4.5 Article

Central leptin regulates heart lipid content by selectively increasing PPAR β/δ expression

Journal

JOURNAL OF ENDOCRINOLOGY
Volume 236, Issue 1, Pages 43-56

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1530/JOE-17-0554

Keywords

leptin; cardiac metabolism; PPAR beta/delta; lipid metabolism

Funding

  1. JCCM [PEII-2014-022-P]
  2. Mineco [BFU2012-39705-C03-01]
  3. UCLM, Spain [GI20174021]
  4. CONACyT from Mexico

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The role of central leptin in regulating the heart from lipid accumulation in lean leptinsen-sitive animals has not been fully elucidated. Herein, we investigated the effects of central leptin infusion on the expression of genes involved in cardiac metabolism and its role in the control of myocardial triacylglyceride (TAG) accumulation in adult Wistar rats. Intracerebroventricular (icv) leptin infusion (0.2 mu g/day) for 7 days markedly decreased TAG levels in cardiac tissue. Remarkably, the cardiac anti-steatotic effects of central leptin were associated with the selective upregulation of gene and protein expression of peroxisome proliferator-activated receptor beta/delta (PPAR beta/delta, encoded by Pparb/d) and their target genes, adipose triglyceride lipase (encoded by Pnpla2, herefater referred to as Atgl), hormone sensitive lipase (encoded by Lipe, herefater referred to as Hsl), pyruvate dehydrogenase kinase 4 (Pdk4) and acyl CoA oxidase 1 (Acox1), involved in myocardial intracellular lipolysis and mitochondrial/peroxisomal fatty acid utilization. Besides, central leptin decreased the expression of stearoyl-CoA deaturase 1 (Scd1) and diacylglycerol acyltransferase 1 (Dgat1) involved in TAG synthesis and increased the CPT-1 independent palmitate oxidation, as an index of peroxisomal beta-oxidation. Finally, the pharmacological inhibition of PPAR beta/delta decreased the effects on gene expression and cardiac TAG content induced by leptin. These results indicate that leptin, acting at central level, regulates selectively the cardiac expression of PPAR beta/delta, contributing in this way to regulate the cardiac TAG accumulation in rats, independently of its effects on body weight.

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