Institut National de la Santé et de la Recherche Médicale (INSERM), U1220, Université Paul Sabatier, UPS, Institut de Recherche en Santé Digestive et Nutrition (IRSD), CHU Purpan, Place du Docteur Baylac, CS 60039, 31024 Toulouse Cedex 3, France; NeuroMicrobiota, European Associated Laboratory (EAL) INSERM/UCL, France.
Institut National de la Santé et de la Recherche Médicale (INSERM), U1048, Université Paul Sabatier, UPS, Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), CHU Rangueil, 1 Avenue Jean Poulhès, BP84225, 31432 Toulouse Cedex 4, France.
Mol Metab. 2018 Apr;10:100-108. doi: 10.1016/j.molmet.2018.01.020. Epub 2018 Jan 31.
Decreasing duodenal contraction is now considered as a major focus for the treatment of type 2 diabetes. Therefore, identifying bioactive molecules able to target the enteric nervous system, which controls the motility of intestinal smooth muscle cells, represents a new therapeutic avenue. For this reason, we chose to study the impact of oral galanin on this system in diabetic mice.
Enteric neurotransmission, duodenal contraction, glucose absorption, modification of gut-brain axis, and glucose metabolism (glucose tolerance, insulinemia, glucose entry in tissue, hepatic glucose metabolism) were assessed.
We show that galanin, a neuropeptide expressed in the small intestine, decreases duodenal contraction by stimulating nitric oxide release from enteric neurons. This is associated with modification of hypothalamic nitric oxide release that favors glucose uptake in metabolic tissues such as skeletal muscle, liver, and adipose tissue. Oral chronic gavage with galanin in diabetic mice increases insulin sensitivity, which is associated with an improvement of several metabolic parameters such as glucose tolerance, fasting blood glucose, and insulin.
Here, we demonstrate that oral galanin administration improves glucose homeostasis via the enteric nervous system and could be considered a therapeutic potential for the treatment of T2D.
降低十二指肠收缩被认为是治疗 2 型糖尿病的主要关注点。因此,鉴定能够靶向控制肠道平滑肌细胞运动的肠神经系统的生物活性分子代表了一种新的治疗途径。出于这个原因,我们选择研究口服甘丙肽对糖尿病小鼠中这个系统的影响。
评估肠神经传递、十二指肠收缩、葡萄糖吸收、肠道-大脑轴的改变以及葡萄糖代谢(葡萄糖耐量、胰岛素血症、组织葡萄糖摄取、肝葡萄糖代谢)。
我们表明,甘丙肽是一种在小肠中表达的神经肽,通过刺激肠神经元释放一氧化氮来减少十二指肠收缩。这与下丘脑一氧化氮释放的改变有关,有利于代谢组织(如骨骼肌、肝脏和脂肪组织)中的葡萄糖摄取。在糖尿病小鼠中,口服慢性甘丙肽灌胃增加了胰岛素敏感性,这与改善多种代谢参数有关,如葡萄糖耐量、空腹血糖和胰岛素。
在这里,我们证明口服甘丙肽给药通过肠神经系统改善葡萄糖稳态,可被视为治疗 2 型糖尿病的潜在治疗方法。