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非胰岛素依赖型糖尿病中的可逆性胰岛素抵抗

Reversible insulin resistance in non-insulin-dependent diabetes mellitus.

作者信息

Karam J H

机构信息

Metabolic Research Unit, University of California, San Francisco, USA.

出版信息

Horm Metab Res. 1996 Sep;28(9):440-4. doi: 10.1055/s-2007-979834.

Abstract

Insulin resistance is a major component of non-insulin-dependent diabetes mellitus (NIDDM). While a genetic contribution is likely, as yet none of several proposed candidate genes have been incriminated in the typically obese patient with NIDDM to explain their insulin resistance. Accordingly, this review focuses on some recent advances in understanding three acquired factors contributing to insulin resistance: visceral obesity, glucotoxicity and lipotoxicity. Newer computerized tomography scans allow quantitation of fat accumulating in visceral organs including the mesentery and omentum. This visceral fat relates much more to the insulin resistance syndrome than does subcutaneous fat. Moreover, exercise, as performed by active Sumo wrestlers, is associated with low visceral fat, absent hyperglycemia and absent dyslipidemia despite massive subcutaneous obesity. It remains to be seen whether exercise programs more moderate than Sumo wrestling will also mobilize visceral fat. A new metabolic pathway has recently been described whereby hexosamines are formed by an increased flux of glucose into fat and muscle. These hexosamine products appear to explain how glucotoxicity results in insulin resistance. They act as a negative feedback system to limit further glucose transport by insulin target tissue during hyperglycemia. Lipotoxicity has previously been implicated in insulin resistance by its inhibitory effect on glucose uptake by muscle because of the Randle-fatty acid cycle. Recently the role of elevated fatty acids in producing "hepatic" resistance to insulin in NIDDM has also been documented, but the site of insulin resistance may be the fat cell rather than the hepatocyte. Therapy consists mainly of hygienic measures, including caloric restriction and exercise, which can reverse all three of these acquired forms of insulin resistance. In addition, pharmacologic measures to reduce hyperglycemia can reduce the glucotoxicity and lipotoxicity. The use of insulin-sparing antihyperglycemia drugs may be particularly useful in the insulin-resistant patient to avoid weight gain while correcting the hyperglycemia.

摘要

胰岛素抵抗是非胰岛素依赖型糖尿病(NIDDM)的主要组成部分。虽然可能存在遗传因素,但在典型的肥胖NIDDM患者中,目前尚未发现几种候选基因与胰岛素抵抗有关。因此,本综述重点关注在理解导致胰岛素抵抗的三个后天因素方面的一些最新进展:内脏肥胖、糖毒性和脂毒性。更新的计算机断层扫描可以对包括肠系膜和网膜在内的内脏器官中积累的脂肪进行定量。这种内脏脂肪与胰岛素抵抗综合征的关系比皮下脂肪更为密切。此外,像活跃的相扑选手那样进行运动,尽管皮下脂肪大量堆积,但内脏脂肪含量低,无高血糖和血脂异常。比相扑运动更适度的运动计划是否也能动员内脏脂肪还有待观察。最近描述了一种新的代谢途径,即葡萄糖流入脂肪和肌肉的通量增加会形成己糖胺。这些己糖胺产物似乎解释了糖毒性如何导致胰岛素抵抗。它们作为一种负反馈系统,在高血糖期间限制胰岛素靶组织进一步的葡萄糖转运。由于兰德尔脂肪酸循环,脂毒性先前因其对肌肉葡萄糖摄取的抑制作用而与胰岛素抵抗有关。最近,也有文献记载了NIDDM中脂肪酸升高在产生“肝脏”胰岛素抵抗中的作用,但胰岛素抵抗的部位可能是脂肪细胞而非肝细胞。治疗主要包括卫生措施,包括热量限制和运动,这些措施可以逆转所有这三种后天形成的胰岛素抵抗形式。此外,降低高血糖的药物措施可以减轻糖毒性和脂毒性。在胰岛素抵抗患者中使用节省胰岛素的抗高血糖药物可能特别有用,可在纠正高血糖的同时避免体重增加。

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