Pacher Pál, Bátkai Sándor, Kunos George
Laboratory of Physiologic Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.
J Physiol. 2004 Jul 15;558(Pt 2):647-57. doi: 10.1113/jphysiol.2004.064824. Epub 2004 Apr 30.
The endocannabinoid anandamide and cannabinoid (CB) receptors have been implicated in the hypotension in various forms of shock and in advanced liver cirrhosis. Anandamide also activates vanilloid TRPV(1) receptors on sensory nerve terminals, triggering the release of calcitonin gene-related peptide which elicits vasorelaxation in isolated blood vessels in vitro. However, the contribution of TRPV(1) receptors to the in vivo hypotensive effect of anandamide is equivocal. We compared the cardiac performance of anaesthetized TRPV(1) knockout (TRPV(1)(-/-)) mice and their wild-type (TRPV(1)(+/+)) littermates and analysed in detail the haemodynamic effects of anandamide using the Millar pressure-volume conductance catheter system. Baseline cardiovascular parameters and systolic and diastolic function at different preloads were similar in TRPV(1)(-/-) and TRPV(1)(+/+) mice. The predominant hypotensive response to bolus intravenous injections of anandamide and the associated decrease in cardiac contractility and total peripheral resistance (TPR) were similar in TRPV(1)(+/+) and TRPV(1)(-/-) mice, as was the ability of the CB(1) receptor antagonist SR141716 to completely block these effects. In TRPV(1)(+/+) mice, this hypotensive response was preceded by a transient, profound drop in cardiac contractility and heart rate and an increase in TPR, followed by a brief pressor response, effects which were unaffected by SR141716 and were absent in TRPV(1)(-/-) mice. These results indicate that mice lacking TRPV(1) receptors have a normal cardiovascular profile and their predominant cardiovascular depressor response to anandamide is mediated through CB(1) receptors. The role of TRPV(1) receptors is limited to the transient activation of the Bezold-Jarisch reflex by very high initial plasma concentrations of anandamide.
内源性大麻素花生四烯乙醇胺和大麻素(CB)受体与多种形式休克及晚期肝硬化中的低血压有关。花生四烯乙醇胺还能激活感觉神经末梢上的香草酸瞬时受体电位1型(TRPV(1))受体,触发降钙素基因相关肽的释放,从而在体外引起离体血管的血管舒张。然而,TRPV(1)受体对花生四烯乙醇胺体内降压作用的贡献尚不明确。我们比较了麻醉状态下TRPV(1)基因敲除(TRPV(1)(-/-))小鼠及其野生型(TRPV(1)(+/+))同窝小鼠的心脏功能,并使用Millar压力-容积传导导管系统详细分析了花生四烯乙醇胺的血流动力学效应。TRPV(1)(-/-)和TRPV(1)(+/+)小鼠的基线心血管参数以及不同前负荷下的收缩和舒张功能相似。TRPV(1)(+/+)和TRPV(1)(-/-)小鼠对静脉推注花生四烯乙醇胺的主要降压反应以及相关的心脏收缩力和总外周阻力(TPR)降低相似,CB(1)受体拮抗剂SR141716完全阻断这些效应的能力也相似。在TRPV(1)(+/+)小鼠中,这种降压反应之前会出现心脏收缩力和心率的短暂、显著下降以及TPR升高,随后是短暂的升压反应,这些效应不受SR141716影响,且在TRPV(1)(-/-)小鼠中不存在。这些结果表明,缺乏TRPV(1)受体的小鼠具有正常的心血管特征,它们对花生四烯乙醇胺的主要心血管降压反应是通过CB(1)受体介导的。TRPV(1)受体的作用仅限于花生四烯乙醇胺初始血浆浓度非常高时对贝佐尔德-雅里什反射的短暂激活。