Department of Cardiovascular Medicine Faculty of Medical Sciences Kyushu University Fukuoka Japan.
Division of Cardiovascular Medicine Research Institute of Angiocardiology Faculty of Medical Sciences Kyushu University Fukuoka Japan.
J Am Heart Assoc. 2021 Apr 6;10(7):e019247. doi: 10.1161/JAHA.120.019247. Epub 2021 Mar 31.
Background Recent accumulating evidence suggests that toll-like receptor 9 (TLR9) is involved in the pathogenesis of cardiovascular diseases. However, its role in pulmonary hypertension remains uncertain. We hypothesized that TLR9 is involved in the development of pulmonary hypertension. Methods and Results A rat model of monocrotaline-induced pulmonary hypertension was used to investigate the effects of TLR9 on hemodynamic parameters, vascular remodeling, and survival. Monocrotaline-exposed rats significantly showed increases in plasma levels of mitochondrial DNA markers, which are recognized by TLR9, TLR9 activation in the lung, and mRNA level in the lung on day 14 after monocrotaline injection. Meanwhile, monocrotaline-exposed rats showed elevated right ventricular systolic pressure, total pulmonary vascular resistance index and vascular remodeling, together with macrophage accumulation on day 21. In the preventive protocol, administration (days -3 to 21 after monocrotaline injection) of selective (E6446) or nonselective TLR9 inhibitor (chloroquine) significantly ameliorated the elevations of right ventricular systolic pressure and total pulmonary vascular resistance index as well as vascular remodeling and macrophage accumulation on day 21. These inhibitors also significantly reduced NF-κB activation and mRNA levels to a similar extent. In the short-term reversal protocol, E646 treatment (days 14-17 after monocrotaline injection) almost normalized NF-κB activation and mRNA level, and reduced macrophage accumulation. In the prolonged reversal protocol, E6446 treatment (days 14-24 after monocrotaline injection) reversed total pulmonary vascular resistance index and vascular remodeling, and improved survival in monocrotaline-exposed rats. Conclusions TLR9 is involved in the development of pulmonary hypertension concomitant via activation of the NF-κB‒IL-6 pathway. Inhibition of TLR9 may be a novel therapeutic strategy for pulmonary hypertension.
最近越来越多的证据表明,Toll 样受体 9(TLR9)参与了心血管疾病的发病机制。然而,其在肺动脉高压中的作用尚不清楚。我们假设 TLR9 参与了肺动脉高压的发生。
使用野百合碱诱导的肺动脉高压大鼠模型来研究 TLR9 对血流动力学参数、血管重构和生存率的影响。野百合碱暴露的大鼠在野百合碱注射后第 14 天明显表现出线粒体 DNA 标志物(TLR9 识别的标志物)的血浆水平升高、肺中 TLR9 激活和肺中 mRNA 水平升高。同时,野百合碱暴露的大鼠在第 21 天表现出右心室收缩压、总肺血管阻力指数和血管重构升高,以及巨噬细胞积聚增加。在预防性方案中,在野百合碱注射后(第-3 天至 21 天)给予选择性(E6446)或非选择性 TLR9 抑制剂(氯喹)可显著改善第 21 天右心室收缩压和总肺血管阻力指数的升高以及血管重构和巨噬细胞积聚。这些抑制剂还以相似的程度显著降低 NF-κB 激活和 mRNA 水平。在短期逆转方案中,E646 治疗(野百合碱注射后第 14-17 天)几乎使 NF-κB 激活和 mRNA 水平正常化,并减少巨噬细胞积聚。在延长的逆转方案中,E6446 治疗(野百合碱注射后第 14-24 天)逆转了总肺血管阻力指数和血管重构,并改善了野百合碱暴露大鼠的生存率。
TLR9 通过激活 NF-κB-IL6 途径参与肺动脉高压的发生。TLR9 的抑制可能是肺动脉高压的一种新的治疗策略。