A critical evaluation of in situ measurement of mitochondrial electrical potentials in single hepatocytes

Détails

ID Serval
serval:BIB_B74BDCD6B80C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A critical evaluation of in situ measurement of mitochondrial electrical potentials in single hepatocytes
Périodique
Biochimica et Biophysica Acta-Bioenergetics
Auteur(s)
Ubl  J. J., Chatton  J. Y., Chen  S., Stucki  J. W.
ISSN
0005-2728
ISSN-L
1879-2650
Statut éditorial
Publié
Date de publication
09/1996
Peer-reviewed
Oui
Volume
1276
Numéro
2
Pages
124-32
Notes
Journal Article Research Support, Non-U.S. Gov't --- Old month value: Sep 12
Résumé
The range of applicability and the critical parameters involved in the assessment of mitochondrial electrical potential (delta psi mit) using epifluorescence microscopy were evaluated based on both theoretical and experimental analysis. Rat hepatocytes loaded with the potential-dependent fluorescent dye rhodamine 123 exhibited the expected heterogeneity of fluorescence distribution with dark regions corresponding to the nucleus and bright regions corresponding to the mitochondria-rich cytosol. Calibration of the signal was performed by permeabilizing the cell membrane for monovalent cations using nystatin and gramicidin, and equilibrating the cell with a K(+)-free bath solution. A voltage-clamp at defined delta psi mit was then achieved after addition of valinomycin in the presence of different K+ concentrations in the bath. Theoretical analysis indicated that the ratio of fluorescence intensity measured in mitochondria-rich and mitochondria-poor regions of cell was related with delta psi mit and yielded quantitative estimates of electrical potential with an accuracy of 10-20 mV. The ratio tended to plateau at potentials more negative than-140 mV, showing a limitation of the technique. Manoeuvres such as imposing a heavy ATP demand or interfering with the mitochondrial respiration depolarized mitochondria, while delta psi mit was not altered in a measurable manner during Ca2+ oscillations consecutive to alpha 1-agonist stimulation.
Mots-clé
Adrenergic alpha-Agonists/pharmacology Animals Cytophotometry/*methods Evaluation Studies Fluorescent Dyes Hypoglycemic Agents/pharmacology Liver/cytology Membrane Potentials/*physiology Metformin/pharmacology Mitochondria, Liver/*physiology Models, Theoretical Phenformin/pharmacology Phenylephrine/pharmacology Rats Reproducibility of Results Rhodamine 123 Rhodamines
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 14:08
Dernière modification de la notice
20/08/2019 16:25
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