- 作者：Ri-Ning Tang ; Lin-Li Lv ; Jian-Dong Zhang ; Hou-Yong Dai ; Qing Li ; Min Zheng ; Jie Ni ; Kun-Ling Ma ; Bi-Cheng Liu ; liubc64@yahoo.com.cn
- 关键词：Cardiac fibrosis ; Diabetes ; Irbesartan ; Endothelial-to-mesenchymal transition ; Rats ; Human aortic endothelial cells
- 刊名：International Journal of Cardiology
- 出版年：2013
- 出版时间：10 January, 2013
- 年：2013
- 卷：162
- 期：2
- 页码：92-99
- 全文大小：2692 K
Background
Emerging evidence has indicated that the endothelial-to-mesenchymal transition (EndMT) is a crucial event during early stages of cardiac fibrosis. In the present study, we first investigated the influence of Irbesartan (Irb) on myocardial EndMT in diabetic rats.Methods
Diabetic rats were divided into two groups: the diabetic group (DM) and the Irb-treated group (DM + Irb). Wistar-Kyoto rats served as controls. The pathological changes were investigated by microscopy. Immunofluorescence was performed to evaluate the co-expression of CD31 and fibroblast-specific protein 1 (FSP1). FSP1 and ¦Á-SMA expressions were detected by RT-PCR and Western blot analysis. EndMT was also studied in human aortic endothelial cells (HAECs) that had been exposed to high glucose (HG) levels.
Results
Increased interstitial fibrosis was detected in the DM group. Double labeling revealed CD31 expression in FSP1-positive cells in the DM group, and this expression was diminished by Irb treatment (P < 0.05). In vitro, we found that HG stimulated angiotensin II synthesis in HAECs. When HAECs were exposed to HG, some of the cells acquired a spindle-shaped morphology and demonstrated a loss of CD31 labeling, which was attenuated by Irb treatment. FSP1 and ¦Á-SMA mRNA and protein expression levels were markedly upregulated in diabetic rats compared to controls, and their expressions were inhibited by Irb treatment (P < 0.05).
Conclusion
The results provide the novel insight that an angiotensin II receptor blocker might prevent diabetic cardiomyopathy by abrogating EndMT in diabetic rats.