Shen Xia, Ye Gang, Metreveli Naira S, Epstein Paul N
Department of Pediatrics, University of Louisville, KY, USA.
Methods Mol Med. 2005;112:379-88. doi: 10.1385/1-59259-879-x:379.
Diabetic cardiomyopathy is a common chronic complication leading to heightened risk of heart failure among diabetic patients. In this chapter, we describe the methods for maintenance and breeding of two diabetic animal models, OVE26 and Agouti mice, for type 1 and type 2 diabetes, respectively. To understand the pathological mechanism, antioxidants such as manganese superoxide dismutase are overexpressed specifically in hearts of diabetic mice. Methods utilized to produce cardiac-targeted transgenic mice are presented in this chapter. Diabetic cardiomyopathy is evaluated in control, diabetic and transgene-protected diabetic animals by measuring contractility of isolated cardiomyocytes. Preparation and contractile analysis of cardiac myocytes are described in detail. Diabetic cardiomyocytes exhibit impaired contractility as well as delayed relaxation, and cardiac-overexpressed antioxidant transgenes are shown to reverse this damage.
糖尿病性心肌病是一种常见的慢性并发症,会增加糖尿病患者发生心力衰竭的风险。在本章中,我们分别描述了用于维持和繁殖两种糖尿病动物模型OVE26和刺豚鼠小鼠的方法,它们分别用于1型和2型糖尿病研究。为了解其病理机制,超氧化物歧化酶等抗氧化剂在糖尿病小鼠心脏中特异性过表达。本章介绍了制备心脏靶向转基因小鼠所采用的方法。通过测量分离心肌细胞的收缩性,对对照、糖尿病和转基因保护的糖尿病动物的糖尿病性心肌病进行评估。详细描述了心肌细胞的制备和收缩性分析。糖尿病心肌细胞表现出收缩性受损以及舒张延迟,而心脏过表达抗氧化剂转基因可逆转这种损伤。