Heat stress‐induced B1 receptor synthesis in the rat: an ex vivo study

1 This ex vivo study was performed to characterize B1 receptor induction in rats submitted to heat stress. Changes in aortic isometric tension were recorded after a 90 min in vitro incubation with [des‐Arg9]‐bradykinin. B1 receptor mRNA were detected in aorta and heart using RT–PCR technique. 2 Aort...

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Published inBritish journal of pharmacology Vol. 125; no. 4; pp. 812 - 816
Main Authors Lagneux, Caroline, Innocenti‐Francillard, Patricia, Godin‐Ribuot, Diane, Bader, Mickael, Ribuot, Christophe
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.10.1998
Nature Publishing
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Summary:1 This ex vivo study was performed to characterize B1 receptor induction in rats submitted to heat stress. Changes in aortic isometric tension were recorded after a 90 min in vitro incubation with [des‐Arg9]‐bradykinin. B1 receptor mRNA were detected in aorta and heart using RT–PCR technique. 2 Aortic rings from sham rats did not respond to [des‐Arg9]‐bradykinin. In contrast, this agonist induced a concentration‐dependent relaxation of aortic rings from rats submitted to lipopolysaccharide (LPS) treatment or to heat stress 24 h earlier. 3 The concentration‐dependent relaxation induced by [des‐Arg9]‐bradykinin on aortic rings from heat‐stressed rats was abolished by [des‐Arg10]‐HOE 140, a selective B1 receptor antagonist. 4 In endothelium denuded aortic rings from heat‐stress rats, [des‐Arg9]‐bradykinin induced a concentration‐dependent constriction. 5 Pretreatment of intact aortic rings from heat‐stress rats with the cyclo‐oxygenase inhibitor, diclofenac (1 μM) did not prevent the concentration‐dependent relaxation in response to [des‐Arg9]‐bradykinin. In contrast, NO synthase inhibition with Nω‐nitro‐L‐arginine methyl ester (30 μM) totally prevented the vasorelaxant response. 6 B1 receptor mRNA were not detected in aorta and heart from sham animals but were present in tissue from heat‐stressed and LPS‐treated rats. 7 In conclusion, our results suggest that heat stress induces a transcriptional activation of the B1 receptor gene. The induction of B1 receptors leads to an endothelium‐ and NO‐dependent vasorelaxant response to [des‐Arg9]‐bradykinin. British Journal of Pharmacology (1998) 125, 812–816; doi:10.1038/sj.bjp.0702146
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ISSN:0007-1188
1476-5381
DOI:10.1038/sj.bjp.0702146