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乙醛对胃细胞增殖的抑制作用。

Inhibition of gastric cell proliferation by acetaldehyde.

作者信息

Matysiak-Budnik T, Kärkkäinen P, Methuen T, Roine R P, Salaspuro M

机构信息

Research Unit of Alcohol Diseases, University of Helsinki, Finland.

出版信息

J Pathol. 1995 Nov;177(3):317-22. doi: 10.1002/path.1711770315.

Abstract

Helicobacter pylori possesses alcohol dehydrogenase activity and is capable of producing acetaldehyde from ethanol in vitro. Acetaldehyde is a toxic and reactive compound and has been shown to inhibit the proliferation of many different cell lines in vitro. To study the effects of acetaldehyde on the proliferation of gastric epithelial cells in vivo, we employed an immunohistochemical method after labelling proliferating cells with 5'-bromo-2'-deoxyuridine in rats receiving acetaldehyde intragastrically. Chronic (16 weeks) exposure of gastric mucosa to acetaldehyde given to rats in their drinking water in concentrations of 10 or 20 mM resulted in significant (P < 0.05) inhibition of gastric epithelial cell proliferation, expressed as 332 +/- 36, 348 +/- 8, and 695 +/- 15 proliferating cells per ten high-power (x 400) fields in the groups drinking 10 mM acetaldehyde, 20 mM acetaldehyde, and in controls respectively. In an acute study, significant inhibition of proliferation was observed after as few as 4 days of exposure to acetaldehyde, but only when a higher dose (50 mM) of acetaldehyde was given (438 +/- 44 versus 615 +/- 19 in controls, P < 0.05). The inhibition of gastric cell renewal by acetaldehyde may play a role in the pathogenesis of ethanol- and/or H. pylori-associated gastric diseases by inhibiting normal gastric mucosal protection and repair.

摘要

幽门螺杆菌具有乙醇脱氢酶活性,在体外能够将乙醇转化为乙醛。乙醛是一种有毒且具有反应活性的化合物,已被证明在体外可抑制多种不同细胞系的增殖。为了研究乙醛对体内胃上皮细胞增殖的影响,我们采用免疫组织化学方法,用5'-溴-2'-脱氧尿苷标记大鼠体内的增殖细胞,这些大鼠经胃内给予乙醛。给大鼠饮用含10或20 mM乙醛的水,使其胃黏膜慢性(16周)暴露于乙醛中,结果导致胃上皮细胞增殖受到显著(P < 0.05)抑制,饮用10 mM乙醛组、20 mM乙醛组和对照组每十个高倍(×400)视野中增殖细胞数分别为332±36、348±8和695±15。在一项急性研究中,仅在给予较高剂量(50 mM)乙醛4天后就观察到增殖受到显著抑制,但对照组为615±19,处理组为438±44(P < 0.05)。乙醛对胃细胞更新的抑制作用可能通过抑制正常胃黏膜保护和修复,在乙醇和/或幽门螺杆菌相关胃病的发病机制中发挥作用。

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