pH REGULATION IN HEART CELLS

心脏细胞的 pH 调节

• 批准号: 7252561
• 负责人: KENNETH W SPITZER
• 金额: $ 16.71万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 1989
• 资助国家: 美国
• 起止时间: 1989-07-01 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7252561
• 关键词: Accounting; Acidosis; Acids; Adverse effects; Area; Arrhythmia; Bicarbonates; Buffers; Cardiac; Cardiac Myocytes; Cells; Coupled; Coupling; Dependence; Diffusion; Fluo-3; Functional disorder; Goals; Heart; Heart Atrium; Image; Individual; Ions; Kinetics; Measures; Mediating; Movement; Muscle; Muscle Cells; Myocardial Ischemia; Myocardium; Patch-Clamp Techniques; Permeability; Property; Protocols documentation; Purkinje Cells; Regulation; Role; Sarcoplasmic Reticulum; System; Techniques; Testing; Title; Ventricular; Work; base; carbonate dehydratase; cell type; design; extracellular; fluorescence imaging; heart cell; insight; research study; response; spatiotemporal

DESCRIPTION (provided by applicant): The broad, long-term goal of this work is to establish a comprehensive understanding of the role of pH in cardiac function at the cellular level. Changes in intracellular pH (pHi) and extracellular pH have profound effects on electrical activity, excitation-contraction coupling and contraction in the heart, which accounts in part for the arrhythmias and contractile dysfunction elicited by myocardial ischemia. Compared to the information available for ventricular muscle, much less is known concerning pHi regulation, the effects of pH on Ca 2+ handling, and intra- and intercellular H+ diffusion in cardiac myocytes that lack transverse tubules (Purkinje and atrial). The protocols described in this project focus primarily on these two cell types and are designed to help fill this gap using fluorescence imaging and patch pipette techniques. The specific aims include: 1. Characterize the effect of intracellular acidosis on excitation-contraction coupling in atria/and Purkinje myocytes. The goal here is to determine the effects of acidosis on Ca 2+ current (L and T type), the spatiotemporal profile of the Ca2+ transient, Ca 2+ handling by the sarcoplasmic reticulum and intracellular Ca 2+ diffusion in these cell types. The response of [Ca2+]i to spatially confined changes in pHi will also be studied. 2. Characterize the electrogenic properties of Na-HCO3 cotransport in ventricular, atrial and Purkinje myocytes. The objective here is to test the hypothesis that Na-HCO3 cotransport is electrogenic in these cell types. 3.Characterize the properties of pH_ regulatory systems in cardiac Purkinje myocytes. The objective here is to determine the kinetic properties and pH-dependence of Na-H exchange (NHE), Na-HCO3 cotransport (NBC) and HCO3-CI exchange (AE) in isolated Purkinje myocytes and to test the hypothesis that CI-OH exchange (CHE) is operational in this cell type. 4. Characterize intra- and intercellular H+ diffusion in atrial and Purkinje cells. The goal here is to determine the intracellular H+ diffusion coefficient within single cells and the junctional permeability H+ coefficient between pairs of electrically coupled myocytes and to test the hypothesis that both parameters are modulated by carbonic anhydrase.

描述（由申请人提供）：这项工作的广泛，长期目标是在细胞水平上建立对pH在心功能中的作用的全面理解。细胞内pH （pHi）和细胞外pH的变化对心脏的电活动、兴奋-收缩耦合和收缩有深远的影响，这是心肌缺血引起心律失常和收缩功能障碍的部分原因。与心室肌的可用信息相比，关于pHi调节，pH对ca2 +处理的影响，以及缺乏横小管的心肌细胞内和细胞间H+扩散的了解要少得多（Purkinje和心房）。在这个项目中描述的协议主要集中在这两种细胞类型，旨在帮助填补这一空白，使用荧光成像和贴片移液技术。具体目标包括：