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在饮食诱导的胰岛素抵抗和高胰岛素血症的纵向发展过程中,夜间游离脂肪酸会独特地升高。

Nocturnal free fatty acids are uniquely elevated in the longitudinal development of diet-induced insulin resistance and hyperinsulinemia.

作者信息

Kim Stella P, Catalano Karyn J, Hsu Isabel R, Chiu Jenny D, Richey Joyce M, Bergman Richard N

机构信息

Department of Physiology and Biophysics, Keck School of Medicine of the University of Southern California, 1333 San Pablo St. MMR 626, Los Angeles, CA 90033, USA.

出版信息

Am J Physiol Endocrinol Metab. 2007 Jun;292(6):E1590-8. doi: 10.1152/ajpendo.00669.2006. Epub 2007 Jan 30.

Abstract

Obesity is strongly associated with hyperinsulinemia and insulin resistance, both primary risk factors for type 2 diabetes. It has been thought that increased fasting free fatty acids (FFA) may be responsible for the development of insulin resistance during obesity, causing an increase in plasma glucose levels, which would then signal for compensatory hyperinsulinemia. But when obesity is induced by fat feeding in the dog model, there is development of insulin resistance and a marked increase in fasting insulin despite constant fasting FFA and glucose. We examined the 24-h plasma profiles of FFA, glucose, and other hormones to observe any potential longitudinal postprandial or nocturnal alterations that could lead to both insulin resistance and compensatory hyperinsulinemia induced by a high-fat diet in eight normal dogs. We found that after 6 wk of a high-fat, hypercaloric diet, there was development of significant insulin resistance and hyperinsulinemia as well as accumulation of both subcutaneous and visceral fat without a change in either fasting glucose or postprandial glucose. Moreover, although there was no change in fasting FFA, there was a highly significant increase in the nocturnal levels of FFA that occurred as a result of fat feeding. Thus enhanced nocturnal FFA, but not glucose, may be responsible for development of insulin resistance and fasting hyperinsulinemia in the fat-fed dog model.

摘要

肥胖与高胰岛素血症和胰岛素抵抗密切相关,这两者都是2型糖尿病的主要危险因素。人们一直认为,空腹游离脂肪酸(FFA)增加可能是肥胖期间胰岛素抵抗发展的原因,导致血糖水平升高,进而引发代偿性高胰岛素血症。但是,在犬类模型中通过高脂喂养诱导肥胖时,尽管空腹FFA和血糖保持恒定,仍会出现胰岛素抵抗和空腹胰岛素显著增加的情况。我们检测了8只正常犬的FFA、葡萄糖和其他激素的24小时血浆谱,以观察任何可能导致高脂饮食诱导的胰岛素抵抗和代偿性高胰岛素血症的潜在餐后或夜间纵向变化。我们发现,在高脂、高热量饮食6周后,出现了显著的胰岛素抵抗和高胰岛素血症,以及皮下和内脏脂肪的堆积,而空腹血糖或餐后血糖均无变化。此外,尽管空腹FFA没有变化,但由于高脂喂养,夜间FFA水平显著升高。因此,在高脂喂养的犬类模型中,夜间FFA增强而非葡萄糖,可能是胰岛素抵抗和空腹高胰岛素血症发展的原因。

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