MoBioFood Research Group, Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, C/Marcel·li Domingo 1, Tarragona, 43007, Spain.
Section for Nutrition Research, Department of Metabolism, Digestion, and Reproduction, Hammersmith Hospital, Imperial College London, London, W12 0NN, UK.
Mol Nutr Food Res. 2020 Aug;64(16):e2000303. doi: 10.1002/mnfr.202000303. Epub 2020 Jul 8.
A grape-seed proanthocyanidin extract (GSPE) interacts at the intestinal level, enhancing glucagon-like peptide-1 (GLP-1) and peptide YY (PYY) release, which modulate appetite and glucose homeostasis. Thus, enhancing L-cell numbers could be a strategy to promote hormone production, providing a potential strategy for obesity and type-2 diabetes mellitus (T2DM) treatment.
Mice ileum organoids are used to evaluate the long-term effects of GSPE and two of its main components, epicatechin (EC) and gallic acid (GA), on intestinal differentiation. Hormone levels are determined using RIA and ELISA kits, and gene expression of transcription factors involved in intestinal cell differentiation, as well as markers of different cell types, are assessed by real-time qPCR. GSPE upregulates enterohormone gene expression and content, as well as the pan-endocrine marker chromogranin A. GSPE also modulates the temporal gene expression profile of early and late transcription factors involved in L-cell differentiation. Furthermore, GSPE upregulates goblet cell (Muc2) and enterocyte (sucraseisomaltase) markers, while downregulating stem cell markers (Lgr5+). Although EC and GA modified enterohormone release, they do not reproduce GSPE effects on transcription factor's profile.
This study shows the potential role of GSPE in promoting enteroendocrine differentiation, effect that is not mediated by EC or GA.
葡萄籽原花青素提取物 (GSPE) 在肠道水平发挥作用,增强胰高血糖素样肽-1 (GLP-1) 和肽 YY (PYY) 的释放,从而调节食欲和葡萄糖稳态。因此,增加 L 细胞数量可能是促进激素产生的一种策略,为肥胖症和 2 型糖尿病 (T2DM) 的治疗提供了一种潜在策略。
使用小鼠回肠类器官来评估 GSPE 及其两种主要成分表儿茶素 (EC) 和没食子酸 (GA) 对肠道分化的长期影响。使用 RIA 和 ELISA 试剂盒测定激素水平,并用实时 qPCR 测定参与肠道细胞分化的转录因子以及不同细胞类型标志物的基因表达。GSPE 上调肠激素基因的表达和含量,以及全内分泌标志物嗜铬粒蛋白 A。GSPE 还调节参与 L 细胞分化的早期和晚期转录因子的时间基因表达谱。此外,GSPE 上调杯状细胞 (Muc2) 和肠细胞 (蔗糖酶异麦芽糖酶) 标志物,同时下调干细胞标志物 (Lgr5+)。尽管 EC 和 GA 改变了肠激素的释放,但它们不能复制 GSPE 对转录因子谱的影响。
本研究表明 GSPE 具有促进肠内分泌细胞分化的潜力,这种作用不是由 EC 或 GA 介导的。