ANESTHETICS AND CARDIAC SIGNAL TRANSDUCTION

麻醉剂和心脏信号传导

• 批准号: 7822167
• 负责人: Zeljko J. Bosnjak
• 金额: $ 2.29万
• 依托单位: MEDICAL COLLEGE OF WISCONSIN
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-06-01 至 2010-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7822167
• 关键词: Acute; Address; Affect; Anesthetics; Biochemical; Cardiac; Cavia; Cell Survival; Characteristics; Clinical; Cytoprotection; Data; Elements; Funding; G Protein-Coupled Receptor Signaling; Goals; Grant; Heart; Heart Atrium; Human; Human Activities; Hypoxia; In Vitro; Infarction; Injury; Inner mitochondrial membrane; Investigation; Ischemic Preconditioning; Laboratories; Lipid Bilayers; MAP Kinase Gene; Mediating; Mediator of activation protein; Membrane; Memory; Mitochondria; Molecular; Muscle Cells; Myocardium; Nucleotides; Oxidative Stress; Pathway interactions; Phase; Play; Potassium; Process; Protein Kinase; Reactive Oxygen Species; Reperfusion Injury; Research Personnel; Research Project Summaries; Research Proposals; Role; Signal Pathway; Signal Transduction; Signaling Protein; Techniques; Testing; clinically relevant; mitochondrial K(ATP) channel; preconditioning; programs

DESCRIPTION (provided by applicant): A growing body of experimental and clinical evidence indicates that certain volatile anesthetics precondition the heart against irreversible ischemia/reperfusion injury by activating endogenous protective cellular mechanisms. This phenomenon has been termed the anesthetic-induced preconditioning (APC). During the previous grant cycle, we obtained data from guinea pig hearts to suggest that opening of the KA/ATP channel by anesthetics contributes to APC. Because APC may vary among species, it is important to establish the mechanisms responsible for APC in human myocardium. Therefore, the objective of our proposal is to investigate the signaling pathways responsible for APC in isolated human atrial myocytes and determine the respective roles of sarc and mitoK/ATP channels in cytoprotection produced by volatile anesthetics. This will be accomplished by the use of electrophysiological, biochemical, molecular and immunohistochemical techniques. The major hypothesis to be tested is that in human myocardium the sarc and mitoKar P channels are involved in cytoprotection afforded by acute APC. To pursue this hypothesis we will address the following specific aims: Aim I: To identify cellular pathways by which acute APC modulates the sarCK/ATP channel in human atrial myocytes. Hypothesis: Volatile anesthetics modulate the human sarCK/ATP channel and its sensitivity to nucleotides, protein kinases (PKC, PTK, MAPK) and reactive oxygen species. Aim II: To characterize how APC affects activity of mitOK/ATP channels in intact myocytes, mitochondrial function and mitoK/ATP channels in planar lipid bilayers. Hypothesis: Volatile anesthetics regulate mitochondrial function and activity of the human mitoKare channel via multiple signaling pathways. Aim III: To characterize the efficacy of acute APC on survival of isolated human atrial myocytes. Hypothesis: Sarc and mitOK/ATP channels play a role in cellular protection against ischemic injury afforded by APC, and this protection is anesthetic specific. In summary, this research project will characterize the importance of the KATP channel in human atrial myocytes and evaluate specific signaling pathways that mediate APC in vitro. This proposal represents a comprehensive approach to the significant and clinically relevant phenomenon of volatile anesthetic-induced cardioprotection against ischemia/reperfusion injury.

描述（由申请人提供）： 越来越多的实验和临床证据表明，某些挥发性麻醉剂通过激活内源性保护性细胞机制来预处理心脏，使其免受不可逆的缺血/再灌注损伤。这种现象被称为麻醉诱导的预适应（APC）。在前一个赠款周期中，我们从豚鼠心脏获得的数据表明，麻醉剂开放KA/ATP通道有助于APC。由于APC可能在物种之间存在差异，因此建立人类心肌中APC的机制非常重要。因此，我们的建议的目的是调查的信号通路，负责APC在分离的人心房肌细胞，并确定各自的作用sarc和mitoK/ATP通道的挥发性麻醉剂产生的细胞保护。这将通过使用电生理学、生物化学、分子和免疫组织化学技术来完成。要测试的主要假设是，在人类心肌中，sarc和mitoKar P通道参与急性APC提供的细胞保护。为了实现这一假设，我们将探讨以下具体目标： 目的一：研究急性APC对人心房肌细胞sarCK/ATP通道的调控途径。假设：挥发性麻醉药调节人sarCK/ATP通道及其对核苷酸、蛋白激酶（PKC、PTK、MAPK）和活性氧的敏感性。 目标二：为了表征APC如何影响完整心肌细胞中的mitoK/ATP通道活性、线粒体功能和平面脂质双层中的mitoK/ATP通道。假设：挥发性麻醉剂通过多种信号通路调节线粒体功能和人线粒体钾通道的活性。 目的III：描述急性APC对离体人心房肌细胞存活的功效。假设：Sarc和mitOK/ATP通道在APC对缺血性损伤的细胞保护中起作用，并且这种保护是麻醉特异性的。总之，本研究项目将表征人心房肌细胞中KATP通道的重要性，并评估体外介导APC的特定信号通路。这一建议代表了一个全面的方法，挥发性麻醉剂诱导的心肌缺血/再灌注损伤的重要和临床相关的现象。