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Difference between revisions of "El-Bacha 2012 Int J Biochem Cell Biol"

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|abstract=Infectious diseases such as those caused by virus, account for a vast proportion of deaths worldwide. Re-emerging aspects of host-virus interactions in recent literature include the vital role played by host metabolism on viral replication and the pro-active participation of mitochondria in this process. Different viruses use distinctive strategies to modulate mitochondrial bioenergetics and enhance viral replication. As a result, energy yielding metabolic pathways are programmed to provide both energy and biosynthetic resources to drive viral protein synthesis and produce infectious particles. Therefore, metabolic antagonists may prove important not only to outline efficient therapy strategies but also to shed light on the pathogenesis of viral infections.
|abstract=Infectious diseases such as those caused by virus, account for a vast proportion of deaths worldwide. Re-emerging aspects of host-virus interactions in recent literature include the vital role played by host metabolism on viral replication and the pro-active participation of mitochondria in this process. Different viruses use distinctive strategies to modulate mitochondrial bioenergetics and enhance viral replication. As a result, energy yielding metabolic pathways are programmed to provide both energy and biosynthetic resources to drive viral protein synthesis and produce infectious particles. Therefore, metabolic antagonists may prove important not only to outline efficient therapy strategies but also to shed light on the pathogenesis of viral infections.
|keywords=Viral infections, mitochondrial bioenergetics, host metabolism, metabolic antagonists
|keywords=Viral infections, mitochondrial bioenergetics, host metabolism, metabolic antagonists
|mipnetlab=BR Rio de Janeiro Da Poian AT, BR Rio de Janeiro Institute Biomedical Chemistry
|mipnetlab=BR Rio de Janeiro Da Poian AT
}}
}}
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Revision as of 14:15, 22 August 2014

Publications in the MiPMap
El-Bacha T and Da Poian AT (2012) Virus-induced changes in mitochondrial bioenergetics as potential targets for therapy. Int J Biochem Cell Biol 45: 41-46.

Β» PMID: 23036789

El-Bacha T, Da Poian AT (2012) Int J Biochem Cell Biol

Abstract: Infectious diseases such as those caused by virus, account for a vast proportion of deaths worldwide. Re-emerging aspects of host-virus interactions in recent literature include the vital role played by host metabolism on viral replication and the pro-active participation of mitochondria in this process. Different viruses use distinctive strategies to modulate mitochondrial bioenergetics and enhance viral replication. As a result, energy yielding metabolic pathways are programmed to provide both energy and biosynthetic resources to drive viral protein synthesis and produce infectious particles. Therefore, metabolic antagonists may prove important not only to outline efficient therapy strategies but also to shed light on the pathogenesis of viral infections. β€’ Keywords: Viral infections, mitochondrial bioenergetics, host metabolism, metabolic antagonists

β€’ O2k-Network Lab: BR Rio de Janeiro Da Poian AT


Labels:

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.  Organism: Human, Mouse  Tissue;cell: Nervous system, Liver  Preparation: Intact cells 



HRR: Oxygraph-2k 

Viral infections