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尼古丁诱导大鼠食管黏膜的体外自由基生成。

In vitro free radical production in rat esophageal mucosa induced by nicotine.

作者信息

Wetscher G J, Bagchi D, Perdikis G, Bagchi M, Redmond E J, Hinder P R, Glaser K, Hinder R A

机构信息

Department of Surgery, Creighton University, Omaha, Nebraska 68131, USA.

出版信息

Dig Dis Sci. 1995 Apr;40(4):853-8. doi: 10.1007/BF02064991.

Abstract

Oxidative stress induced by nicotine was investigated in the esophageal mucosa of rats. The homogenized mucosa was incubated for 30 min with 50, 100, 200, 400, and 800 ng/mg protein/ml nicotine or with 200 ng/mg protein/ml nicotine for 15, 30, 45, and 60 min. Esophageal mucosa was also incubated for 30 min with 200 ng/mg protein/ml nicotine with or without the scavengers superoxide dismutase (SOD), catalase, SOD+catalase, inactivated SOD, inactivated catalase, or albumin. Incubation with 0.9% NaCl served as control. There was a strong correlation between chemiluminescence and the nicotine dose (r = 0.75) or the nicotine incubation time (r = 0.77). Thirty-minute incubation of the esophageal mucosa with 200 ng/mg protein/ml nicotine increased chemiluminescence 5.5-fold and lipid peroxidation 3.3-fold. This response was dampened by SOD or catalase and abolished by SOD+catalase. Inactivated enzymes or albumin had no scavenging effect. These results demonstrate that nicotine causes oxidative stress to the esophageal mucosa.

摘要

在大鼠食管黏膜中研究了尼古丁诱导的氧化应激。将匀浆后的黏膜与浓度为50、100、200、400和800 ng/mg蛋白质/毫升的尼古丁孵育30分钟,或与浓度为200 ng/mg蛋白质/毫升的尼古丁孵育15、30、45和60分钟。食管黏膜还与浓度为200 ng/mg蛋白质/毫升的尼古丁一起孵育30分钟,同时分别添加或不添加清除剂超氧化物歧化酶(SOD)、过氧化氢酶、SOD + 过氧化氢酶、失活的SOD、失活的过氧化氢酶或白蛋白。用0.9%氯化钠孵育作为对照。化学发光与尼古丁剂量(r = 0.75)或尼古丁孵育时间(r = 0.77)之间存在很强的相关性。食管黏膜与浓度为200 ng/mg蛋白质/毫升的尼古丁孵育30分钟后,化学发光增加了5.5倍,脂质过氧化增加了3.3倍。这种反应被SOD或过氧化氢酶减弱,并被SOD + 过氧化氢酶消除。失活的酶或白蛋白没有清除作用。这些结果表明尼古丁会对食管黏膜造成氧化应激。

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