Leander J D, Zerbe R L, Hart J C
J Pharmacol Exp Ther. 1985 Aug;234(2):463-9.
The effects of agonists at kappa, mu and delta opioid receptors were determined on vasopressin levels in water-deprived rats. Bremazocine and U-50, 488 (kappa agonists) markedly suppressed vasopressin levels, whereas morphine and methadone (mu agonists) and metkephamid (a mixed mu and delta agonist) did not suppress vasopressin levels. Likewise, clonidine, a potent diuretic in normally hydrated rats, did not clearly suppress vasopressin levels. Metkephamid was shown to have a modest diuretic effect in normally hydrated rats but not in water-deprived rats. The diuretic effects of bremazocine were blocked completely by simultaneous treatment with desmopressin, a synthetic vasopressin-like analog. Desmopressin also blocked the diuretic effect of a waterload, but only partially attenuated the diuretic effect of clonidine. These results support the hypothesis that kappa opioid agonists produce a diuretic effect by suppressing plasma levels of vasopressin, and at higher doses produce a pattern of urination similar to animals lacking vasopressin. By comparison, mu and delta opioid agonists have little effect on vasopressin levels in water-deprived rats.
研究了κ、μ和δ阿片受体激动剂对缺水大鼠血管加压素水平的影响。布瑞马唑辛和U-50,488(κ激动剂)显著抑制血管加压素水平,而吗啡和美沙酮(μ激动剂)以及美普他酚(一种μ和δ混合激动剂)并未抑制血管加压素水平。同样,可乐定在正常水合大鼠中是一种强效利尿剂,但并未明显抑制血管加压素水平。美普他酚在正常水合大鼠中显示出适度的利尿作用,但在缺水大鼠中则没有。布瑞马唑辛的利尿作用可通过同时给予去氨加压素(一种合成的血管加压素样类似物)而完全阻断。去氨加压素也阻断了水负荷的利尿作用,但仅部分减弱了可乐定的利尿作用。这些结果支持了以下假设:κ阿片受体激动剂通过抑制血管加压素的血浆水平产生利尿作用,并且在较高剂量时产生类似于缺乏血管加压素的动物的排尿模式。相比之下,μ和δ阿片受体激动剂对缺水大鼠的血管加压素水平几乎没有影响。