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来自Goto-Kakizaki和链脲佐菌素诱导的糖尿病大鼠模型的离体动脉的功能异常。

Functional abnormalities in isolated arteries from Goto-Kakizaki and streptozotocin-treated diabetic rat models.

作者信息

Brøndum E, Nilsson H, Aalkjaer C

机构信息

The Water and Salt Research Center, Institute of Physiology and Biophysics, University of Aarhus, Denmark.

出版信息

Horm Metab Res. 2005 Apr;37 Suppl 1:56-60. doi: 10.1055/s-2005-861370.

Abstract

Several different rat models have been developed for both type 1 and type 2 diabetes with the aim of displaying specific traits of diabetes. For example, a review on nephropathy associated with type 2 diabetes included 16 different rodent models ; new models are still being developed. The large number of different models developed for different traits makes it difficult to choose the right model for a given study. It is often a problem that the models are not sufficiently characterized, which makes it easy to misinterpret data or even come to the wrong conclusions. In this brief review, we will concentrate on the functional responses obtained in vitro from mesenteric arteries and aortic segments from rat models of diabetes. Since it is beyond the scope of this review to overview all different rodent models of diabetes, we will focus on two commonly used models of diabetes, namely the streptozotocin (STZ)-induced type 1 diabetic rat model and the inbred type 2 diabetic Goto-Kakizaki (GK)-rat model.

摘要

为了展现糖尿病的特定特征,已经开发了几种不同的1型和2型糖尿病大鼠模型。例如,一篇关于2型糖尿病相关肾病的综述纳入了16种不同的啮齿动物模型;新的模型仍在不断开发中。针对不同特征开发的大量不同模型使得为特定研究选择合适的模型变得困难。模型特征不够充分往往是个问题,这很容易导致数据解读错误甚至得出错误结论。在这篇简短的综述中,我们将专注于从糖尿病大鼠模型的肠系膜动脉和主动脉段体外获得的功能反应。由于概述所有不同的糖尿病啮齿动物模型超出了本综述的范围,我们将重点关注两种常用的糖尿病模型,即链脲佐菌素(STZ)诱导的1型糖尿病大鼠模型和近交系2型糖尿病Goto-Kakizaki(GK)大鼠模型。

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