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Fatty Acid Metabolic Remodeling During Type 2 Diabetes Remission After Bariatric Surgery

机译:减肥手术后2型糖尿病缓解期间的脂肪酸代谢重塑

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摘要

Hypertrophic remodeling of white adipose tissues is associated with overexposure of lean organs to circulating triglycerides (TGs) and nonesterified fatty acids (NEFAs), ultimately leading to insulin resistance. Bariatric surgery promotes type 2 diabetes (T2D) remission through a succession of weight loss-dependent and -independent mechanisms. However, the longitudinal contribution of adipocyte size reduction and fatty acid metabolic handling remain unknown. Here we show that severely obese participants with T2D display hypertriglyceridemia and excessive systemic lipolysis during intravenous lipid overload. Three days after biliopancreatic diversion with duodenal switch (DS), whole-body glycerol turnover was normalized and associated with lower HOMA-insulin resistance index. A mean excess weight loss of 84% was achieved 12 months after DS. The smaller subcutaneous adipocyte size predicted better glycemic control in T2D. TG disposal and acyi-camitine production during lipid overload, along with muscle insulin sensitivity, improved with weight loss. Nevertheless, systemic NEFA fluxes and NEFA spillover remained similar, suggesting that increased NEFA storage capacity per volume of adipose tissue exactly compensated for the decrease in fat mass during weight loss. In conclusion, T2D remission after DS is mainly associated with greater circulating TG disposal, lower systemic lipolysis, and better fatty acid handling by lean tissues.
机译:白色脂肪组织的肥大重塑与瘦身器官过度暴露于循环甘油三酸酯(TGs)和非酯化脂肪酸(NEFAs)有关,最终导致胰岛素抵抗。减肥手术通过一系列依赖于体重减轻和非依赖性的机制来促进2型糖尿病(T2D)的缓解。然而,脂肪细胞尺寸减小和脂肪酸代谢处理的纵向贡献仍然未知。在这里,我们显示严重肥胖的T2D参与者在静脉脂质超负荷期间显示出高甘油三酯血症和全身性脂解过多。经十二指肠开关(DS)转移胆胰后三天,全身甘油更新正常,且与较低的HOMA-胰岛素抵抗指数相关。 DS后12个月,平均体重减轻了84%。较小的皮下脂肪细胞大小预示着T2D的血糖控制更好。脂质超负荷期间TG的处置和酰基-卡马汀的产生以及肌肉胰岛素敏感性随着体重减轻而改善。然而,全身性NEFA通量和NEFA溢出仍然相似,这表明增加的每单位脂肪组织的NEFA储藏容量正好弥补了减肥过程中脂肪量的减少。总之,DS后T2D缓解主要与循环TG处理量增加,全身脂解降低和瘦肉组织对脂肪酸的更好处理有关。

著录项

  • 来源
    《Diabetes》 |2017年第11期|2743-2755|共13页
  • 作者单位

    Department of Medicine, Division of Endocrinology, Centre de recherche du CHUS, Universite de Sherbrooke, Sherbrooke, Quebec, Canada,Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Department of Medicine, Division of Endocrinology, Centre de recherche du CHUS, Universite de Sherbrooke, Sherbrooke, Quebec, Canada;

    University of Lyon, CARMEN INSERM U1060, INSA-Lyon, Villeurbanne, France;

    Department of Medicine, Division of Endocrinology, Centre de recherche du CHUS, Universite de Sherbrooke, Sherbrooke, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Universite Laval, Quebec City, Quebec, Canada;

    Department of Medicine, Division of Endocrinology, Centre de recherche du CHUS, Universite de Sherbrooke, Sherbrooke, Quebec, Canada;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:46:03

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