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甘珀酸、醛固酮和脱氧皮质酮对大鼠的胃抗溃疡及抗分泌作用

Gastric antiulcer and antisecretory effects of carbenoxolone, aldosterone and desoxycorticosterone in rats.

作者信息

Dajani E Z, Bianchi R G, Casler J J, Weet J F

出版信息

Arch Int Pharmacodyn Ther. 1979 Nov;242(1):128-38.

PMID:543742
Abstract

The beneficial antiulcer actions of carbenoxolone may possibly be due to an aldosterone-like component on the gastric mucosa. This suggests that aldosterone and possibly other corticoids may have antiulcer actions. The potential gastric antisecretory and antiulcer actions of aldosterone (ALDO) and desoxycorticosterone acetate (DOCA) were studied in the rat in comparison to the reference standard carbenoxolone. Stress ulcers were induced in fasted rats by the the forced exertion technique. Gastric secretion was evaluated in the five-hour pyloric ligated Shay rat model. The renal mineralocorticoid actions of these drugs were also studied in the adrenalectomized rat. Intragastric administration of carbenoxolone and DOCA, but not ALDO, significantly inhibited gastric ulcer formation in rats. Carbenoxolone given subcutaneously (s.c.) did not inhibit ulcer formation. ALDO exhibited antiulcer actions only when multiple s.c. injections were made. The antiulcer actions of DOCA and ALDO are not mediated via an inhibitory effect on gastric secretion. At all doses tested DOCA and ALDO showed significant renal effect, while carbenoxolone exhibited this effect only at the highest tested dose. These results suggest that the beneficial antiulcerogenic action of carbenoxolone is due to a direct effect on gastric mucosa and is not related to an aldosterone-like component.

摘要

生胃酮的有益抗溃疡作用可能归因于其对胃黏膜的一种类似醛固酮的成分。这表明醛固酮以及可能的其他皮质激素可能具有抗溃疡作用。与参考标准生胃酮相比,研究了醛固酮(ALDO)和醋酸去氧皮质酮(DOCA)在大鼠中的潜在胃泌素分泌抑制和抗溃疡作用。通过强制运动技术在禁食大鼠中诱导应激性溃疡。在五小时幽门结扎的 Shay 大鼠模型中评估胃分泌。还在肾上腺切除的大鼠中研究了这些药物的肾盐皮质激素作用。胃内给予生胃酮和 DOCA,但不给予 ALDO,可显著抑制大鼠胃溃疡的形成。皮下注射生胃酮不能抑制溃疡形成。只有多次皮下注射时,ALDO 才表现出抗溃疡作用。DOCA 和 ALDO 的抗溃疡作用不是通过对胃分泌的抑制作用介导的。在所有测试剂量下,DOCA 和 ALDO 均显示出显著的肾脏作用,而生胃酮仅在最高测试剂量下才表现出这种作用。这些结果表明,生胃酮有益的抗溃疡作用是由于其对胃黏膜的直接作用,与类似醛固酮的成分无关。

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