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Azelnidipine, unique calcium channel blocker could prevent stress-induced cardiac dysfunction like α·β blocker
Yuri Takano1, Takashi Ueyama, Fuminobu Ishikura
1School of Allied Health Sciences, Osaka University, Faculty of Medicine, Osaka, Japan.
Insights
Azelnidipine, a unique calcium blocker, protects against emotional stress-induced cardiac dysfunction by preventing a drop in heart function. This study shows azelnidipine offers protective effects similar to alpha and beta blockers.
Area of Science:
- Cardiology
- Pharmacology
- Stress Physiology
Background:
- Alpha and beta-adrenergic blockers are known to protect against cardiac dysfunction induced by emotional stress.
- Azelnidipine is a distinct calcium channel blocker that does not elevate heart rate.
Purpose of the Study:
- To evaluate the efficacy of azelnidipine in preventing cardiac dysfunction caused by acute stress.
Main Methods:
- Rats were pretreated with azelnidipine (0.3 mg/kg), labetalol (3 mg/kg), or vehicle.
- Immobilization stress (IMO) was induced for 30 minutes, followed by anesthesia.
- Cardiac function (fractional area change - FAC), blood pressure, and heart rate were monitored via echocardiography.
Main Results:
- During IMO, mean blood pressure was significantly lower in the azelnidipine and labetalol groups compared to the vehicle group.
- Post-IMO, fractional area change (FAC) was significantly higher in both azelnidipine and labetalol groups versus the vehicle group.
- Labetalol group showed a transiently lower FAC during IMO compared to azelnidipine and vehicle groups.
Conclusions:
- Acute administration of azelnidipine effectively prevents the decline in cardiac function following acute stress.
- Azelnidipine demonstrates a protective effect against stress-induced cardiac dysfunction, comparable to alpha and beta-adrenergic blockers.
Background:
We have reported that α and β adrenergic blockers could protect against emotional stress-induced cardiac dysfunction. Azelnidipine is a unique calcium blocker which does not increase heart rate. The purpose of this study is to evaluate the effect of azelnidipine to prevent stress-induced cardiac dysfunction.
Methods And Results:
Rats premedicated with azelnidipine (0.3 mg/kg), labetalol (3 mg/kg), or vehicle, were restrained for 30 min (immobilization stress: IMO) to reproduce emotional stress, and anesthetized to release stress. We measured the fractional area change (FAC) by echocardiography, blood pressure, and heart rate at the end of IMO and every 10 min for 60 min after IMO. During IMO, FAC in the labetalol group was significantly lower than that in the other two groups. At 20 min after IMO, FAC in the azelnidipine or labetalol group was significantly higher than that in the vehicle group (86 ± 9%, 73 ± 5% vs. 56 ± 11%, p<0.05). During IMO, mean blood pressure in the azelnidipine or labetalol group was significantly lower than that in the vehicle group (107 ± 5 mmHg, 106 ± 17 mmHg vs. 124 ± 5 mmHg, p<0.05).
Conclusion:
Acute administration of azelnidipine could prevent a sudden drop of cardiac function after acute stress like IMO. Azelnidipine might have a protective effect on stress-induced cardiac dysfunction like α and β adrenergic blockers.
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