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http://hdl.handle.net/1942/4572Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | LEYSSENS, Anne | - |
| dc.contributor.author | Nowicky, A.V. | - |
| dc.contributor.author | Patterson, L. | - |
| dc.contributor.author | Compton, M. | - |
| dc.contributor.author | Duchen, M.R. | - |
| dc.date.accessioned | 2007-12-20T15:50:41Z | - |
| dc.date.available | 2007-12-20T15:50:41Z | - |
| dc.date.issued | 1996 | - |
| dc.identifier.citation | The journal of physiology, 496(1). p. 111-128 | - |
| dc.identifier.uri | http://hdl.handle.net/1942/4572 | - |
| dc.description.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. | - |
| dc.language.iso | en | - |
| dc.title | The relationship between mitochondrial state, ATP hydrolysis, [Mg2+]i and [Ca2+]i studied in isolated rat cardiomyocytes | - |
| dc.type | Journal Contribution | - |
| dc.identifier.epage | 128 | - |
| dc.identifier.issue | 1 | - |
| dc.identifier.spage | 111 | - |
| dc.identifier.volume | 496 | - |
| dc.bibliographicCitation.oldjcat | - | |
| dc.identifier.url | http://jp.physoc.org/cgi/content/abstract/496/Pt_1/111 | - |
| item.fullcitation | LEYSSENS, Anne; Nowicky, A.V.; Patterson, L.; Compton, M. & Duchen, M.R. (1996) The relationship between mitochondrial state, ATP hydrolysis, [Mg2+]i and [Ca2+]i studied in isolated rat cardiomyocytes. In: The journal of physiology, 496(1). p. 111-128. | - |
| item.contributor | LEYSSENS, Anne | - |
| item.contributor | Nowicky, A.V. | - |
| item.contributor | Patterson, L. | - |
| item.contributor | Compton, M. | - |
| item.contributor | Duchen, M.R. | - |
| item.fulltext | No Fulltext | - |
| item.accessRights | Closed Access | - |
| Appears in Collections: | Research publications | |
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