INDY as a Therapeutic Target for Cardio-Metabolic Disease

被引:1
|
作者
Pesta, Dominik [1 ,2 ,3 ]
Jordan, Jens [1 ]
机构
[1] German Aerosp Ctr DLR, Inst Aerosp Med, D-51147 Cologne, Germany
[2] Univ Hosp Cologne, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50931 Cologne, Germany
[3] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
关键词
citrate transport; cardiovascular disease; metabolic disease; INDY (I'm Not Dead; Yet); SLC13A5; diabetes; insulin resistance; longevity; obesity; FATTY LIVER-DISEASE; CARDIOVASCULAR OUTCOMES; INSULIN SENSITIVITY; NEPRILYSIN INHIBITION; HEPATIC STEATOSIS; DROSOPHILA INDY; ACID SYNTHESIS; HEART-RATE; LIFE-SPAN; RECEPTOR;
D O I
10.3390/metabo12030244
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Decreased expression of the plasma membrane citrate transporter INDY (acronym I'm Not Dead, Yet) promotes longevity and protects from high-fat diet- and aging-induced metabolic derangements. Preventing citrate import into hepatocytes by different strategies can reduce hepatic triglyceride accumulation and improve hepatic insulin sensitivity, even in the absence of effects on body composition. These beneficial effects likely derive from decreased hepatic de novo fatty acid biosynthesis as a result of reduced cytoplasmic citrate levels. While in vivo and in vitro studies show that inhibition of INDY prevents intracellular lipid accumulation, body weight is not affected by organ-specific INDY inhibition. Besides these beneficial metabolic effects, INDY inhibition may also improve blood pressure control through sympathetic nervous system inhibition, partly via reduced peripheral catecholamine synthesis. These effects make INDY a promising candidate with bidirectional benefits for improving both metabolic disease and blood pressure control.
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页数:10
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