Bátkai Sándor, Pacher Pál, Osei-Hyiaman Douglas, Radaeva Svetlana, Liu Jie, Harvey-White Judith, Offertáler László, Mackie Ken, Rudd M Audrey, Bukoski Richard D, Kunos George
Laboratory of Physiologic Studies, National Institute on Alcohol Abuse & Alcoholism, National Institutes of Health, Bethesda, Md 20892-8115, USA.
Circulation. 2004 Oct 5;110(14):1996-2002. doi: 10.1161/01.CIR.0000143230.23252.D2. Epub 2004 Sep 27.
Endocannabinoids are novel lipid mediators with hypotensive and cardiodepressor activity. Here, we examined the possible role of the endocannabinergic system in cardiovascular regulation in hypertension.
In spontaneously hypertensive rats (SHR), cannabinoid-1 receptor (CB1) antagonists increase blood pressure and left ventricular contractile performance. Conversely, preventing the degradation of the endocannabinoid anandamide by an inhibitor of fatty acid amidohydrolase reduces blood pressure, cardiac contractility, and vascular resistance to levels in normotensive rats, and these effects are prevented by CB1 antagonists. Similar changes are observed in 2 additional models of hypertension, whereas in normotensive control rats, the same parameters remain unaffected by any of these treatments. CB1 agonists lower blood pressure much more in SHR than in normotensive Wistar-Kyoto rats, and the expression of CB1 is increased in heart and aortic endothelium of SHR compared with Wistar-Kyoto rats.
We conclude that endocannabinoids tonically suppress cardiac contractility in hypertension and that enhancing the CB1-mediated cardiodepressor and vasodilator effects of endogenous anandamide by blocking its hydrolysis can normalize blood pressure. Targeting the endocannabinoid system offers novel therapeutic strategies in the treatment of hypertension.
内源性大麻素是具有降压和心脏抑制活性的新型脂质介质。在此,我们研究了内源性大麻素系统在高血压心血管调节中的可能作用。
在自发性高血压大鼠(SHR)中,大麻素-1受体(CB1)拮抗剂可升高血压并增强左心室收缩功能。相反,通过脂肪酸酰胺水解酶抑制剂阻止内源性大麻素花生四烯乙醇胺的降解,可将血压、心脏收缩力和血管阻力降低至正常血压大鼠的水平,而这些作用可被CB1拮抗剂阻断。在另外两种高血压模型中也观察到类似变化,而在正常血压对照大鼠中,相同参数不受任何这些处理的影响。CB1激动剂在SHR中降低血压的作用比在正常血压的Wistar-Kyoto大鼠中更强,与Wistar-Kyoto大鼠相比,SHR心脏和主动脉内皮中CB1的表达增加。
我们得出结论,内源性大麻素在高血压中可调节性抑制心脏收缩力,通过阻断内源性花生四烯乙醇胺的水解来增强CB1介导的心脏抑制和血管舒张作用可使血压正常化。靶向内源性大麻素系统为高血压治疗提供了新的治疗策略。