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在分离的大鼠心肌细胞中研究线粒体状态、ATP水解、细胞内镁离子浓度([Mg2+]i)和细胞内钙离子浓度([Ca2+]i)之间的关系。

The relationship between mitochondrial state, ATP hydrolysis, [Mg2+]i and [Ca2+]i studied in isolated rat cardiomyocytes.

作者信息

Leyssens A, Nowicky A V, Patterson L, Crompton M, Duchen M R

机构信息

Department of Physiology, University College London, UK.

出版信息

J Physiol. 1996 Oct 1;496 ( Pt 1)(Pt 1):111-28. doi: 10.1113/jphysiol.1996.sp021669.

Abstract
  1. As ATP has a higher affinity for Mg2+ than ADP, the cytosolic magnesium concentration rises upon ATP hydrolysis. We have therefore used the Mg(2+)-sensitive fluorescent indicator Magnesium Green (MgG) to provide an index of changing ATP concentration in single rat cardiomyocytes in response to altered mitochondrial state. 2. In response to FCCP, [Mg2+]i rose towards a plateau coincident with the progression to rigor, which signals ATP depletion. Contamination of the MgG signal by changes in intracellular free Ca2+ concentration (the KD of MgG for Ca2+ is 4.7 microM) was excluded by simultaneous measurement of [Ca2+]i and [Mg2+]i in cells dual loaded with fura-2 and MgG. The response to FCCP was independent of external Mg2+, confirming an intracellular source for the rise in [Mg2+]i. 3. Simultaneous measurements of mitochondrial NAD(P)H autofluorescence and mitochondrial potential (delta psi m; .-1 fluorescence) and of autofluorescence and MgG allowed closer study of the relationship between [Mg2+]i and mitochondrial state. Oligomycin abolished the FCCP-induced rise in [Mg2+]i without altering the change in autofluorescence. Thus, the rise in [Mg2+]i in response to FCCP is consistent with the release of intracellular Mg2+ following ATP hydrolysis by the mitochondrial F1F0-ATPase. 4. The rise in [Mg2+]i was correlated with cell-attached recordings of ATP-sensitive K+ channel (KATP) activity. In response to FCCP, an increase in KATP channel activity was seen only as [Mg2+]i reached a plateau. In response to blockade of mitochondrial respiration and glycolysis with cyanide (CN-) and 2-deoxyglucose (DOG), [Mg2+]i rose more slowly but again KATP channel opening increased only when [Mg2+]i reached a plateau and the cells shortened. 5. Oligomycin decreased the rate of rise of [Mg2+]i delayed the onset of rigor and increased the rate of mitochondrial depolarization in response to CN-_DOG. Thus, with blockade of mitochondrial respiration delta psi m is maintained by the mitochondrial F1F0-ATPase at the expense of ATP reserves. 6. In response to CN-_DOG, the initial rise in [Mg2+]i was accompanied by a small rise in [Ca2+]i. After [Mg2+]i reached a plateau and rigor developed, [Ca2+]i rose progressively. On reperfusion, in hypercontracted cells, [Ca2+]i recovered before [Mg2+]i and [ca2+]i oscillations were sustained while [Mg2+]i decreased. Thus on reperfusion, full recovery of [ATP]i is slow, but the activation of contractile elements and the restoration of [Ca2+]i does not require the re-establishment of millimolar concentrations of ATP.
摘要
  1. 由于ATP对Mg2+的亲和力高于ADP,ATP水解时胞质镁浓度会升高。因此,我们使用对Mg(2+)敏感的荧光指示剂镁绿(MgG)来提供单个大鼠心肌细胞中ATP浓度变化的指标,以响应线粒体状态的改变。2. 响应FCCP时,[Mg2+]i升高至平台期,这与发展为僵硬状态同时发生,表明ATP耗尽。通过在同时加载fura-2和MgG的细胞中同时测量[Ca2+]i和[Mg2+]i,排除了细胞内游离Ca2+浓度变化对MgG信号的干扰(MgG对Ca2+的解离常数为4.7 microM)。对FCCP的反应与细胞外Mg2+无关,证实了[Mg2+]i升高的细胞内来源。3. 同时测量线粒体NAD(P)H自发荧光和线粒体电位(Δψm;.-1荧光)以及自发荧光和MgG,有助于更深入地研究[Mg2+]i与线粒体状态之间的关系。寡霉素消除了FCCP诱导的[Mg2+]i升高,而不改变自发荧光的变化。因此,响应FCCP时[Mg2+]i的升高与线粒体F1F0 - ATP酶水解ATP后细胞内Mg2+的释放一致。4. [Mg2+]i的升高与ATP敏感性钾通道(KATP)活性的细胞贴附记录相关。响应FCCP时,仅当[Mg2+]i达到平台期时,KATP通道活性才会增加。用氰化物(CN-)和2 - 脱氧葡萄糖(DOG)阻断线粒体呼吸和糖酵解时,[Mg2+]i升高得更慢,但同样只有当[Mg2+]i达到平台期且细胞缩短时,KATP通道才会开放增加。5. 寡霉素降低了[Mg2+]i的升高速率,延迟了僵硬状态的出现,并增加了响应CN-_DOG时线粒体去极化的速率。因此,在阻断线粒体呼吸时,线粒体F1F0 - ATP酶维持Δψm,代价是消耗ATP储备。6. 响应CN-_DOG时,[Mg2+]i的初始升高伴随着[Ca2+]i的小幅升高。在[Mg2+]i达到平台期且僵硬状态发展后,[Ca2+]i逐渐升高。再灌注时,在过度收缩的细胞中,[Ca2+]i在[Mg2+]i之前恢复,并且[Ca2+]i振荡持续存在,而[Mg2+]i下降。因此,再灌注时,[ATP]i的完全恢复很慢,但收缩元件的激活和[Ca2+]i的恢复并不需要重新建立毫摩尔浓度的ATP。

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