Down-regulation of the human ether-a-go-go-related gene in rat cardiac hypertrophy

• Published in: The American journal of the medical sciences Vol. 341; no. 2; p. 119
• Main Authors: Hu, Chuangjia, Yan, Chunying, Lin, Jijin, Liu, Shukai, Li, Yanyan
• Format: Journal Article
• Language: English
• Published: United States 01.02.2011
• Subjects: Animals; Aorta, Abdominal; Aortic Coarctation - complications; Base Sequence; Disease Models, Animal; DNA Primers - genetics; Down-Regulation; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels - genetics; Ether-A-Go-Go Potassium Channels - metabolism; Female; Humans; Hypertrophy, Left Ventricular - complications; Hypertrophy, Left Ventricular - genetics; Hypertrophy, Left Ventricular - metabolism; Hypertrophy, Left Ventricular - pathology; Long QT Syndrome - etiology; Long QT Syndrome - genetics; Long QT Syndrome - metabolism; Male; Rats; Rats, Sprague-Dawley; RNA, Messenger - genetics; RNA, Messenger - metabolism
• ISSN: 1538-2990
• DOI: 10.1097/MAJ.0b013e3181f73f81

Cardiac hypertrophy is a risk factor for QT prolongation and cardiac sudden death. In this study, the authors examined the expressional regulation on the rat human ether-a-go-go-related gene (HERG), which encodes a structural subunit of the rapid component of the delayed rectifier potassium current (I(Kr)), during myocardial hypertrophy using rat as a model system. Cardiac hypertrophy was established in Sprague-Dawley rats by coarctation of the abdominal aorta [left ventricular hypertrophy (LVH) group]. Sham-operated rats were defined as control group (Ctrl group). Hemodynamic, morphologic and histologic parameters were recorded 6 weeks after operation. In addition, the expression of HERG was also determined using a combination of real-time polymerase chain reaction, Western blot and immunohistochemical analyses. Compared with the sham-operated Ctrl group, abdominal aortic coarctation induced LVH in the LVH group, as evidenced by significantly increased ratios of heart weight/left ventricular weight to body weight and enlarged left ventricular myocytes in the histologic sections. The hemodynamic profile revealed significant increases in heart rate and left ventricular end-diastolic pressure, as well as a decrease in the maximal rate of left ventricular pressure fall in the LVH rats, when compared with the Ctrl rats. Electrocardiograms showed prolonged QT and corrected QT intervals. On the molecular level, a significant reduction of HERG, messengerRNA and protein was observed in LVH group, which was inversely correlated with prolonged corrected QT (r = -0.842, P = 0.000). The expressional down-regulation of HERG gene may constitute a novel mechanism for QT prolongation during cardiac hypertrophy.