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:王为服[1] 张元芳[2] 丁强[2] 徐一甄[3] 凌治萍[4]
机构地区:[1]海南省人民医院泌尿外科,海口570311 [2]上海医科大学华山医院泌尿外科 [3]上海医科大学华山医院 [4]上海医科大学电镜室
出 处:《中华泌尿外科杂志》1999年第10期628-631,共4页Chinese Journal of Urology
摘 要:目的 探讨糖尿病(DM) 性阴茎勃起功能障碍(ED) 的发病机理。 方法 SD 大鼠注射链脲佐菌素制造DM 动物模型后,注射阿朴吗啡观察6 周、8 周及12 周大鼠阴茎勃起情况,筛选DM 性ED 大鼠模型,观察其阴茎海绵体组织超微结构的改变。 结果 DM 性ED 大鼠模型阴茎海绵体内皮细胞及平滑肌细胞超微结构均有明显的病理改变:线粒体退变、内质网扩张,糖原颗粒、吞饮小泡及微丝减少。此外,还可见大量间质组织增生及微血管腔闭塞。随DM 病程不同,其改变程度不同,8 周时以内皮细胞损害为明显,12 周时以平滑肌细胞损害为明显。 结论 DM 严重影响阴茎勃起功能,海绵体组织超微结构的病理改变可能是DM 性ED 发病机理之一。Objective To study the ultrastructure of cavernous tissue in impotent rats with diabetes mellitus (DM). Methods Sprague Dewley rats were injected intraperitoneally with streptozotocin(STZ) to make experimental models of DM.Injected with apomorphine,penile erections in rats with DM and in controls were observed and noted on the sixth week,the eighth week and the twelfth week from the fourth day of injecting STZ.The experimental models of impotent rats with DM were then selected and the ultrastructure of the cavernous tissues studied. Results The significant pathological changes were observed in the endothelial and smooth muscle cells of cavernous tissue of impotent rats with DM:these were the degeneration of mitochondria,the dilatation of endoplasmic reticulum,the reduce of glycogen particle,pinocytotic vesicle and microfilament.The proliferation of messenchymal tissue and obturation of microvessel were also observed.The change extent of cavernous tissue was positively correlated with the duration of DM,the changes of endothelial and smooth muscle cells being obvious on the eight or twelve week. Conclusions The function of penile erection is affected seriously by DM,and these pathological changes of cavernous tissue may be one of the most important mechanisms of impotence with DM.
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:216.73.216.28