已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Bifidobacterium bifidum reduces apoptosis in the intestinal epithelium in necrotizing enterocolitis

双歧杆菌 细胞凋亡 体内 医学 坏死性小肠结肠炎 免疫学 生物 内科学 双歧杆菌 生物化学 发酵 生物技术 乳酸菌
作者
Ludmila Khailová,Sarah K. Mount Patrick,Kelly M. Arganbright,Melissa D. Halpern,Toshi Kinouchi,Bohuslav Dvořák
出处
期刊:American Journal of Physiology-gastrointestinal and Liver Physiology [American Physiological Society]
卷期号:299 (5): G1118-G1127 被引量:132
标识
DOI:10.1152/ajpgi.00131.2010
摘要

Necrotizing enterocolitis (NEC) is a devastating intestinal disease of neonates, and clinical studies suggest the beneficial effect of probiotics in NEC prevention. Recently, we have shown that administration of Bifidobacterium bifidum protects against NEC in a rat model. Intestinal apoptosis can be suppressed by activation of cyclooxygenase-2 (COX-2) and increased production of prostaglandin E(2) (PGE(2)). The present study investigates the effect of B. bifidum on intestinal apoptosis in the rat NEC model and in an intestinal epithelial cell line (IEC-6), as a mechanism of protection against mucosal injury. Premature rats were divided into the following three groups: dam fed, hand fed with formula (NEC), or hand fed with formula supplemented with B. bifidum (NEC + B. bifidum). Intestinal Toll-like receptor-2 (TLR-2), COX-2, PGE(2), and apoptotic regulators were measured. The effect of B. bifidum was verified in IEC-6 cells using a model of cytokine-induced apoptosis. Administration of B. bifidum increased expression of TLR-2, COX-2, and PGE(2) and significantly reduced apoptosis in the intestinal epithelium of both in vivo and in vitro models. The Bax-to-Bcl-w ratio was shifted toward cell survival, and the number of cleaved caspase-3 positive cells was markedly decreased in B. bifidum-treated rats. Experiments in IEC-6 cells showed anti-apoptotic effect of B. bifidum. Inhibition of COX-2 signaling blocked the protective effect of B. bifidum treatment in both in vivo and in vitro models. In conclusion, oral administration of B. bifidum activates TLR-2 in the intestinal epithelium. B. bifidum increases expression of COX-2, which leads to higher production of PGE(2) in the ileum and protects against intestinal apoptosis associated with NEC. This study indicates the ability of B. bifidum to downregulate apoptosis in the rat NEC model and in IEC-6 cells by a COX-2-dependent matter and suggests a molecular mechanism by which this probiotic reduces mucosal injury and preserves intestinal integrity.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Jasper应助大侦探皮卡丘采纳,获得10
4秒前
12秒前
SciGPT应助浚稚采纳,获得10
16秒前
敲一下叮关注了科研通微信公众号
16秒前
21秒前
王永文发布了新的文献求助10
22秒前
Ava应助btbu2015采纳,获得10
23秒前
25秒前
xiao完成签到,获得积分10
25秒前
泥巴发布了新的文献求助10
25秒前
25秒前
STZHEN完成签到,获得积分10
27秒前
香蕉又夏完成签到,获得积分10
28秒前
29秒前
顾天宇发布了新的文献求助10
31秒前
dew完成签到,获得积分20
37秒前
SciGPT应助wzz采纳,获得10
37秒前
小二郎应助btbu2015采纳,获得10
39秒前
43秒前
香蕉又夏发布了新的文献求助10
49秒前
顾天宇完成签到,获得积分10
51秒前
寻道图强应助Micheal采纳,获得10
51秒前
532完成签到 ,获得积分10
53秒前
chen某完成签到,获得积分10
55秒前
1分钟前
浚稚发布了新的文献求助10
1分钟前
可爱的函函应助xiao采纳,获得10
1分钟前
big佳完成签到,获得积分10
1分钟前
ccm应助qyn1234566采纳,获得10
1分钟前
1分钟前
1分钟前
1分钟前
big佳发布了新的文献求助10
1分钟前
1分钟前
1分钟前
1分钟前
赫鲁晓夫发布了新的文献求助10
1分钟前
泥巴发布了新的文献求助10
1分钟前
xiao发布了新的文献求助10
1分钟前
cxin发布了新的文献求助10
1分钟前
高分求助中
Teaching Social and Emotional Learning in Physical Education 900
Plesiosaur extinction cycles; events that mark the beginning, middle and end of the Cretaceous 800
Chinese-English Translation Lexicon Version 3.0 500
Recherches Ethnographiques sue les Yao dans la Chine du Sud 500
Two-sample Mendelian randomization analysis reveals causal relationships between blood lipids and venous thromboembolism 500
[Lambert-Eaton syndrome without calcium channel autoantibodies] 460
Aspect and Predication: The Semantics of Argument Structure 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2395099
求助须知:如何正确求助?哪些是违规求助? 2098519
关于积分的说明 5288648
捐赠科研通 1825913
什么是DOI,文献DOI怎么找? 910359
版权声明 559972
科研通“疑难数据库(出版商)”最低求助积分说明 486551