Astaxanthin as a Peroxisome Proliferator-Activated Receptor (PPAR) Modulator: Its Therapeutic Implications

Mar Drugs. 2019 Apr 23;17(4):242. doi: 10.3390/md17040242.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are part of the nuclear hormone receptors superfamily that plays a pivotal role in functions such as glucose and lipid homeostasis. Astaxanthin (ASX) is a lipid-soluble xanthophyll carotenoid synthesized by many microorganisms and various types of marine life that is known to possess antioxidant, anti-inflammatory, antidiabetic, anti-atherosclerotic, and anticancer activities. As such, it is a promising nutraceutical resource. ASX-mediated modulation of PPARs and its therapeutic implications in various pathophysiological conditions are described in this review. ASX primarily enhances the action of PPARα and suppresses that of PPARβ/δ and PPARγ, but it has also been confirmed that ASX displays the opposite effects on PPARs, depending on the cell context. Anti-inflammatory effects of ASX are mediated by PPARγ activation, which induces the expression of pro-inflammatory cytokines in macrophages and gastric epithelial cells. The PPARγ-agonistic effect of ASX treatment results in the inhibition of cellular growth and apoptosis in tumor cells. Simultaneous and differential regulation of PPARα and PPARγ activity by ASX has demonstrated a hepatoprotective effect, maintaining hepatic lipid homeostasis and preventing related hepatic problems. Considering additional therapeutic benefits of ASX such as anti-gastric, cardioprotective, immuno-modulatory, neuroprotective, retinoprotective, and osteogenic effects, more studies on the association between ASX-mediated PPAR regulation and its therapeutic outcomes in various pathophysiological conditions are needed to further elucidate the role of ASX as a novel nutraceutical PPAR modulator.

Keywords: PPAR modulator; anti-inflammation; anticancer; astaxanthin; lipid and glucose metabolism; peroxisome proliferator-activated receptors (PPARs).

Publication types

  • Review

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Glucose / metabolism
  • Homeostasis / drug effects
  • Humans
  • Inflammation / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • PPAR alpha / metabolism*
  • PPAR gamma / metabolism*
  • Transcription Factors / metabolism
  • Xanthophylls / pharmacology

Substances

  • Cytokines
  • PPAR alpha
  • PPAR gamma
  • Transcription Factors
  • Xanthophylls
  • astaxanthine
  • Glucose