Valle 1986 Biochem Biophys Res Commun: Difference between revisions
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|journal=Biochem Biophys Res Commun | |journal=Biochem Biophys Res Commun | ||
|abstract=This communication describes experiments showing that safranine, at the concentrations usually employed as a probe of mitochondrial membrane potential, causes significant undesirable side effects on Ca2+ transport by liver mitochondria. The major observations are: (i) safranine potentiates the spontaneous Ca2+ release from liver mitochondria induced by phosphate or acetoacetate. This is paralelled by potentiation of the release of state-4 respiration and of the rate of mitochondrial swelling, indicating a generalized effect of the dye on the mitochondrial membrane; (ii) the efflux of mitochondrial Ca2+ stimulated by hydroperoxide is irreversible in the presence of safranine even if membrane stabilizers such as Mg2+ and ATP are present. It is concluded that the use of safranine to monitor the changes in membrane potential during Ca2+ transport by mitochondria should be avoided or special care be taken. | |abstract=This communication describes experiments showing that safranine, at the concentrations usually employed as a probe of mitochondrial membrane potential, causes significant undesirable side effects on Ca2+ transport by liver mitochondria. The major observations are: (i) safranine potentiates the spontaneous Ca2+ release from liver mitochondria induced by phosphate or acetoacetate. This is paralelled by potentiation of the release of state-4 respiration and of the rate of mitochondrial swelling, indicating a generalized effect of the dye on the mitochondrial membrane; (ii) the efflux of mitochondrial Ca2+ stimulated by hydroperoxide is irreversible in the presence of safranine even if membrane stabilizers such as Mg2+ and ATP are present. It is concluded that the use of safranine to monitor the changes in membrane potential during Ca2+ transport by mitochondria should be avoided or special care be taken. | ||
|mipnetlab=BR Campinas Vercesi AE | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|tissues=Liver | |tissues=Liver | ||
|topics=Ion;substrate transport, mt-Membrane potential | |||
|couplingstates=LEAK | |couplingstates=LEAK | ||
|additional=Safranine, Ca2+, mt-swelling | |additional=Safranine, Ca2+, mt-swelling | ||
}} | }} | ||
Latest revision as of 17:05, 27 March 2018
| Valle VG, Pereira-da-Silva L, Vercesi AE (1986) Undesirable feature of safranine as a probe for mitochondrial membrane potential. Biochem Biophys Res Commun 135: 189-195. |
Valle VG, Pereira-da-Silva L, Vercesi AE (1986) Biochem Biophys Res Commun
Abstract: This communication describes experiments showing that safranine, at the concentrations usually employed as a probe of mitochondrial membrane potential, causes significant undesirable side effects on Ca2+ transport by liver mitochondria. The major observations are: (i) safranine potentiates the spontaneous Ca2+ release from liver mitochondria induced by phosphate or acetoacetate. This is paralelled by potentiation of the release of state-4 respiration and of the rate of mitochondrial swelling, indicating a generalized effect of the dye on the mitochondrial membrane; (ii) the efflux of mitochondrial Ca2+ stimulated by hydroperoxide is irreversible in the presence of safranine even if membrane stabilizers such as Mg2+ and ATP are present. It is concluded that the use of safranine to monitor the changes in membrane potential during Ca2+ transport by mitochondria should be avoided or special care be taken.
• O2k-Network Lab: BR Campinas Vercesi AE
Labels:
Tissue;cell: Liver
Regulation: Ion;substrate transport, mt-Membrane potential
Coupling state: LEAK
Safranine, Ca2+, mt-swelling
