MYOCARDIAL PROTECTION BY NHE-1 INHIBITION

NHE-1 抑制对心肌的保护

• 批准号: 6662580
• 负责人: Raul Jaime Gazmuri
• 金额: $ 27.3万
• 依托单位: ROSALIND FRANKLIN UNIV OF MEDICINE & SCI
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-09-30 至 2006-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6662580
• 关键词: cardiopulmonary resuscitation; cardiovascular injury; chemoprevention; cytoprotection; eicosanoids; heart disorder chemotherapy; high energy compound; inhibitor /antagonist; ischemia; myocardium; nonhuman therapy evaluation; oxidative stress; sodium hydrogen exchanger; swine; vasomotion; ventricular fibrillation

DESCRIPTION (provided by applicant): The current proposal is for studies on the mechanisms of myocardial protection associated with inhibition of the sarcolemmal Na+-H+ exchanger isoform-1 (NHE-1). Studies are conducted in a porcine model of whole-body ischemia induced by ventricular fibrillation (VF) in which resuscitation is either attempted using conventional closed-chest resuscitation or simulated using peripheral cardiopulmonary bypass, according to four specific aims designed to study 1) the mechanisms by which NHE-1 inhibition ameliorates ischemic contracture during resuscitation from VF, 2) the mechanisms by which post-resuscitation ventricular ectopic activity is reduced after NHE-1inhibition, 3) the late post-resuscitation effects of NHE-1 inhibition on cardiovascular and neurological function, and 4) the effects of NHE-1 inhibition when instituted before the onset of VF on subsequent resuscitation and survival. The mechanisms of ischemic contracture are investigated by measuring myocardial blood flow (fluorescent microspheres) and oxidative injury (isoprostane levels) in a closed-chest resuscitation model and by measuring myocardial Na+ and high-energy nucleotides under conditions of controlled coronary blood flow using cardiopulmonary bypass. The mechanisms of post-resuscitation ectopic activity are investigated by recording monophasic action potentials in relation to NHE-1 inhibition, Na+-Ca2+ exchanger inhibition, and sarcolemmal K+ATP channel blockade. The late post-resuscitation outcome is assess by using implantable sensors measuring blood pressure, the electrocardiogram, temperature, and mobility over a period of 7 days post-resuscitation. Finally, the effects of pretreatment with NHE-1 inhibition are compared with those when treatment is started during the resuscitation effort. Interventions that can increase outcome after onset of VF (even by a small fraction) could have a dramatic public health effect by saving thousands of lives.

描述（由申请人提供）： 目前的建议是研究与心肌保护有关的机制， 抑制肌膜Na+-H+交换器亚型-1（NHE-1）。 研究是在一个 由心室纤维性颤动（VF）诱导的全身缺血的猪模型，其中使用常规的闭胸复苏尝试复苏或使用外周心肺转流模拟复苏，根据四个特定的目的，设计用于研究1）NHE-1抑制改善VF复苏期间缺血性挛缩的机制，2）NHE-1抑制后复苏后心室异位活动减少的机制，3）NHE-1抑制对心血管和神经功能的复苏后晚期效应，以及4）在VF发作之前开始抑制NHE-1对随后的复苏和存活的影响。 通过测量心肌血流量来研究缺血性挛缩的机制 （荧光微球）和氧化损伤（异前列腺素水平），并通过在使用心肺转流术的受控冠状动脉血流的条件下测量心肌Na+和高能核苷酸。 的机制 复苏后异位活动的研究通过记录单相动作电位， 与NHE-1抑制、Na+-Ca 2+交换抑制和肌膜K+ATP通道的关系 封锁 通过使用植入式传感器测量复苏后7天内的血压、心电图、体温和活动性来评估复苏后晚期结果。 最后，将用NHE-1抑制预处理的效果与在复苏努力期间开始治疗的效果进行比较。 可以增加VF发作后的结果（即使是一小部分）的干预措施可以通过挽救数千人的生命而产生巨大的公共卫生影响。