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单基因肥胖小鼠中的糖尿病:db/db小鼠及其在心脏后果研究中的应用。

Diabetes in mice with monogenic obesity: the db/db mouse and its use in the study of cardiac consequences.

作者信息

Belke Darrell D, Severson David L

机构信息

The University of Calgary, Calgary, AB, Canada.

出版信息

Methods Mol Biol. 2012;933:47-57. doi: 10.1007/978-1-62703-068-7_4.

Abstract

The leptin receptor deficient db/db mouse has served as a rodent model for obesity and type 2 diabetes for more than 40 years. Diabetic features in db/db mice follow an age-dependent progression, with early insulin resistance followed by an insulin secretory defect resulting in profound hyperglycemia. Diabetic db/db mice have been utilized to assess the cardiac consequences of diabetes, specifically evidence for a distinct diabetic cardiomyopathy. The db/db model is characterized by a contractile function deficit in the heart which becomes manifest 8-10 weeks after birth. Metabolic changes include an increased reliance on fatty acids and a decreased reliance on glucose as a fuel source for oxidative metabolism within the heart. As a mouse model for type 2 diabetes, both drug treatment and transgenic manipulation have proven beneficial towards improving metabolism and contractile function. The db/db mouse model has provided a useful resource to understand and treat the type 2 diabetic condition.

摘要

瘦素受体缺陷的db/db小鼠作为肥胖和2型糖尿病的啮齿动物模型已超过40年。db/db小鼠的糖尿病特征呈年龄依赖性进展,早期出现胰岛素抵抗,随后出现胰岛素分泌缺陷,导致严重的高血糖。糖尿病db/db小鼠已被用于评估糖尿病的心脏后果,特别是明确的糖尿病性心肌病的证据。db/db模型的特征是心脏收缩功能缺陷,在出生后8-10周表现出来。代谢变化包括心脏内氧化代谢对脂肪酸的依赖性增加,对葡萄糖作为燃料来源的依赖性降低。作为2型糖尿病的小鼠模型,药物治疗和转基因操作已被证明对改善代谢和收缩功能有益。db/db小鼠模型为理解和治疗2型糖尿病提供了有用的资源。

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