Vargas H M, Brezenoff H E
Department of Pharmacology, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark 07103.
J Hypertens. 1988 Sep;6(9):739-45. doi: 10.1097/00004872-198809000-00008.
Experiments were conducted to determine the effects of chronic depletion of brain acetylcholine (ACh) on the development and maintenance of hypertension in spontaneously hypertensive rats (SHR). Synthesis of brain ACh was inhibited by chronic infusion of hemicholinium-3 (HC-3) into the cerebral ventricles, and systolic blood pressure was monitored by tail cuff occlusion. In 5-week-old SHR, infusion of HC-3 (0.25 micrograms/h) suppressed development of hypertension when compared to saline-infused control SHR during the 21 days of infusion (140 versus 190 mmHg on day 21). Hypothalamic and brain-stem ACh during this period was reduced by 50% and by 60-75%, respectively. In 18-week-old SHR with established hypertension, HC-3 (0.25 and 0.5 micrograms/h) reduced systolic blood pressure by 35-40 mmHg for 8 days, after which pressures returned to control hypertensive levels (191 mmHg) by day 14. The increase in blood pressure was accompanied by recovery of hypothalamic ACh levels to 75% of control. The specificity and physiological effectiveness of HC-3 was shown by its ability to inhibit the centrally mediated pressor response to physostigmine but not to oxotremorine. Infusion of HC-3 did not affect body growth, water consumption, body temperature or gross behavior. From this study, it can be concluded that brain cholinergic neurons are an important component in the development and the maintenance of hypertension in the SHR.
进行实验以确定脑内乙酰胆碱(ACh)长期耗竭对自发性高血压大鼠(SHR)高血压发生发展及维持的影响。通过向脑室长期注入半胱氨酸-3(HC-3)来抑制脑内ACh的合成,并用尾套法监测收缩压。在5周龄的SHR中,与注入生理盐水的对照SHR相比,注入HC-3(0.25微克/小时)在21天的注入期内抑制了高血压的发展(第21天分别为140 mmHg和190 mmHg)。在此期间,下丘脑和脑干的ACh分别减少了50%和60 - 75%。在已患高血压的18周龄SHR中,HC-3(0.25和0.5微克/小时)使收缩压在8天内降低了35 - 40 mmHg,之后到第14天血压恢复到对照高血压水平(191 mmHg)。血压升高伴随着下丘脑ACh水平恢复到对照水平的75%。HC-3的特异性和生理效应表现在它能够抑制对毒扁豆碱的中枢介导的升压反应,但不能抑制对氧化震颤素的反应。注入HC-3不影响身体生长、水消耗、体温或总体行为。从这项研究可以得出结论,脑胆碱能神经元是SHR高血压发生发展及维持的重要组成部分。