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Respiratory inhibition of isolated mammalian mitochondria by salivary antifungal peptide histatin-5.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2003 Nov 28; Vol. 311 (4), pp. 1034-40. - Publication Year :
- 2003
-
Abstract
- Histatin-5 is a peptide secreted in the human saliva, which possesses powerful antifungal activity. Previous studies have shown that this peptide exerts its candidacidal activity, through the inhibition of both mitochondrial respiration and the formation of reactive oxygen species. The purpose of the present study was to investigate the biological consequences of histatin-5 action on mammalian mitochondria to verify if the toxic mechanism exerted on mitochondria from Candida albicans is an exclusive for fungal cells. Moreover, hypothesising that the damage exerted on mitochondria may induce programmed cellular death pathways, we evaluated two main markers of apoptosis: the mitochondrial membrane potential (DeltaPsi) and the release of cytochrome c. The results obtained show that exposure of isolated mammalian mitochondria to histatin-5 determines: (i) a large inhibition of the respiratory chain at the level of complex I, (ii) a slight decrease in the mitochondrial membrane potential, and (iii) no release of cytochrome c.
- Subjects :
- Animals
Antifungal Agents pharmacology
Apoptosis drug effects
Apoptosis physiology
Cells, Cultured
Dose-Response Relationship, Drug
Histatins
Mitochondria ultrastructure
Rats
Rats, Sprague-Dawley
Cell Respiration drug effects
Cell Respiration physiology
Cytochromes c metabolism
Membrane Potentials drug effects
Membrane Potentials physiology
Mitochondria drug effects
Mitochondria physiology
Salivary Proteins and Peptides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 311
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 14623286
- Full Text :
- https://doi.org/10.1016/j.bbrc.2003.10.104