Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Front Endocrinol (Lausanne). 2022 May 4;13:884501. doi: 10.3389/fendo.2022.884501. eCollection 2022.
Decreased circulating levels of food-intake-regulating gut hormones have been observed in type 2 diabetes and obesity. However, it is still unknown if this is due to decreased secretion from the gut mucosal cells or due to extra-intestinal processing of hormones.
We measured intestinal hormone content and assessed morphological differences in the intestinal mucosa by histology and immunohistochemistry. Secretion of hormones and absorption of glucose and bile acids (BA) were assessed in isolated perfused mouse intestine.
GIP (glucose-dependent insulinotropic polypeptide) and SS (somatostatin) contents were higher in the duodenum of control mice (p < 0.001, and <0.01). Duodenal GLP-1 (glucagon-like peptide-1) content (p < 0.01) and distal ileum PYY content were higher in DIO mice (p < 0.05). Villus height in the jejunum, crypt depth, and villus height in the ileum were increased in DIO mice (p < 0.05 and p = 0.001). In the distal ileum of DIO mice, more immunoreactive GLP-1 and PYY cells were observed (p = 0.01 and 0.007). There was no difference in the absorption of glucose and bile acids. Distal secretion of SS tended to be higher in DIO mice (p < 0.058), whereas no difference was observed for the other hormones in response to glucose or bile acids.
Our data suggest that differences regarding production and secretion are unlikely to be responsible for the altered circulating gut hormone levels in obesity, since enteroendocrine morphology and hormone secretion capacity were largely unaffected in DIO mice.
在 2 型糖尿病和肥胖症患者中,观察到调节食物摄入的肠道激素循环水平降低。然而,目前尚不清楚这是由于肠道黏膜细胞分泌减少,还是由于激素的肠外处理所致。
我们通过组织学和免疫组织化学方法测量了肠道激素含量,并评估了肠道黏膜的形态学差异。通过分离灌注的小鼠肠道评估激素分泌以及葡萄糖和胆汁酸(BA)的吸收。
与对照组相比,(p < 0.001 和 <0.01),控制组小鼠十二指肠中 GIP(葡萄糖依赖性胰岛素释放多肽)和 SS(生长抑素)含量较高。(p < 0.01),DIO 小鼠十二指肠 GLP-1(胰高血糖素样肽-1)含量和回肠 PYY 含量较高(p < 0.05)。DIO 小鼠空肠绒毛高度、隐窝深度和回肠绒毛高度增加(p < 0.05 和 p = 0.001)。在 DIO 小鼠的回肠远端,观察到更多的 GLP-1 和 PYY 免疫反应细胞(p = 0.01 和 0.007)。葡萄糖和胆汁酸的吸收没有差异。DIO 小鼠的 SS 远端分泌倾向于更高(p < 0.058),而葡萄糖或胆汁酸对其他激素的反应没有差异。
我们的数据表明,生产和分泌方面的差异不太可能是肥胖症中循环肠道激素水平改变的原因,因为 DIO 小鼠的肠内分泌形态和激素分泌能力基本不受影响。