Effects of beta3-adrenergic receptors agonist on beating rate and cAMP levels in cultured cardiomyocytes of rats.
- Author:
Yi-hui KONG
1
;
Wei-min LI
;
Ying TIAN
Author Information
- Publication Type:Journal Article
- MeSH: Adrenergic beta-Agonists; pharmacology; Animals; Animals, Newborn; Cells, Cultured; Cyclic AMP; metabolism; Ethanolamines; pharmacology; Myocytes, Cardiac; drug effects; metabolism; RNA, Messenger; genetics; Rats; Rats, Wistar; Receptors, Adrenergic, beta-3; metabolism
- From: Chinese Journal of Applied Physiology 2003;19(2):109-113
- CountryChina
- Language:Chinese
-
Abstract:
AIMTo evaluate the effects of beta3-adrenergic receptors (ARs) agonist (BRL-37344) on beating rate and cAMP levels and investigate the influence on the chronotropic action of beta3-ARs in cultured cardiomyocyte of rats.
METHODSCultured neonatal rat cardiomyocytes were divided randomly into eight groups, control group, ISO group, Nadolol + ISO group, BRL group, PIX + BRL group, L-NAME + BRL group, Nadolol + BRL group and Bupranolol + BRL group. Beating rate of culture neonatal rat cardiomyocytes was observed and cAMP measured by enzyme immunoassay kit. Expression levels of beta3-ARs mRNA in cardiomyocytes was evaluated by reverse transcription-polymerase chain reaction (RT-PCR).
RESULTSISO, nonspecific beta-ARs agonist increased beating rate and intracellular cAMP production, antagonized by Nadolol, beta1, beta2-ARs antagonist. BRL37344 decreased beating rate and intracellular cAMP levels. FPTX, Gi protein inhibitor and Bupranolol, nonspecific beta-ARs antagonist totally blocked the effect and L-NAME, nitric oxide synthase (NOS) inhibitor partly blocked the effect, but Nadolol did not. There was the expression of beta3-AR mRNA in cardiomyocytes by RT-PCR.
CONCLUSIONSBeta3-ARs showed in cardiomyocytes and produced negative chronotropic effects. beta1, beta2-ARs antagonist did not affect it. It suggested beta3-ARs signal transduction was related with G1 protein. The negative inotropic effect of beta3-ARs stimulation was mediated by activation of the NOS pathway.