肠道激素作为外周抗肥胖靶点。

Caroline J Small, Stephen R Bloom
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引用次数: 27

摘要

许多多肽是由胃肠道合成和释放的。虽然它们在调节胃肠功能方面的作用已经为人所知有一段时间了,但现在很明显,它们也会影响饮食行为,从而成为潜在的抗肥胖目标。肽YY (PYY)与胰高血糖素样肽1 (GLP-1)和氧调素一起在餐后从胃肠道l细胞释放。小鼠、大鼠或人外周给药pyy3 -36 (PYY的循环形式)后,对食物摄入有明显的抑制作用。pyy3 -36被认为通过NPY Y2 GPCR介导其作用。肥胖受试者空腹基础PYY水平较低,餐后升高幅度较小。然而,肥胖似乎与PYY抵抗无关(与瘦素无关),外源性输注PYY 3-36导致肥胖组食物摄入量减少30%,瘦组减少31%。胰高血糖素前前基因的产物GLP-1或oxyntomodulin在外周或直接进入中枢神经系统时可减少食物摄入量。此外,两者都被证明可以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。胃促生长素,一种由胃产生的巨大激素,在禁食一段时间后循环增加。通过外周或直接进入中枢神经系统的胃促生长素会增加食物摄入量,长期服用会导致肥胖。进一步注射到正常健康志愿者体内会增加食物摄入量和食欲。胃饥饿素被认为是通过生长激素促分泌受体(GHS-R)起作用的。肥胖是目前英国过早死亡的主要原因,每周导致近1000人死亡。在世界范围内,它的流行正在加速。自然产生的肠道激素的管理可能提供一个长期的治疗方法来控制体重。在这里,我们考虑一些肠道激素的治疗潜力,以及它们在治疗肥胖方面的作用。
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Gut hormones as peripheral anti obesity targets.

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.

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