Korean J Physiol Pharmacol.
1998 Feb;2(1):55-62.
Effects of alpha-, beta-adrenergic, and calcium channel blockers on
renin- angiotensin system in perfused rat heart
- Affiliations
-
- 1Department of Pharmacology, Keimyung University, School of Medicine, Taegu 700-712, Korea.
Abstract
-
alpha-,beta-Adrenergics, and calcium channels were known to be related
to inducing cardiac hypertrophy. Recently, it was reported that the
cardiac renin-angiotensin system (RAS) was an important factor in
ventricular hypertrophy. The present study was aimed to investigate the
effects of alpha-, beta-adrenergic, and calcium channel blockers that
might be involved in the regulation of cardiac RAS. The reverse
transcription-polymerase chain reaction (RT-PCR) was used to detect the
expression of renin gene in the perfused rat heart. Changes in
angiotensin converting enzyme (ACE) activity and cyclic AMP (cAMP)
content which were thought to play a role in inducing cardiac
hypertrophy were measured in the perfused rat heart. The expression of
renin gene was not only increased by isoproterenol with
metoprolol-pretreatment but also increased by vasopressin treatment in
the presence of calcium channel blocker, nifedipine or verapamil.
Either prazosin alone or norepinephrine with prazosin-pretreatment
significantly increased the ACE activity. However, isoproterenol with
metoprolol-pretreatment significantly decreased the ACE activity. On
the other hand, the ACE activity was not changed by vasopressin,
nifedipine, or verapamil treatments. The content of cAMP was
significantly increased by either isoproterenol or vasopressin
treatment. According to these results, renin gene expression was
associated with beta2-adrenoceptor and calcium channel. ACE activity
was associated with alpha- and beta2- adrenoceptor. In conclusion,
beta2-adrenoceptor was important in cardiac renin gene expression and
ACE activity and alpha-, beta-adrenergic, and calcium channel blockers
might be involved in the regulation of cardiac RAS in a complicated
way.