Fasting-induced HMGCS2 expression in the kidney does not contribute to circulating ketones

Andrea H. Venable, Lauren E. Lee, Kyle Feola, John Santoyo, Tatyana Broomfield, Sarah C. Huen

Research output: Contribution to journalArticlepeer-review

Abstract

Mitochondrial hydroxymethylglutaryl-CoA synthase 2 (HMGCS2) is the rate-limiting enzyme in ketogenesis. The liver expresses high levels of HMGCS2 constitutively as the main ketogenic organ. It has been suggested that the kidney could be ketogenic as HMGCS2 is expressed in the kidney during fasting and diabetic conditions. However, definitive proof of the capacity for the kidney to produce ketones is lacking. We demonstrated that during fasting, HMGCS2 expression is induced in the proximal tubule of the kidney and is peroxisome proliferator activated receptor-a dependent. Mice with kidney-specific Hmgcs2 deletion showed a minor, likely physiologically insignificant, decrease in circulating ketones during fasting. Conversely, liver-specific Hmgcs2 knockout mice exhibited a complete loss of fasting ketosis. Together, these findings indicate that renal HMGCS2 does not significantly contribute to global ketone production and that during fasting, the increase in circulating ketones is solely dependent on hepatic HMGCS2. Proximal tubule HMGCS2 serves functions other than systemic ketone provision. NEW & NOTEWORTHY The mitochondrial enzyme hydroxymethylglutaryl-CoA synthase 2 (HMGCS2) catalyzes the rate-limiting step of ketogenesis. Although the liver constitutively expresses HMGCS2 and is considered the main ketogenic organ, HMGCS2 is induced in the kidney during fasting, leading to the proposal that the kidney contributes to fasting ketosis. We showed kidney HMGCS2 does not contribute to circulating ketones during fasting and cannot compensate for hepatic ketogenic insufficiency.

Original languageEnglish (US)
Pages (from-to)F460-F467
JournalAmerican Journal of Physiology - Renal Physiology
Volume322
Issue number4
DOIs
StatePublished - Apr 2022

Keywords

  • Circulating ketones
  • Fasting ketogenesis
  • Hydroxymethylglutaryl-coenzyme A synthase 2
  • Kidney
  • Liver

ASJC Scopus subject areas

  • Physiology
  • Urology

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