Karpov Andrei A, Vachrushev Nikita S, Shilenko Leonid A, Smirnov Sergey S, Bunenkov Nikolay S, Butskih Maxim G, Chervaev Al-Khalim A, Vaulina Dariya D, Ivkin Dmitry Yu, Moiseeva Olga M, Galagudza Michael M
Institute of Experimental Medicine, Almazov National Medical Research Centre, 2 Akkuratova Street, 197341 St. Petersburg, Russia.
Department of Experimental Pharmacology, State Federal-Funded Educational Institution of Higher Education, Saint Petersburg State Chemical and Pharmaceutical University of the Ministry of Healthcare of the Russian Federation, 14 Professora Popova Street, 197022 St. Petersburg, Russia.
J Cardiovasc Dev Dis. 2023 Jan 23;10(2):40. doi: 10.3390/jcdd10020040.
Chronic thromboembolic pulmonary hypertension (CTEPH) develops in 1.5-2.0% of patients experiencing pulmonary embolism (PE) and is characterized by stable pulmonary artery obstruction, heart failure, and poor prognosis. Little is known about involvement of autonomic nervous system (ANS) in the mechanisms of CTEPH. This study was aimed at evaluation of the effect of vagal and sympathetic denervation, as well as stimulation of the parasympathetic nervous system, on the outcomes of CTEPH in rats. CTEPH was induced by multiple intravenous injections of alginate microspheres. Sympathetic and vagal denervation was performed using unilateral surgical ablation of the stellate ganglion and vagotomy, respectively. Stimulation of the parasympathetic nervous system was carried out by administering pyridostigmine. The effect of neuromodulatory effects was assessed in terms of hemodynamics, histology, and gene expression. The results demonstrated the key role of ANS in the development of CTEPH. Sympathetic denervation as well as parasympathetic stimulation resulted in attenuated pulmonary vascular remodeling. These salutary changes were associated with altered MMP2 and TIMP1 expression in the lung and decreased FGFb level in the blood. Unilateral vagotomy had no effect on physiological and morphological outcomes of the study. The data obtained contribute to the identification of new therapeutic targets for CTEPH treatment.
慢性血栓栓塞性肺动脉高压(CTEPH)在1.5%-2.0%的肺栓塞(PE)患者中发生,其特征为肺动脉阻塞稳定、心力衰竭且预后不良。关于自主神经系统(ANS)在CTEPH发病机制中的作用知之甚少。本研究旨在评估迷走神经和交感神经去神经支配以及副交感神经系统刺激对大鼠CTEPH结局的影响。通过多次静脉注射海藻酸盐微球诱导CTEPH。分别采用单侧手术切除星状神经节和迷走神经切断术进行交感神经和迷走神经去神经支配。通过给予吡啶斯的明刺激副交感神经系统。从血流动力学、组织学和基因表达方面评估神经调节作用的效果。结果表明ANS在CTEPH的发生发展中起关键作用。交感神经去神经支配以及副交感神经刺激导致肺血管重塑减轻。这些有益变化与肺中MMP2和TIMP1表达改变以及血液中FGFb水平降低有关。单侧迷走神经切断术对本研究的生理和形态学结局无影响。所获得的数据有助于确定CTEPH治疗的新靶点。