Murugesan Priya, Zhang Yixuan, Youn Ji Youn, Cai Hua
Division of Molecular Medicine, Department of Anesthesiology, Division of Cardiology, Department of Medicine, David Geffen School of Medicine at University of California Los Angeles, United States.
Division of Molecular Medicine, Department of Anesthesiology, Division of Cardiology, Department of Medicine, David Geffen School of Medicine at University of California Los Angeles, United States.
Redox Biol. 2022 Sep;55:102348. doi: 10.1016/j.redox.2022.102348. Epub 2022 May 26.
Limited medical therapies have been implemented for the treatment of the devastating cardiorespiratory disease of pulmonary hypertension (PH) while none of which is sufficiently effective to stop or regress development of PH. We have previously shown that netrin-1, an axon-guiding protein during development, protects against ischemia reperfusion injury induced myocardial infarction via modest and stable production of nitric oxide (NO) and attenuation of oxidative stress. Since NO deficiency and oxidative stress-mediated vascular remodeling play important roles in the pathogenesis of PH, our present study investigated therapeutic effects on PH of netrin-1 and its derived small peptides. Infused into mice for 3 weeks during exposure to hypoxia, netrin-1 and netrin-1 derived small peptides V1, V2 or V3 substantially alleviated pathophysiological and molecular features of PH, as indicated by abrogated increases in mean pulmonary artery pressure (mPAP) and right ventricular systolic pressure (RVSP), attenuated right ventricular hypertrophy, diminished vascular remodeling of medial thickening and upregulation in smooth muscle alpha-actin (SMA) and proliferative cell nuclear antigen (PCNA), and alleviated perivascular and peribronchial fibrosis reflected by collagen deposition. NO bioavailability was substantially improved by treatment with netrin-1 and netrin-1 derived small peptides, while hypoxia induced increases in total superoxide production and eNOS uncoupling activity were all attenuated. These dual mechanisms of increasing NO bioavailability and decreasing oxidative stress at the same time, underlie robust protective effects on PH of netrin-1 and its derived small peptides, which are different from existing medications that primarily target NO signaling alone. Our data for the first time demonstrate intriguing findings that netrin-1 and netrin-1 derived small peptides can be used as novel and robust therapeutics for the treatment of PH.
针对肺动脉高压(PH)这种毁灭性的心肺疾病,目前实施的医学治疗方法有限,而且没有一种方法能充分有效地阻止或逆转PH的发展。我们之前已经表明,netrin-1是一种发育过程中的轴突导向蛋白,它通过适度稳定地产生一氧化氮(NO)和减轻氧化应激,来保护心脏免受缺血再灌注损伤诱导的心肌梗死。由于NO缺乏和氧化应激介导的血管重塑在PH的发病机制中起重要作用,我们目前的研究调查了netrin-1及其衍生的小肽对PH的治疗效果。在暴露于低氧环境的小鼠中输注3周后,netrin-1及其衍生的小肽V1、V2或V3显著减轻了PH的病理生理和分子特征,表现为平均肺动脉压(mPAP)和右心室收缩压(RVSP)的升高被消除,右心室肥厚减轻,血管中层增厚的重塑减弱,平滑肌α-肌动蛋白(SMA)和增殖细胞核抗原(PCNA)的上调减少,以及胶原沉积所反映的血管周围和支气管周围纤维化减轻。用netrin-1及其衍生的小肽治疗可显著提高NO的生物利用度,同时低氧诱导的总超氧化物生成增加和eNOS解偶联活性均减弱。增加NO生物利用度和同时降低氧化应激的这两种双重机制,是netrin-1及其衍生的小肽对PH具有强大保护作用的基础,这与主要单独靶向NO信号的现有药物不同。我们的数据首次证明了有趣的发现,即netrin-1及其衍生的小肽可作为治疗PH的新型强效疗法。