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不同内源性阿片受体在大鼠胃十二指肠溃疡形成中的可能作用

On the possible role of different endogenous opiate receptors in gastroduodenal ulceration of the rat.

作者信息

Balint G A, Nafradi J

机构信息

First Department of Medicine, Albert Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Agents Actions. 1990 Aug;31(1-2):164-9. doi: 10.1007/BF02003238.

Abstract

In Wistar rats of both sexes stress(restraint)- and drug (indomethacin)-induced gastric, as well, as cysteamine-induced duodenal ulceration was treated by morphine and nalorphine, given either alone or in combination. Neither morphine nor nalorphine had a significant anti-ulcerogenic effect. In contrast, the combined morphine + nalorphine treatment showed a highly significant anti-ulcerogenic action in the case of gastric ulceration but it was ineffective on duodenal ulcer formation. It seems that the chi and sigma endogenous opiate receptors play a significant role in the anti-ulcerogenic effect, while the mu receptors are involved to a considerably lesser degree. Moreover, the experimental results strengthen the view that gastric and duodenal ulceration are two different pathological entities and that ulcer formation is only a common consequence.

摘要

在雄性和雌性Wistar大鼠中,通过单独或联合给予吗啡和烯丙吗啡,对压力(束缚)诱导、药物(吲哚美辛)诱导的胃溃疡以及半胱胺诱导的十二指肠溃疡进行治疗。吗啡和烯丙吗啡均无显著的抗溃疡作用。相比之下,吗啡 + 烯丙吗啡联合治疗对胃溃疡显示出高度显著的抗溃疡作用,但对十二指肠溃疡形成无效。似乎κ和σ内源性阿片受体在抗溃疡作用中起重要作用,而μ受体的参与程度要小得多。此外,实验结果强化了以下观点:胃溃疡和十二指肠溃疡是两种不同的病理实体,溃疡形成只是一个共同的结果。

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