Protective effect of olmesartan against cardiac ischemia/reperfusion injury in spontaneously hypertensive rats

被引:9
作者
Lu, Xin [1 ,2 ]
Bi, Yan-Wen [1 ]
Chen, Ke-Biao [2 ]
Wang, Hong-Yue [2 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Cardiovasc Surg, 107 Wen Hua Xi Rd, Jinan 250012, Shandong, Peoples R China
[2] Taian City Cent Hosp, Dept Cardiovasc Surg, Tai An 271000, Shandong, Peoples R China
关键词
spontaneously hypertensive rats; ischemia/reperfusion injury; high mobility group box 1; hypoxia-inducible factor-1 alpha; olmesartan;
D O I
10.3892/etm.2015.2373
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Olmesartan, as a new angiotensin II receptor blocker, has shown beneficial effects on cardiovascular diseases. Nevertheless, the effect of olmesartan on ischemia/reperfusion (I/R) injury in the hypertensive heart has not been investigated. Therefore, the present study aimed to investigate the effect of olmesartan on I/R injury in spontaneously hypertensive rats (SHRs). Experimental groups were designed with a 2x2 factorial design for olmesartan and I/R effects. In the I/R group, the left anterior descending coronary artery (LAD) was ligated for 40 min followed by a 180-min reperfusion. In the sham group, SHRs underwent the same surgical procedure as the I/R group, with the exception that the suture passed under the LAD without being tightened. In the Olm-I/R group, the SHRs received olmesartan (5 mg/kg) for 4 weeks prior to surgery and other procedures were the same as for the I/R group. In the Olm-sham group, the SHRs received olmesartan (5 mg/kg) for 4 weeks prior to surgery and other procedures were the same as for the sham group. Infarct size was measured for the I/R and Olm-I/R groups. Blood pressure (BP), serum creatine kinase (CK), left ventricular mass index (LVMI), high mobility group box 1 (HMGB1) protein expression levels and hypoxia-inducible factor-1 alpha (HIF-1 alpha) mRNA expression levels were measured for all four groups. Olmesartan significantly reduced BP and LVMI in the olmesartan-treated SHRs compared with those in the SHRs that were not treated with olmesartan. HMGB1 and HIF-1 alpha expression levels were significantly decreased in the Olm-sham and Olm-I/R groups compared with those in the sham and I/R groups, respectively. The proportional increase in HIF-1 alpha expression due to I/R was greater in the olmesartan-treated rats than in the untreated rats. Serum CK levels were significantly reduced in the Olm-I/R group compared with those in the I/R group. In conclusion, olmesartan ameliorates left ventricular hypotrophy and protects the heart against I/R injury in addition to lowing BP in SHRs. The protective effect of olmesartan may be partly due to its antioxidative and anti-inflammatory properties.
引用
收藏
页码:2081 / 2087
页数:7
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