Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: The beta(1)-adrenoceptor site activated by CGP12177 varies in behavior according to the estrous cycle phase and stress
Author: Santos, IN
Marcondes, FK
Spadari-Bratfisch, RC
Abstract: The aim of this work was to assess whether stress and estrous cycle phases affected the beta(1)-adrenoceptor (beta(1)-AR) site activated by CGP12177 in the right atria of rats. The chronotropic response to CGP12177 in the absence or presence of antagonists was determined in atria from rats submitted to one daily foot-shock session for 3 consecutive days. Blood was collected for hormonal assays. The pD(2) for CGP12177 in atria from females was lower than in atria from males and was unaltered by stress or the estrous cycle. Propranolol (200 nM) or CGP20712A (3 muM) shifted the concentration-response curves to CGP12177 to the right in control and stressed estrus or control diestrus rats. Atria from stressed diestrus rats were resistant to blockade by propranolol or CGP20712A, indicating that the effect of beta-adrenoceptor antagonists on the response to CGP12177 is influenced by estrous cycle phases. The stress-induced increase in serum corticosterone levels was independent of the estrous cycle or gender, but the estradiol/progesterone ratio was affected differently in the two groups of female rats. In the diestrus group, serum estradiol levels decreased after the first foot-shock session and remained low until the day of sacrifice, whereas in the estrus group the serum levels of estradiol did not decrease after stress and peaked on the second day, which corresponded to proestrus. These data do not indicate whether there is a direct or indirect effect of stress hormones and (or) sex steroids on cardiac beta(1)-AR sensitivity. However, they do show that the classic and low-affinity binding sites of the beta(1)-AR are independently regulated and that the beta(1)-AR atypical site affinity for antagonists depends on the estrous cycle.
Subject: allosterism
receptor active site
steroid hormones
Country: Canadá
Editor: Natl Research Council Canada
Citation: Canadian Journal Of Physiology And Pharmacology. Natl Research Council Canada, v. 81, n. 5, n. 459, n. 468, 2003.
Rights: fechado
Identifier DOI: 10.1139/Y03-057
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000182787500006.pdf436.07 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.