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在起始饲料中添加阿斯巴甜可加速断奶前羔羊小肠上皮细胞周期,并刺激胰高血糖素样肽-2 的分泌。

Aspartame supplementation in starter accelerates small intestinal epithelial cell cycle and stimulates secretion of glucagon-like peptide-2 in pre-weaned lambs.

机构信息

Laboratory of Gastrointestinal Microbiology, Jiangsu Key Laboratory of Gastrointestinal Nutrition and Animal Health, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.

National Centre for International Research on Animal Gut Nutrition, Nanjing Agricultural University, Nanjing, China.

出版信息

J Anim Physiol Anim Nutr (Berl). 2019 Sep;103(5):1338-1350. doi: 10.1111/jpn.13159. Epub 2019 Jul 25.

Abstract

The objective of this study was to test the hypothesis that aspartame supplementation in starter diet accelerates small intestinal cell cycle by stimulating secretion and expression of glucagon-like peptide -2 (GLP-2) in pre-weaned lambs using animal and cell culture experiments. In vivo, twelve 14-day-old lambs were selected and allocated randomly to two groups; one was treated with plain starter diet (Con, n = 6) and the other was treated with starter supplemented with 200 mg of aspartame/kg starter (APM, n = 6). Results showed that the lambs received APM treatment for 35 d had higher (p < .05) GLP-2 concentration in the plasma and greater jejunum weight/live body weight (BW) and jejunal crypt depth. Furthermore, APM treatment significantly upregulated (p < .05) the mRNA expression of cyclin D1 in duodenum; and cyclin A2, cyclin D1, cyclin-dependent kinases 6 (CDK6) in jejunum; and cyclin A2, cyclin D1, CDK4 in ileum. Moreover, APM treatment increased (p < .05) the mRNA expression of glucagon (GCG), insulin-like growth factor 1 (IGF-1) in the jejunum and ileum and mRNA expression of GLP-2 receptor (GLP-2R) in the jejunum. In vitro, when jejunal cells were treated with GLP-2 for 2 hr, the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) OD, IGF-1 concentration, and the mRNA expression of IGF-1, cyclin D1 and CDK6 were increased (p < .05). Furthermore, IGF-1 receptor (IGF-1R) inhibitor decreased (p < .05) the mRNA expression of IGF-1, cyclin A2, cyclin D1 and CDK6 in GLP-2 treatment jejunal cells. These results suggest that aspartame supplementation in starter accelerates small intestinal cell cycle that may, in part, be related to stimulate secretion and expression of GLP-2 in pre-weaning lambs. Furthermore, GLP-2 can indirectly promote the proliferation of jejunal cells mainly through the IGF-1 pathway. These findings provide new insights into nutritional interventions that promote the development of small intestines in young ruminants.

摘要

本研究旨在通过动物和细胞培养实验验证阿斯巴甜(甜味剂)补充启动饲料可通过刺激胰高血糖素样肽-2(GLP-2)分泌和表达来加速断奶前羔羊的小肠细胞周期这一假说。在体内,选择 12 只 14 日龄羔羊并随机分配到两组;一组用普通启动饲料(Con,n=6)处理,另一组用添加 200mg/kg 阿斯巴甜的启动饲料(APM,n=6)处理。结果表明,接受 APM 处理 35d 的羔羊血浆中 GLP-2 浓度更高(p<0.05),空肠重量/活体重(BW)和空肠隐窝深度更大。此外,APM 处理显著上调(p<0.05)十二指肠中环素 D1 mRNA 的表达;空肠中环素 A2、环素 D1、细胞周期蛋白依赖性激酶 6(CDK6)和回肠中环素 A2、环素 D1、细胞周期蛋白依赖性激酶 4(CDK4)的表达。此外,APM 处理增加了空肠和回肠中胰高血糖素(GCG)、胰岛素样生长因子 1(IGF-1)mRNA 的表达和空肠中 GLP-2 受体(GLP-2R)的表达。在体外,当用 GLP-2 处理空肠细胞 2 小时时,3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四唑溴盐(MTT)OD、IGF-1 浓度以及 IGF-1、环素 D1 和 CDK6 的 mRNA 表达均增加(p<0.05)。此外,IGF-1 受体(IGF-1R)抑制剂降低了 GLP-2 处理空肠细胞中 IGF-1、环素 A2、环素 D1 和 CDK6 的 mRNA 表达(p<0.05)。这些结果表明,在启动饲料中添加阿斯巴甜可加速小肠细胞周期,这在一定程度上可能与刺激断奶前羔羊 GLP-2 的分泌和表达有关。此外,GLP-2 可以通过 IGF-1 途径间接促进空肠细胞的增殖。这些发现为促进幼反刍动物小肠发育的营养干预提供了新的见解。

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