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硫代葡萄糖金致肥胖小鼠肥胖发生过程中,丙酮酸脱氢酶复合体对葡萄糖负荷反应的组织差异。

Tissue differences in the response of the pyruvate dehydrogenase complex to a glucose load during the development of obesity in gold-thioglucose-obese mice.

作者信息

Bryson J M, Cooney G J, Wensley V R, Phuyal J L, Caterson I D

机构信息

Department of Endocrinology, Royal Prince Alfred Hospital, Sydney, N.S.W., Australia.

出版信息

Biochem J. 1995 Feb 1;305 ( Pt 3)(Pt 3):811-6. doi: 10.1042/bj3050811.

Abstract

The activity of pyruvate dehydrogenase (PDHC), a key enzyme complex in the oxidative disposal of glucose, was measured after an oral glucose load in the heart, liver, quadriceps muscle, white adipose tissue (WAT) and brown adipose tissue (BAT) of gold-thioglucose (GTG)-obese mice at different stages during the development of obesity and in age-matched controls. Significant responses to the glucose load were seen 30 min post-gavage in heart, WAT and BAT of control mice but no change was observed in quadriceps muscle. The increase in activity of the active form of PDHC (PDHCa) in response to glucose in heart was reduced 2 weeks after the induction of GTG-obesity with no response in 5 or 10 week obese mice. A 2-3-fold increase in the PDHCa response in both WAT and BAT of 2 week obese mice was absent in 5 and 10 week obese animals. Basal PDHCa activity in quadriceps muscle was increased in 2 week obese mice but subsequently returned to control levels as obesity progressed. The glucose load produced no change in the activity of PDHCa in quadriceps muscle of obese mice. These results demonstrate that changes in the capacity for oxidative glucose disposal in different tissues, as indicated by changes in PDHCa activity, may contribute to glucose-intolerance and insulin-resistance in GTG-obese mice and that the response of the PDHC to insulin during the development of obesity varies in different tissues.

摘要

在肥胖发展的不同阶段,对硫代葡萄糖金(GTG)诱导肥胖的小鼠以及年龄匹配的对照小鼠,口服葡萄糖负荷后,测定了丙酮酸脱氢酶(PDHC)的活性,PDHC是葡萄糖氧化代谢中的关键酶复合物。在心脏、肝脏、股四头肌、白色脂肪组织(WAT)和棕色脂肪组织(BAT)中进行了该测定。对照小鼠在灌胃后30分钟,心脏、WAT和BAT对葡萄糖负荷有显著反应,但股四头肌未观察到变化。诱导GTG肥胖2周后,心脏中PDHC活性形式(PDHCa)对葡萄糖的反应性增加减弱,在5周或10周肥胖小鼠中无反应。2周龄肥胖小鼠的WAT和BAT中PDHCa对葡萄糖的反应增加2 - 3倍,在5周和10周肥胖动物中未出现。2周龄肥胖小鼠股四头肌中的基础PDHCa活性增加,但随着肥胖进展随后恢复到对照水平。肥胖小鼠股四头肌中葡萄糖负荷未导致PDHCa活性改变。这些结果表明,如PDHCa活性变化所示,不同组织中葡萄糖氧化代谢能力的改变可能导致GTG肥胖小鼠的葡萄糖不耐受和胰岛素抵抗,并且肥胖发展过程中PDHC对胰岛素的反应在不同组织中有所不同。

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In vivo insulin sensitivity of the pyruvate dehydrogenase complex in tissues of the rat.
Am J Physiol. 1993 Jul;265(1 Pt 1):E102-7. doi: 10.1152/ajpendo.1993.265.1.E102.

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