Peroxisome Proliferate Activated Receptor Delta - Pipeline Review: Humans Treated with PPARD Exhibit Enhanced Insulin Sensitivity


Published on : Sep 20, 2019

Albany, New York, September 20, 2019: The peroxisome proliferate activated receptors (PPARs) are usually ligand-activated transcription factors that are involved in energy homeostasis. PPARs natural ligands tend to be fatty acids and there are three different PPAR isoforms; PPARG; PPARA and PPARD. Nonetheless, PPARs are encoded have distinct functions and are encoded by separate genes owing to tissue expression and affinity for ligands.

Over the last decade, PPARD has received increased attention with its role in fatty acid catabolism and energy homeostasis being acknowledged ever since the specific ligand GW501516 was synthesized.

These insights are according to the intelligence report, titled, “Peroxisome Proliferate Activated Receptors Delta—Pipeline Review, H2 2019,” which has been freshly added to Market Research Hub’s (MRH) overarching repository.

While PPARA has its say on genes involved in fatty acid oxidation, peroxisome proliferate activated receptor delta (PPARD) controls genes implicated in lipoprotein and lipid oxidation metabolism. Humans treated with a PPARD agonist showed increased HDL and decreased LDL cholesterol levels, enhanced insulin sensitivity, thereby making it an accepted drug option for treatment of metabolic disease. Of late, PPARD has become instrumental in macrophages by inducing a transition from proinflammatory (M1) to anti-inflammatory (M2) macropages.

Accordingly, significance of PPARD on lipid metabolism makes it an obvious target for treatment of insulin resistance and obesity. Further, several studies in mice reveal the significance of PPARD in the embryonic development, in the brain, skin and in the regulation of inflammatory macrophages in adipose tissue and liver.

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