Potassium 2-(1-hydroxypentyl)-benzoate attenuated hydrogen peroxide-induced apoptosis in neuroblastoma SK-N-SH cells

被引:18
作者
Hu, Yanli [1 ,2 ]
Peng, Ying [1 ,2 ]
Long, Yan [1 ,2 ]
Xu, Shaofeng [1 ,2 ]
Feng, Nan [1 ,2 ]
Wang, Ling [1 ,2 ]
Wang, Xiaoliang [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Medicines, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
关键词
PHPB; Apoptosis; PKC; Hydrogen peroxide; Alzheimer's disease; Stroke; ACUTE ISCHEMIC-STROKE; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; CEREBRAL-ISCHEMIA; DEATH; INJURY; BRAIN; DAMAGE; ANTIOXIDANT; PROTECTS;
D O I
10.1016/j.ejphar.2012.01.031
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Potassium 2-(1-hydroxypentyl)-benzoate (dl-PHPB) has been shown to have potent neuroprotective effects, such as reducing the infarct volume and improving neurobehavioral deficits in the transient focal cerebral ischemic rat model. The present study is to evaluate the neuroprotective effect of dl-PHPB on hydrogen peroxide (H2O2)-induced apoptosis and the possible mechanism in the human neuroblastoma SK-N-SH cells. Our results showed that dl-PHPB significantly attenuated H2O2-induced cell death, and reduced neuronal apoptosis. Dl-PHPB partially reversed the decrease of B-cell CLL/lymphoma 2 (Bcl-2) protein level induced by H2O2. Furthermore, dl-PHPB inhibited the elevation of pro-apoptotic Bcl-2-associated X protein (Bax) and caspase3, and alleviated the down-regulation of protein kinase C alpha (PKC alpha). The PKC inhibitor, Calphostin C significantly attenuated the protective effects of dl-PHPB. The findings suggest that dl-PHPB may protect neurons against H2O2-induced apoptosis by modulating apoptosis-related proteins, and PKC signaling pathway may be involved in the neuroprotection of dl-PHPB. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:49 / 54
页数:6
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