Impact of new 1,4‑dihydrothiopyridine derivatives with analgesic activity on gastric mucosa

E. Bibik, A. Myazina, K. Frolov, V. Dotsenko, S. Krivokolysko
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引用次数: 0

Abstract

In clinical practice, the occurrence of such a side effect as gastrotoxicity can occur in patients taking NSAIDs with any route of administration. In this case, damage not only to the upper parts of the digestive tract is noted, but also to the intestine as a whole, since NSAID-induced enteropathy is manifested by the intestinal permeability disorder with protein exudation and diapedesis of erythrocytes, as well as by the development of erosions, ulcers, and life-threatening complications: bleeding, perforation, intestinal obstruction, and the appearance of circular folds [1]. The purpose of the study: to investigate the morphofunctional state of the stomach after exposure to non-steroidal anti-inflammatory drugs and novel heterocyclic compounds synthesized by us which have been proven to have high analgesic activity in white rats.
具有镇痛活性的新型1,4 -二氢硫代吡啶衍生物对胃粘膜的影响
在临床实践中,服用任何给药途径的非甾体抗炎药都可能发生胃毒性等副作用。在这种情况下,不仅消化道上部受到损害,整个肠道也受到损害,因为nsaid引起的肠病表现为肠通透性障碍,伴有蛋白质渗出和红细胞渗出,以及糜烂、溃疡和危及生命的并发症:出血、穿孔、肠梗阻和环状褶皱的出现[1]。本研究目的:探讨非甾体类抗炎药和我们合成的新型杂环化合物对大鼠胃的形态功能影响,这些化合物已被证明具有较高的镇痛活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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