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Role of extracellular proton-sensing OGR1 in regulation of insulin secretion and pancreatic β-cell functions

机译:细胞外质子感应OGR1在调节胰岛素分泌和胰腺β细胞功能中的作用

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References(74) Cited-By(4) Insulin secretion with respect to pH environments has been investigated for a long time but its mechanism remains largely unknown. Extracellular pH is usually maintained at around 7.4 and, its change has been thought to occur in non-physiological situations. Acidification takes place under ischemic and inflammatory microenvironments, where stimulation of anaerobic glycolysis results in the production of lactic acid. In addition to ionotropic ion channels, such as transient receptor potential V1 (TRPV1) and acid-sensing ion channels (ASICs), metabotropic proton-sensing G protein-coupled receptors (GPCRs) have also been identified recently as proton-sensing machineries. While ionotropic ion channels usually sense strong acidic pH, proton-sensing GPCRs sense pH of 7.6 to 6.0 and have been shown to mediate a variety of biological actions in neutral and mildly acidic pH environments. Studies with receptor knockout mice have revealed that proton-sensing receptors, including ovarian cancer G protein-coupled receptor 1 (OGR1), a proton-sensing GPCRs, play a role in the regulation of insulin secretion and glucose metabolism under physiological conditions. Small molecule 3,5-disubstituted isoxazoles have recently been identified as OGR1 agonists working at neutral pH and have been shown to stimulate pancreatic β-cell differentiation and insulin synthesis. Thus, proton-sensing OGR1 may be an important player for insulin secretion and a potential target for improving β-cell function.
机译:参考文献(74)By-By(4)关于pH值环境的胰岛素分泌已进行了很长时间的研究,但其机理仍不清楚。细胞外pH通常维持在7.4左右,并且其变化被认为是在非生理情况下发生的。酸化发生在缺血性和炎症性微环境下,其中厌氧糖酵解的刺激导致乳酸的产生。除了离子型离子通道,例如瞬态受体电位V1(TRPV1)和酸敏感离子通道(ASICs)外,近代质子敏感的G蛋白偶联受体(GPCR)也已被鉴定为质子敏感的机器。离子型离子通道通常可感应强酸性pH,而质子感应GPCR可感应7.6至6.0的pH,并已证明在中性和弱酸性pH环境中可介导多种生物学作用。对受体敲除小鼠的研究表明,质子敏感受体,包括卵巢癌G蛋白偶联受体1(OGR1),质子敏感GPCR,在生理条件下可调节胰岛素分泌和葡萄糖代谢。小分子3,5-二取代异恶唑最近被鉴定为在中性pH下起作用的OGR1激动剂,并已显示出可刺激胰腺β细胞分化和胰岛素合成。因此,质子感应OGR1可能是胰岛素分泌的重要参与者,也是改善β细胞功能的潜在目标。

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