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Pharmacological correction of obesity-induced autophagy arrest using calcium channel blockers

  • Hwan Woo Park
  • , Haeli Park
  • , Ian A. Semple
  • , Insook Jang
  • , Seung Hyun Ro
  • , Myungjin Kim
  • , Victor A. Cazares
  • , Edward L. Stuenkel
  • , Jung Jae Kim
  • , Jeong Sig Kim
  • , Jun Hee Lee*
  • *Corresponding author for this work
  • University of Michigan, Ann Arbor
  • Nanyang Technological University
  • Department of Obstetrics and Gynecology
  • Soonchunhyang University

Research output: Contribution to journal › Article › peer-review

Abstract

Autophagy deregulation during obesity contributes to the pathogenesis of diverse metabolic disorders. However, without understanding the molecular mechanism of obesity interference in autophagy, development of therapeutic strategies for correcting such defects in obese individuals is challenging. Here we show that a chronic increase of the cytosolic calcium concentration in hepatocytes during obesity and lipotoxicity attenuates autophagic flux by preventing the fusion between autophagosomes and lysosomes. As a pharmacological approach to restore cytosolic calcium homeostasis in vivo, we administered the clinically approved calcium channel blocker verapamil to obese mice. Such treatment successfully increases autophagosome-lysosome fusion in liver, preventing accumulation of protein inclusions and lipid droplets and suppressing inflammation and insulin resistance. As calcium channel blockers have been safely used in clinics for the treatment of hypertension for more than 30 years, our results suggest they may be a safe therapeutic option for restoring autophagic flux and treating metabolic pathologies in obese patients.

Original languageEnglish
Article number4834
JournalNature Communications
Volume5
DOIs
Publication statusPublished - 2014
Externally publishedYes

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