Neuroprotective effects of carboxymethylated chitosan on hydrogen peroxide induced apoptosis in Schwann cells

被引:27
|
作者
He, Bin [1 ]
Tao, Hai-Ying [1 ]
Liu, Shi-Qing [1 ]
机构
[1] Wuhan Univ, Dept Orthoped, Renmin Hosp, Wuhan 430060, Hubei Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Schwann cells; Survival; Hydrogen peroxide; Apoptosis; Carboxymethylatecl chitosan; DIABETIC-NEUROPATHY; BAX TRANSLOCATION; OXIDATIVE STRESS; PERIPHERAL-NERVE; IN-VITRO; BCL-2; EXPRESSION; DEATH; PROLIFERATION; MITOCHONDRIA;
D O I
10.1016/j.ejphar.2014.07.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The protective and promotion effects of Carboxymethylated chitosan (CMCS) on peripheral nerve and cultured Schwann cells (SCs) have been demonstrated, but few studies discussed the protective roles of CMCS on SCs apoptosis. We explored the anti-apoptotic activities of CMCS in SCs to enhance cells survival in this present study. Rat SCs were isolated and cultured in vitro, hydrogen peroxide (H2O2) was used to establish the apoptosis models of SCs. Cells proliferative activity was assessed by CCK-8 assay. The apoptosis of SCs was detected by flow cytometry (FCM) analysis. Superoxide dismutase (SOD) and malondiadlehyde (MDA) activities were detected by the corresponding assay kit. The nuclear appearance of apoptotic SCs was observed by nuclear staining with Hoechst 33342. The real-time PCR was performed to detect the levels of Bcl-2, Bax, Caspase-3 and -9 mRNA. Detection of caspase-3 and -9 was fulfilled by using Western blot analysis. FCM assay and Hoechst33342 staining results indicated that CMCS could protect SCs from apoptosis with close and time-dependent manner. SOD and MIDA analysis results indicated that CMCS could promote SOD activity and reduce the MDA levels in H2O2 induced SCs. The decreased caspase-3, -9 and Bax activities and increased Bcl-2 activity were observed in CMCS treated SCs. The present study indicates CMCS has the neuroprotective effect on peripheral nerves and inhibit SCs apoptosis. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 134
页数:8
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