Targeted Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Ochang, Chungbuk 363-883; Department of Biomolecular Science, University of Science and Technology, Daejeon 305-350, Korea.
Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology, Ochang, Chungbuk 363-883; Department of Functional Genomics, University of Science and Technology, Daejeon 305-350, Korea.
BMB Rep. 2014 Mar;47(3):173-8. doi: 10.5483/bmbrep.2014.47.3.272.
There is rapidly growing interest in the human microbiome because of its implication in metabolic disorders and inflammatory diseases. Consequently, understanding the biology of short chain fatty acids and their receptors has become very important for identifying novel therapeutic avenues. GPR41 and GPR43 have been recognized as the cognate receptors for SCFAs and their roles in metabolism and inflammation have drawn much attention in recent years. GPR43 is highly expressed on immune cells and has been suggested to play a role in inflammatory diseases such as inflammatory bowel disease. Both GPR41 and GPR43 have been implicated in diabetes and obesity via the regulation of adipose tissue and gastrointestinal hormones. So far, many studies have provided contradictory results, and therefore further research is required to validate these receptors as drug targets. We will also discuss the synthetic modulators of GPR41 and GPR43 that are critical to understanding the functions of these receptors.
由于其在代谢紊乱和炎症性疾病中的作用,人类微生物组引起了人们越来越多的兴趣。因此,了解短链脂肪酸及其受体的生物学特性对于确定新的治疗途径变得非常重要。GPR41 和 GPR43 已被确认为 SCFA 的同源受体,近年来,它们在代谢和炎症中的作用引起了广泛关注。GPR43 在免疫细胞上高度表达,并被认为在炎症性疾病(如炎症性肠病)中发挥作用。GPR41 和 GPR43 都通过调节脂肪组织和胃肠道激素与糖尿病和肥胖有关。到目前为止,许多研究提供了相互矛盾的结果,因此需要进一步的研究来验证这些受体作为药物靶点的作用。我们还将讨论 GPR41 和 GPR43 的合成调节剂,这对于理解这些受体的功能至关重要。