Mohn Nutrition Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
Hormone Laboratory, Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.
Diabetes. 2020 Sep;69(9):1903-1916. doi: 10.2337/db19-1174. Epub 2020 Jun 25.
Circulating branched-chain amino acids (BCAAs) associate with insulin resistance and type 2 diabetes. 3-Hydroxyisobutyrate (3-HIB) is a catabolic intermediate of the BCAA valine. In this study, we show that in a cohort of 4,942 men and women, circulating 3-HIB is elevated according to levels of hyperglycemia and established type 2 diabetes. In complementary cohorts with measures of insulin resistance, we found positive correlates for circulating 3-HIB concentrations with HOMA2 of insulin resistance, as well as a transient increase in 3-HIB followed by a marked decrease after bariatric surgery and weight loss. During differentiation, both white and brown adipocytes upregulate BCAA utilization and release increasing amounts of 3-HIB. Knockdown of the 3-HIB-forming enzyme 3-hydroxyisobutyryl-CoA hydrolase decreases release of 3-HIB and lipid accumulation in both cell types. Conversely, addition of 3-HIB to white and brown adipocyte cultures increases fatty acid uptake and modulated insulin-stimulated glucose uptake in a time-dependent manner. Finally, 3-HIB treatment decreases mitochondrial oxygen consumption and generation of reactive oxygen species in white adipocytes, while increasing these measures in brown adipocytes. Our data establish 3-HIB as a novel adipocyte-derived regulator of adipocyte subtype-specific functions strongly linked to obesity, insulin resistance, and type 2 diabetes.
循环支链氨基酸(BCAAs)与胰岛素抵抗和 2 型糖尿病有关。3-羟基异丁酸(3-HIB)是支链氨基酸缬氨酸的代谢中间产物。在这项研究中,我们表明,在 4942 名男性和女性的队列中,根据高血糖和已确立的 2 型糖尿病的水平,循环 3-HIB 升高。在具有胰岛素抵抗测量值的补充队列中,我们发现循环 3-HIB 浓度与 HOMA2 的胰岛素抵抗呈正相关,并且在减肥手术后和体重减轻后 3-HIB 短暂增加后明显减少。在分化过程中,白色和棕色脂肪细胞均上调 BCAA 利用并释放越来越多的 3-HIB。3-HIB 形成酶 3-羟基异丁酰辅酶 A 水解酶的敲低会减少两种细胞类型中 3-HIB 的释放和脂质积累。相反,将 3-HIB 添加到白色和棕色脂肪细胞培养物中会以时间依赖性方式增加脂肪酸摄取和胰岛素刺激的葡萄糖摄取。最后,3-HIB 处理可降低白色脂肪细胞中线粒体耗氧量和活性氧的产生,而在棕色脂肪细胞中则增加这些参数。我们的数据将 3-HIB 确立为一种新型脂肪细胞衍生调节剂,可强烈调节与肥胖,胰岛素抵抗和 2 型糖尿病密切相关的脂肪细胞亚型特异性功能。