Please use this identifier to cite or link to this item:
Title: Caspase-dependent and -independent cell death induced by 3-nitropropionic acid in rat cortical neurons
Authors: Almeida, Sandra 
Brett, Ana C. 
Góis, Inês N. 
Oliveira, Catarina R. 
Rego, A. Cristina 
Issue Date: 2006
Citation: Journal of Cellular Biochemistry. 98:1 (2006) 93-101
Abstract: Mitochondria play a critical role in cell death by releasing apoptogenic factors, such as cytochrome c and apoptosis-inducing factor (AIF), from the intermembrane space into the cytoplasm. Because mitochondrial dysfunction has been shown to be involved in several neurodegenerative diseases, mitochondrial toxins are largely used to model these disorders. These include 3-nitropropionic acid (3-NP), an irreversible inhibitor of succinate dehydrogenase, which has been used to model Huntington's disease and was previously reported by us to induce apoptotic cell death through caspase activation. In the present study, we evaluated the involvement of caspase-independent neuronal cell death induced by 3-NP (1 mM) and the effect of z-VDVAD-fmk, an inhibitor of caspase-2, using cortical neurons in culture. Our results highly suggest that 3-NP induces both caspase-dependent and -independent cell death. We showed that z-VDVAD-fmk prevented both caspase-2 and -3-like activities evoked by 3-NP, but only partly prevented chromatin fragmentation/condensation. However, z-VDVAD-fmk did not avoid 3-NP-induced release of cytochrome c or AIF from mitochondria nor did it affect the levels of mitochondrial Bax. Furthermore, 3-NP-mediated decrease in plasma membrane integrity was not affected by z-VDVAD-fmk. Under these conditions, the inhibitor prevented the caspase-dependent cell death. J. Cell. Biochem. 98: 93-101, 2006. © 2005 Wiley-Liss, Inc.
DOI: 10.1002/jcb.20748
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat
obra.pdf237.92 kBAdobe PDFView/Open
Show full item record


checked on Feb 18, 2020

Citations 5

checked on Aug 2, 2022

Page view(s) 50

checked on Aug 8, 2022


checked on Aug 8, 2022

Google ScholarTM




Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.