Department of Medicine, Queen's University, Kingston, Ontario, Canada.
Physiol Res. 2024 Nov 29;73(S2):S493-S510. doi: 10.33549/physiolres.935431.
Hypoxic pulmonary vasoconstriction (HPV) rapidly and reversibly matches lung ventilation (V) and perfusion (Q), optimizing oxygen uptake and systemic oxygen delivery. HPV occurs in small pulmonary arteries (PA), which uniquely constrict to hypoxia. Although HPV is modulated by the endothelium the core mechanism of HPV resides in PA smooth muscle cells (PASMC). The PASMC's mitochondrial oxygen sensor lies within the electron transport chain (ETC) and includes NDUFS2 in ETC Complex-I. PASMC mitochondria respond to hypoxia by varying production of reactive oxygen species (ROS) and hydrogen peroxide in proportion to alveolar oxygen tension. Hypoxic ROS inhibition results in a state of reduction which triggers a redox-mediated inhibition of oxygen-sensitive, voltage-gated, potassium channels, including Kv1.5 and Kv2.1. Kv channel inhibition depolarizes the PASMC, opening of large-conductance calcium channels (CaL), elevating cytosolic calcium and activating the contractile apparatus. HPV is strongest in small PAs where sensors (hypoxia-responsive mitochondria) and effectors (oxygen-sensitive K+ channels) are enriched. Oxygenation at birth reverses fetal HPV, contributing to the rapid neonatal drop in pulmonary vascular resistance (PVR). A similar mitochon-drial-K+ channel sensor-effector mechanism exists in the ductus arteriosus (DA), however in DASMC it is oxygen-induced increases in mitochondrial ROS that inhibit DASMC K+ channels, causing DA constriction. Atelectasis and pneumonia elicit HPV, which optimises V/Q matching, increasing systemic oxygenation. Whilst HPV in response to localized hypoxia in a single lung lobe does not increase PA pressure; global airway hypoxia, as occurs with altitude or sleep apnea, causes pulmonary hypertension. HPV can be inhibited by drugs, including calcium channel blockers, or used to maintain a dry operative field during single lung anesthesia for lung surgery. HPV does not normally cause lung edema but excessive, heterogenous HPV contributes to high altitude pulmonary edema. HPV is suppressed in COVID-19 pneumonia by a SARS-CoV-2 mitochondriopathy. HPV is a component of the body's homeostatic oxygen sensing system. Keywords: Ductus arteriosus, Redox, NDUFS2, Oxygen sensitive potassium, Channels, High altitude pulmonary edema (HAPE), Mitochondrial electron transport chain, COVID-19 pneumonia, Atelectasis.
低氧性肺血管收缩(HPV)可迅速而可逆地使肺通气(V)和灌注(Q)相匹配,从而优化摄氧量和全身氧输送。HPV 发生于小肺动脉(PA),其独特之处在于对低氧的收缩。尽管 HPV 受内皮细胞调节,但 HPV 的核心机制存在于 PA 平滑肌细胞(PASMC)中。PASMC 的线粒体氧传感器位于电子传递链(ETC)内,ETC 复合物 I 中的 NDUFS2 也包含其中。PASMC 线粒体通过改变活性氧(ROS)和过氧化氢的产生来对低氧做出反应,其产生量与肺泡氧张力成比例。低氧 ROS 抑制导致还原状态,从而触发氧敏感、电压门控、钾通道(包括 Kv1.5 和 Kv2.1)的还原调节抑制。Kv 通道抑制使 PASMC 去极化,大电导钙通道(CaL)开放,细胞浆钙升高,激活收缩装置。HPV 在传感器(低氧反应性线粒体)和效应器(氧敏感 K+通道)丰富的小 PA 中最强。出生时的氧合作用逆转胎儿 HPV,导致肺血管阻力(PVR)的新生儿迅速下降。在动脉导管(DA)中存在类似的线粒体-K+通道传感器-效应器机制,然而,在 DA 平滑肌细胞(DASMC)中,抑制 DASMC K+通道的是线粒体 ROS 的氧诱导增加,导致 DA 收缩。肺不张和肺炎引发 HPV,优化 V/Q 匹配,增加全身氧合。虽然单侧肺叶局部低氧时的 HPV 不会增加 PA 压力;但全身性气道低氧,如高原或睡眠呼吸暂停时发生的低氧,会导致肺动脉高压。HPV 可被药物抑制,包括钙通道阻滞剂,或用于在单肺麻醉期间维持干燥的手术视野,以便进行肺手术。HPV 通常不会引起肺水肿,但过度、异质性的 HPV 导致高原肺水肿。SARS-CoV-2 线粒体病抑制 COVID-19 肺炎中的 HPV。HPV 是人体恒态氧感应系统的一部分。关键词:动脉导管、氧化还原、NDUFS2、氧敏感钾通道、高原肺水肿(HAPE)、线粒体电子传递链、COVID-19 肺炎、肺不张。