume 72, Article number: 2 (2022) Cite this article

Abstract

We recently reported a positive relationship between occlusal disharmony and cardiovascular disease via activation of β-adrenergic signaling in mice. Furthermore, inhibition of type 5 adenylyl cyclase (AC5), a major cardiac subtype in adults, protects the heart against oxidative stress. Here, we examined the role of AC5 in the development of occlusal-disharmony-induced cardiovascular disease in bite-opening (BO) mice, prepared by cementing a suitable appliance onto the mandibular incisor. We first examined the effects of BO treatment on cardiac function in mice treated or not treated for 2 weeks with vidarabine, which we previously identified as an inhibitor of cardiac AC. Cardiac function was significantly decreased in the BO group compared to the control group, but vidarabine ameliorated the dysfunction. Cardiac fibrosis, myocyte apoptosis and myocyte oxidative DNA damage were significantly increased in the BO group, but vidarabine blocked these changes. The BO-induced cardiac dysfunction was associated with increased phospholamban phosphorylation at threonine-17 and serine-16, as well as increased activation of the Ca2+-calmodulin-dependent protein kinase II/receptor-interacting protein 3 signaling pathway. These data suggest that AC5 inhibition with vidarabine might be a new therapeutic approach for the treatment of cardiovascular disease associated with occlusal disharmony.

Introduction

Oral health decrease with age, and this is a major risk factor for many diseases, including cardiovascular disease [1]. In addition, aging-related loss of teeth, poor periodontal status and low alveolar bone levels can lead to occlusal disharmony [1, 2]. Increased sympathetic nervous activity was recently recognized as a hallmark feature that links aging with increased cardiovascular risk [3], and it is also involved in the etiology of oral frailty [4,5,6].

Adenylyl cyclase (AC) is the target enzyme of β-adrenergic receptor (β-AR) signaling stimulation. At least 9 isoforms are known, 7 of which are expressed in the heart; the type 5 isoform (AC5) is a major adult cardiac isoform, while type 6 is a major fetal isoform [7,8,9]. We have developed a mouse model with knock-out of AC5 (AC5KO) [10] and we have also identified vidarabine as a cardiac AC inhibitor in mice [11]. Using these models, we found that genetic disruption and pharmacological inhibition of AC5 are associated with resistance to the development of heart failure [10, 12, 13] and increased longevity [13, 14].

We previously examined the effects of occlusal disharmony on cardiac remodeling (fibrosis and myocyte apoptosis), cardiac function and susceptibility to atrial fibrillation in bite-opening mice (BO), in which a 0.7-mm BO was introduced by cementing a suitable appliance onto the mandibular incisor. We found that BO-induced cardiac dysfunction and susceptibility to atrial fibrillation are ameliorated by co-treatment with propranolol, a non-selective β-blocker [15, 16]. These findings indicate that activation of β-AR signaling might play a part in the cardiac dysfunction induced by occlusal disharmony.

However, β-blockers have several critical side effects. The inhibition of sympathetic signaling reduces cardiac function [17, 18], and great caution is required in the use of β-blockers for the treatment of heart failure and arrhythmia in aged patients [18]. We therefore proposed the usefulness of AC isoform-specific therapy, and we showed that vidarabine, which we previously identified as an inhibitor of cardiac AC, prevented the development of post-myocardial infarction heart failure and catecholamine-induced arrhythmia without worsening cardiac dysfunction [19, 20]. Therefore, in this work we examined the effects of AC isoform-specific therapy with vidarabine on occlusal-disharmony-induced cardiac dysfunction.

However, the role of AC5 in the occlusal-disharmony-induced cardiac deterioration remains poorly understood. In this study, therefore, we examined the effects of AC5 inhibition with vidarabine on cardiac function, cardiac fibrosis, myocyte apoptosis, and oxidative DNA damage induced by occlusal disharmony in mice (Fig. 1a, b, Additional file 1: Fig. S1). Acute and chronic treatment with vidarabine does not alter basal cardiac function in healthy animals, unlike β-blocker administration [20, 21]. More importantly, vidarabine has been used as an anti-viral drug for many years in humans [11, 20]. Therefore, vidarabine, rather than β-blocker, might be a safe and immediately clinically available drug for the treatment or prevention of cardiac dysfunction induced by occlusal disharmony.

Fig. 1
figure 1

Schematic illustrations of experimental procedure and bite-opening treatment, and comparison of body weight, cardiac muscle weight and lung weight among the groups. a Male 16-week-old C57BL/6 mice were divided into four groups: a normal control group (CTRL), a bite-opening (BO)-treated group, a vidarabine-treated group (V), and a BO plus vidarabine-treated (BO + V) group. Long-term infusion of vidarabine was performed for 14 days at a dose of 15 mg/kg/day with the osmotic mini-pumps, and the indicated measurements were made. b Schematic representation of a bite-opening (BO) in the form of a 0.7 mm increase in the vertical height of occlusion, obtained by cementing a composite resin onto the mandibular incisors to cause occlusal disharmony in mice. c Body weight was measured daily for all animals throughout the 2-week experimental period. ****P < 0.0001 (Control (n = 5) vs. BO (n = 5), ####P < 0.0001 (Control vs. BO + V (n = 5), ‡‡‡‡P < 0.0001 (BO vs. V (n = 5)), ※※※※P < 0.0001 (V vs. BO + V) by two-way repeated-measures ANOVA followed by the Bonferroni post hoc test. d, e No significant difference in heart (d) or lung (e) size in terms of weight per tibial length ratio (mg/mm) at 2 weeks after BO treatment (Control (n = 5), BO (n = 5), vidarabine (n = 5) and BO + vidarabine (n = 5) groups; P = NS, not significantly different, vs. Control by one-way ANOVA) followed by the Tukey–Kramer post hoc test. Data are presented as mean ± SD

Full size image

Materials and methods

Mice and experimental protocols

All experiments were performed on male 12-week-old C57BL/6 mice obtained from CLEA Japan (Tokyo, Japan). Mice were group-housed at 23 °C under a 12–12 light/dark cycle with lights on at 8:00 AM in accordance with the standard conditions for mouse studies by our group [15, 16, 22, 23]. Both food and water were available ad libitum.

Occlusal disharmony in mice was induced by introducing a 0.7-mm BO, employing our standard method of cementing a suitable appliance onto the mandibular incisor under intraperitoneal anesthesia with medetomidine (0.03 mg/ml), midazolam (0.4 mg/ml), and butorphanol (0.5 mg/ml) [15, 16, 24]. Mice were divided into four groups: a normal control group (Control), a BO-only treatment group (BO), a vidarabine-only treatment group (V), and a BO plus vidarabine treatment group (BO + V) (Fig. 1a, b). Chronic infusion of vidarabine dissolved in DMSO (#359-13471; Sigma, St. Louis MO, USA) was performed for 14 days at a dose of 15 mg/kg/day delivered with osmotic mini-pumps (Model 2002; ALZET, Cupertino, CA, USA) [20, 25]. The dose of vidarabine (15 mg/kg/day) was selected based upon that used in previous studies: this dose did not eliminate the inotropic effects of acute isoproterenol, did not depress cardiac function at baseline, and retained high selectivity for AC5 [20]. Because the BO mice cannot easily eat the standard pellet food (CE-2: 334.9 kcal/100 g; CLEA Japan), but can take paste food, the standard pellet food was changed to paste food 3 days before the BO treatment in all groups, as in previous studies [24, 26]. Body weight (BW) (n = 5 each) (Fig. 1c), food intake (Control: n = 4, BO: n = 6, V: n = 4, BO + V: n = 6) (Additional file 1: Fig. S2a) and water intake (Control: n = 4, BO: n = 5, V: n = 5, BO + V: n = 6) (Additional file 1: Fig. S2b) were monitored throughout the 2-week experimental period.

Physiological experiments

Mice (Control: n = 6, BO: n = 6, V: n = 7, BO + V: n = 6) were anesthetized via a mask with isoflurane vapor (1.0–1.5% v/v) titrated to maintain the lightest anesthesia possible, and echocardiographic measurements were performed by means of ultrasonography (TUS-A300, Toshiba, Tokyo, Japan) at 14 days after BO treatment [27].

Evaluation of fibrosis

Among several quantitative methods available to determine interstitial fibrotic regions [23, 28, 29], we employed Masson-trichrome staining using the Accustatin Trichrome Stain Kit (#HT15-1KT; Sigma-Aldrich, St. Louis, MO, USA) in accordance with the manufacturer’s protocol, as described previously [15, 16, 22, 23]. Cross sections (10 μm) were cut with a cryostat (CM1900; Leica Microsystems, Nussloch, Germony). The sections were air-dried and fixed with 4% paraformaldehyde (v/v) in 0.1 M phosphate-buffered saline (pH 7.5) (Control: n = 4, BO: n = 5, V: n = 4, BO + V: n = 4) [15, 16, 22, 23]. We quantified interstitial fibrotic regions using freely available image analysis software (Image J 1.48; https://imagej.nih.gov/ij/download.html) to evaluate the percentage of blue area in the Masson-trichrome sections [15, 16, 22, 23].

Evaluation of apoptosis

Apoptosis was determined by terminal deoxyribonucleotidyl transferase (TdT)-mediated biotin-16-deoxyuridine (TUNEL) staining using an Apoptosis in situ Detection Kit (#293-71501; Wako, Osaka, Japan). TUNEL-positive nuclei per field of view were manually counted in six sections of each of the four groups (Control: n = 4, BO: n = 5, V: n = 5, BO + V: n = 4) over a microscopic field of 20 x, then averaged and expressed as the ratio of TUNEL-positive nuclei (%) [27, 30]. By limiting the counting of total nuclei and TUNEL-positive nuclei to areas containing true cross sections of myocytes, we could selectively count only those nuclei that were clearly located within myocytes.

Western blotting

Cardiac muscle excised from mice (Control: n = 10, BO: n = 8, V: n = 6, BO + V: n = 8) was homogenized in a Polytron (Kinematica AG, Lucerne, Switzerland) in ice-cold RIPA buffer (Thermo Fisher Scientific, Waltham, MA, USA: 25 mM Tris–HCl (pH 7.6), 150 mM NaCl, 1% NP-40, 1% sodium deoxycholate, 0.1% SDS) without addition of inhibitors [31], and the homogenate was centrifuged at 13,000 × g for 10 min at 4 °C. The supernatant was collected and the protein concentration was measured using a DC protein assay kit (Bio-Rad, Hercules, CA, USA). Equal amounts of protein (5 μg) were subjected to 12.5% SDS–polyacrylamide gel electrophoresis and blotted onto 0.2 mm PVDF membrane (Millipore, Billerica, MA, USA).

Western blotting was conducted with commercially available antibodies [10, 27, 30]. Primary antibodies against α-smooth muscle actin (α-SMA) (1:1000, #19245), calmodulin kinase II (CaMKII) (1:1000, #3362), phospho-CaMKII (1:1000, Thr-286, #3361), B cell lymphoma 2 (BCL-2) (1:1000, #3498), BCL-2 associated X (Bax) (1:1000, #2772), receptor-interacting protein 3 (RIP3) (1:1000, #95702), phospho-RIP3 (1:1000, Thr-231/Ser-232, #91702), p38 (1:1000, #8690), phospho-p38 (1:1000, Thr-180/Tyr-182, #4511), apoptosis signal-regulatory kinase 1 (ASK1) (1:1000, #8662) and phospho-ASK1 (1:1000, Thr-845, #3765) were purchased from Cell Signaling Technology (Boston, MA, USA), primary antibodies against glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (1:200, sc-25778) were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and primary antibodies against phospho-phospholamban (PLN) (1:5000, Thr-17, #A010-13; 1:5000, Ser-16, #A010-12) and PLN (1:5000, #A010-14) were purchased from Badrilla (Leeds, UK). Primary antibodies against nicotinamide adenine dinucleotide phosphate oxidase (NOX) 4 (1:1000, #ab133303), NOX2 (1:1000, #ab80508) and xanthine oxidase (XO) (1:1000, #ab109235) were purchased from Abcam (Cambridge, UK) and AC5 (1:1000, #SAB4500206) were purchased from Sigma. Horseradish peroxide-conjugated anti-rabbit (1:5000, #NA934) or anti-mouse IgG (1:5000, #NA931) purchased from GB Healthcare was used as the secondary antibody. The primary and secondary antibodies were diluted in Tris-buffered saline (pH 7.6) with 0.1% Tween 20 and 5% bovine serum albumin. The blots were visualized with enhanced chemiluminescence solution (ECL: Prime Western Blotting Detection Reagent, GE Healthcare, Piscataway, NJ, USA) and scanned with a densitometer (LAS-1000, Fuji Photo Film, Tokyo, Japan). Note that there are different numbers of samples in different western blotting figures (Figs. 2, 3, 4, 5, 6) because we excluded outliers (extremely low or high values compared to others in the same groups).

Fig. 2
figure 2

Effect of vidarabine on BO-induced fibrosis in the heart. a Representative images of Masson-trichrome-stained sections of cardiac muscle in the Control (CTRL) (upper left), BO (upper right), vidarabine (V) (lower left) and BO + V; lower right) groups. b The area of fibrosis was significantly increased in the BO group (n = 5), but this increase was blocked in the BO + V group (n = 4). **P < 0.01, ***P < 0.001 by one-way repeated-measures ANOVA followed by the Tukey–Kramer post hoc test. c Expression of α-SMA, a fibrosis-related gene, was significantly increased in the BO group (n = 4), but this increase was blocked in the BO + V group (n = 4). *P < 0.05, **P < 0.01 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Data are presented as mean ± SD. Full-size images of immunoblots are presented in Additional file 1: Fig. S3

Full size image
Fig. 3
figure 3

Effect of vidarabine on BO-induced cardiac myocyte apoptosis. a TUNEL-positive nuclei (black arrows) in representative TUNEL-stained sections were counted in cardiac muscle in the Control (CTRL; upper left), BO (upper right), Vidarabine (V; lower left) and BO + V (lower right) groups. b The number of TUNEL-positive nuclei was significantly increased in the BO group (n = 5), but this increase was blocked in the BO + V group (n = 4). *P < 0.05 by one-way ANOVA followed by the Tukey–Kramer post hoc test. c The Bax/BCL-2 ratio was significantly increased in the BO group (n = 4), but this increase was blocked in the BO + V group (n = 5). *P < 0.05 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Data are presented as mean ± SD. Full-size images of immunoblots are presented in Additional file 1: Fig. S4

Full size image
Fig. 4
figure 4

Effect of vidarabine on BO-induced oxidative stress in cardiac muscle. a Representative immunohistochemical images of oxidative DNA damage (8-OHdG) in cardiac muscle in the Control (CTRL; upper left), BO (upper right), vidarabine (V; lower left) and BO + V (lower right) groups. b 8-OHdG-positive nuclei were significantly increased in the BO group (n = 5), but this increase was blocked in the BO + V group (n = 4). *P < 0.05 by one-way ANOVA followed by the Tukey–Kramer post hoc test. c Representative SDS-PAGE of oxidized proteins in cardiac muscle homogenate prepared from Control (CTRL; lane 1), BO (lane 2), V (lane 3) and BO + V (lane 4) groups using the OxiSelectTM Protein Carbonyl Immunoblot Kit. Full-size images of immunoblots are presented in Additional file 1: Fig. S6. d Oxidized proteins were significantly increased in the BO group (n = 5), but this increase was blocked in the BO + V group (n = 4). *P < 0.05, **P < 0.01 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Data are presented as mean ± SD

Full size image
Fig. 5
figure 5

Effect of vidarabine on AC5, NOX4/2, XO, phospho-p38 and phospho-ASK1 in the heart of BO mice. a AC5 expression was similar in all four groups. NS, not significantly different, by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S7. b NOX4 expression was significantly increased in the BO group (n = 8), and this increase was significantly blocked in the BO + V group (n = 8). **P < 0.01, ***P < 0.001 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S8. c NOX2 expression was similar among the four groups (n = 5 each). NS, not significantly different, by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S9. d Expression of XO was significantly increased in the BO group (n = 5), and this increase was significantly blocked in the BO + V group (n = 7). **P < 0.01, ***P < 0.001, ***P < 0.001 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S10. e Expression of phospho-p38 was significantly increased in the BO group (n = 4) and this was significantly blocked in the BO + V group (n = 5). *P < 0.05 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S11. f Expression of phospho-ASK1 (Thr-845) was significantly increased in the BO group (n = 4) and this increase was significantly blocked in the BO + V group (n = 5). *P < 0.05 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S12. Data are presented as mean ± SD

Full size image
Fig. 6
figure 6

Effect of vidarabine on BO-induced RIP3, phospho-CaMKII and phospho-PLN in the heart of BO mice. a Expression of RIP3, a key mediator of necroptosis, was significantly increased in the BO group (n = 4), but this increase was significantly blocked in the BO + V group (n = 4). **P < 0.01, ***P < 0.001 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S13. b Expression of phospho-CaMKII (Thr-286) was significantly increased in the BO group (n = 5), but this increase was significantly blocked in the BO + V group (n = 4). *P < 0.05, **P < 0.01, ***P < 0.001 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S14. c Expression of phospho-PLN (Thr-17) was significantly increased in the BO group (n = 5), but this increase was blocked in the BO + V group (n = 4). *P < 0.05, **P < 0.01 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S15. d Expression of phospho-PLN (Ser-16) was significantly increased in the BO group (n = 5), but this increase was significantly blocked in the BO + V group (n = 5). *P < 0.05, **P < 0.01 by one-way ANOVA followed by the Tukey–Kramer post hoc test. Full-size images of immunoblots are presented in Additional file 1: Fig. S16. Data are presented as expressed as mean ± SD

Full size image

Immunostaining

Oxidative DNA damage in the myocardium was evaluated by immunostaining for 8-hydroxy-2’-deoxyguanosine (8-OHdG) using the Vector M.O.M Immunodetection system (Control: n = 4, BO: n = 5, V: n = 5, BO + V: n = 4) (#PK-2200, Vector Laboratories, Inc. Burlingame, CA, USA) under our standard conditions [15, 16]. Cross sections were cut at 10 μm with a cryostat at − 20 ºC, air-dried and fixed with 4% paraformaldehyde (v/v) in TBS-T for 5 min at room temperature. Antigen retrieval was achieved with 0.1% citrate plus 1% Triton X-100 for 30 min at room temperature, then the sections were washed with TBS-T, incubated with 0.3% horse serum in TBS-T for 1 h at room temperature, and blocked with M.O.M. blocking reagent (Vector Laboratories, Burlingame, CA, USA) overnight at 4 ºC. For the positive control, sections were incubated with 0.3% H2O2 in TBS-T before the anti-8-OHdG antibody treatment. The sections were incubated with anti-8-OHdG antibody (8.3 μg/ml in M.O.M. Dilute; clone N45.1 monoclonal antibody; Japan Institute for the Control of Aging, Shizuoka, Japan) overnight at 4ºC in a humidified chamber, then incubated with 0.3% H2O2 in 0.3% horse serum for 1 h at room temperature to inactivate endogenous peroxidase, rinsed with TBS-T, incubated with anti-mouse IgG in M.O.M. Diluent, and processed with an ABC kit (Vector Laboratories, Inc. Burlingame, CA, USA). The ratio of 8-OHdG nuclei with oxidative DNA damage (stained dark brown) per total cell number was evaluated.

Statistical analysis

Data are presented as means ± standard deviation (SD). Comparisons were performed using two-way repeated-measures ANOVA followed by the Bonferroni post hoc test (Fig. 1c, Additional file 1: Fig. S2a, b) or one-way ANOVA followed by Tukey’s post hoc test (Figs. 1d, e, 2b, c, 3b, c, 4b, d, 5a–f, 6a–d). Differences were considered significant when P < 0.05.

Results

Effects of BO on body weight with/without vidarabine co-treatment

The BW in the control and vidarabine groups showed no significant change during the experimental period (Fig. 1c). However, BW gradually decreased in the BO and BO plus vidarabine treatment groups (BO + vidarabine), reaching a minimum at 4–6 days after the BO treatment, in accordance with previous findings by our group [15] and others [24, 32]. After that, the BW of the BO and BO + vidarabine groups gradually increased, but did not reach the preoperative level during the experimental period (Fig. 1c).

Effects of BO on the consumption of food and drinking water

We monitored the daily consumption of pellet food and water per mouse, measured as an average of the animals in each cage, during the 2-week experimental period. Consumption levels of food (Additional file 1: Fig. S2a) and water (Additional file 1: Fig. S2b) in the Control and vidarabine groups were similar and did not show significant changes during the period. The BO and BO + vidarabine groups might have some difficulty eating and the consumption of food and water was minimum at 1 day after the BO treatment. However, consumption recovered to preoperative levels within 6 days and no significant difference was observed among the four groups at 2 weeks. Changes in the consumption of water showed a similar tendency to those of food (Additional file 1: Fig. S2b).

Effects of BO on heart size and lung weight with/without vidarabine co-treatment

We examined the effect of BO with/without vidarabine on heart size in terms of cardiac muscle mass per tibial length ratio (Fig. 1d) and the effect on wet lung weight in terms of wet lung weight per tibial length ratio (Fig. 1e). Similar results were obtained among the four groups (n = 5 each).

These data suggest that BO did not induce cardiac hypertrophy or lung edema during the experimental period.

Vidarabine inhibits BO-induced cardiac fibrosis

We examined cardiac fibrosis in BO mice with/without vidarabine by means of Masson-trichrome staining (Fig. 2a, b). BO treatment significantly increased the area of fibrosis in cardiac muscle (Control (n = 4) vs. BO (n = 5); 0.9 ± 0.4% vs. 2.5 ± 0.8%, P < 0.01 vs. Control) in accordance with our previous finding [15]. Vidarabine alone did not alter the area of fibrosis, but it blocked the BO-induced increase of fibrosis (BO (n = 5) vs. BO + vidarabine (n = 4); 2.5 ± 0.8% vs. 1.1 ± 0.5%, P < 0.001 vs. BO).

We also evaluated cardiac fibrosis by measuring the level of α-SMA expression at 2 weeks after the start of BO, because this parameter is closely associated with cardiac fibrosis [33]. Expression of α-SMA was significantly increased in cardiac muscle of BO mice (Control (n = 5) vs. BO (n = 4); 1.0 ± 0.4 vs. 2.5 ± 0.9 arbitrary unit (A.U.), P < 0.05 vs. Control), and the increase was significantly suppressed by vidarabine (BO (n = 4) vs. BO + vidarabine (n = 4); 2.5 ± 0.9 vs. 0.7 ± 0.5 A.U., P < 0.01 vs. BO) (Fig. 2c).

These data, together with our previous findings [20], suggest that cardiac fibrosis induced by BO might be mediated at least in part through the activation of AC5.

Vidarabine inhibits BO-induced cardiac myocyte apoptosis

We also examined cardiac myocyte apoptosis in BO mice with/without vidarabine by means of TUNEL staining (Fig. 3a, b). BO treatment significantly increased cardiac myocyte apoptosis (Control (n = 4) vs. BO (n = 5); 1.6 ± 1.3% vs. 4.2 ± 1.7%, P < 0.05 vs. Control) in accordance with our previous findings [15]. Vidarabine alone (n = 5) had no effects on the number of TUNEL-positive cardiac myocytes, but it blocked the BO-induced increase of TUNEL-positive cardiac myocytes (BO (n = 5) vs. BO + vidarabine (n = 4); 4.2 ± 1.7% vs. 1.3 ± 0.7%, P < 0.05 vs. Control).

We also evaluated cardiac myocyte apoptosis by examining the ratio of Bax protein, an accelerator of apoptosis, and BCL-2 protein, a regulator of apoptosis, in the heart (Fig. 3c).

BO treatment significantly increased the ratio of Bax/BCL-2 in the heart (Control (n = 4) vs. BO (n = 4); 1.0 ± 0.6% vs. 5.9 ± 2.6 A.U., P < 0.05 vs. Control). Vidarabine alone (n = 5) had no effects on the ratio of Bax/BCL-2, but it blocked the BO-induced increase in the Bax/BCL-2 ratio (BO (n = 4) vs. BO + vidarabine (n = 5); 5.9 ± 2.6 vs. 1.3 ± 1.0 A.U., P < 0.05 vs. Control) (Fig. 3c).

These and earlier results [11] support the idea that the increase of TUNEL-positive cardiac myocytes induced by BO treatment might be mediated at least in part through the activation of AC5.

Vidarabine inhibits BO-induced cardiac dysfunction

We performed echocardiography to evaluate cardiac function in terms of left ventricular cardiac function (EF) and fractional shortening (%FS) (Table 1). Both parameters were significantly decreased in the BO group compared to the control mice (EF: Control (n = 6) vs. BO (n = 6); 68 ± 1.1% vs. 61 ± 3.0%, P < 0.001 vs. Control; %FS: Control (n = 6) vs. BO (n = 6); 33 ± 0.8% vs. 28 ± 1.9%, P < 0.001 vs. Control). Vidarabine alone (n = 7) had no effect on EF or %FS, but blocked the BO-induced decrease of EF and %FS (EF: BO (n = 6) vs. BO + vidarabine (n = 6); 61 ± 3.0% vs. 66 ± 1.4%, P < 0.01 vs. Control; %FS: BO (n = 6) vs. BO + vidarabine (n = 6); 28 ± 1.9% vs. 31 ± 1.0%, P < 0.01 vs. Control).

Table 1 Cardiac function assessed by echocardiography at 2 weeks after BO
Full size table

These data suggest that BO treatment decreases cardiac function at least in part through the activation of AC5.

Vidarabine inhibits BO-induced oxidative stress

We evaluated oxidative stress in the myocardium by means of 8-OHdG immunostaining (Fig. 4a, b) and western blotting of oxidized proteins (Fig. 4c, d).

We first prepared positive and negative control sections by incubating cells with (positive control)/without (negative control) 0.3% H2O2 in TBS-T for 1 h at room temperature before the anti-8-OHdG antibody treatment and confirmed that the 8-OHdG staining procedure could clearly discriminate 8-OHdG-positive and non-positive nuclei (Additional file 1: Fig. S5).

The ratio of 8-OHdG-positive/total cells was significantly increased in the BO group (Control (n = 4) vs. BO (n = 5); 1.1 ± 0.6% vs. 3.0 ± 1.4%, P < 0.05 vs. Control), and the increase was suppressed by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 4); 3.0 ± 1.4% vs. 1.1 ± 0.4%, P < 0.05 vs. Control).

The amount of oxidized proteins, measured using the OxiSelectTM protein kit, was also significantly increased (Control (n = 4) vs. BO (n = 5); 1.0 ± 0.1 vs. 2.7 ± 1.0 A.U., P < 0.01 vs. Control), and again the increase was suppressed by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 4); 2.7 ± 1.0 vs. 1.1 ± 0.4 A.U., P < 0.05 vs. Control).

These results, together with the data shown in Figs. 2, 3 and Table 1, indicate that BO treatment increases oxidative stress-induced myocardial damage at least in part through the activation of AC5, which might contribute to the cardiac remodeling and dysfunction in BO mice.

Effects of BO on AC5 expression

We first examined the effects of BO treatment on AC5 expression with/without vidarabine, since AC5 was previously found to be increased by chronic catecholamine stress [12]. However, BO treatment did not alter AC5 expression and similar results were obtained in all four groups (Fig. 5a).

Vidarabine inhibits BO-mediated NOX4 and XO expression

Reactive oxygen species (ROS) are produced through a number of pathways, including NOX and XO, and may be involved in various physiological and pathological processes in the heart, including fibrosis, apoptosis and heart failure [34,35,36,37].

Two NOX isoforms, NOX2 and NOX4, are expressed in the heart, and their activity is regulated by their expression level [35, 38]. We therefore examined NOX4 and NOX2 protein expression in the heart among the four groups. NOX4 expression was significantly increased in the BO group (Control (n = 10) vs. BO (n = 8); 1.0 ± 0.2 vs. 1.6 ± 0.4 A.U., P < 0.001 vs. Control). This increase was significantly inhibited by vidarabine (BO (n = 8) vs. BO + vidarabine (n = 8); 1.6 ± 0.4 vs. 1.1 ± 0.2 A.U., P < 0.01 vs. BO) (Fig. 5b). We also examined NOX2 protein expression and found that it was similar among the four groups (n = 5 each) (Fig. 5c).

We next examined XO expression in the heart in the four groups. XO expression was significantly increased in the BO group (Control (n = 8) vs. BO (n = 5); 1.0 ± 0.2 vs. 2.1 ± 0.7 A.U., P < 0.001 vs. Control). This increase was significantly inhibited by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 7); 2.1 ± 0.7 vs. 1.1 ± 0.4 A.U., P < 0.01 vs. BO) (Fig. 5d).

These data suggest that activation of AC5 might contribute, at least in part, to the upregulation of NOX4 and XO.

Vidarabine inhibits BO-mediated activation of p38 MAPK

Overproduction of ROS derived from NOX4 and XO triggers oxidative stress and subsequently activates the p38 mitogen-activated protein kinase (MAPK) signaling pathway, leading to cardiac dysfunction [38,39,40]. We therefore examined the phosphorylation levels of p38 MAPK and found that p38 MAPK phosphorylation was significantly increased in the BO group (Control (n = 4) vs. BO (n = 5); 1.0 ± 0.3 vs. 2.8 ± 1.7 A.U., P < 0.05 vs. Control). This increase was significantly inhibited by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 5); 2.8 ± 1.7 vs. 1.1 ± 0.4 A.U., P < 0.05 vs. Control) (Fig. 5e).

These data suggest that overproduction of ROS derived from BO-induced upregulation of NOX4 and XO activates the p38 MAPK signaling pathway, which might lead to cardiac remodeling and dysfunction.

Vidarabine inhibits BO-mediated activation of ASK1

ROS production was recently demonstrated to increase activation of ASK1, which signals selectively to p38 MAPK and orchestrates cardiac remodeling in response to pressure overload, chronic catecholamine stress and hypertensive heart disease [41,42,43]. We thus examined phosphorylation of ASK1 (Thr-845) and found that it was significantly increased in the BO group (Control (n = 4) vs. BO (n = 4); 1.0 ± 0.3 vs. 2.6 ± 1.4, P < 0.05 vs. Control). This increase was significantly inhibited by vidarabine (BO (n = 4) vs. BO + vidarabine (n = 5); 2.6 ± 1.4 vs. 0.5 ± 0.2, P < 0.01 vs. BO) (Fig. 5f).

These data suggest that ROS production derived from BO-induced NOX4 upregulation activates ASK1, leading to p38 MAPK and cardiac remodeling and dysfunction.

Vidarabine inhibits BO-induced necroptosis

Overproduction of ROS derived from NOX4 was recently demonstrated to cause myocardial apoptosis and necroptosis, leading to heart failure via activation of RIP3 in cardiac myocytes [44]. We therefore examined the amount of phospho-RIP3 (Thr-231/Ser-232) and found that it was significantly increased in the heart of BO mice (Control (n = 5) vs. BO (n = 4); 1.0 ± 0.3 vs. 5.4 ± 2.3 A.U., P < 0.001 vs. Control) (Fig. 6a). Again, this increase was significantly attenuated by vidarabine (BO (n = 4) vs. BO + vidarabine (n = 4); 5.4 ± 2.3 vs. 1.7 ± 0.5 A.U., P < 0.01 vs. BO) (Fig. 6a).

These data suggest that activation of AC5 might contribute, at least in part, to the upregulation of NOX4 and XO.

Vidarabine inhibits BO-induced CaMKII phosphorylation

RIP3-mediated myocardial apoptosis and necroptosis were recently demonstrated to be dependent upon the activation of CaMKII [44]. We therefore examined the amount of phospho-CaMKII (Thr-286) in the heart of BO mice and found that it was significantly increased at 2 weeks after BO (Control (n = 4) vs. BO (n = 5); 1.0 ± 0.2 vs. 1.9 ± 0.2 A.U., P < 0.001 vs. Control). The increase was significantly attenuated by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 4); 1.9 ± 0.2 vs. 1.2 ± 0.3, P < 0.01 vs. BO) (Fig. 6b).

These data suggest that BO treatment might activate NOX4/RIP3/CaMKII signaling via activation of AC5.

Vidarabine inhibits BO-induced PLN phosphorylation

The elevation of diastolic sarcoplasmic reticulum Ca2+ leakage mediated by PLN phosphorylation contributes considerably to the pathogenesis of cardiac remodeling and dysfunction via ROS derived from NOX4 [45, 46]. We therefore examined the effect of BO on PLN phosphorylation at Thr-17 and Ser-16, which are phosphorylated by CaMKII and by protein kinase A (Fig. 6c, d).

Phospho-PLN (Thr-17) was significantly increased in cardiac muscle of BO mice (Control (n = 4) vs. BO (n = 5); 1.0 ± 0.2 vs. 2.6 ± 1.3 A.U., P < 0.05 vs. Control) (Fig. 6c). This increase was significantly attenuated by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 5); 2.6 ± 1.3% vs. 0.7 ± 0.2 A.U., P < 0.01 vs. BO) (Fig. 6c).

Phospho-PLN (Ser-16) was also significantly increased in cardiac muscle of BO mice (Control (n = 4) vs. BO (n = 5); 1.0 ± 0.5 vs. 2.2 ± 0.8 A.U., P < 0.05 vs. Control). Again, the increase was significantly attenuated by vidarabine (BO (n = 5) vs. BO + vidarabine (n = 5); 2.2 ± 0.8 vs. 0.8 ± 0.1 A.U., P < 0.01 vs. BO) (Fig. 6d).

These data, together with the previous results, suggest that BO might increase PLN phosphorylation, leading to ROS-mediated elevation of diastolic sarcoplasmic reticulum Ca2+ leakage in cardiac myocytes.

Discussion

Oral health is important for maintaining general health and is associated with physical activity, including the status of the cardiovascular system [47]. Extensive studies have shown that the link between oral health and cardiovascular disease (CVD) may be explained by chronic inflammation and repeated bacteremia from the oral cavity, as inflammation plays an important role in the pathogenesis of CVD [1]. However, periodontal status may not completely explain the oral health–CVD relationship, and other factors such as occlusal disharmony, might also contribute [48].

Occlusal disharmony due to BO treatment causes muscle dysfunction and susceptibility to muscle fatigue in masseter and suprahyoid muscles via accumulation of ROS in rats [49, 50]. In addition, occlusal-disharmony-induced ROS production in the oral cavity might cause not only local pathogenic disturbance, but also systemic diseases, including heart disease, in patients [51]. Importantly, we previously showed that cardiac fibrosis and myocyte apoptosis were significantly increased in cardiac muscle of BO mice, together with accumulation of ROS, leading to cardiac dysfunction and susceptibility to atrial fibrillation via activation of β-AR signaling [15, 16]. Here, we examined whether AC5, a major cardiac AC isoform, is a mediator of the β-AR signaling leading to occlusal-disharmony-induced cardiac dysfunction, because AC5 is known to be a major regulator of oxidative stress in the heart [52, 53].

AC transduces the signal generated by binding of a ligand, most commonly norepinephrine, to β-AR and Gsα, resulting in the conversion of ATP to cAMP [54]. There are nine major mammalian isoforms of AC, with AC6 being the major fetal cardiac AC isoform, and AC5, the major cardiac isoform in adults [9, 54, 55]. We showed that in AC5KO, the heart was protected against the stress of chronic pressure overload [30] and chronic catecholamine stimulation [12]. Interestingly, however, AC5 inhibition appears to have multiple effects. For example, AC5 gene knockout or pharmacological AC5 inhibition increases longevity in mice [14, 20].

Inhibition of AC activity by P-site inhibitors including vidarabine is poor when AC is not fully stimulated [19, 56]. We have previously demonstrated that inhibition of AC5 by acute and chronic treatment with vidarabine did not affect cardiac function at baseline, but improved the response to pathological stress such as chronic catecholamine stress and permanent coronary artery occlusion [19, 20]. In addition, inhibition of AC5 also protects against physical frailty, enhances exercise capacity, and protects against diabetes, obesity and diabetic cardiomyopathy [14, 20, 52].

Several epidemiological surveys have confirmed a positive relationship between oral health and physical frailty, including cardiovascular disease [1, 57]. Tooth loss could contribute to occlusal disharmony or impaired masticatory performance [58,59,60]. More recently, a relationship between occlusal disharmony and cardiovascular disease was demonstrated in a Japanese urban population [1, 61]. However, the mechanism remains poorly understood.

In this study, pharmacological AC5 inhibition with vidarabine was shown to protect the heart from occlusal-disharmony-induced oxidative stress in BO mice, a well-established model of occlusal disharmony [15, 16, 24, 62]. In particular, our findings indicate that AC5 inhibition in BO mice has a cardioprotective effect mediated at least in part by a decrease of NOX4 overexpression and CaMKII phosphorylation, leading to reduced phospholamban phosphorylation on serine-16 and threonine-17 (Fig. 7).

Fig. 7
figure 7

This scheme illustrates the proposed role of β-AR/Gsα/AC5 signaling in the heart of BO mice. β-AR/Gsα/AC5 signaling is activated by the BO treatment, leading to oxidative stress via activation of NOX4/ASK1/p38 and phosphorylation of CaMKII (Thr-286), which mediates PLN phosphorylation at Thr-17. In addition, cAMP derived from AC5 mediates oxidative stress and PLN phosphorylation at Ser-16. These changes might cause fibrosis, myocyte apoptosis and oxidative stress in the heart of BO mice, leading to cardiac dysfunction

Full size image

NOX2 and NOX4 are the major isoforms of the NOX family enzymes in the heart, and both isoforms play an important role in mediating oxidative stress at baseline and under stress [35]. NOX2 is predominantly localized at the plasma membrane and NOX4 is predominantly localized in mitochondria [63, 64]. Therefore, upregulation of NOX4, but not NOX2, increases mitochondrial dysfunction, leading to apoptosis of cardiac myocytes and heart failure in response to pressure overload and chronic catecholamine stimulation [63, 65]. In addition, we demonstrated previously that disruption of the AC5 gene plays a protective role against the development of heart failure in response to pressure overload and chronic catecholamine stress, potentially through limiting the incidence of myocardial apoptosis [12, 30]. These data suggest that occlusal-disharmony-induced CVD might occur, at least in part, through the upregulation of NOX4 induced by activation of AC5 (Fig. 7).

We previously identified vidarabine as a candidate AC5 inhibitor by computer-based drug screening, and its inhibitory activity was confirmed in an in vitro cAMP accumulation assay in cardiac myocytes and also in AC assay using a crude membrane preparation [11, 19, 20]. The major finding of the current investigation is that inhibition of AC5 by vidarabine ameliorates the development of occlusal-disharmony-induced cardiac dysfunction by reducing the oxidative stress generated via the RIP3/NOX4 signaling pathway in a cAMP-dependent mechanism (Fig. 7). We have previously reported that vidarabine inhibits the development of catecholamine-induced heart failure and atrial fibrillation in mice without suppressing cardiac function [20, 66].

In previous studies, we demonstrated that vidarabine inhibits AC5 more potently than AC2 or AC3, which are more abundant in the lungs and pancreas, respectively [11]. Since β-AR is expressed in the pulmonary bronchus and pancreas, β-AR blockers cause bronchial smooth muscle contraction and inhibition of insulin release, leading to bronchospasm and glucose intolerance [67, 68]. Our current findings suggest that the use of vidarabine to suppress only the activity of AC5, and not the entire β-AR signaling pathway, may be preferable to β-AR blockade therapy for the treatment of CVD associated with occlusal-disharmony.

Conclusion

Our current and previous findings suggest that vidarabine might broadly inhibit stress-induced cardiomyopathy, leading to improved longevity and reduced physical frailty. Since vidarabine is a clinically approved drug, an early clinically trial should be feasible.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

AC5:

Type 5 adenylyl cyclase

BO:

Bite-opening

AC:

Adenylyl cyclase

AC5KO:

Mouse model with knock-out of AC5

BO:

Bite-opening

β-AR:

β-Adrenergic receptor

BW:

Body weight

TUNEL:

Terminal deoxyribonucleotidyl transferase (TdT)-mediated biotin-16-deoxyuridine

α-SMA:

α-Smooth muscle actin

CaMKII:

Calmodulin kinase II

BCL-2:

B cell lymphoma 2

Bax:

BCL-2 associated X

RIP3:

Receptor-interacting protein 3

ASK1:

Apoptosis signal-regulatory kinase 1

GAPDH:

Glyceraldehyde-3-phosphate dehydrogenase

PLN:

Phospholamban

NOX:

Nicotinamide adenine dinucleotide phosphate oxidase

XO:

Xanthine oxidase

8-OHdG:

8-Hydroxy-2’-deoxyguanosine

A.U.:

Arbitrary unit

EF:

Left ventricular cardiac function

%FS:

%Fractional shortening

ROS:

Reactive oxygen species

MAPK:

Mitogen-activated protein kinase

CVD:

Cardiovascular disease

References

  1. Ogawa M, Satomi-Kobayashi S, Yoshida N, Tsuboi Y, Komaki K, Nanba N, Izawa KP, Sakai Y, Akashi M, Hirata K (2021) Relationship between oral health and physical frailty in patients with cardiovascular disease. J Cardiol 77:131–138. https://doi.org/10.1016/j.jjcc.2020.07.016

    Article  PubMed  Google Scholar 

  2. An JY, Darveau R, Kaeberlein M (2018) Oral health in geroscience: animal models and the aging oral cavity. Geroscience 40:1–10. https://doi.org/10.1007/s11357-017-0004-9

    Article  PubMed  Google Scholar 

  3. Balasubramanian P, Hall D, Subramanian M (2019) Sympathetic nervous system as a target for aging and obesity-related cardiovascular diseases. Geroscience 41:13–24. https://doi.org/10.1007/s11357-018-0048-5

    Article  CAS  PubMed  Google Scholar 

  4. Segovia M, Ganzinelli S, Reina S, Borda E, Sterin-Borda L (2012) Role of anti-β1 adrenergic antibodies from patients with periodontitis in cardiac dysfunction. J Oral Pathol Med 41:242–248. https://doi.org/10.1111/j.1600-0714.2011.01090.x

    Article  CAS  PubMed  Google Scholar 

  5. Collin HL, Niskanen L, Uusitupa M, Töyry J, Collin P, Koivisto AM, Viinamäki H, Meurman JH (2000) Oral symptoms and signs in elderly patients with type 2 diabetes mellitus. A focus on diabetic neuropathy. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 90:299–305. https://doi.org/10.1067/moe.2000.107536

    Article  CAS  PubMed  Google Scholar 

  6. Shimizu Y, Hosomichi J, Kaneko S, Shibutani N, Ono T (2011) Effect of sympathetic nervous activity on alveolar bone loss induced by occlusal hypofunction in rats. Arch Oral Biol 56:1404–1411. https://doi.org/10.1016/j.archoralbio.2011.05.004

    Article  PubMed  Google Scholar 

  7. Ishikawa Y, Katsushika S, Chen L, Halnon NJ, Kawabe J, Homcy CJ (1992) Isolation and characterization of a novel cardiac adenylylcyclase cDNA. J Biol Chem 267:13553–13557

    Article  CAS  Google Scholar 

  8. Katsushika S, Chen L, Kawabe J, Nilakantan R, Halnon NJ, Homcy CJ, Ishikawa Y (1992) Cloning and characterization of a sixth adenylyl cyclase isoform: types V and VI constitute a subgroup within the mammalian adenylyl cyclase family. Proc Natl Acad Sci U S A 89:8774–8778. https://doi.org/10.1073/pnas.89.18.8774

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Tobise K, Ishikawa Y, Holmer SR, Im MJ, Newell JB, Yoshie H, Fujita M, Sussannnie EE, Homcy CJ (1994) Changes in type VI adenylyl cyclase isoform expression correlate with a decreased capacity for cAMP generation in the aging ventricle. Circ Res 74:596–603. https://doi.org/10.1161/01.res.74.4.596

    Article  CAS  PubMed  Google Scholar 

  10. Okumura S, Kawabe J, Yatani A, Takagi G, Lee MC, Hong C, Liu J, Takagi I, Sadoshima J, Vatner DE, Ishikawa Y (2003) Type 5 adenylyl cyclase disruption alters not only sympathetic but also parasympathetic and calcium-mediated cardiac regulation. Circ Res 93:364–371. https://doi.org/10.1161/01.res.0000086986.35568.63

    Article  CAS  PubMed  Google Scholar 

  11. Iwatsubo K, Minamisawa S, Tsunematsu T, Nakagome M, Toya Y, Tomlinson JE, Umemura S, Scarborough RM, Levy DE, Ishikawa Y (2004) Direct inhibition of type 5 adenylyl cyclase prevents myocardial apoptosis without functional deterioration. J Biol Chem 279:40938–40945. https://doi.org/10.1074/jbc.M314238200

    Article  CAS  PubMed  Google Scholar 

  12. Okumura S, Vatner DE, Kurotani R, Bai Y, Gao S, Yuan Z, Iwatsubo K, Ulucan C, Kawabe J, Ghosh K, Vatner SF, Ishikawa Y (2007) Disruption of type 5 adenylyl cyclase enhances desensitization of cyclic adenosine monophosphate signal and increases Akt signal with chronic catecholamine stress. Circulation 116:1776–1783. https://doi.org/10.1161/circulationaha.107.698662

    Article  CAS  PubMed  Google Scholar 

  13. Iwatsubo K, Suzuki S, Li C, Tsunematsu T, Nakamura F, Okumura S, Sato M, Minamisawa S, Toya Y, Umemura S, Ishikawa Y (2007) Dopamine induces apoptosis in young, but not in neonatal, neurons via Ca2+-dependent signal. Am J Physiol Cell Physiol 293:C1498–C1508. https://doi.org/10.1152/ajpcell.00088.2007

    Article  CAS  PubMed  Google Scholar 

  14. Yan L, Vatner DE, O’Connor JP, Ivessa A, Ge H, Chen W, Hirotani S, Ishikawa Y, Sadoshima J, Vatner SF (2007) Type 5 adenylyl cyclase disruption increases longevity and protects against stress. Cell 130:247–258. https://doi.org/10.1016/j.cell.2007.05.038

    Article  CAS  PubMed  Google Scholar 

  15. Yagisawa Y, Suita K, Ohnuki Y, Ishikawa M, Mototani Y, Ito A, Matsuo I, Hayakawa Y, Nariyama M, Umeki D, Saeki Y, Amitani Y, Nakamura Y, Tomonari H, Okumura S (2020) Effects of occlusal disharmony on cardiac fibrosis, myocyte apoptosis and myocyte oxidative DNA damage in mice. PLoS ONE 15:e0236547. https://doi.org/10.1371/journal.pone.0236547

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Suita K, Yagisawa Y, Ohnuki Y, Umeki D, Nariyama M, Ito A, Hayakawa Y, Matsuo I, Mototani Y, Saeki Y, Okumura S (2020) Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice. Sci Rep 10:13765. https://doi.org/10.1038/s41598-020-70791-8

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Vatner DE, Asai K, Iwase M, Ishikawa Y, Shannon RP, Homcy CJ et al (1999) Beta-adrenergic receptor-G protein-adenylyl cyclase signal transduction in the failing heart. Am J Cardiol 83(12a):80h-h85. https://doi.org/10.1016/s0002-9149(99)00266-0

    Article  CAS  PubMed  Google Scholar 

  18. Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JGF, Coats AJS et al (2016) 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J 37(27):2129–2200. https://doi.org/10.1093/eurheartj/ehw128

    Article  Google Scholar 

  19. Suita K, Fujita T, Cai W, Hidaka Y, Jin H, Prajapati R et al (2018) Vidarabine, an anti-herpesvirus agent, prevents catecholamine-induced arrhythmias without adverse effect on heart function in mice. Pflugers Arch 470(6):923–935. https://doi.org/10.1007/s00424-018-2121-4

    Article  CAS  PubMed  Google Scholar 

  20. Iwatsubo K, Bravo C, Uechi M, Baljinnyam E, Nakamura T, Umemura M, Lai L, Gao S, Yan L, Zhao X, Park M, Qiu H, Okumura S, Iwatsubo M, Vatner DE, Vatner SF, Ishikawa Y (2012) Prevention of heart failure in mice by an antiviral agent that inhibits type 5 cardiac adenylyl cyclase. Am J Physiol Heart Circ Physiol 302:H2622–H2628. https://doi.org/10.1152/ajpheart.00190.2012

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Wada T, Nakamura Y, Cao X, Ohara H, Izumi-Nakaseko H, Ando K, Nakazato Y, Sugiyama A (2016) Antiviral drug vidarabine possessing cardiac type 5 adenylyl cyclase inhibitory property did not affect cardiohemodynamic or electrophysiological variables in the halothane-anesthetized dogs. J Toxicol Sci 41:115–122. https://doi.org/10.2131/jts.41.115

    Article  CAS  PubMed  Google Scholar 

  22. Kawamura N, Ohnuki Y, Matsuo I, Suita K, Ishikawa M, Mototani Y, Shiozawa K, Ito A, Yagisawa Y, Hayakawa Y, Nariyama Y, Umeki D, Ujiie Y, Gomi K, Okumura S (2019) Effects of chronic Porphyromonas gingivalis lipopolysaccharide infusion on skeletal muscles in mice. J Physiol Sci 69:503–511. https://doi.org/10.1007/s12576-019-00670-z

    Article  CAS  PubMed  Google Scholar 

  23. Ito A, Ohnuki Y, Suita K, Ishikawa M, Mototani Y, Shiozawa K, Kawamura N, Yagisawa Y, Nariyama M, Umeki D, Nakamura Y, Okumura S (2019) Role of β-adrenergic signaling in masseter muscle. PLoS ONE 14:e0215539. https://doi.org/10.1371/journal.pone.0215539

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Shimizu Y, Khan M, Kato G, Aoki K, Ono T (2018) Occlusal disharmony-induced stress causes osteopenia of the lumbar vertebrae and long bones in mice. Sci Rep 8:173. https://doi.org/10.1038/s41598-017-18037-y

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Bai Y, Tsunematsu T, Jiao Q, Ohnuki Y, Mototani Y, Shiozawa K, Jin M, Cai W, Jin HL, Fujita T, Ichikawa Y, Suita K, Kurotani R, Yokoyama U, Sato M, Iwatsubo K, Ishikawa Y, Okumura S (2012) Pharmacological stimulation of type 5 adenylyl cyclase stabilizes heart rate under both microgravity and hypergravity induced by parabolic flight. J Pharmacol Sci 119:381–389. https://doi.org/10.1254/jphs.12102fp

    Article  CAS  PubMed  Google Scholar 

  26. Umeki D, Ohnuki Y, Mototani Y, Shiozawa K, Suita K, Fujita T, Nakamura Y, Saeki Y, Okumura S (2015) Protective effects of clenbuterol against dexamethasone-induced masseter muscle atrophy and myosin heavy chain transition. PLoS ONE 10:e0128263. https://doi.org/10.1371/journal.pone.0128263

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Okumura S, Fujita T, Cai W, Jin M, Namekata I, Mototani Y, Jin H, Ohnuki Y, Tsuneoka Y, Kurotani R, Suita K, Kawakami Y, Hamaguchi S, Abe T, Kiyonari H, Tsunematsu T, Bai Y, Suzuki S, Hidaka Y, Umemura M, Ichikawa Y, Yokoyama U, Sato M, Ishikawa F, Izumi-Nakaseko H, Adachi-Akahane S, Tanaka H, Ishikawa Y (2014) Epac1-dependent phospholamban phosphorylation mediates the cardiac response to stresses. J Clin Invest 124:2785–2801. https://doi.org/10.1172/jci64784

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Yan J, Thomson JK, Wu X, Zhao W, Pollard AE, Ai X (2014) Novel methods of automated quantification of gap junction distribution and interstitial collagen quantity from animal and human atrial tissue sections. PLoS ONE 9:e104357. https://doi.org/10.1371/journal.pone.0104357

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Stromp TA, Spear TJ, Holtkamp RM, Andres KN, Kaine JC, Alghuraibawi WH, Leung SW, Fornwalt BK, Vandsburger MH (2018) Quantitative gadolinium-free cardiac fibrosis imaging in end stage renal disease patients reveals a longitudinal correlation with structural and functional decline. Sci Rep 8:16972. https://doi.org/10.1038/s41598-018-35394-4

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Okumura S, Takagi G, Kawabe J, Yang G, Lee MC, Hong C, Liu J, Vatner DE, Sadoshima J, Vatner SF, Ishikawa Y (2003) Disruption of type 5 adenylyl cyclase gene preserves cardiac function against pressure overload. Proc Natl Acad Sci U S A 100:9986–9990. https://doi.org/10.1073/pnas.1733772100

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Yu H, He Y, Zhang X, Peng Z, Yang Y, Zhu R, Bai J, Tian Y, Li X, Chen W, Fang D, Wang R (2011) The rat IgGFcγBP and Muc2 C-terminal domains and TFF3 in two intestinal mucus layers bind together by covalent interaction. PLoS ONE 6:e20334. https://doi.org/10.1371/journal.pone.0020334

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Mori D, Katayama T, Miyake H, Fujiwara S, Kubo KY (2013) Occlusal disharmony leads to learning deficits associated with decreased cellular proliferation in the hippocampal dentate gyrus of SAMP8 mice. Neurosci Lett 534:228–232. https://doi.org/10.1016/j.neulet.2012.12.004

    Article  CAS  PubMed  Google Scholar 

  33. Villalobos E, Criollo A, Schiattarella GG, Altamirano F, French KM, May HI, Jiang N, Nguyen NUN, Romero D, Roa JC, Garcia L, Diaz-Araya G, Morselli E, Ferdous A, Conway SJ, Sadek HA, Gillette TG, Lavandero S, Hill JA (2019) Fibroblast primary cilia are required for cardiac fibrosis. Circulation 139:2342–2357. https://doi.org/10.1161/circulationaha.117.028752

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Wilkinson-Berka JL, Rana I, Armani R, Agrotis A (2013) Reactive oxygen species, Nox and angiotensin II in angiogenesis: implications for retinopathy. Clin Sci (Lond) 124:597–615. https://doi.org/10.1042/cs20120212

    Article  CAS  Google Scholar 

  35. Kuroda J, Sadoshima J (2010) NADPH oxidase and cardiac failure. J Cardiovasc Transl Res 3:314–320. https://doi.org/10.1007/s12265-010-9184-8

    Article  PubMed  PubMed Central  Google Scholar 

  36. Yang Y, Zhao J, Qiu J, Li J, Liang X, Zhang Z, Zhang X, Fu H, Korantzopoulos P, Letas KP, Tse G, Li G, Liu T (2018) Xanthine oxidase inhibitor allopurinol prevents oxidative stress-mediated atrial remodeling in alloxan-induced diabetes mellitus rabbits. J Am Heart Assoc 7:e008807. https://doi.org/10.1161/jaha.118.008807

    Article  PubMed  PubMed Central  Google Scholar 

  37. Boueiz A, Damarla M, Hassoun PM (2008) Xanthine oxidoreductase in respiratory and cardiovascular disorders. Am J Physiol Lung Cell Mol Physiol 294:L830–L840. https://doi.org/10.1152/ajplung.00007.2008

    Article  CAS  PubMed  Google Scholar 

  38. Zhao H, Zhang M, Zhou F, Cao W, Bi L, Xie Y, Yang Q, Wang S (2016) Cinnamaldehyde ameliorates LPS-induced cardiac dysfunction via TLR4-NOX4 pathway: the regulation of autophagy and ROS production. J Mol Cell Cardiol 101:11–24. https://doi.org/10.1016/j.yjmcc.2016.10.017

    Article  CAS  PubMed  Google Scholar 

  39. Bode JG, Ehlting C, Häussinger D (2012) The macrophage response towards LPS and its control through the p38(MAPK)-STAT3 axis. Cell Signal 24:1185–1194. https://doi.org/10.1016/j.cellsig.2012.01.018

    Article  CAS  PubMed  Google Scholar 

  40. Matesanz N, Lafuente N, Azcutia V, Martín D, Cuadrado A, Nevado J, Rodriguez-Manas L, Sanchez-Ferrer CF, Peiro C (2007) Xanthine oxidase-derived extracellular superoxide anions stimulate activator protein 1 activity and hypertrophy in human vascular smooth muscle via c-Jun N-terminal kinase and p38 mitogen-activated protein kinases. J Hypertens 25:609–618. https://doi.org/10.1097/HJH.0b013e328013e7c4

    Article  CAS  PubMed  Google Scholar 

  41. Tsujimoto I, Hikoso S, Yamaguchi O, Kashiwase K, Nakai A, Takeda T et al (2005) The antioxidant edaravone attenuates pressure overload-induced left ventricular hypertrophy. Hypertension 45(5):921–926. https://doi.org/10.1161/01.HYP.0000163461.71943.e9

    Article  CAS  PubMed  Google Scholar 

  42. Meijles DN, Cull JJ, Markou T, Cooper STE, Haines ZHR, Fuller SJ et al (2020) Redox regulation of cardiac ASK1 (apoptosis signal-regulating kinase 1) controls p38-MAPK (mitogen-activated protein kinase) and orchestrates cardiac remodeling to hypertension. Hypertension 76(4):1208–18. https://doi.org/10.1161/hypertensionaha.119.14556

    Article  CAS  PubMed  Google Scholar 

  43. Zhang GX, Kimura S, Nishiyama A, Shokoji T, Rahman M, Yao L et al (2004) Cardiac oxidative stress in acute and chronic isoproterenol-infused rats. Cardiovasc Res 65(1):230–238. https://doi.org/10.1016/j.cardiores.2004.08.013

    Article  CAS  Google Scholar 

  44. Zhang T, Zhang Y, Cui M, Jin L, Wang Y, Lv F, Liu Y, Zheng W, Shang H, Zhang J, Zhang M, Wu H, Guo J, Zhang X, Hu X, Cao CM, Xiao RP (2016) CaMKII is a RIP3 substrate mediating ischemia- and oxidative stress-induced myocardial necroptosis. Nat Med 22:175–182. https://doi.org/10.1038/nm.4017

    Article  CAS  PubMed  Google Scholar 

  45. Chen WJ, Chang SH, Chan YH, Lee JL, Lai YJ, Chang GJ, Tsai FC, Yeh YH (2019) Tachycardia-induced CD44/NOX4 signaling is involved in the development of atrial remodeling. J Mol Cell Cardiol 135:67–78. https://doi.org/10.1016/j.yjmcc.2019.08.006

    Article  CAS  PubMed  Google Scholar 

  46. Cheng H, Lederer WJ (2008) Calcium sparks. Physiol Rev 88:1491–1545. https://doi.org/10.1152/physrev.00030.2007

    Article  CAS  PubMed  Google Scholar 

  47. Mattila KJ, Nieminen MS, Valtonen VV, Rasi VP, Kesaniemi YA, Syrjala SL, Jungell PS, Isoluoma M, Hietaniemi K, Jokinen MJ (1989) Association between dental health and acute myocardial infarction. BMJ 298:779–781. https://doi.org/10.1136/bmj.298.6676.779

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Joshipura KJ, Douglass CW, Willett WC (1998) Possible explanations for the tooth loss and cardiovascular disease relationship. Ann Periodontol 3:175–183. https://doi.org/10.1902/annals.1998.3.1.175

    Article  CAS  PubMed  Google Scholar 

  49. Wu D, Liu J (2019) Occlusal interference induces oxidative stress and increases the expression of UCP3 in the masseter muscle: a rat model. Arch Oral Biol 102:249–255. https://doi.org/10.1016/j.archoralbio.2019.04.022

    Article  CAS  PubMed  Google Scholar 

  50. Iyomasa MM, de Souza GC, Dias FJ, Pitol DL, Watanabe IS, Issa JPM (2009) Histological and histochemical effects after occlusion alteration in suprahyoid muscles. Micron 40:239–246. https://doi.org/10.1016/j.micron.2008.08.001

    Article  CAS  PubMed  Google Scholar 

  51. Buczko P, Zalewska A, Szarmach I (2015) Saliva and oxidative stress in oral cavity and in some systemic disorders. J Physiol Pharmacol 66:3–9

    CAS  PubMed  Google Scholar 

  52. Vatner SF, Park M, Yan L, Lee GJ, Lai L, Iwatsubo K, Ishikawa Y, Pessin J, Vater DE (2013) Adenylyl cyclase type 5 in cardiac disease, metabolism, and aging. Am J Physiol Heart Circ Physiol 305:H1–H8. https://doi.org/10.1152/ajpheart.00080.2013

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Vatner SF, Pachon RE, Vatner DE (2015) Inhibition of adenylyl cyclase type 5 increases longevity and healthful aging through oxidative stress protection. Oxid Med Cell Longev 2015:250310. https://doi.org/10.1155/2015/250310

    Article  PubMed  PubMed Central  Google Scholar 

  54. Ishikawa Y, Homcy CJ (1997) The adenylyl cyclases as integrators of transmembrane signal transduction. Circ Res 80:297–304. https://doi.org/10.1161/01.res.80.3.297

    Article  CAS  PubMed  Google Scholar 

  55. Espinasse I, Iourgenko V, Defer N, Samson F, Hanoune J, Mercadier JJ (1995) Type V, but not type VI, adenylyl cyclase mRNA accumulates in the rat heart during ontogenic development. Correlation with increased global adenylyl cyclase activity. J Mol Cell Cardiol 27:1789–1795. https://doi.org/10.1016/0022-2828(95)90002-0

    Article  CAS  PubMed  Google Scholar 

  56. Onda T, Hashimoto Y, Nagai M, Kuramochi H, Saito S, Yamazaki H et al (2001) Type-specific regulation of adenylyl cyclase. Selective pharmacological stimulation and inhibition of adenylyl cyclase isoforms. J Biol Chem 276(51):47785–93. https://doi.org/10.1074/jbc.M107233200

    Article  CAS  PubMed  Google Scholar 

  57. Hung HC, Joshipura KJ, Colditz G, Manson JE, Rimm EB, Speizer FE, Willett WC (2004) The association between tooth loss and coronary heart disease in men and women. J Public Health Dent 64:209–215. https://doi.org/10.1111/j.1752-7325.2004.tb02755.x

    Article  PubMed  Google Scholar 

  58. Ikebe K, Matsuda K, Kagawa R, Enoki K, Okada T, Yoshida M, Maeda Y (2012) Masticatory performance in older subjects with varying degrees of tooth loss. J Dent 40:71–76. https://doi.org/10.1016/j.jdent.2011.10.007

    Article  PubMed  Google Scholar 

  59. Ikebe K, Matsuda K, Kagawa R, Enoki K, Yoshida M, Maeda Y, Nokubi T (2011) Association of masticatory performance with age, gender, number of teeth, occlusal force and salivary flow in Japanese older adults: is ageing a risk factor for masticatory dysfunction? Arch Oral Biol 56:991–996. https://doi.org/10.1016/j.archoralbio.2011.03.019

    Article  PubMed  Google Scholar 

  60. Kugimiya Y, Watanabe Y, Igarashi K, Hoshino D, Motokawa K, Edahiro A, Ueda T, Takano T, Sakurai K, Taniguchi Y, Kitamura A, Nasu I, Shinkai S, Hirano H (2020) Factors associated with masticatory performance in community-dwelling older adults: a cross-sectional study. J Am Dent Assoc 151:118–126. https://doi.org/10.1016/j.adaj.2019.10.003

    Article  PubMed  Google Scholar 

  61. Iwashima Y, Kokubo Y, Ono T, Yoshimuta Y, Kida M, Kosaka T, Maeda Y, Kawano Y, Miyamoto Y (2014) Additive interaction of oral health disorders on risk of hypertension in a Japanese urban population: the Suita Study. Am J Hypertens 27:710–719. https://doi.org/10.1093/ajh/hpt227

    Article  PubMed  Google Scholar 

  62. Katayama T, Mori D, Miyake H, Fujiwara S, Ono Y, Takahashi T, Onozuka M, Kubo K (2012) Effect of bite-raised condition on the hippocampal cholinergic system of aged SAMP8 mice. Neurosci Lett 520:77–81. https://doi.org/10.1016/j.neulet.2012.05.035

    Article  CAS  PubMed  Google Scholar 

  63. Ago T, Kuroda J, Pain J, Fu C, Li H, Sadoshima J (2010) Upregulation of Nox4 by hypertrophic stimuli promotes apoptosis and mitochondrial dysfunction in cardiac myocytes. Circ Res 106(7):1253–1264. https://doi.org/10.1161/circresaha.109.213116

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Maejima Y, Kuroda J, Matsushima S, Ago T, Sadoshima J (2011) Regulation of myocardial growth and death by NADPH oxidase. J Mol Cell Cardiol 50(3):408–416. https://doi.org/10.1016/j.yjmcc.2010.12.018

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Ma X, Song Y, Chen C, Fu Y, Shen Q, Li Z et al (2011) Distinct actions of intermittent and sustained β-adrenoceptor stimulation on cardiac remodeling. Sci China Life Sci 54(6):493–501. https://doi.org/10.1007/s11427-011-4183-9

    Article  CAS  PubMed  Google Scholar 

  66. Suita K, Fujita T, Hasegawa N, Cai W, Jin H, Hidaka Y, Prajapati R, Umemura M, Yokoyama U, Sato M, Okumura S, Ishikawa Y (2015) Norepinephrine-induced adrenergic activation strikingly increased the atrial fibrillation duration through β1- and α1-adrenergic receptor-mediated signaling in mice. PLoS ONE 10:e0133664. https://doi.org/10.1371/journal.pone.0133664

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Lawrence DS, Sahay JN, Chatterjee SS, Cruickshank JM (1982) Asthma and beta-blockers. Eur J Clin Pharmacol 22(6):501–509. https://doi.org/10.1007/bf00609622

    Article  CAS  PubMed  Google Scholar 

  68. Holm G, Johansson S, Vedin A, Wilhelmsson C, Smith U (1980) The effect of beta-blockade on glucose tolerance and insulin release in adult diabetes. Acta Med Scand 208(3):187–191. https://doi.org/10.1111/j.0954-6820.1980.tb01175.x

    Article  CAS  PubMed  Google Scholar 

  69. Kilkenny C, Parsons N, Kadyszewski E, Festing MFW, Cuthill IC, Fry D, Hutton J, Altman DG (2009) Survey of the quality of experimental design, statistical analysis and reporting of research using animals. PLoS ONE 4:e7824. https://doi.org/10.1371/journal.pone.0007824

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals (2011). Guide for the Care and Use of Laboratory Animals. 8th edition. Washington (DC): National Academies Press (US) The National Academy of Science. https://doi.org/10.17226/12910

Download references

Acknowledgements

None.

Funding

This study was supported in part by the Japan Society for the Promotion of Science. (JSPS) KAKENHI Grant (20K10304 to YO, 20K10305 to KS, 19K24109, 21K17171 to AI and 18K06862, 21K10242 to SO).

Author information

Authors and Affiliations

  1. Department of Physiology, Tsurumi University School of Dental Medicine, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama, 230-8501, Japan

    Yoshio Hayakawa, Kenji Suita, Yoshiki Ohnuki, Yasumasa Mototani, Akinaka Morii, Kenichi Kiyomoto, Michinori Tsunoda, Ichiro Matsuo & Satoshi Okumura

  2. Department of Dental Anesthesiology, Tsurumi University School of Dental Medicine, Yokohama, 230-8501, Japan

    Yoshio Hayakawa & Hiroshi Kawahara

  3. Department of Oral Anatomy, Tsurumi University School of Dental Medicine, Yokohama, 230-8501, Japan

    Misao Ishikawa

  4. Department of Orthodontics, Tsurumi University School of Dental Medicine, Yokohama, 230-8501, Japan

    Aiko Ito

  5. Department of Pediatric Dentistry, Tsurumi University School of Dental Medicine, Yokohama, 236-8501, Japan

    Megumi Nariyama

  6. Department of Periodontology, Tsurumi University School of Dental Medicine, Yokohama, 230-8501, Japan

    Akinaka Morii, Kenichi Kiyomoto, Michinori Tsunoda & Ichiro Matsuo

Authors
  1. Yoshio Hayakawa
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Kenji Suita
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Yoshiki Ohnuki
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Yasumasa Mototani
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Misao Ishikawa
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Aiko Ito
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Megumi Nariyama
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Akinaka Morii
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Kenichi Kiyomoto
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Michinori Tsunoda
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Ichiro Matsuo
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Hiroshi Kawahara
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Satoshi Okumura
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Y.H., K.S., Y.O., S.O. conceived and designed the research. Y.H., K.S., M.I., A.I., I.M. performed the experiments. Y.M., M.N., A.M., K.K., M.T., H.K. contributed reagents/materials/analysis tools. S.O. wrote the paper. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Satoshi Okumura.

Ethics declarations

Ethics approval and consent to participate

All animal experiments complied with the ARRIVE guidelines [69] and were carried out in accordance with the National Institutes of Health guide for the care and use of laboratory animals [70] and institutional guidelines. The experimental protocol was approved by the Animal Care and Use Committee of Tsurumi University (No. 29A041).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Figure S1.

The original photo of Fig. 1b. The box outlined in black, indicated by the arrow, corresponds to the cropped part shown in the main article. Figure S2. Food consumption and (a) and drinking water (b) throughout the 2-week experimental period. C: Control, B: BO, V: Vidarabine, BO + V: BO + Vidarabine. Fig. S3. Representative full-length western blotting of Fig. 2c. The amounts of activated α-SMA (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S4. Representative full-length western blotting of Fig. 3c. The amounts of Bax (left panel) and BCL-2 (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped parts of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S5. Representative images of negative (left) and positive (right) controls of 8-OHdG immunostaining. Fig. S6. Representative full-length western blotting of Fig. 4c. The amounts of activated oxidized protein (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot. C: control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S7. Representative full-length western blotting of Fig. 5a. The amounts of AC5 (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S8. Representative full-length western blotting of Fig. 5b. The amounts of NOX4 (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S9. Representative full-length western blotting of Fig. 5c. The amounts of NOX2 (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S10. Representative full-length western blotting of Fig. 5d. The amounts of XO (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S11. Representative full-length western blotting of Fig. 5e. The amounts of phosphorylated p38 at Thr-180/Tyr-182 (left panel) and total p38 (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S12. Representative full-length western blotting of Fig. 5f. The amounts of phosphorylated ASK-1 at Thr-845 (left panel) and total ASK-1 (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S13. Representative full-length western blotting of Fig. 6a. The amounts of RIP3 (left panel) and GAPDH (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S14. Representative full-length western blotting of Fig. 6b. The amounts of phosphorylated CaMKII at Thr-286 (left panel) and total CaMKII (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S15. Representative full-length western blotting of Fig. 6c. The amounts of phosphorylated PLB at Thr-17 (left panel) and total PLB (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine. Fig. S16. Representative full-length western blotting of Fig. 6d. The amounts of phosphorylated PLB at Ser-16 (left panel) and total PLB (right panel) are shown. The box outlined in black in each panel, indicated by the arrow, corresponds to the cropped part of the blot shown in the main article. C: Control, B: BO, V: Vidarabine, BOV: BO + Vidarabine.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hayakawa, Y., Suita, K., Ohnuki, Y. et al. Vidarabine, an anti-herpes agent, prevents occlusal-disharmony-induced cardiac dysfunction in mice. J Physiol Sci 72, 2 (2022). https://doi.org/10.1186/s12576-022-00826-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12576-022-00826-4

Keywords

The Journal of Physiological Sciences

ISSN: 1880-6562

Contact us