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:杨曙[1] 谢鼎华[1] 伍伟景[1] 肖自安[1] 刘嘉[1] 杨新明[1] 田丰[1]
机构地区:[1]中南大学湘雅二医院耳鼻咽喉科,长沙410011
出 处:《听力学及言语疾病杂志》2002年第3期156-158,T001,共4页Journal of Audiology and Speech Pathology
基 金:国家自然科学基金资助项目 (项目编号 39770 795 )
摘 要:目的 通过检测乙酰胆碱对蒙古沙鼠耳蜗中一氧化氮合酶 (nitricoxidesynthase ,NOS)的影响 ,初步探讨耳蜗中NOS的调节机制。方法 蒙古沙鼠耳蜗经还原型辅酶Ⅱ -黄递酶 (NADPH -黄递酶 )染色后行耳蜗铺片 ,分别以同一动物两侧耳蜗为实验组和对照组进行对比观察 ,检测乙酰胆碱 (ACh)对耳蜗NOS活性的影响 ,其染色深度的差异通过HPIAS - 10 0 0高清晰度彩色病理图像免疫组化测量系统判断。结果 蒙古沙鼠耳蜗外毛细胞基底部传出神经末梢呈现NADPH -黄递酶染色阳性反应 ,ACh处理后染色深度明显增强 ,其平均灰度值从 74.2 8± 11.71减低至 46 .5± 7.78(P <0 .0 1)。结论 蒙古沙鼠耳蜗外毛细胞基底部的传出神经末梢可见NOS分布 ,ACh能增强其活性 。Objective To investigate the influence of acetylcholine (ACh) on the activity of NOS so as to primarily elucidate the regulating mechanism of NOS. Methods After stained with NADPH-diaphorase, surface preparation of Mongolian gerbil cochleae was performed. For evaluating the influence of ACh on the activities of NOS, the depth of NADPH-diaphorase staining in both cochleae of the same animal, which was measured with High Resolution Image Analysis System (HPIAS-1000), was compared, one for ACh-treated group and another for control.Results The NADPH-diaphorase staining was labeled in the efferent endings at base of outer hair cells (OHCs). After ACh treatment, the depth of the HADPH-diaphorase staining significantly increased, showing that the average gray level of the staining in the efferent endings was decreased from 74.28±11.71 to 46.5±7.78 (P<0.01).Conclusion In the cochlea of Mongolian gerbils, NOS staining was labeled in the auditory efferent endings at the base of OHCs,and ACh treatment could increase the NOS activity. These results indicate that ACh plays an important role by NO, a second messenger molecule, in the regulation of auditory physiology.
关 键 词:乙酰胆碱 一氧化氮合酶 还原型辅酶Ⅱ-黄递酶 耳蜗
分 类 号:R764.35[医药卫生—耳鼻咽喉科]
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:18.188.195.92