Chia Chee W, Carlson Olga D, Liu David D, González-Mariscal Isabel, Santa-Cruz Calvo Sara, Egan Josephine M
Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland
Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.
Am J Physiol Endocrinol Metab. 2017 Sep 1;313(3):E359-E366. doi: 10.1152/ajpendo.00080.2017. Epub 2017 Jun 27.
The mechanisms regulating incretin secretion are not fully known. Human obesity is associated with altered incretin secretion and elevated endocannabinoid levels. Since cannabinoid receptors (CBRs) are expressed on incretin-secreting cells in rodents, we hypothesized that endocannabinoids are involved in the regulation of incretin secretion. We compared plasma glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) responses during oral glucose tolerance test (OGTT) in 20 lean and 20 obese participants from the Baltimore Longitudinal Study of Aging (BLSA). Next, we recruited 20 healthy men to evaluate GIP and GLP-1 responses during OGTT after administering placebo or nabilone (CBR agonist) in a randomized, double-blind, crossover fashion. Compared with the BLSA lean group, the BLSA obese group had significantly higher fasting and post-OGTT GIP levels, but similar fasting GLP-1 and significantly lower post-OGTT GLP-1 levels. In the nabilone vs. placebo study, when compared with placebo, nabilone resulted in significantly elevated post-dose fasting GIP levels and post-OGTT GIP levels, but no change in post-dose fasting GLP-1 levels together with significantly lower post-OGTT GLP-1 levels. Glucose levels were not different with both interventions. We conclude that elevated GIP levels in obesity are likely a consequence of increased endocannabinoid levels. CBRs exert tonic control over GIP secretion, which may have a homeostatic effect in suppressing GLP-1 secretion. This raises the possibility that gut hormones are influenced by endocannabinoids.
调节肠促胰岛素分泌的机制尚未完全明确。人类肥胖与肠促胰岛素分泌改变及内源性大麻素水平升高有关。由于啮齿动物中肠促胰岛素分泌细胞表达大麻素受体(CBRs),我们推测内源性大麻素参与肠促胰岛素分泌的调节。我们比较了巴尔的摩纵向衰老研究(BLSA)中20名瘦人和20名肥胖参与者在口服葡萄糖耐量试验(OGTT)期间血浆葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽-1(GLP-1)的反应。接下来,我们招募了20名健康男性,以随机、双盲、交叉方式在服用安慰剂或纳必隆(CBR激动剂)后评估OGTT期间的GIP和GLP-1反应。与BLSA瘦人组相比,BLSA肥胖组空腹和OGTT后GIP水平显著更高,但空腹GLP-1水平相似,OGTT后GLP-1水平显著更低。在纳必隆与安慰剂的研究中,与安慰剂相比,纳必隆导致给药后空腹GIP水平和OGTT后GIP水平显著升高,但给药后空腹GLP-1水平无变化,同时OGTT后GLP-1水平显著更低。两种干预措施下血糖水平无差异。我们得出结论,肥胖中GIP水平升高可能是内源性大麻素水平升高的结果。CBRs对GIP分泌发挥张力性控制作用,这可能在抑制GLP-1分泌方面具有稳态效应。这增加了肠道激素受内源性大麻素影响的可能性。