Small Caroline J, Bloom Stephen R
Department of Metabolic Medicine, Division of Investigative Science, Imperial College London, Hammersmith Campus, Du Cane Road, London, W12 ONN, UK.
Curr Drug Targets CNS Neurol Disord. 2004 Oct;3(5):379-88. doi: 10.2174/1568007043336950.
Many peptides are synthesised and released from the gastrointestinal tract. Whilst their roles in regulation of gastrointestinal function have been known for some time, it is now evident that they also influence eating behaviour and thus potential anti obesity targets. Peptide YY (PYY) is released post prandially from the gastrointestinal L-cells with glucagon-like peptide 1 (GLP-1) and oxyntomodulin. Following peripheral administration of PYY 3-36, the circulating form of PYY, to mouse, rat or human there is marked inhibition of food intake. PYY 3-36 is thought to mediate its actions through the NPY Y2 GPCR. Obese subjects have lower basal fasting PYY levels and have a smaller post prandial rise. However, obesity does not appear to be associated with resistance to PYY (as it is with leptin) and exogenous infusion of PYY 3-36 results in a reduction in food intake by 30% in an obese group and 31% in a lean group. GLP-1 or oxyntomodulin, products of the prepreglucagon gene, decrease food intake when administered either peripherally or directly into the CNS. In addition, both have been shown to decrease food intake in humans. These effects are thought to be mediated by the GLP-1 receptor. Ghrelin, a huger hormone produced by the stomach, increases in the circulation following a period of fasting. Administration of ghrelin either peripherally or directly into the CNS increases food intake and chronic administration leads to obesity. Further infusion into normal healthy volunteers increases both food intake and appetite. Ghrelin is thought to act through the growth hormone secretagogue receptor (GHS-R). Obesity is the current major cause of premature death in the UK, killing almost 1000 people a week. Worldwide its prevalence is accelerating. The administration of the naturally occurring gut hormone may offer a long-term therapeutic approach to weight control. Here we consider the therapeutic potential of some gut hormones, and the GPCR's through which they act, in the treatment of obesity.
许多肽类物质在胃肠道合成并释放。虽然它们在调节胃肠功能方面的作用已为人所知一段时间,但现在很明显,它们也会影响进食行为,因此是潜在的抗肥胖靶点。餐后,肽YY(PYY)与胰高血糖素样肽1(GLP-1)和胃泌酸调节素一起从胃肠道的L细胞释放出来。给小鼠、大鼠或人类外周注射循环形式的PYY 3-36后,食物摄入量会受到显著抑制。据认为,PYY 3-36通过NPY Y2 G蛋白偶联受体(GPCR)介导其作用。肥胖受试者的基础空腹PYY水平较低,餐后升高幅度较小。然而,肥胖似乎与对PYY的抵抗无关(与瘦素不同),对外源注射PYY 3-36,肥胖组的食物摄入量减少30%,瘦组减少31%。胰高血糖素原基因的产物GLP-1或胃泌酸调节素,无论是外周给药还是直接注入中枢神经系统,都会减少食物摄入量。此外,两者都已被证明能减少人类的食物摄入量。这些作用被认为是由GLP-1受体介导的。胃饥饿素是一种由胃产生的饥饿激素,禁食一段时间后其在循环中的水平会升高。外周或直接向中枢神经系统注射胃饥饿素会增加食物摄入量,长期给药会导致肥胖。进一步向正常健康志愿者注射会增加食物摄入量和食欲。胃饥饿素被认为通过生长激素促分泌素受体(GHS-R)发挥作用。肥胖是英国目前过早死亡的主要原因,每周导致近1000人死亡。在全球范围内,其患病率正在加速上升。给予天然存在的肠道激素可能为体重控制提供一种长期的治疗方法。在这里,我们考虑一些肠道激素及其作用的GPCR在肥胖治疗中的治疗潜力。