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链脲佐菌素诱导的糖尿病大鼠肝脏微粒体脂肪酸链延长中酶的位点特异性变化。

Enzyme site-specific changes in hepatic microsomal fatty acid chain elongation in streptozotocin-induced diabetic rats.

作者信息

Suneja S K, Osei P, Cook L, Nagi M N, Cinti D L

机构信息

Department of Pharmacology, University of Connecticut Health Center, Farmington 06032.

出版信息

Biochim Biophys Acta. 1990 Jan 16;1042(1):81-5. doi: 10.1016/0005-2760(90)90059-7.

Abstract

The hepatic microsomal fatty acid chain elongation of palmitoyl-CoA and gamma-linolenoyl-CoA was diminished by 40-50% in male Sprague-Dawley rats made diabetic for 2 and 4 weeks following the intravenous administration of a single dose (65 mg/kg) of streptozotocin. Analysis of the activities of the four enzymatic components showed that only one enzyme, the condensing enzyme, which catalyzes the initial and rate-limiting step in chain elongation, was altered by the diabetic state. Both chain elongation and condensation activities were depressed to the same extent, whereas beta-ketoacyl-CoA reductase, beta-hydroxyacyl-CoA dehydrase and trans-2-enoyl-CoA reductase activities were the same as the values obtained with non-diabetic controls. 2 week administration of 10 units of insulin per day to rats which were diabetic for a 2-week period resulted in the reversal of the reduced palmitoyl-CoA elongation and condensation activities to control values. However, neither the condensation nor the elongation of gamma-linolenoyl was reversed by the insulin treatment. These results support the notion of multiple condensing enzymes or chain elongation systems.

摘要

在静脉注射单剂量(65毫克/千克)链脲佐菌素后,使雄性斯普拉格-道利大鼠患糖尿病2周和4周,其肝脏微粒体中棕榈酰辅酶A和γ-亚麻酰辅酶A的脂肪酸链延长减少了40%-50%。对四种酶成分活性的分析表明,只有一种酶,即催化链延长起始和限速步骤的缩合酶,会因糖尿病状态而改变。链延长和缩合活性均降低到相同程度,而β-酮酰辅酶A还原酶、β-羟酰辅酶A脱水酶和反式-2-烯酰辅酶A还原酶的活性与非糖尿病对照组的值相同。对患糖尿病2周的大鼠每天给予10单位胰岛素,持续给药2周,可使降低的棕榈酰辅酶A延长和缩合活性恢复到对照值。然而,胰岛素治疗并未使γ-亚麻酸的缩合或延长恢复正常。这些结果支持了存在多种缩合酶或链延长系统的观点。

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