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对乙酰氨基酚在组织培养中对胃黏膜细胞保护作用的巯基介导

Sulphydryl mediation in the protection of gastric mucosal cells in tissue culture by acetaminophen.

作者信息

Romano M, Razandi M, Raza A, Szabo S, Ivey K J

机构信息

Department of Medicine, Long Beach VA Medical Center, California.

出版信息

Ital J Gastroenterol. 1991 Nov;23(8):481-6.

PMID:1751823
Abstract

Acetaminophen protects gastric mucosa in vivo against acute drug-induced damage and has also been shown to protect gastric epithelial cells in vitro. Protection afforded by acetaminophen in vitro is not associated with increased prostaglandin output. The present study evaluated whether protection of gastric epithelial cells by acetaminophen in vitro may be mediated by endogenous sulphydryls. Monolayers from a well-differentiated human gastric epithelial cell line were studied. Sodium taurocholate was used as a damaging agent and cell damage was assessed by the 51Cr release assay. Acetaminophen dose-dependently protected gastric cell monolayers against damage induced by sodium taurocholate. The sulphydryl blocker iodoacetamide dose-dependently decreased the concentration of nonprotein glutathione and cysteine and counteracted the protection afforded by acetaminophen. This suggests that sulphydryl compounds may mediate the protection of gastric epithelial cells by acetaminophen in vitro.

摘要

对乙酰氨基酚在体内可保护胃黏膜免受急性药物诱导的损伤,并且在体外也已显示出能保护胃上皮细胞。对乙酰氨基酚在体外提供的保护作用与前列腺素产量增加无关。本研究评估了对乙酰氨基酚在体外对胃上皮细胞的保护作用是否可能由内源性巯基介导。使用来自高分化人胃上皮细胞系的单层细胞进行研究。牛磺胆酸钠用作损伤剂,并通过51Cr释放试验评估细胞损伤。对乙酰氨基酚剂量依赖性地保护胃细胞单层免受牛磺胆酸钠诱导的损伤。巯基阻断剂碘乙酰胺剂量依赖性地降低非蛋白谷胱甘肽和半胱氨酸的浓度,并抵消了对乙酰氨基酚提供的保护作用。这表明巯基化合物可能介导对乙酰氨基酚在体外对胃上皮细胞的保护作用。

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