检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:张惠君[1] 曾园山[2] 聂俊辉[2] 张伟[2]
机构地区:[1]中山大学中山医学院解剖学教研室,广州510080 [2]中山大学中山医学院组织学胚胎学教研室,神经科学研究室,广州510080
出 处:《解剖学报》2003年第5期553-555,共3页Acta Anatomica Sinica
基 金:教育部留学回国人员科研启动基金 [教 (启 ) 99 2 81]
摘 要:目的 探讨吗啡对钳夹损伤坐骨神经后其传入纤维终末在脊髓Ⅱ板层分布的影响。 方法 用显示抗氟化物酸性磷酸酶 (FRAP)组织化学方法 ,借助图像分析仪测量损伤坐骨神经后 15d和 30d吗啡组和对照组大鼠脊髓Ⅱ板层FRAP阳性反应物面积。 结果 损伤坐骨神经后吗啡组和对照组大鼠脊髓Ⅱ板层FRAP阳性反应区均有不同程度的缺失 ;对照组损伤坐骨神经后 30d的FRAP阳性反应物面积比 15d的FRAP阳性反应物面积增大 40 %。吗啡组损伤坐骨神经后 30d的FRAP阳性反应物面积比 15d的FRAP阳性反应物面积增大 2 2 %;同时也比对照组损伤坐骨神经后 30d的FRAP阳性反应物面积增大 19%。 结论 随着损伤坐骨神经后大鼠存活时间延长 ,其脊髓Ⅱ板层FRAP阳性反应物面积呈恢复性增大 ;吗啡能使坐骨神经损伤大鼠脊髓Ⅱ板层的FRAP阳性反应物面积明显增大。Objective To explore the effects of morphine on the terminal of primary afferent fiber distributing in spinal lamina Ⅱ after the sciatic nerve crush. Methods The positive reactive areas of fluoride-resistant acid phosphatase(FRAP) at spinal lamina Ⅱ were measured by the FRAP histochemistry and microcomputer image analysis techniques, after sciatic nerve was injured 15 days and 30 days both in morphine and control groups of rats. Results The positive reactive areas of FRAP at spinal lamina Ⅱ were depleted on different degree in two groups of rat after sciatic nerve was injured. The positive reactive areas of FRAP were greater 40% on injured sciatic nerve in 30 days than in 15 days in control group. In morphine group, the positive reactive areas of FRAP were larger 22% on injured sciatic nerve in 30 days than in 15 days; simulaneously also were bigger 19% than on injured sciatic nerve 30 days of control group.Conclusion The positive reactive areas of FRAP at spinal lamina Ⅱ show recovering enlargement as the surviving time lengthens in both groups of rats injured sciatic nerve.Morphine may enhance the positive reactive area of FRAP at spinal lamina Ⅱ in rat of sciatic nerve crush.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.31