Hilzendeger Aline M, Shenoy Vinayak, Raizada Mohan K, Katovich Michael J
Department of Pharmacodynamics, University of Florida, PO Box 100487, Gainesville, FL, 32610, USA.
Curr Hypertens Rep. 2014 Sep;16(9):469. doi: 10.1007/s11906-014-0469-1.
Pulmonary hypertension (PH) is a progressive lung disease characterized by elevated pressure in the lung vasculature, resulting in right-sided heart failure and premature death. The pathogenesis of PH is complex and multifactorial, involving a dysregulated autonomic nervous system and immune response. Inflammatory mechanisms have been linked to the development and progression of PH; however, these are usually restricted to systemic and/or local lung tissue. Inflammation within the CNS, often referred to as neuroinflammation involves activation of the microglia, the innate immune cells that are found specifically in the brain and spinal cord. Microglial activation results in the release of several cytokines and chemokines that trigger neuroinflammation, and has been implicated in the pathogenesis of several disease conditions such as Alzheimer's, Parkinson's, hypertension, atherosclerosis, and metabolic disorders. In this review, we introduce the concept of neuroinflammation in the context of PH, and discuss possible strategies that could be developed for PH therapy based on this concept.
肺动脉高压(PH)是一种进行性肺部疾病,其特征是肺血管系统压力升高,导致右心衰竭和过早死亡。PH的发病机制复杂且多因素,涉及自主神经系统和免疫反应失调。炎症机制与PH的发生和发展有关;然而,这些通常局限于全身和/或局部肺组织。中枢神经系统内的炎症,通常称为神经炎症,涉及小胶质细胞的激活,小胶质细胞是专门存在于脑和脊髓中的固有免疫细胞。小胶质细胞激活导致几种细胞因子和趋化因子的释放,引发神经炎症,并与多种疾病的发病机制有关,如阿尔茨海默病、帕金森病、高血压、动脉粥样硬化和代谢紊乱。在本综述中,我们在PH的背景下介绍神经炎症的概念,并讨论基于这一概念可能开发的用于PH治疗的策略。