Lemaire I, Tseng R, Lemaire S
Proc Natl Acad Sci U S A. 1978 Dec;75(12):6240-2. doi: 10.1073/pnas.75.12.6240.
In normal adult rats anesthetized with urethane, intravenous injections of beta-endorphin (30--150 micrograms kg-1) induced a transient fall of blood pressure followed by a small hypertension and a prolonged hypotension. Prior administration of naloxone completely blocked these effects, whereas naloxone, given 1 hr after beta-endorphin, did not reverse the prolonged depressor phase of the opioid peptide. The effects of beta-endorphin on the arterial blood pressure were greatly reduced in animals pretreated with p-chlorophenylalanine, a specific depletor of serotonin. Moreover, in rats pretreated with potent serotonin antagonists such as cyproheptadine, mianserin, and metergoline, beta-endorphin did not produce a significant hypotension. Furthermore, the depressor effect of beta-endorphin was potentiated by fluoxetine, a specific serotonin uptake inhibitor. These observations suggest the participation of a serotonergic pathway in the action of beta-endorphin on the arterial blood pressure.
在用乌拉坦麻醉的正常成年大鼠中,静脉注射β-内啡肽(30 - 150微克/千克)会导致血压短暂下降,随后出现轻微高血压和持续低血压。预先给予纳洛酮可完全阻断这些效应,而在β-内啡肽给药1小时后给予纳洛酮,则不会逆转阿片肽的持续降压阶段。在用对氯苯丙氨酸(一种特异性血清素耗竭剂)预处理的动物中,β-内啡肽对动脉血压的影响大大降低。此外,在用强效血清素拮抗剂如赛庚啶、米安色林和麦角乙脲预处理的大鼠中,β-内啡肽不会产生明显的低血压。此外,β-内啡肽的降压作用被特异性血清素摄取抑制剂氟西汀增强。这些观察结果表明血清素能途径参与了β-内啡肽对动脉血压的作用。