The selected pathophysiological aspects of PPARs activation

B Kieć-Wilk1, A Dembińska-Kieć, A Olszanecka

  • 1Department of Clinical Biochemistry, Medical College Jagiellonian University, Kopernika 15a, 30-504 Krakow, Poland. mbkiec@cyf-kr.edu.pl

Insights

Peroxisome proliferator activated receptors (PPARs) regulate metabolism and offer cardiovascular protection. However, PPARs activation may cause lipotoxicity in cardiomyocytes, contributing to cardiac hypertrophy in metabolic diseases.

Area of Science:

  • Cardiovascular Biology
  • Metabolic Regulation
  • Molecular Endocrinology

Background:

  • Peroxisome proliferator activated receptors (PPARs) are nuclear transcription factors regulating glucose and lipid metabolism.
  • Three PPAR isoforms (alpha, beta/delta, gamma) exist, with diverse tissue distribution and functions.
  • PPARs exhibit anti-atherogenic, anti-inflammatory, and anti-hypertensive properties, including cardioprotection in hypertension-induced cardiac hypertrophy.

Purpose of the Study:

  • To review the dual role of PPARs activation in cardiac pathophysiology.
  • To explore the potential unfavorable effects of PPARs on lipid metabolism in cardiomyocytes.
  • To discuss the implications of PPARs activation in conditions like diabetes, metabolic syndrome, and obesity.

Main Methods:

  • Literature review of experimental reports and hypotheses.
  • Analysis of existing evidence on PPARs function and dysfunction.
  • Synthesis of pathophysiological aspects of PPARs activation in cardiac hypertrophy.

Main Results:

  • PPARs activation demonstrates cardioprotective effects in hypertension-induced cardiac hypertrophy.
  • Emerging evidence suggests PPARs activation can induce lipotoxicity in cardiomyocytes.
  • This lipotoxicity may contribute to pathological cardiac hypertrophy in metabolic diseases.

Conclusions:

  • PPARs possess a complex role in cardiac health, with both beneficial and detrimental effects.
  • Understanding the balance of PPARs activation is crucial for managing metabolic and cardiovascular diseases.
  • Further research is needed to elucidate the precise mechanisms of PPARs-induced lipotoxicity and its clinical relevance.

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