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本文引用的文献

1
Oxidative phosphorylation: unique regulatory mechanism and role in metabolic homeostasis.氧化磷酸化:独特的调节机制及其在代谢稳态中的作用
J Appl Physiol (1985). 2017 Mar 1;122(3):611-619. doi: 10.1152/japplphysiol.00715.2016. Epub 2016 Oct 27.
2
Regulation of metabolism: the work-to-rest transition in skeletal muscle.新陈代谢的调节:骨骼肌的工作-休息转换
Am J Physiol Endocrinol Metab. 2016 Apr 15;310(8):E633-E642. doi: 10.1152/ajpendo.00512.2015. Epub 2016 Feb 2.
3
Regulation of metabolism: the rest-to-work transition in skeletal muscle.新陈代谢的调节:骨骼肌从休息到工作的转变。
Am J Physiol Endocrinol Metab. 2015 Nov 1;309(9):E793-801. doi: 10.1152/ajpendo.00355.2015. Epub 2015 Sep 22.
4
Mitochondrial cytochrome c oxidase: Mechanism of action and role in regulating oxidative phosphorylation: Reply to Pannala, Beard, and Dash.线粒体细胞色素c氧化酶:作用机制及在调节氧化磷酸化中的作用:对帕纳拉、比尔德和达什的回复
J Appl Physiol (1985). 2015 Jul 15;119(2):158. doi: 10.1152/japplphysiol.00349.2015.
5
Letter to the Editor: Mitochondrial cytochrome c oxidase: mechanism of action and role in regulating oxidative phosphorylation.致编辑的信:线粒体细胞色素c氧化酶:作用机制及在调节氧化磷酸化中的作用
J Appl Physiol (1985). 2015 Jul 15;119(2):157. doi: 10.1152/japplphysiol.00290.2015.
6
Programming and regulation of metabolic homeostasis.代谢稳态的编程与调控
Am J Physiol Endocrinol Metab. 2015 Mar 15;308(6):E506-17. doi: 10.1152/ajpendo.00544.2014. Epub 2015 Jan 20.
7
Mitochondrial cytochrome c oxidase: mechanism of action and role in regulating oxidative phosphorylation.线粒体细胞色素c氧化酶:作用机制及在调节氧化磷酸化中的作用
J Appl Physiol (1985). 2014 Dec 15;117(12):1431-9. doi: 10.1152/japplphysiol.00737.2014. Epub 2014 Oct 16.
8
Mitochondrial cytochrome c oxidase and control of energy metabolism: measurements in suspensions of isolated mitochondria.线粒体细胞色素c氧化酶与能量代谢调控:分离线粒体悬液中的测量
J Appl Physiol (1985). 2014 Dec 15;117(12):1424-30. doi: 10.1152/japplphysiol.00736.2014. Epub 2014 Oct 16.
9
Eukaryotic origins: How and when was the mitochondrion acquired?真核生物的起源:线粒体是如何以及何时获得的?
Cold Spring Harb Perspect Biol. 2014 Jul 18;6(12):a015990. doi: 10.1101/cshperspect.a015990.
10
Regulation of cellular metabolism: programming and maintaining metabolic homeostasis.细胞代谢的调控:编程与维持代谢稳态
J Appl Physiol (1985). 2013 Dec;115(11):1583-8. doi: 10.1152/japplphysiol.00894.2013. Epub 2013 Oct 10.

氧化磷酸化:调节作用及其在细胞和组织代谢中的作用。

Oxidative phosphorylation: regulation and role in cellular and tissue metabolism.

机构信息

Department of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

出版信息

J Physiol. 2017 Dec 1;595(23):7023-7038. doi: 10.1113/JP273839. Epub 2017 Oct 29.

DOI:10.1113/JP273839
PMID:29023737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5709332/
Abstract

Oxidative phosphorylation provides most of the ATP that higher animals and plants use to support life and is responsible for setting and maintaining metabolic homeostasis. The pathway incorporates three consecutive near equilibrium steps for moving reducing equivalents between the intramitochondrial [NAD ]/[NADH] pool to molecular oxygen, with irreversible reduction of oxygen to bound peroxide at cytochrome c oxidase determining the net flux. Net flux (oxygen consumption rate) is determined by demand for ATP, with feedback by the energy state ([ATP]/[ADP][P ]) regulating the pathway. This feedback affects the reversible steps equally and independently, resulting in the rate being coupled to ([ATP]/[ADP][P ]) . With increasing energy state, oxygen consumption decreases rapidly until a threshold is reached, above which there is little further decrease. In most cells, [ATP] and [P ] are much higher than [ADP] and change in [ADP] is primarily responsible for the change in energy state. As a result, the rate of ATP synthesis, plotted against [ADP], remains low until [ADP] reaches about 30 μm and then increases rapidly with further increase in [ADP]. The dependencies on energy state and [ADP] near the threshold can be fitted by the Hill equation with a Hill coefficients of about -2.6 and 4.2, respectively. The homeostatic set point for metabolism is determined by the threshold, which can be modulated by the PO2 and intramitochondrial [NAD ]/[NADH]. The ability of oxidative phosphorylation to precisely set and maintain metabolic homeostasis is consistent with it being permissive of, and essential to, development of higher plants and animals.

摘要

氧化磷酸化提供了高等动物和植物用来支持生命的大部分 ATP,并负责设定和维持代谢稳态。该途径整合了三个连续的近平衡步骤,用于将还原当量从线粒体内部的[NAD]/[NADH]池转移到分子氧,不可逆地将氧还原为与细胞色素 c 氧化酶结合的过氧化物,决定净流量。净流量(耗氧量)由 ATP 的需求决定,能量状态([ATP]/[ADP][P ])的反馈调节途径。这种反馈对可逆步骤产生同等和独立的影响,导致该速率与[ATP]/[ADP][P ]耦合。随着能量状态的增加,耗氧量迅速下降,直到达到一个阈值,超过这个阈值,耗氧量几乎没有进一步下降。在大多数细胞中,[ATP]和[P ]都远远高于[ADP],[ADP]的变化主要负责能量状态的变化。因此,以[ADP]为横坐标绘制的 ATP 合成速率在[ADP]达到约 30 μm 之前一直保持较低水平,然后随着[ADP]的进一步增加而迅速增加。在接近阈值时,对能量状态和[ADP]的依赖性可以用 Hill 方程拟合,Hill 系数分别约为-2.6 和 4.2。代谢的稳态设定点由阈值决定,阈值可以通过 PO2 和线粒体内部[NAD]/[NADH]进行调节。氧化磷酸化能够精确地设定和维持代谢稳态,这与其对高等植物和动物的发育是允许的和必不可少的是一致的。