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. 2019 Oct 31;20(21):5422. doi: 10.3390/ijms20215422

Table 1.

PPARs tissue distribution and biological functions.

Isoforms Tissues Distribution Target Genes Functions Synthetic Ligands Natural Ligands
PPARγ White and brown adipose tissue, the large intestine, skeletal muscle, spleen, pancreas, and brain. aP2,
FATP,
FAT/CD36.
Regulation of adipogenesis, energy balance,
lipogenesis,
gluconeogenesis,
lipid storage,
glucose uptake,
metabolism uptake and differentiation.
Rosiglitazone,
Pioglitazone,
Troglitazone,
T3D-959,
DBZ.
9-HODE,
13-HODE,
15d-PGJ2,
EPA.
PPARα Liver, heart, skeletal muscle, intestinal mucosa, white and brown adipose tissue, pancreas, and brain. Acyl-CoA oxidase,
Thiolase,
Apolipoprotein A-I, Apolipoprotein A-II,
CYP8B1,
FATP,
FAT/CD36, and
Lipoprotein lipase.
Fatty acid metabolism,
inflammation, thermogenesis, ketogenesis, glucose uptake, fatty acid oxidation and
lipid storage.
Wy-14643,
GW-2331,
GW-9578,
K-877
Fibrates.
Palmitic acid,
Oleic acid,
Linoleic acid,
Arachidonic acid, DHA, oleoylethanolamide.
PPARβ/δ Liver, intestine, kidney, abdominal white and brown adipose tissue, skeletal muscle, heart, pancreas, and brain. Genes involved in lipid uptake, metabolism, and efflux, Lpin2, St3gal5. Fatty acid oxidation, fatty acid metabolism, regulates blood cholesterol,
glucose uptake, glucose utilization, insulin secretion, ketogenesis and inflammation.
L-796449,
L-783483,
GW-2433,
MBX-8025,
T3D-959,
GW501516,
GW610742.
Dihomo-γ-linolenic acid,
Arachidonic acid,
Methyl palmitate,
2-bromopalmitic acid,
prostacyclin I2,
4-HNE.