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新型拮抗剂表明CB1大麻素受体参与了花生四烯乙醇胺的降压作用。

Novel antagonist implicates the CB1 cannabinoid receptor in the hypotensive action of anandamide.

作者信息

Varga K, Lake K, Martin B R, Kunos G

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0613, USA.

出版信息

Eur J Pharmacol. 1995 May 24;278(3):279-83. doi: 10.1016/0014-2999(95)00181-j.

Abstract

In anaesthetised rats, the endogenous cannabinoid anandamide has potent cardiovascular effects that include a brief pressor effect and a more prolonged depressor response. The depressor response is attenuated after transection of the cervical spinal cord or blockade of alpha-adrenergic receptors by phentolamine, and is dose-dependently inhibited by a selective antagonist of the CB1 cannabinoid receptor. The pressor component is not affected by any of these interventions. This suggests that the depressor response is due to inhibition of sympathetic tone mediated by CB1 receptors, whereas the pressor component is due to a peripheral action that does not involve the same receptors or the sympathetic nervous system.

摘要

在麻醉大鼠中,内源性大麻素花生四烯乙醇胺具有强大的心血管效应,包括短暂的升压效应和更持久的降压反应。在颈脊髓横断或用酚妥拉明阻断α-肾上腺素能受体后,降压反应减弱,并且被CB1大麻素受体的选择性拮抗剂剂量依赖性抑制。升压成分不受这些干预措施的任何影响。这表明降压反应是由于CB1受体介导的交感神经张力抑制,而升压成分是由于不涉及相同受体或交感神经系统的外周作用。

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