Rauchova 2005 Biochem Biophys Res Comm: Difference between revisions

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|area=Respiration
|area=Respiration
|injuries=RONS; Oxidative Stress
|injuries=RONS; Oxidative Stress
|substratestates=CII, GpDH, Other combinations
|substratestates=CII, CGpDH, Other combinations
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|discipline=Pharmacology; Biotechnology
|discipline=Pharmacology; Biotechnology
}}
}}

Revision as of 14:36, 19 February 2015

Publications in the MiPMap
Rauchova H, Vrbacky M, Bergamini C, Fato R, Lenaz G, Houstek J, Drahota Z (2005) Inhibition of glycerophosphate-dependent H2O2 generation in brown fat mitochondria by idebenone. Biochem Biophys Res Comm 339:362-6.

Β» PMID: 16300743

Rauchova H, Vrbacky M, Bergamini C, Fato R, Lenaz G, Houstek J, Drahota Z (2005) Biochem. Biophys. Res. Commun.

Abstract: The established protective effect of coenzyme Q (CoQ) analogs is dependent on the location of reactive oxygen species (ROS) generation. One of these analogsβ€”idebenone (hydroxydecyl-ubiquinone) is used as an antioxidative therapeutic drug. We tested its scavenging effect on the glycerophosphate (GP)-dependent ROS production as this enzyme was shown as a new site in the mitochondrial respiratory chain where ROS can be generated. We observed that idebenone inhibits both GP- and succinate-dependent ROS production. Idebenone and CoQ1 were found to be more efficient in the scavenging activity (IC50 : 0.052 and 0.075 ΞΌM, respectively) than CoQ3 (IC50 : 45.8 ΞΌM). Idebenone also inhibited ferricyanide (FeCN)-activated, GP-dependent ROS production. Our data thus extend previous findings on the scavenging effect of idebenone and show that it can also eliminate GP-dependent ROS generation β€’ Keywords: Mitochondrial glycerophosphate dehydrogenase, Succinate dehydrogenase, Reactive oxygen species, debenone, Coenzyme Q analogs

β€’ O2k-Network Lab: CZ Prague Houstek J, IT Bologna Lenaz G


Labels: MiParea: Respiration 

Stress:RONS; Oxidative Stress"RONS; Oxidative Stress" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property. 




HRR: Oxygraph-2k 


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