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大鼠小肠中的慢性缺氧与谷胱甘肽依赖性解毒作用

Chronic hypoxia and glutathione-dependent detoxication in rat small intestine.

作者信息

LeGrand T S, Aw T Y

机构信息

Department of Physiology and Biophysics, Louisiana State University Medical Center, Shreveport 71130-3932, USA.

出版信息

Am J Physiol. 1996 Apr;270(4 Pt 1):G725-9. doi: 10.1152/ajpgi.1996.270.4.G725.

DOI:10.1152/ajpgi.1996.270.4.G725
PMID:8928804
Abstract

It has previously been found that chronic O2 deficiency decreases activity of the enzymes of the glutathione (GSH) redox system in the liver. To study the effects of O2 deficiency on intestinal detoxication capacity, pair-fed (16 g food/day) Sprague-Dawley rats were exposed to air (20.9% O2; n = 4) or 10% O2 (n = 4) for 10 days. Animals were killed, and intestinal mucosal homogenate (20% wt/vol) was obtained and assayed for activities of glucose-6-phosphate dehydrogenase (G6PD), GSH peroxidase (GSHPx), GSH disulfide reductase (GSSGRd), and gamma-glutamyl cysteine synthetase (gamma-GCS). Hypoxia decreases activities of GSHPx, GSSGRd, and gamma-GCS by approximately 50%, which suggests compromised detoxication. A proximal-to-distal reduction in enzymatic capacity indicates impairment of detoxication may be more pronounced in the distal intestine. G6PD, a key enzyme in NADPH production, remains unchanged. Urinary malondialdehyde was also monitored. Hypoxic rats exhibited a threefold increase in thiobarbituric acid-reactive substance, consistent with a generalized oxidative stress in these animals. Taken together, the results indicate that chronic hypoxia promotes tissue oxidative stress and impairs the ability of the enterocyte to metabolize ingested oxidants.

摘要

先前已发现,慢性缺氧会降低肝脏中谷胱甘肽(GSH)氧化还原系统的酶活性。为了研究缺氧对肠道解毒能力的影响,将成对喂养(每天16克食物)的斯普拉格-道利大鼠暴露于空气(20.9%氧气;n = 4)或10%氧气(n = 4)中10天。处死动物后,获取肠黏膜匀浆(20%重量/体积),并检测葡萄糖-6-磷酸脱氢酶(G6PD)、谷胱甘肽过氧化物酶(GSHPx)、谷胱甘肽二硫化物还原酶(GSSGRd)和γ-谷氨酰半胱氨酸合成酶(γ-GCS)的活性。缺氧使GSHPx、GSSGRd和γ-GCS的活性降低约50%,这表明解毒功能受损。酶活性从近端到远端的降低表明,解毒功能受损在远端肠道可能更为明显。G6PD是NADPH生成中的关键酶,其活性保持不变。还监测了尿丙二醛。缺氧大鼠的硫代巴比妥酸反应性物质增加了三倍,这与这些动物普遍存在的氧化应激一致。综上所述,结果表明慢性缺氧会促进组织氧化应激,并损害肠细胞代谢摄入氧化剂的能力。

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