Difference between revisions of "Brazdova 2017 MiP2017"
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{{Abstract | {{Abstract | ||
|title=[[ | |title=[[File:BrazdovaA.jpg|left|90px|Brazdova Andrea]] Pleiotropic effects of biguanides on mitochondrial reactive oxygen species production. | ||
|info=[[MiP2017]] | |info=[[MiP2017]] | ||
|authors=Brazdova A, Pecinova A, Drahota Z, Kovalcikova J, Kovarova N, Pecina P, Alan L, Zima M, Houstek J, Mracek T | |||
|year=2017 | |year=2017 | ||
|event=MiP2017 | |event=MiP2017 | ||
|abstract=[[Image:MITOEAGLE-logo.jpg|left|100px|link=http://www.mitoglobal.org/index.php/MITOEAGLE|COST Action MITOEAGLE]] | |abstract=[[Image:MITOEAGLE-logo.jpg|left|100px|link=http://www.mitoglobal.org/index.php/MITOEAGLE|COST Action MITOEAGLE]] Metformin is widely prescribed as a first-choice anti-hyperglycemic drug for treatment of type 2 diabetes mellitus and recent epidemiological studies demonstrated its utility also in cancer therapy. Despite its beneficial therapeutic effects and long term use in clinical practice, its molecular target, either for anti-hyperglycemic or anti-neoplastic action, remains elusive. However, the body of the research on metformin effect oscillates around mitochondrial metabolism, including the function of oxidative phosphorylation (OXPHOS) apparatus. | ||
We focused on direct inhibitory mechanism of biguanides (metformin and phenformin) on OXPHOS complexes and its functional impact using the model of isolated brown adipose tissue mitochondria. We demonstrated that biguanides non-specifically target the activities of all respiratory chain dehydrogenases (mitochondrial NADH, succinate and glycerophosphate dehydrogenases), but only at very high concentrations (10<sup>-2</sup> – 10<sup>-1</sup> M) that highly exceeded cellular concentrations observed during the treatment. In addition, these concentrations of biguanides also triggered burst of reactive oxygen species production which, in combination with pleiotropic OXPHOS inhibition, could be toxic for the organism. | |||
We conclude that the favorable effect of biguanides should probably be associated with subtler mechanism, different from the generalized inhibition of the respiratory chain. | |||
|editor=[[Kandolf G]] | |editor=[[Kandolf G]] | ||
|mipnetlab=CZ Prague Houstek J, CZ Hradec Kralove Cervinkova Z, CZ Prague Kalous M | |||
}} | |||
{{Labeling | |||
|area=Respiration, Pharmacology;toxicology | |||
|diseases=Diabetes | |||
|tissues=Fat | |||
|preparations=Isolated mitochondria | |||
|pathways=F, N, NS | |||
|instruments=Oxygraph-2k | |||
|additional=Metformin, | |||
}} | }} | ||
== Affiliations and support == | |||
== Affiliations == | ::::Dept Bioenergetics, Inst Physiology, Czech Academy Sciences, Prague, Czech Republic. - andrea.brazdova@fgu.cas.cz | ||
::::Supported by the Grant Agency of the Czech Republic (16-12726S). | |||
Latest revision as of 04:20, 12 February 2020
 |
Link: MiP2017
Brazdova A, Pecinova A, Drahota Z, Kovalcikova J, Kovarova N, Pecina P, Alan L, Zima M, Houstek J, Mracek T (2017)
Event: MiP2017
Metformin is widely prescribed as a first-choice anti-hyperglycemic drug for treatment of type 2 diabetes mellitus and recent epidemiological studies demonstrated its utility also in cancer therapy. Despite its beneficial therapeutic effects and long term use in clinical practice, its molecular target, either for anti-hyperglycemic or anti-neoplastic action, remains elusive. However, the body of the research on metformin effect oscillates around mitochondrial metabolism, including the function of oxidative phosphorylation (OXPHOS) apparatus.
We focused on direct inhibitory mechanism of biguanides (metformin and phenformin) on OXPHOS complexes and its functional impact using the model of isolated brown adipose tissue mitochondria. We demonstrated that biguanides non-specifically target the activities of all respiratory chain dehydrogenases (mitochondrial NADH, succinate and glycerophosphate dehydrogenases), but only at very high concentrations (10-2 – 10-1 M) that highly exceeded cellular concentrations observed during the treatment. In addition, these concentrations of biguanides also triggered burst of reactive oxygen species production which, in combination with pleiotropic OXPHOS inhibition, could be toxic for the organism.
We conclude that the favorable effect of biguanides should probably be associated with subtler mechanism, different from the generalized inhibition of the respiratory chain.
• Bioblast editor: Kandolf G
• O2k-Network Lab: CZ Prague Houstek J, CZ Hradec Kralove Cervinkova Z, CZ Prague Kalous M
Labels: MiParea: Respiration, Pharmacology;toxicology Pathology: Diabetes
Tissue;cell: Fat
Preparation: Isolated mitochondria
Pathway: F, N, NS HRR: Oxygraph-2k
Metformin
Affiliations and support
- Dept Bioenergetics, Inst Physiology, Czech Academy Sciences, Prague, Czech Republic. - andrea.brazdova@fgu.cas.cz
- Supported by the Grant Agency of the Czech Republic (16-12726S).
