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PPARδ:: a dagger in the heart of the metabolic syndrome

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 116, Issue 3, Pages 590-597

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI27955

Keywords

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Funding

  1. NHLBI NIH HHS [P50HL56989, P50 HL056989] Funding Source: Medline
  2. NIDDK NIH HHS [1F32DK071478, F32 DK071478, U19DK62434, U19 DK062434] Funding Source: Medline

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Obesity is a growing threat to global health by virtue of its association with insulin resistance, glucose intolerance, hypertension, and dyslipidemia, collectively known as the metabolic syndrome or syndrome X. The nuclear receptors PPAR alpha and PPAR gamma are therapeutic targets for hypertriglyceridemia and insulin resistance, respectively, and drugs that modulate these receptors are currently in clinical use. More recent work on the less-described PPAR isotype PPAR delta has uncovered a dual benefit for both hypertriglyceridemia and insulin resistance, highlighting the broad potential of PPAR delta in the treatment of metabolic disease. PPAR delta enhances fatty acid catabolism and energy uncoupling in adipose tissue and muscle, and it suppresses macrophage-derived inflammation. Its combined activities in these and other tissues make it a multifaceted therapeutic target for the metabolic syndrome with the potential to control weight gain, enhance physical endurance, improve insulin sensitivity, and ameliorate atherosclerosis.

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