Nejvíce citovaný článek - PubMed ID 26047380
Melanocortin-4 receptor gene mutations in obese Slovak children
Leptin-melanocortin pathway plays an essential role in the body weight regulation. Enhanced melanocortin signaling in the hypothalamus results in both decreased food intake and increased energy expenditure. The discovery of monogenic obesities with dysfunction of melanocortin-4 receptor (MC4R) greatly contributed to understanding of energy balance regulation. This review presents phenotypical characterization and prevalence of the MC4R gene mutations. Genome-wide association studies revealed that MC4R gene is significantly related not only to monogenic obesities but also to common obesity. An interaction of variants in the MC4R gene with fat mass and obesity associated (FTO) gene significantly increases the risk for obesity, particularly in adolescence. On the other hand, about 15 % of the MC4R gene variants result in a gain of function that protects against obesity and is associated with favorable metabolic profile. Long-term attempts to activate the MC4R have recently been finalized by a discovery of setmelanotide, a novel specific MC4R agonist that is devoid of untoward cardiovascular side-effects. The employment of specific MC4R agonists may open new horizons not only in the treatment of rare monogenic obesities but also in some common obesities where stimulation of MC4R could be achieved.
- MeSH
- alfa-MSH farmakologie MeSH
- celogenomová asociační studie MeSH
- cílená molekulární terapie MeSH
- látky proti obezitě farmakologie MeSH
- lidé MeSH
- mutace * MeSH
- obezita farmakoterapie genetika metabolismus MeSH
- receptor melanokortinový typ 4 genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- alfa-MSH MeSH
- látky proti obezitě MeSH
- receptor melanokortinový typ 4 MeSH