
浏览全部资源
扫码关注微信
1. 重庆医科大学中医药学院骨科教研室
2. 重庆医科大学附属第一医院骨科
纸质出版日期:2010,
扫 描 看 全 文
[1]黄英如,蒋电明,曹文富,欧云生,安洪.雷公藤多甙对冷保存坐骨神经雪旺细胞凋亡及免疫原性的影响[J].重庆医科大学学报,2010,35(06):833-836.
HUANG Ying-ru, et al. Effects of tripterygium glycoside on schwann’s cell apoptosis and immunogenicity of cold preserved sciatic nerve[J]. Journal of Chongqing Medical University, 2010,35(6):833-836.
[1]黄英如,蒋电明,曹文富,欧云生,安洪.雷公藤多甙对冷保存坐骨神经雪旺细胞凋亡及免疫原性的影响[J].重庆医科大学学报,2010,35(06):833-836. DOI: 10.13406/j.cnki.cyxb.2010.06.003.
HUANG Ying-ru, et al. Effects of tripterygium glycoside on schwann’s cell apoptosis and immunogenicity of cold preserved sciatic nerve[J]. Journal of Chongqing Medical University, 2010,35(6):833-836. DOI: 10.13406/j.cnki.cyxb.2010.06.003.
目的:观察雷公藤多甙(Tripterygium glycoside
TG)对冷保存大鼠坐骨神经雪旺细胞凋亡和主要组织相容性复合体(Major histocompatibility complex
MHC)表达的影响。方法:Wistar大鼠坐骨神经在0、200、400、800mg/LTG溶液(A、B、C、D组)中
4℃保存24h、3d、7d
HE染色光镜观察
免疫组化检测Bcl-2表达
TUNEL法检测细胞凋亡。用TG溶液保存24h的Wistar大鼠坐骨神经桥接对应组SD大鼠(A’、B’、C’、D’组)坐骨神经10mm缺损
E’组为新鲜异体移植
移植后1、2、4周
行大体及光镜观察
免疫组化检测移植物MHC-Ⅰ、Ⅱ分子表达。结果:冷保存不同时间
各组神经纤维结构正常。保存24h
各组间细胞凋亡差异无统计学意义(P>0.05)。保存3、7d时
Bcl-2表达B、C组高于A、D组(P<0.05)
而B组与C组间、A组与D组间差异无统计学意义(均P>0.05);细胞凋亡A组高于B、C、D组
B、D组高于C组(均P<0.05)
但B、D组间差异无统计学意义(P>0.05)。移植术后移植物与周围组织粘连、炎症细胞入侵
B’、C’、D’组比A’、E’组轻;移植物MHC-Ⅰ、Ⅱ分子表达
术后第1周出现高峰
同一时相B’、C’、D’组低于A’、E’组
C’、D’组低于B’组(均P<0.05)
但A’与E’组间、C’与D’组间差异无统计学意义(均P>0.05)。结论:一定浓度的TG能抑制冷保存大鼠坐骨神经雪旺细胞凋亡和主要组织相容性抗原表达
降低异体移植后排斥反应。
Objective:To investigate the effects of Tripterygium glycoside(TG) on Schwann’s cell apoptosis and major histocompatibility complex (MHC) of cold preserved sciatic nerve in rats. Methods:At 4℃
Wistar rat sciatic nerve segments were preserved in 0
200
400
800 mg/L TG solution(groups A
B
C
D)for 24 hours
3 days and 7 days. The sciatic nerves were observed by HE staining
the expression of Bcl- 2 was detected by immunohistochemical staining
and the apoptosis of Schwann’s cell by TUNEL. The Wistar rat sciatic nerve segments preserved for 24 hours were transplanted to the corresponding SD rats (groups A’
B’
C’
D’)
and group E’ received fresh nerve allograft. After allograft
the gross appearance and the pathology were observed at 1
2 and 4 weeks
and the expression of MHC-I
II of the allografts were detected by immunohistochemical staining. Results:The microstructure of sciatic nerves cold preserved were normal. The apoptosis of cold preserved sciatic nerves had no significant difference among the groups after preserved for 24 hours (P>0.05). After preserved for 3 days or 7 days
the expression of Bcl-2 in groups B and C were significantly higher than those in groups A and D P<0.05)
but there was no significant difference between group B and group C
between group A and group D (P>0.05);the apoptosis index in group A was significantly higher than those in groups B
C and D
higher in groups B and D than in group C(P<0.05)
but there was no significant differences between group B and group D(P>0.05). The adhesions between allografts and connective tissue
and the inflammatory cell infiltration in groups B’
C’and D’were better than those in groups A’and E’.The expression ofMHC-I
II ofthe allografts reached the peak at the first week. At the same time
the expression ofMHC-Ⅰ、Ⅱin groups B’
C’and D’were significantly lower than those in groups A’and E’
lower in groups C’and D’than in group B’
but there was no significant differences between group A’and group E’
between group C’and group D’(P>0.05). Conclusion:Certain concentration of TG can inhibit the apoptosis of Schwann’s cell and the expression of major histocompatibility antigen of cold preserved sciatic nerve in rats
and decrease rejection after nerve allograft.
雷公藤多甙异体神经移植冷保存雪旺细胞凋亡移植免疫
Tripterygium glycosideNerve allograftCold preser vationSchwann’s cell apoptosisTransplantation immunity
0
浏览量
78
下载量
1
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621