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Mechanisms of Bile Acid Signaling and Metabolism following Gastric Bypass

Mechanisms of Bile Acid Signaling and Metabolism following Gastric Bypass
胃绕道手术后胆汁酸信号传导和代谢的机制
批准号:
8927341
负责人:
Vance L Albaugh
金额:
$4.23万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-02 至 2016-04-29

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中文摘要
翻译
描述(由申请人提供):肥胖和糖尿病被认为是新的世界性流行病。Roux-en-Y胃旁路手术(RYGB)是治疗肥胖和相关2型糖尿病最有效的方法。有趣的是,RYGB后的改善在减肥之前就开始了,这些效果的机制尚不清楚。我们实验室最近的发现已经确定胆汁酸对这种代谢改善的重要部分负责。我们的实验室已经成功地建立了与人类相似的RYGB小鼠模型。为了了解胆汁酸在RYGB代谢改善中的潜在作用,我们创建了一种新的小鼠模型,可以在不改变胃解剖结构的情况下将胆汁酸转移到小肠的各个部分。我们的初步研究表明,与RYGB相比,胆道转移到回肠可以更好地减轻体重和防止高脂肪饮食引起的肥胖。这些发现表明胆酸可能是RYGB后肥胖改善和糖尿病治愈的主要信号。与RYGB相比,本研究将研究胆道转移如何改变胆汁酸代谢/动力学和信号传导的分子机制,以产生更有效和持续的体重减轻和对饮食性肥胖的抵抗。这项工作可能会确定新的抗糖尿病和抗肥胖药物靶点,但更重要的是可以确定更简单但更有效的手术治疗肥胖和糖尿病。
英文摘要
DESCRIPTION (provided by applicant): Obesity and diabetes are considered the new worldwide epidemics. It is well accepted that Roux-en-Y gastric bypass (RYGB) surgery is the most effective treatment for obesity and the associated type 2 diabetes. Interestingly, the improvements following RYGB start occurring before weight loss, and the mechanism for these effects is unknown. Recent findings in our laboratory have identified bile acids to be responsible for a significant portion of such metabolic improvements. Our laboratory has been successful in establishing mouse models of RYGB similar to those performed in humans. In an attempt to understand the potential role of bile acids in the metabolic improvements seen with RYGB, we have created a new mouse model that enables diversion of bile acids to various segments of the small intestine without altering the anatomy of the stomach. Our preliminary studies show that biliary diversion to the ileum produces better weight loss and protection from high fat diet-induced obesity than RYGB. These findings suggest that bile acids may be a major signal leading to amelioration of obesity and cure of diabetes after RYGB. This proposal will examine the molecular mechanisms of how bile acid metabolism/kinetics and signaling are altered by biliary diversion to produce more effective and sustained weight loss and resistance to diet- induced obesity compared to RYGB. This work may identify new anti-diabetes and anti-obesity drug targets, but more importantly could identify simpler but more effective surgical treatments for obesity and diabetes.
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Mechanisms of Bile Acid Signaling and Metabolism following Gastric Bypass
Mechanisms of Bile Acid Signaling and Metabolism following Gastric Bypass
ACUTE EFFECTS OF OLANZAPINE ON PLASMA LEPTIN, GLUCOSE TOLERANCE FREE FATTY ACIDS
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