Capillary-Mitochondrial Oxygen Transport in Muscle: Paradigm Shifts.

IF 3.8 Q2 CELL BIOLOGY Function (Oxford, England) Pub Date : 2023-01-01 DOI:10.1093/function/zqad013
David C Poole, Timothy I Musch
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引用次数: 1

Abstract

When exercising humans increase their oxygen uptake (V̇O2) 20-fold above rest the numbers are staggering: Each minute the O2 transport system - lungs, cardiovascular, active muscles - transports and utilizes 161 sextillion (10 21) O2 molecules. Leg extension exercise increases the quadriceps muscles' blood flow 100-times; transporting 17 sextillion O2 molecules per kilogram per minute from microcirculation (capillaries) to mitochondria powering their cellular energetics. Within these muscles, the capillary network constitutes a prodigious blood-tissue interface essential to exchange O2 and carbon dioxide requisite for muscle function. In disease, microcirculatory dysfunction underlies the pathophysiology of heart failure, diabetes, hypertension, pulmonary disease, sepsis, stroke and senile dementia. Effective therapeutic countermeasure design demands knowledge of microvascular/capillary function in health to recognize and combat pathological dysfunction. Dated concepts of skeletal muscle capillary (from the Latin capillus meaning 'hair') function prevail despite rigorous data-supported contemporary models; hindering progress in the field for future and current students, researchers and clinicians. Following closely the 100th anniversary of August Krogh's 1920 Nobel Prize for capillary function this Evidence Review presents an anatomical and physiological development of this dynamic field: Constructing a scientifically defensible platform for our current understanding of microcirculatory physiological function in supporting blood-mitochondrial O2 transport. New developments include: 1. Putative roles of red blood cell aquaporin and rhesus channels in determining tissue O2 diffusion. 2. Recent discoveries regarding intramyocyte O2 transport. 3. Developing a comprehensive capillary functional model for muscle O2 delivery-to-V̇O2 matching. 4. Use of kinetics analysis to discriminate control mechanisms from collateral or pathological phenomena.

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肌肉中的毛细血管-线粒体氧运输:范式转变。
当人们运动时,他们的氧气吸吸量(V / O2)是休息时的20倍,这个数字是惊人的:每分钟氧气运输系统——肺、心血管、活动肌肉——运输和使用161万亿(10 / 21)个氧气分子。腿部伸展运动使股四头肌的血流量增加100倍;每公斤每分钟从微循环(毛细血管)向线粒体输送17万亿氧分子,为细胞能量提供动力。在这些肌肉中,毛细血管网络构成了一个巨大的血液组织界面,对交换肌肉功能所必需的氧气和二氧化碳至关重要。在疾病中,微循环功能障碍是心衰、糖尿病、高血压、肺病、败血症、中风和老年性痴呆的病理生理学基础。有效的治疗对策设计需要微血管/毛细血管功能的健康知识,以识别和对抗病理功能障碍。尽管有严格的数据支持的现代模型,但骨骼肌毛细血管(源自拉丁语capillus,意为“毛发”)功能的过时概念仍然盛行;阻碍了未来和现在的学生、研究人员和临床医生在该领域的进步。紧跟奥古斯特·克拉夫(August Krogh)获得1920年诺贝尔毛细血管功能奖100周年,本证据综述介绍了这一动态领域的解剖学和生理学发展:为我们目前对支持血液-线粒体O2运输的微循环生理功能的理解构建一个科学的可辩护的平台。新的发展包括:1;红细胞水通道蛋白和恒河通道在决定组织氧扩散中的假定作用。2. 关于心肌细胞内氧转运的最新发现。3.建立肌肉O2输送- v / O2匹配的综合毛细血管功能模型。4. 利用动力学分析来区分控制机制与附带现象或病理现象。
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审稿时长
3 weeks
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