Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, Japan.
Hypertens Res. 2010 Dec;33(12):1305-11. doi: 10.1038/hr.2010.189. Epub 2010 Oct 14.
Connective tissue growth factor (CTGF) is a secreted protein that regulates fibrosis. We hypothesized that CTGF is induced in a pressure-overloaded (PO) heart and that blocking the angiotensin II type 1 receptor would reduce CTGF expression. Accordingly, we administered olmesartan and compared its effects with other antihypertensive drugs in a PO heart. CTGF induction was determined in a rat PO model, and olmesartan, hydralazine or saline was continuously administered. The effects of olmesartan on CTGF induction, myocyte hypertrophy and fibrosis were evaluated. The effect of olmesartan on cardiac function was also examined in CTGF- and transforming growth factor-beta 1 (TGF-β1)-infused rats. CTGF was increased in the PO heart 3 days after aortic banding and was markedly distributed around the perivascular fibrotic area. After 28 days, blood pressure was not significantly different in the olmesartan and hydralazine groups, but olmesartan treatment reduced CTGF distribution in PO hearts. Olmesartan was associated with a significantly reduced myocyte hypertrophy index (4.77±0.48 for olmesartan and 6.05±1.45 for saline, P<0.01), fibrosis area (32.0±15.5% compared with the saline group, P<0.05) and serum TGF-β1 level (62.6±10.6 ng ml⁻¹ for olmesartan and 84.4±7.2 ng ml⁻¹ for hydralazine, P<0.05). In addition, cardiac function was significantly preserved in the olmesartan group compared with the saline group. Finally, olmesartan ameliorated the cardiac dysfunction in CTGF- and TGF-β1-infused rats. Olmesartan attenuated CTGF induction, reduced perivascular fibrosis and ameliorated cardiac dysfunction in a PO heart. Our results provide insight into the beneficial effects of olmesartan on PO hearts, independent of blood-pressure lowering.
结缔组织生长因子(CTGF)是一种调节纤维化的分泌蛋白。我们假设 CTGF 在压力超负荷(PO)心脏中被诱导,并且阻断血管紧张素 II 型 1 受体将减少 CTGF 的表达。因此,我们给予奥美沙坦并在 PO 心脏中比较其与其他降压药物的效果。在大鼠 PO 模型中确定 CTGF 诱导,连续给予奥美沙坦、肼屈嗪或生理盐水。评估奥美沙坦对 CTGF 诱导、心肌细胞肥大和纤维化的影响。还在 CTGF 和转化生长因子-β1(TGF-β1)输注大鼠中检查奥美沙坦对心脏功能的影响。主动脉缩窄后 3 天 PO 心脏中 CTGF 增加,并且明显分布在血管周围纤维化区域周围。28 天后,奥美沙坦和肼屈嗪组的血压无显著差异,但奥美沙坦治疗可减少 PO 心脏中的 CTGF 分布。奥美沙坦与心肌细胞肥大指数的显著降低相关(奥美沙坦组为 4.77±0.48,生理盐水组为 6.05±1.45,P<0.01),纤维化面积(与生理盐水组相比为 32.0±15.5%,P<0.05)和血清 TGF-β1 水平(奥美沙坦组为 62.6±10.6ng/ml,肼屈嗪组为 84.4±7.2ng/ml,P<0.05)。此外,奥美沙坦组与生理盐水组相比心脏功能明显保存。最后,奥美沙坦改善了 CTGF 和 TGF-β1 输注大鼠的心脏功能障碍。奥美沙坦减弱了 PO 心脏中的 CTGF 诱导,减少了血管周围纤维化并改善了心脏功能障碍。我们的结果提供了奥美沙坦对 PO 心脏有益作用的见解,独立于降压作用。