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2-氨基己二酸可预防肥胖和糖尿病。

2-Aminoadipic acid protects against obesity and diabetes.

机构信息

State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine of Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Biotecan Medical Diagnostics Co., Ltd, Zhangjiang Center for Translational Medicine, Shanghai, China.

出版信息

J Endocrinol. 2019 Nov;243(2):111-123. doi: 10.1530/JOE-19-0157.

DOI:10.1530/JOE-19-0157
PMID:31454789
Abstract

Obesity and type 2 diabetes (T2D) are both complicated endocrine disorders resulting from an interaction between multiple predisposing genes and environmental triggers, while diet and exercise have key influence on metabolic disorders. Previous reports demonstrated that 2-aminoadipic acid (2-AAA), an intermediate metabolite of lysine metabolism, could modulate insulin secretion and predict T2D, suggesting the role of 2-AAA in glycolipid metabolism. Here, we showed that treatment of diet-induced obesity (DIO) mice with 2-AAA significantly reduced body weight, decreased fat accumulation and lowered fasting glucose. Furthermore, Dhtkd1-/- mice, in which the substrate of DHTKD1 2-AAA increased to a significant high level, were resistant to DIO and obesity-related insulin resistance. Further study showed that 2-AAA induced higher energy expenditure due to increased adipocyte thermogenesis via upregulating PGC1α and UCP1 mediated by β3AR activation, and stimulated lipolysis depending on enhanced expression of hormone-sensitive lipase (HSL) through activating β3AR signaling. Moreover, 2-AAA could alleviate the diabetic symptoms of db/db mice. Our data showed that 2-AAA played an important role in regulating glycolipid metabolism independent of diet and exercise, implying that improving the level of 2-AAA in vivo could be developed as a strategy in the treatment of obesity or diabetes.

摘要

肥胖和 2 型糖尿病(T2D)都是复杂的内分泌紊乱,是由多个易感基因与环境触发因素相互作用引起的,而饮食和运动对代谢紊乱有重要影响。先前的报告表明,赖氨酸代谢中间产物 2-氨基己二酸(2-AAA)可以调节胰岛素分泌并预测 T2D,这表明 2-AAA 在糖脂代谢中发挥作用。在这里,我们表明,用 2-AAA 治疗饮食诱导的肥胖(DIO)小鼠可显著减轻体重、减少脂肪堆积和降低空腹血糖。此外,Dhtkd1-/- 小鼠中 DHTKD1 的底物 2-AAA 增加到显著高水平,对 DIO 和肥胖相关的胰岛素抵抗具有抗性。进一步的研究表明,2-AAA 通过激活β3AR 信号转导,通过上调 PGC1α 和 UCP1 增加脂肪细胞产热,诱导更高的能量消耗,从而导致更高的能量消耗,这是由于脂肪细胞产热增加所致,并且依赖于激素敏感脂肪酶(HSL)表达的增强来刺激脂肪分解。此外,2-AAA 可以减轻 db/db 小鼠的糖尿病症状。我们的数据表明,2-AAA 在调节糖脂代谢方面发挥着重要作用,独立于饮食和运动,这意味着提高体内 2-AAA 的水平可以作为治疗肥胖或糖尿病的策略。

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