Branched-chain keto acids inhibit mitochondrial pyruvate carrier and suppress gluconeogenesis in hepatocytes

被引:16
作者
Nishi, Kiyoto [1 ,3 ]
Yoshii, Akira [1 ]
Abell, Lauren [1 ]
Zhou, Bo [1 ]
Frausto, Ricardo [4 ]
Ritterhoff, Julia [1 ]
McMillen, Timothy S. [1 ]
Sweet, Ian [2 ]
Wang, Yibin [4 ,5 ]
Gao, Chen [4 ,6 ]
Tian, Rong [1 ]
机构
[1] Univ Washington, Mitochondria & Metab Ctr, Dept Anesthesiol & Pain Med, 850 Republican St, Seattle, WA 98109 USA
[2] Univ Washington, Med Diabet Inst, 750 Republican St, Seattle, WA 98109 USA
[3] Shiga Univ Med Sci, Dept Pharmacol, Otsu, Shiga 5202182, Japan
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Anesthesiol, Cardiovasc Res Labs, Los Angeles, CA 90095 USA
[5] Duke NUS Sch Med, Signature Program Cardiovasc & Metab Dis, Singapore, Singapore
[6] Univ Cincinnati, Coll Med, Dept Pharmacol & Syst Physiol, Cincinnati, OH 45267 USA
来源
CELL REPORTS | 2023年 / 42卷 / 06期
基金
美国国家卫生研究院;
关键词
AMINO-ACIDS; INSULIN-RESISTANCE; GLUCOSE-METABOLISM; CATABOLISM; TRANSPORT; HEART;
D O I
10.1016/j.celrep.2023.112641
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Branched-chain amino acid (BCAA) metabolism is linked to glucose homeostasis, but the underlying signaling mechanisms are unclear. We find that gluconeogenesis is reduced in mice deficient of Ppm1k, a positive regulator of BCAA catabolism, which protects against obesity-induced glucose intolerance. Accu-mulation of branched-chain keto acids (BCKAs) inhibits glucose production in hepatocytes. BCKAs suppress liver mitochondrial pyruvate carrier (MPC) activity and pyruvate-supported respiration. Pyruvate-supported gluconeogenesis is selectively suppressed in Ppm1k-deficient mice and can be restored with pharmacolog-ical activation of BCKA catabolism by BT2. Finally, hepatocytes lack branched-chain aminotransferase that alleviates BCKA accumulation via reversible conversion between BCAAs and BCKAs. This renders liver MPC most susceptible to circulating BCKA levels hence a sensor of BCAA catabolism.
引用
收藏
页数:18
相关论文
共 50 条
  • [21] Expression of mitochondrial branched-chain aminotransferase and α-keto-acid dehydrogenase in rat brain: implications for neurotransmitter metabolism
    Cole, Jeffrey T.
    Sweatt, Andrew J.
    Hutson, Susan M.
    FRONTIERS IN NEUROANATOMY, 2012, 6
  • [22] The contradictory role of branched-chain amino acids in lifespan and insulin resistance
    Yao, He
    Li, Kai
    Wei, Jie
    Lin, Yajun
    Liu, Yinghua
    FRONTIERS IN NUTRITION, 2023, 10
  • [23] Association of circulating branched-chain amino acids with risk of moyamoya disease
    Zeng, Chaofan
    Ge, Peicong
    Liu, Chenglong
    Yu, Xiaofan
    Zhai, Yuanren
    Liu, Wei
    He, Qiheng
    Li, Junsheng
    Liu, Xingju
    Wang, Jia
    Ye, Xun
    Zhang, Qian
    Wang, Rong
    Zhang, Yan
    Zhao, Jizong
    Zhang, Dong
    FRONTIERS IN NUTRITION, 2022, 9
  • [24] Branched-Chain Amino Acids as Pharmacological Nutrients in Chronic Liver Disease
    Kawaguchi, Takumi
    Izumi, Namiki
    Charlton, Michael R.
    Sata, Michio
    HEPATOLOGY, 2011, 54 (03) : 1063 - 1070
  • [25] Whole-body metabolic fate of branched-chain amino acids
    Blair, Megan C.
    Neinast, Michael D.
    Arany, Zoltan
    BIOCHEMICAL JOURNAL, 2021, 478 (04) : 765 - 776
  • [26] Loss of Mitochondrial Pyruvate Carrier 2 in the Liver Leads to Defects in Gluconeogenesis and Compensation via Pyruvate-Alanine Cycling
    McCommis, Kyle S.
    Chen, Zhouji
    Fu, Xiaorong
    McDonald, William G.
    Colca, Jerry R.
    Kletzien, Rolf F.
    Burgess, Shawn C.
    Finck, Brian N.
    CELL METABOLISM, 2015, 22 (04) : 682 - 694
  • [27] Insulin resistance and the metabolism of branched-chain amino acids
    Jingyi Lu
    Guoxiang Xie
    Weiping Jia
    Wei Jia
    Frontiers of Medicine, 2013, 7 : 53 - 59
  • [28] Branched-chain amino acids for people with hepatic encephalopathy
    Gluud, Lise Lotte
    Dam, Gitte
    Les, Inigo
    Cordoba, Juan
    Marchesini, Giulio
    Borre, Mette
    Aagaard, Niels Kristian
    Vilstrup, Hendrik
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2015, (09): : CD001939
  • [29] Mitochondrial pyruvate carrier inhibition initiates metabolic crosstalk to stimulate branched chain amino acid catabolism
    Ferguson, Daniel
    Eichler, Sophie J.
    Yiew, Nicole K. H.
    Colca, Jerry R.
    Cho, Kevin
    Patti, Gary J.
    Shew, Trevor M.
    Lutkewitte, Andrew J.
    Mukherjee, Sandip
    McCommis, Kyle S.
    Niemi, Natalie M.
    Finck, Brian N.
    MOLECULAR METABOLISM, 2023, 70
  • [30] Branched-chain amino acids and atherosclerosis: friends or foes?
    Grajeda-Iglesias, Claudia
    Rom, Oren
    Aviram, Michael
    CURRENT OPINION IN LIPIDOLOGY, 2018, 29 (02) : 166 - 169