免疫系统
肠道菌群
菌群(微生物学)
炎症
免疫学
免疫
糖尿病
抗生素
2型糖尿病
医学
生物
细菌
微生物学
内分泌学
遗传学
作者
Sweta Patel,Dipeeka Mandaliya,Bhumika Prajapati,Sunny Kumar,Sriram Seshadri
出处
期刊:Endocrine, metabolic & immune disorders
[Bentham Science Publishers]
日期:2019-01-09
卷期号:19 (3): 349-357
被引量:7
标识
DOI:10.2174/1871530319666181224122115
摘要
Gut microbiota is currently targeted for various diseases especially metabolic disorders such as diabetes. Our strategy is to alter gut microflora via specific antibiotic to reduce load of inflammation in the liver that increases as a result of high carbohydrate diet. Th1, Th17 and Treg are important immune cell types which decide the type of inflammatory response. Liver is tolerogenic in nature with low Th17/Treg ratio. In diabetics, this ratio decreases even more, and can cause liver trauma.The present study tries to find relationship between gut flora and immune cells such as Th1/Th17/Treg and their role in liver metabolism using diet induced diabetic mice model.Upon alteration of flora using Cefdinir in different forms, one could help lower the level of Treg cells thus increasing the ratio. Gut flora is strongly associated with the immunity in the liver. Targeted alteration of gut flora helps us to restore insulin sensitivity.Colon targeted Cefdinir gives more promising results, opens colonic bacteria as target for improving gut, liver inflammation and insulin sensitivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI