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Differential caspase activity in the cortex and striatum with chronic infusion of 3-nitropropionic acid
被引:8
|作者:
Cho, Kyoung Joo
[1
]
Kim, Gyung Whan
[1
]
机构:
[1] Yonsei Univ, Coll Med, Dept Neurol, Severance Hosp, Seoul 120752, South Korea
关键词:
3-Nitropropionic acid;
Apoptosis signal-regulating kinase 1;
siRNA;
Caspase-6;
Caspase-3;
NEUROTROPHIC FACTOR;
MITOCHONDRIAL TOXIN;
OXIDATIVE STRESS;
DISEASE MODELS;
DEGENERATION;
INVOLVEMENT;
APOPTOSIS;
DEATH;
PHOSPHORYLATION;
EXCITOTOXICITY;
D O I:
10.1016/j.bbrc.2015.08.075
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Systemic administration of 3-nitropropionic acid (3-NP) facilitates the development of select striatal lesions, and some reports provide clues about this pathology. In this study, we investigated the relationship between reduced levels of brain-derived neurotrophic factor (BDNF) in lesioned brain regions and caspase activity, as well as involvement of apoptosis signal-regulating kinase 1 (ASK!) in caspase activation. We analyzed apoptotic cell death, BDNF distribution, caspase-3 activity, caspase-6 activity, ASKI expression level, and active ASK1 in the cortex and striatum. There were different levels and distributions of these factors within each sub-region. Caspase-6 activity was reduced with downregulation of ASK1 in the cortex. BDNF protein levels did not decrease in the cortex, but there was replenishment of severely reduced BDNF in the striatum. The present study suggests that an increase in ASK1 in the damaged cortex is related to caspase-6 activation and is involved in cortical depletion of BDNF in the striatum. Furthermore, with systemic infusion of 3-NP, differential expression of ASK1 in the cortex and striatum suggests that this kinase may modulate caspase activation and striatal degeneration. (C) 2015 Elsevier Inc. All rights reserved.
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页码:631 / 637
页数:7
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