Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Drahota 2002 J Bioenerg Biomembr"

From Bioblast
Line 1: Line 1:
{{Publication
{{Publication
|title=Drahota Z, Chowdhury SKR, Floryk D, Mrácek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J (2002) Glycerophosphate-dependent hydrogen peroxide production by brown adipose tissue mitochondria and ist activation by ferricyanide. J Bioenerg Biomembr 34:105-13.
|title=Drahota Z, Roy Chowdhury SK, Floryk D, Mrácek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J (2002) Glycerophosphate-dependent hydrogen peroxide production by brown adipose tissue mitochondria and ist activation by ferricyanide. J Bioenerg Biomembr 34:105-13.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/12018887 PMID: 12018887]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/12018887 PMID: 12018887]
|authors=Drahota Z, Chowdhury SKR, Floryk D, Mracek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J
|authors=Drahota Z, Roy Chowdhury SK, Floryk D, Mracek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J
|year=2002
|year=2002
|journal=J Bioenerg Biomembr
|journal=J Bioenerg Biomembr
Line 11: Line 11:
}}
}}
{{Labeling
{{Labeling
|area=Respiration
|tissues=Fat
|tissues=Fat
|preparations=Isolated mitochondria
|preparations=Isolated mitochondria

Revision as of 17:27, 12 February 2016

Publications in the MiPMap
Drahota Z, Roy Chowdhury SK, Floryk D, Mrácek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J (2002) Glycerophosphate-dependent hydrogen peroxide production by brown adipose tissue mitochondria and ist activation by ferricyanide. J Bioenerg Biomembr 34:105-13.

» PMID: 12018887

Drahota Z, Roy Chowdhury SK, Floryk D, Mracek T, Wilhelm J, Rauchova H, Lenaz G, Houstek J (2002) J Bioenerg Biomembr

Abstract: Oxidation of glycerophosphate (GP) by brown adipose tissue mitochondria in the presence of antimycin A was found to be accompanied by significant production of hydrogen peroxide. GP-dependent hydrogen peroxide production could be detected by p-hydroxyphenylacetate fluorescence changes or as an antimycin A-insensitive oxygen consumption. One-electron acceptor, potassium ferricyanide, highly stimulated the rate of GP-dependent antimycin A-insensitive oxygen uptake, which was prevented by inhibitors of mitochondrial GP dehydrogenase (mGPDH) or by coenzyme Q(CoQ). GP-dependent ferricyanide-induced peroxide production was also determined luminometrically, using mitochondria or partially purified mGPDH. Ferricyanide-induced peroxide production was negligible, when succinate or NADH was used as a substrate. These results indicate that hydrogen peroxide is produced directly by mGPDH and reflect the differences in the transport of reducing equivalents from mGPDH and succinate dehydrogenase to the CoQ pool. The data suggest that more intensive production of reactive oxygen species may be present in mammalian cells with active mGPDH. Keywords: Brown adipose tissue, Mitochondrial glycerophosphate dehydrogenase, Ferricyanide, Hydrogen peroxide

O2k-Network Lab: CZ Prague Houstek J, CZ Hradec Kralove Cervinkova Z, CA Winnipeg Fernyhough P, IT Bologna Lenaz G


Labels: MiParea: Respiration 

Stress:Oxidative stress;RONS 

Tissue;cell: Fat  Preparation: Isolated mitochondria 



HRR: Oxygraph-2k