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脂质超载与外溢:代谢性损伤与代谢综合征

Lipid overload and overflow: metabolic trauma and the metabolic syndrome.

作者信息

Unger Roger H

机构信息

University of Texas Southwestern Medical Center, Dallas, TX 75390-8854, USA.

出版信息

Trends Endocrinol Metab. 2003 Nov;14(9):398-403. doi: 10.1016/j.tem.2003.09.008.

Abstract

Approximately two-thirds of the US population are overweight, which means that insulin resistance is probably the most common metabolic abnormality in the USA. I propose three novel concepts concerning the causes and consequences of insulin resistance that challenge current thinking. First, there is the evidence that resistance to insulin-stimulated glucose metabolism is not a primary event in obesity, but is secondary to lipid accumulation resulting from full responsiveness to insulin-stimulated lipogenic activity. Second, resistance to insulin-stimulated glucose metabolism, now considered detrimental to health, might be a protective mechanism that reduces lipid-induced damage to tissue by excluding glucose from cells, thus decreasing glucose-derived lipogenesis. Third, I suggest that lipid-induced insulin resistance and the accompanying metabolic syndrome are secondary to leptin resistance, resulting in breakdown in the normal partitioning of surplus lipids in the adipocyte compartment.

摘要

大约三分之二的美国人口超重,这意味着胰岛素抵抗可能是美国最常见的代谢异常情况。我提出了三个关于胰岛素抵抗的原因和后果的新观点,这些观点挑战了当前的认知。首先,有证据表明,对胰岛素刺激的葡萄糖代谢的抵抗并非肥胖中的原发性事件,而是继发于对胰岛素刺激的脂肪生成活性产生充分反应后导致的脂质积累。其次,对胰岛素刺激的葡萄糖代谢的抵抗,目前被认为对健康有害,它可能是一种保护机制,通过将葡萄糖排除在细胞外从而减少脂质诱导的组织损伤,进而减少葡萄糖衍生的脂肪生成。第三,我认为脂质诱导的胰岛素抵抗及伴随的代谢综合征继发于瘦素抵抗,导致脂肪细胞中多余脂质的正常分配出现紊乱。

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