Cantalamessa F, de Caro G, Massi M, Micossi L G
Arch Int Pharmacodyn Ther. 1982 Mar;256(1):10-21.
Naloxone, administered to rats subcutaneously or by i.c.v. route, produces a dose-dependent inhibition of water intake elicited by angiotensin II or water deprivation. However, doses of the drug which do not affect drinking inhibit the antidipsic effect of subcutaneous morphine. The larger is the dose of morphine, the larger is the antimorphinic effect evoked by naloxone. These data would suggest that, at least in respect to the effects of narcotics on water intake, naloxone is a partial agonist of the nalorphine type, but the slopes of naloxone and of morphine dose-response regression lines are not in keeping with this hypothesis. Thus, the mechanism of the anti-morphic effect elicited by naloxone on drinking behaviour remains to be clarified.
皮下注射或脑室内注射纳洛酮可使大鼠因血管紧张素II或缺水引起的饮水呈剂量依赖性抑制。然而,不影响饮水的药物剂量可抑制皮下注射吗啡的抗利尿作用。吗啡剂量越大,纳洛酮引起的抗吗啡作用就越大。这些数据表明,至少就麻醉品对饮水的影响而言,纳洛酮是烯丙吗啡类型的部分激动剂,但纳洛酮和吗啡剂量反应回归线的斜率与这一假设不符。因此,纳洛酮对饮水行为产生的抗吗啡作用机制仍有待阐明。