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Vasodilatory Effects of CNP on Aortic Arteries of RabbitsChinese Full Text

CHEN Li1,LI Qi-yong2,LIAO Shi-ping3,JIANG Rong-jian2,KONG Hong2,LAI Jin-chuan2,CHENG Biao2,SHU Yan2.1.Department of Physiology,West China School of Preclinical and Forensic Medicine,Sichuan University,Chengdu 610041,China;2.Department of Cardiology,Sichuan Academy of Medical Sciences & Sichuan Provincial People’s Hospital,Chengdu 610072,China;3.Department of Experiments of Functional Science,West China School of Preclinical and Forensic Medicine,Sichuan University,Chengdu 610041,China

Abstract: Objective To investigate the mechanism of vasodilatory effects of C-type natriuretic peptide(CNP).Methods Tension changes in aortic rings of rabbits were recorded with the presence of CNP or C-type natriuretic peptide receptor(NPR-C) agonist(cANF4-23) after pretreatment with epinephrine(NE) or 60 mmol/L KCl.The vasodilatory effects of four types of potassium channel blocker and NPR-C antagonist(cANF4-28) were also tested.Results A maximal vasorelaxant effects of(33.5±5.9)% and(38.4±10.6)% were recorded in the presence of 1 μmol/L CNP and cANF4-23,respectively.cANF4-28 attenuated the action of CNP((19.8±8.3)%).The vasorelaxant effects of CNP and cANF4-23 decreased significantly after pretreatment with 60 mmol/L KCl(P<0.01).Glibenclamide and BaCl2 also attenuated the relaxant activities of CNP(P<0.05).But only BaCl2 decreased the vasodilatory action of cANF4-23(P<0.05).Conclusion The relaxant activity of CNP is mediated through three paths: NPR-B/KATP,NPR-C/KIR and NPR-C/calcium channels.
  • DOI:

    10.13464/j.scuxbyxb.2010.05.046

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  • Classification Code:

    R965.2

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