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Effects of sorbitol dehydrogenase deficiency on nerve conduction in experimental diabetic mice.山梨醇脱氢酶缺乏对实验性糖尿病小鼠神经传导的影响。
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Is sorbitol dehydrogenase gene expression affected by streptozotocin-diabetes in the rat?大鼠中链脲佐菌素诱导的糖尿病会影响山梨醇脱氢酶基因的表达吗?
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Comparison of the effects of inhibitors of aldose reductase and sorbitol dehydrogenase on neurovascular function, nerve conduction and tissue polyol pathway metabolites in streptozotocin-diabetic rats.链脲佐菌素诱导的糖尿病大鼠中醛糖还原酶和山梨醇脱氢酶抑制剂对神经血管功能、神经传导及组织多元醇途径代谢产物影响的比较
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Plasma Insulin/Erythrocytic Aldose Reductase Ratio as a Predictor for Hepatocellular Carcinoma among Type II Diabetics and Hepatitis C Virus-infected Patients.血浆胰岛素/红细胞醛糖还原酶比值作为 2 型糖尿病和丙型肝炎病毒感染患者肝细胞癌的预测指标。
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Caloric restriction counteracts age-related changes in the activities of sorbitol metabolizing enzymes from mouse liver.热量限制可抵消小鼠肝脏中山梨醇代谢酶活性的年龄相关变化。
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Colocalization of polyol-metabolizing enzymes and immunological detection of fructated proteins in the female reproductive system of the rat.大鼠雌性生殖系统中多元醇代谢酶的共定位及果糖化蛋白的免疫检测
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本文引用的文献

1
Distribution of alcohol and sorbitol dehydrogenases. Assessment of mRNA species in mammalian tissues.乙醇脱氢酶和山梨醇脱氢酶的分布。哺乳动物组织中mRNA种类的评估。
Eur J Biochem. 1993 Jul 15;215(2):497-503. doi: 10.1111/j.1432-1033.1993.tb18059.x.
2
Is sorbitol dehydrogenase gene expression affected by streptozotocin-diabetes in the rat?大鼠中链脲佐菌素诱导的糖尿病会影响山梨醇脱氢酶基因的表达吗?
Biochim Biophys Acta. 1994 May 25;1226(2):213-8. doi: 10.1016/0925-4439(94)90031-0.
3
Glycation of albumin: reaction with glucose, fructose, galactose, ribose or glyceraldehyde measured using four methods.白蛋白的糖基化:使用四种方法测量与葡萄糖、果糖、半乳糖、核糖或甘油醛的反应。
J Biochem Biophys Methods. 1994 Mar;28(2):115-21. doi: 10.1016/0165-022x(94)90025-6.
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DNA cleavage induced by glycation of Cu,Zn-superoxide dismutase.铜锌超氧化物歧化酶糖基化诱导的DNA切割
Biochem J. 1994 Nov 15;304 ( Pt 1)(Pt 1):219-25. doi: 10.1042/bj3040219.
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Inhibition of sorbitol dehydrogenase. Effects on vascular and neural dysfunction in streptozocin-induced diabetic rats.山梨醇脱氢酶的抑制作用。对链脲佐菌素诱导的糖尿病大鼠血管和神经功能障碍的影响。
Diabetes. 1995 Feb;44(2):234-42. doi: 10.2337/diab.44.2.234.
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In vivo glycation of aldehyde reductase, a major 3-deoxyglucosone reducing enzyme: identification of glycation sites.醛糖还原酶(一种主要的3-脱氧葡萄糖酮还原酶)的体内糖基化:糖基化位点的鉴定
Biochemistry. 1995 Jan 31;34(4):1433-8. doi: 10.1021/bi00004a038.
7
Immunological detection of glycated proteins in normal and streptozotocin-induced diabetic rats using anti hexitol-lysine IgG.使用抗己糖醇赖氨酸IgG对正常和链脲佐菌素诱导的糖尿病大鼠中的糖化蛋白进行免疫检测。
Biochim Biophys Acta. 1995 Oct 17;1272(2):73-9. doi: 10.1016/0925-4439(95)00067-e.
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Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
9
Intestinal absorption of sorbitol and effects of its acute administration on glucose homeostasis in normal rats.山梨醇在正常大鼠肠道中的吸收及其急性给药对葡萄糖稳态的影响。
Br J Nutr. 1985 Jul;54(1):53-62. doi: 10.1079/bjn19850092.
10
Glycation and inactivation of human Cu-Zn-superoxide dismutase. Identification of the in vitro glycated sites.人铜锌超氧化物歧化酶的糖基化与失活。体外糖基化位点的鉴定。
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正常及糖尿病大鼠中山梨醇脱氢酶的糖基化作用与失活

Glycation and inactivation of sorbitol dehydrogenase in normal and diabetic rats.

作者信息

Hoshi A, Takahashi M, Fujii J, Myint T, Kaneto H, Suzuki K, Yamasaki Y, Kamada T, Taniguchi N

机构信息

Department of Biochemistry, Osaka University Medical School, Japan.

出版信息

Biochem J. 1996 Aug 15;318 ( Pt 1)(Pt 1):119-23. doi: 10.1042/bj3180119.

DOI:10.1042/bj3180119
PMID:8761460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1217596/
Abstract

Sorbitol dehydrogenase (SDH) is involved in the polyol pathway, which plays an important role in the pathogenesis of diabetic complications. We have measured the tissue distributions of SDH mRNA, both the immunoreactive enzyme levels and the enzyme activity. SDH mRNA was especially abundant in liver, kidney and testis. Both the activity and enzyme content are high in liver and kidney but not in testis. The discrepancy between mRNA and immunoreactive enzyme levels and the activity of SDH observed in testis was also seen in livers of streptozotocin-induced diabetic rats. SDH was found to exist in both glycated and non-glycated forms, with larger amounts of the glycated protein in the diabetic liver. Moreover, after incubation of purified enzyme with glucose or fructose, its activity was markedly decreased. These results indicate that glycation causes a decrease in SDH activity in liver under diabetic conditions. The same post-transcriptional event might occur to decrease the activity of SDH in testis in normal animals.

摘要

山梨醇脱氢酶(SDH)参与多元醇途径,该途径在糖尿病并发症的发病机制中起重要作用。我们测定了SDH mRNA的组织分布、免疫反应性酶水平和酶活性。SDH mRNA在肝脏、肾脏和睾丸中特别丰富。肝脏和肾脏中的活性和酶含量都很高,但睾丸中则不然。在链脲佐菌素诱导的糖尿病大鼠的肝脏中也观察到睾丸中SDH mRNA与免疫反应性酶水平和活性之间的差异。发现SDH以糖化和非糖化两种形式存在,糖尿病肝脏中糖化蛋白的含量更高。此外,将纯化的酶与葡萄糖或果糖孵育后,其活性明显降低。这些结果表明,在糖尿病条件下,糖基化会导致肝脏中SDH活性降低。在正常动物的睾丸中,可能会发生相同的转录后事件以降低SDH的活性。