Document Detail


Nano-copper induces oxidative stress and apoptosis in kidney via both extrinsic and intrinsic pathways.
MedLine Citation:
PMID:  22000994     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
In the modern medicine nano particle has been used as a power tool but recently it has been established that nano particle pathophysiologically affects different organs. Recently, we have investigated the role of copper nano particle in liver dysfunction. In the literature, practically little is known about the nano-copper induced renal dysfunction. We, therefore, conducted the present study as a continuation of our earlier one to investigate the molecular mechanism in nano-copper induced kidney dysfunction. Nano-copper exposure increased the production of reactive oxygen species (ROS), reactive nitrogen species (RNS) and altered the levels of oxidative stress related biomarkers in kidney tissue. Signal transduction mechanism studies showed that nano copper exposure reciprocally regulated Bcl-2 family protein expression, disturbed mitochondrial membrane potential and subsequently helped releasing cytochrome c from mitochondria to cytosol. Apoptotic nature of cell death is confirmed by activation of caspases 3 which is also supported by histological study. In addition, we also observed the activation of Fas, caspase 8 and tBid in kidney tissue in this pathophysiology, suggesting the involvement of extrinsic pathways. Combining all, results suggest that nano copper can trigger both intrinsic and extrinsic apoptotic pathways in oxidative stress mediated kidney dysfunction.
Authors:
Abhijit Sarkar; Joydeep Das; Prasenjit Manna; Parames C Sil
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-10-5
Journal Detail:
Title:  Toxicology     Volume:  -     ISSN:  1879-3185     ISO Abbreviation:  -     Publication Date:  2011 Oct 
Date Detail:
Created Date:  2011-10-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0361055     Medline TA:  Toxicology     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011. Published by Elsevier Ireland Ltd.
Affiliation:
Division of Molecular Medicine, Bose Institute, P-1/12, CIT Scheme VIIM, Calcutta 700054, West Bengal, India.
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