• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于细胞内ADP扩散受限迁移率的心脏磷酸肌酸能量转运穿梭的理论支持。

Theoretical support for the heart phosphocreatine energy transport shuttle based on the intracellular diffusion limited mobility of ADP.

作者信息

Jacobus W E

出版信息

Biochem Biophys Res Commun. 1985 Dec 31;133(3):1035-41. doi: 10.1016/0006-291x(85)91240-9.

DOI:10.1016/0006-291x(85)91240-9
PMID:4084301
Abstract

Flux rates for phosphate metabolites were calculated using the equation for radial diffusion, assuming heart intracellular conditions and a 5% concentration gradient. The data show that while the flux of phosphocreatine is about 3 times faster than ATP, both are more than two orders of magnitude greater than the known maximum rate of ATP utilization. In contrast, since the concentration of free ADP is very low, its flux is below the maximum rate of ATP turnover, while the flux of creatine is almost 3 orders of magnitude greater than ADP. The data suggest that the rate of high-energy phosphate production could be limited by ADP diffusion, with creatine thus substituting as the primary cytoplasmic-mitochondrial phosphate acceptor.

摘要

在假定心肌细胞内环境及5%浓度梯度的情况下,使用径向扩散方程计算了磷酸代谢物的通量率。数据显示,虽然磷酸肌酸的通量比ATP快约3倍,但两者均比已知的ATP最大利用速率大两个数量级以上。相比之下,由于游离ADP的浓度非常低,其通量低于ATP周转的最大速率,而肌酸的通量几乎比ADP大3个数量级。数据表明,高能磷酸生成速率可能受ADP扩散限制,因此肌酸可作为主要的细胞质-线粒体磷酸受体。

相似文献

1
Theoretical support for the heart phosphocreatine energy transport shuttle based on the intracellular diffusion limited mobility of ADP.基于细胞内ADP扩散受限迁移率的心脏磷酸肌酸能量转运穿梭的理论支持。
Biochem Biophys Res Commun. 1985 Dec 31;133(3):1035-41. doi: 10.1016/0006-291x(85)91240-9.
2
Theoretical modelling of some spatial and temporal aspects of the mitochondrion/creatine kinase/myofibril system in muscle.肌肉中线粒体/肌酸激酶/肌原纤维系统某些时空方面的理论建模。
Mol Cell Biochem. 1998 Jul;184(1-2):249-89.
3
A simple analysis of the "phosphocreatine shuttle".“磷酸肌酸穿梭”的简单分析
Am J Physiol. 1984 May;246(5 Pt 1):C365-77. doi: 10.1152/ajpcell.1984.246.5.C365.
4
Role of phosphocreatine in energy transport in skeletal muscle of bullfrog studied by 31P-NMR.用31P-核磁共振研究磷酸肌酸在牛蛙骨骼肌能量转运中的作用。
Biochim Biophys Acta. 1990 Feb 19;1051(2):144-50. doi: 10.1016/0167-4889(90)90186-h.
5
Respiratory control and the integration of heart high-energy phosphate metabolism by mitochondrial creatine kinase.呼吸控制与线粒体肌酸激酶对心脏高能磷酸代谢的整合作用。
Annu Rev Physiol. 1985;47:707-25. doi: 10.1146/annurev.ph.47.030185.003423.
6
Energy transport from mitochondria to myofibril by a creatine phosphate shuttle in cardiac cells.心肌细胞中通过磷酸肌酸穿梭机制实现能量从线粒体到肌原纤维的转运。
Am J Physiol. 1983 Nov;245(5 Pt 1):C423-7. doi: 10.1152/ajpcell.1983.245.5.C423.
7
Myocardial adaptation during acute hibernation: mechanisms of phosphocreatine recovery.急性冬眠期间的心肌适应性:磷酸肌酸恢复机制
Cardiovasc Res. 1993 Nov;27(11):2044-51. doi: 10.1093/cvr/27.11.2044.
8
Compartmentalized energy transfer in cardiomyocytes: use of mathematical modeling for analysis of in vivo regulation of respiration.心肌细胞中的区室化能量转移:利用数学模型分析体内呼吸调节
Biophys J. 1997 Jul;73(1):428-45. doi: 10.1016/S0006-3495(97)78082-2.
9
Bioenergetic consequences of cardiac phosphocreatine depletion induced by creatine analogue feeding.肌酸类似物喂养诱导的心脏磷酸肌酸耗竭的生物能量后果
J Biol Chem. 1991 Oct 25;266(30):20296-304.
10
Subcellular distribution of phosphagens in isolated perfused rat heart.磷酸原在离体灌注大鼠心脏中的亚细胞分布
FEBS Lett. 1980 Apr 7;112(2):273-6. doi: 10.1016/0014-5793(80)80196-7.

引用本文的文献

1
Timing mechanisms to control heart rhythm and initiate arrhythmias: roles for intracellular organelles, signalling pathways and subsarcolemmal Ca.控制心律和引发心律失常的时间机制:细胞内细胞器、信号通路和肌小节下 Ca 的作用。
Philos Trans R Soc Lond B Biol Sci. 2023 Jun 19;378(1879):20220170. doi: 10.1098/rstb.2022.0170. Epub 2023 May 1.
2
Non-invasive investigation of myocardial energetics in cardiac disease using P magnetic resonance spectroscopy.使用磷磁共振波谱对心脏病患者心肌能量代谢进行无创性研究。
Cardiovasc Diagn Ther. 2020 Jun;10(3):625-635. doi: 10.21037/cdt-20-275.
3
Maturation of Cardiac Energy Metabolism During Perinatal Development.
围产期心脏能量代谢的成熟
Front Physiol. 2018 Jul 19;9:959. doi: 10.3389/fphys.2018.00959. eCollection 2018.
4
Assessing Metabolism and Injury in Acute Human Traumatic Brain Injury with Magnetic Resonance Spectroscopy: Current and Future Applications.利用磁共振波谱评估急性人类创伤性脑损伤中的代谢与损伤:现状与未来应用
Front Neurol. 2017 Sep 12;8:426. doi: 10.3389/fneur.2017.00426. eCollection 2017.
5
Protective effects of traditional Chinese medicine formula NaoShuanTong capsule on haemorheology and cerebral energy metabolism disorders in rats with blood stasis.中药复方脑栓通胶囊对血瘀型大鼠血液流变学及脑能量代谢紊乱的保护作用
Biotechnol Biotechnol Equip. 2014 Jan 2;28(1):140-146. doi: 10.1080/13102818.2014.901678.
6
Incubating isolated mouse EDL muscles with creatine improves force production and twitch kinetics in fatigue due to reduction in ionic strength.在离子强度降低导致疲劳的情况下,用肌酸孵育分离的小鼠 EDL 肌肉可提高其力的产生和抽搐动力学特性。
PLoS One. 2011;6(8):e22742. doi: 10.1371/journal.pone.0022742. Epub 2011 Aug 5.
7
Spatial patterning of metabolism by mitochondria, oxygen, and energy sinks in a model cytoplasm.线粒体、氧气和能量汇在模型细胞质中对代谢的空间模式形成。
Curr Biol. 2008 Apr 22;18(8):586-91. doi: 10.1016/j.cub.2008.03.038. Epub 2008 Apr 10.
8
Nucleotide-gated KATP channels integrated with creatine and adenylate kinases: amplification, tuning and sensing of energetic signals in the compartmentalized cellular environment.与肌酸激酶和腺苷酸激酶整合的核苷酸门控KATP通道:在细胞区室化环境中对能量信号的放大、调节和传感
Mol Cell Biochem. 2004 Jan-Feb;256-257(1-2):243-56. doi: 10.1023/b:mcbi.0000009872.35940.7d.
9
Diffusion control of protein phosphorylation in signal transduction pathways.信号转导通路中蛋白质磷酸化的扩散控制
Biochem J. 2000 Sep 15;350 Pt 3(Pt 3):901-7.
10
In vivo (31)P-NMR diffusion spectroscopy of ATP and phosphocreatine in rat skeletal muscle.大鼠骨骼肌中ATP和磷酸肌酸的体内(31)P-NMR扩散光谱分析
Biophys J. 2000 Apr;78(4):1657-64. doi: 10.1016/S0006-3495(00)76717-8.