Center for Clinical Metabolic Research, Gentofte Hospital, University of Copenhagen, Hellerup, Denmark.
Steno Diabetes Center Copenhagen, Gentofte, Denmark.
Obesity (Silver Spring). 2020 Nov;28(11):2163-2174. doi: 10.1002/oby.22973.
Changes in the secretion of gut-derived peptide hormones have been associated with the metabolic benefits of Roux-en-Y gastric bypass (RYGB) surgery. In this study, the effects of RYGB on anthropometrics, postprandial plasma hormone responses, and mRNA expression in small intestinal mucosa biopsy specimens before and after RYGB were evaluated.
In a cross-sectional study, 20 individuals with obesity undergoing RYGB underwent mixed meal tests and upper enteroscopy with retrieval of small intestinal mucosa biopsy specimens 3 months before and after surgery. Concentrations of circulating gut and pancreatic hormones during mixed meal tests as well as full mRNA sequencing of biopsy specimens were evaluated.
RYGB-induced improvements of body weight and composition, insulin resistance, and circulating cholesterols were accompanied by significant changes in postprandial plasma responses of pancreatic and gut hormones. Global gene expression analysis of biopsy specimens identified 2,437 differentially expressed genes after RYGB, including changes in genes that encode prohormones and G protein-coupled receptors.
RYGB affects the transcription of a wide range of genes, indicating that the observed beneficial metabolic effects of RYGB may rely on a changed expression of several genes in the gut. RYGB-induced changes in the expression of genes encoding signaling peptides and G protein-coupled receptors may disclose new gut-derived treatment targets against obesity and diabetes.
肠道来源的肽激素分泌的变化与 Roux-en-Y 胃旁路(RYGB)手术的代谢益处有关。本研究评估了 RYGB 对肥胖患者 RYGB 前后的人体测量学、餐后血浆激素反应和小肠黏膜活检标本 mRNA 表达的影响。
在一项横断面研究中,20 名接受 RYGB 的肥胖患者在手术前 3 个月进行混合餐试验和上消化道内窥镜检查,并采集小肠黏膜活检标本。评估混合餐试验期间循环肠道和胰腺激素的浓度以及活检标本的全长 mRNA 测序。
RYGB 诱导的体重和成分改善、胰岛素抵抗和循环胆固醇的改善伴随着餐后胰腺和肠道激素反应的显著变化。活检标本的全基因表达分析确定 RYGB 后有 2437 个差异表达基因,包括编码前激素和 G 蛋白偶联受体的基因的变化。
RYGB 影响广泛范围的基因转录,表明 RYGB 观察到的有益代谢效应可能依赖于肠道中几种基因表达的改变。RYGB 诱导的编码信号肽和 G 蛋白偶联受体的基因表达变化可能揭示针对肥胖和糖尿病的新的肠道来源的治疗靶点。