Interaction of Potent Mitochondrial Uncouplers with Thiol-Containing Antioxidants.
FCCP
fluazinam
isolated mitochondria
membrane potential
mitochondrial uncoupler
planar bilayer lipid membrane
reactive oxygen species
respiration rate
thiol-containing antioxidants
Journal
Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981
Informations de publication
Date de publication:
23 Jun 2019
23 Jun 2019
Historique:
received:
11
04
2019
revised:
20
06
2019
accepted:
21
06
2019
entrez:
26
6
2019
pubmed:
27
6
2019
medline:
27
6
2019
Statut:
epublish
Résumé
It is generally considered that reactive oxygen species (ROS) are involved in the development of numerous pathologies. The level of ROS can be altered via the uncoupling of oxidative phosphorylation by using protonophores causing mitochondrial membrane depolarization. Here, we report that the uncoupling activity of potent protonophores, such as carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP), carbonyl cyanide 3-chlorophenylhydrazone (CCCP), and fluazinam, can be abrogated by the addition of thiol-containing antioxidants to isolated mitochondria. In particular, N-acetylcysteine, glutathione, cysteine, and dithiothreitol removed both a decrease in the mitochondrial membrane potential and an increase in the respiration rate that is caused by FCCP. The thiols also reduced the electrical current that is induced by FCCP and CCCP across planar bilayer lipid membranes. Thus, when speculating on the mechanistic roles of ROS level modulation by mitochondrial uncoupling based on the antioxidant reversing certain FCCP and CCCP effects on cellular processes, one should take into account the ability of these protonophoric uncouplers to directly interact with the thiol-containing antioxidants.
Identifiants
pubmed: 31234606
pii: antiox8060194
doi: 10.3390/antiox8060194
pmc: PMC6616877
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Russian Science Foundation
ID : 16-14-10025
Références
J Biol Chem. 2002 Sep 27;277(39):36204-15
pubmed: 12121989
J Neurochem. 2003 Sep;86(5):1101-7
pubmed: 12911618
Biochemistry. 1963 Mar-Apr;2:357-61
pubmed: 13954345
J Biol Chem. 1964 Feb;239:452-4
pubmed: 14169144
J Bioenerg Biomembr. 2004 Aug;36(4):353-6
pubmed: 15377871
Biochim Biophys Acta. 1992 Jul 6;1101(1):41-7
pubmed: 1633176
Cardiovasc Res. 2006 Nov 1;72(2):313-21
pubmed: 16950237
Oncol Rep. 2007 Jul;18(1):71-6
pubmed: 17549348
Drug Metab Dispos. 2009 Sep;37(9):1797-800
pubmed: 19541825
Adv Exp Med Biol. 1977;78:67-82
pubmed: 197811
Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):865-77
pubmed: 20175987
Int J Mol Med. 2011 Apr;27(4):575-81
pubmed: 21258765
Neurotoxicology. 2011 Dec;32(6):702-10
pubmed: 21907236
Cell Death Dis. 2014 Nov 13;5:e1524
pubmed: 25393480
Chem Biol Interact. 2015 Sep 5;239:100-10
pubmed: 26115783
Nat Commun. 2016 Jun 30;7:12109
pubmed: 27357649
Alzheimers Dement. 2017 May;13(5):582-591
pubmed: 27599210
J Biol Chem. 2017 Oct 6;292(40):16697-16708
pubmed: 28848050
J Med Chem. 2018 Jun 14;61(11):4641-4655
pubmed: 29156129
Arch Biochem Biophys. 1989 Mar;269(2):623-38
pubmed: 2919886
Biochim Biophys Acta Bioenerg. 2019 Apr 1;1860(4):310-316
pubmed: 30710552
Biochim Biophys Acta. 1979 Jul 4;585(3):462-76
pubmed: 39629
Biochim Biophys Acta. 1965 Sep 27;109(1):284-92
pubmed: 4379418
Biochem J. 1973 Jul;134(3):707-16
pubmed: 4749271
Biochim Biophys Acta. 1982 Nov 15;682(2):289-92
pubmed: 7171582
Hoppe Seylers Z Physiol Chem. 1980 Jan;361(1):9-15
pubmed: 7358335
J Biol Chem. 1994 Jan 7;269(1):71-6
pubmed: 8276873
Biosci Rep. 1997 Jun;17(3):259-72
pubmed: 9337481
FEBS Lett. 1997 Oct 13;416(1):15-8
pubmed: 9369223
J Cell Biol. 1998 Jun 15;141(6):1423-32
pubmed: 9628898
FEBS Lett. 1976 Oct 1;68(2):191-7
pubmed: 976474
J Biol Chem. 1976 Oct 25;251(20):6183-8
pubmed: 977564