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α2-肾上腺素能受体阻断后布马佐辛和U-50,488对大鼠的抗利尿作用。

Antidiuretic effect of bremazocine and U-50,488 in rats after alpha 2-adrenoceptor blockade.

作者信息

Bianchi G

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

J Pharm Pharmacol. 1991 Mar;43(3):212-6. doi: 10.1111/j.2042-7158.1991.tb06670.x.

Abstract

The role of alpha 2-adrenoceptors and kappa-opioid receptors in urination was studied in rats. In water-loaded rats (40 mL kg-1 p.o.) the kappa-opioid agonist bremazocine (0.05 0.2 mg kg-1 i.p.) induced a dose-related diuretic response in the second hour after administration, but had no effect in the first hour. When rats were pretreated with the alpha 2-adrenoceptor antagonist idazoxan (1 mg kg-1 s.c.), bremazocine induced a dose-related antidiuretic response in the first hour; thereafter the rats showed an increase of urination similar to that with bremazocine alone. The antidiuretic effect of bremazocine was dependent on the dose of idazoxan with maximal response after 1-3 mg kg-1. Similar results were obtained with bremazocine in the presence of yohimbine (1 mg kg-1 s.c.). The antidiuretic profile of bremazocine after idazoxan was shared by U-50,488 (2.5-10 mg kg-1 i.p.), although this compound alone at the high dose reduces urine output in the first hour. The antidiuresis induced by bremazocine in the presence of idazoxan in water-loaded rats was completely antagonized by 10 but not 2 mg kg-1 i.p. of the opioid antagonist naloxone. Thus, kappa-opioid agonists, in addition to their diuretic effect, also produce an antidiuretic response which may be mediated by alpha 2-adrenoceptors.

摘要

研究了α2-肾上腺素能受体和κ-阿片受体在大鼠排尿中的作用。在经口给予40 mL/kg水负荷的大鼠中,κ-阿片激动剂布瑞马佐辛(0.050.2 mg/kg,腹腔注射)在给药后第二小时诱导出剂量相关的利尿反应,但在第一小时无作用。当大鼠预先皮下注射α2-肾上腺素能受体拮抗剂咪唑克生(1 mg/kg)时,布瑞马佐辛在第一小时诱导出剂量相关的抗利尿反应;此后,大鼠的排尿量增加,与单独使用布瑞马佐辛时相似。布瑞马佐辛的抗利尿作用取决于咪唑克生的剂量,在13 mg/kg后出现最大反应。在育亨宾(1 mg/kg,皮下注射)存在的情况下,布瑞马佐辛也得到了类似的结果。U-50,488(2.5~10 mg/kg,腹腔注射)在咪唑克生给药后也呈现出布瑞马佐辛的抗利尿特征,尽管该化合物单独使用高剂量时在第一小时会减少尿量。在水负荷大鼠中,咪唑克生存在时布瑞马佐辛诱导的抗利尿作用被腹腔注射10 mg/kg而非2 mg/kg的阿片受体拮抗剂纳洛酮完全拮抗。因此,κ-阿片激动剂除了具有利尿作用外,还会产生一种可能由α2-肾上腺素能受体介导的抗利尿反应。

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