Pettinger W A, Tanaka K, Keeton K, Campbell W B, Brooks S N
Proc Soc Exp Biol Med. 1975 Mar;148(3):625-30. doi: 10.3181/00379727-148-38597.
In our attempt to find an anesthetic agent which did not influence the renin-angiotensin system in the rat, the effect of widely used injectable and gaseous anesthetics and narcotic agents on renin release was chacterized. All of the agents studied induced dose- and time-related increases in serum renin activity when administered in anesthetic doses. Preliminary experiments in anesthetic doses. Preliminary experiments indicated that cardiovascular effects were highly variable, giving little insight into the relationship between renin release and cardiovascular changes. Propranolol impaired most of the anesthesia-induced renin release and impaired aldosterone release with the one agent (urethane) studied. Renin release by two anesthetic agents (ketamine and urethane) appeared to be mediated premarily through the beta-adrenermediated primarily through the beta-adrenergic receptor mechanism, but equivocal results were obtained with other agents (pentobarbital and morphine). It is possible that other anesthetics, as with urethane, may induce aldosterone release by way of renin release. This anesthesia-induced renin release and the extensive biologic activities of angiotensin and aldosterone suggest a potential for influencing many investigations, particularly those involving cardiovascular and endocrine systems.
在我们试图寻找一种不影响大鼠肾素-血管紧张素系统的麻醉剂的过程中,对广泛使用的注射用和气态麻醉剂以及麻醉性镇痛药对肾素释放的影响进行了表征。当以麻醉剂量给药时,所有研究的药物均引起血清肾素活性与剂量和时间相关的增加。在麻醉剂量下进行的初步实验表明,心血管效应变化很大,几乎无法深入了解肾素释放与心血管变化之间的关系。普萘洛尔可减弱大多数麻醉诱导的肾素释放,并在所研究的一种药物(乌拉坦)作用下减弱醛固酮释放。两种麻醉剂(氯胺酮和乌拉坦)引起的肾素释放似乎主要通过β-肾上腺素能受体机制介导,但其他药物(戊巴比妥和吗啡)的结果不明确。与乌拉坦一样,其他麻醉剂有可能通过肾素释放诱导醛固酮释放。这种麻醉诱导的肾素释放以及血管紧张素和醛固酮广泛的生物活性表明,其有可能影响许多研究,尤其是那些涉及心血管和内分泌系统的研究。