The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult

Neuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhi...

Full description

Bibliographic Details
Main Authors: Madhuri Roy, Robert M Sapolsky
Format: Article
Language:English
Published: Elsevier 2003-10-01
Series:Neurobiology of Disease
Subjects:
p35
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996103000834
id doaj-540aebc0713746509951a39b7f3778c3
record_format Article
spelling doaj-540aebc0713746509951a39b7f3778c32021-03-20T04:48:33ZengElsevierNeurobiology of Disease1095-953X2003-10-0114119The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insultMadhuri Roy0Robert M Sapolsky1Department of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USADepartment of Biological Sciences, Stanford University, Stanford, CA 94305-5020, USANeuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhibitors, p35 and crmA, following domoic acid-induced excitotoxicity in hippocampal neurons. We show that though p35 and crmA rescued neurons from toxicity, they did so under conditions of negligible caspase activation and morphological apoptosis. Thus, we characterized the novel neuroprotective effects of p35 and crmA and found that they attenuated the drop in the mitochondrial potential and blunted the decline in ATP levels. These data, to our knowledge, are the first detailed descriptions of the cell death mechanisms following domoic acid treatment of neurons. Moreover, in demonstrating the previously unexplored modulation of these processes, these data underline the capacity for classically “anti-apoptotic” proteins to alter other branches of cell death processes.http://www.sciencedirect.com/science/article/pii/S0969996103000834HippocampusApoptosisDomoic acidcrmAp35Caspase
collection DOAJ
language English
format Article
sources DOAJ
author Madhuri Roy
Robert M Sapolsky
spellingShingle Madhuri Roy
Robert M Sapolsky
The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
Neurobiology of Disease
Hippocampus
Apoptosis
Domoic acid
crmA
p35
Caspase
author_facet Madhuri Roy
Robert M Sapolsky
author_sort Madhuri Roy
title The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
title_short The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
title_full The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
title_fullStr The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
title_full_unstemmed The neuroprotective effects of virally-derived caspase inhibitors p35 and crmA following a necrotic insult
title_sort neuroprotective effects of virally-derived caspase inhibitors p35 and crma following a necrotic insult
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2003-10-01
description Neuronal excitotoxicity causes energetic impairment and the ensuing cell death has historically been regarded as necrotic. Recent findings, however, indicate that apoptosis may participate in excitotoxicity. Here we examined the neuroprotective mechanisms of the well-characterized viral caspase inhibitors, p35 and crmA, following domoic acid-induced excitotoxicity in hippocampal neurons. We show that though p35 and crmA rescued neurons from toxicity, they did so under conditions of negligible caspase activation and morphological apoptosis. Thus, we characterized the novel neuroprotective effects of p35 and crmA and found that they attenuated the drop in the mitochondrial potential and blunted the decline in ATP levels. These data, to our knowledge, are the first detailed descriptions of the cell death mechanisms following domoic acid treatment of neurons. Moreover, in demonstrating the previously unexplored modulation of these processes, these data underline the capacity for classically “anti-apoptotic” proteins to alter other branches of cell death processes.
topic Hippocampus
Apoptosis
Domoic acid
crmA
p35
Caspase
url http://www.sciencedirect.com/science/article/pii/S0969996103000834
work_keys_str_mv AT madhuriroy theneuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult
AT robertmsapolsky theneuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult
AT madhuriroy neuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult
AT robertmsapolsky neuroprotectiveeffectsofvirallyderivedcaspaseinhibitorsp35andcrmafollowinganecroticinsult
_version_ 1724212119620026368