FAT/CD36 Participation in Human Skeletal Muscle Lipid Metabolism: A Systematic Review.
Arnulfo Ramos-JiménezRuth A Zavala-LiraVerónica Moreno-BritoEverardo González-RodríguezPublished in: Journal of clinical medicine (2022)
Fatty acid translocase/cluster of differentiation 36 (FAT/CD36) is a multifunctional membrane protein activated by a high-fat diet, physical exercise, fatty acids (FAs), leptin, and insulin. The principal function of FAT/CD36 is to facilitate the transport of long-chain fatty acids through cell membranes such as myocytes, adipocytes, heart, and liver. Under high-energy expenditure, the different isoforms of FAT/CD36 in the plasma membrane and mitochondria bind to the mobilization and oxidation of FAs. Furthermore, FAT/CD36 is released in its soluble form and becomes a marker of metabolic dysfunction. Studies with healthy animals and humans show that physical exercise and a high-lipid diet increase FAT/CD36 expression and caloric expenditure. However, several aspects such as obesity, diabetes, Single Nucleotide polymorphisms (SNPs), and oxidative stress affect the normal FAs metabolism and function of FAT/CD36, inducing metabolic disease. Through a comprehensive systematic review of primary studies, this work aimed to document molecular mechanisms related to FAT/CD36 in FAs oxidation and trafficking in skeletal muscle under basal conditions, physical exercise, and diet in healthy individuals.
Keyphrases
- fatty acid
- adipose tissue
- high fat diet
- skeletal muscle
- insulin resistance
- systematic review
- oxidative stress
- type diabetes
- nk cells
- physical activity
- metabolic syndrome
- cardiovascular disease
- weight loss
- heart failure
- endothelial cells
- stem cells
- poor prognosis
- single cell
- long non coding rna
- dna damage
- mesenchymal stem cells
- high fat diet induced
- hydrogen peroxide
- glycemic control
- heat shock
- signaling pathway
- induced apoptosis
- case control