Morrell Eric D, Tsai Ben M, Crisostomo Paul R, Wang Meijing, Markel Troy A, Lillemoe Keith D, Meldrum Daniel R
Sections of General and Cardiothoracic Surgery, Department of Surgery, Indiana University Medical Center, Indianapolis, IN 46202, USA.
J Mol Cell Cardiol. 2006 Jun;40(6):751-60. doi: 10.1016/j.yjmcc.2006.03.431. Epub 2006 May 11.
Hypoxic pulmonary vasoconstriction (HPV) and pulmonary hypertension present a common and formidable clinical problem for practicing intensivists, thoracic, transplant, and trauma surgeons. The Redox Theory for the mechanisms of HPV has provided researchers with a new understanding of the etiology behind HPV that has opened the door to many new avenues of therapy for the disease. Potassium channels have been proposed to be the main mediator contributing to HPV, and treatment concepts that attempt to manipulate the function and number of those channels have been explored. Additionally, attempts to transfer genes that express the formation of specific potassium channels directly into pulmonary hypertensive lungs have proven to be very promising. Finally, rho kinase (ROK) has been discovered to play a very central role in the formation of hypoxia-induced pulmonary hypertension, and the advent of very specific ROK inhibitors has shown positive clinical results. The purposes of this review are to: (1) briefly discuss some of the basic mechanisms that undergird HPV, including the Redox Theory for the mechanisms of HPV; (2) address current research involving treatments concepts related to ion channels; (3) report on research involving gene therapy to combat pulmonary hypertension; and (4) examine potential therapeutic avenues associated with inhibition of rho kinase.
低氧性肺血管收缩(HPV)和肺动脉高压是执业重症医学专家、胸外科医生、移植外科医生和创伤外科医生面临的一个常见且棘手的临床问题。HPV机制的氧化还原理论为研究人员提供了对HPV病因的新认识,为该疾病开辟了许多新的治疗途径。钾通道被认为是导致HPV的主要介质,人们已经探索了试图操纵这些通道功能和数量的治疗理念。此外,将表达特定钾通道形成的基因直接导入肺动脉高压肺的尝试已被证明非常有前景。最后,已发现rho激酶(ROK)在低氧诱导的肺动脉高压形成中起核心作用,非常特异性的ROK抑制剂的出现已显示出积极的临床结果。本综述的目的是:(1)简要讨论支撑HPV的一些基本机制,包括HPV机制的氧化还原理论;(2)阐述当前涉及与离子通道相关治疗理念的研究;(3)报告涉及对抗肺动脉高压基因治疗的研究;(4)探讨与抑制rho激酶相关的潜在治疗途径。