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速尿对离体培养豚鼠血管纹毒性作用的观察
引用本文:张运东,孔维佳. 速尿对离体培养豚鼠血管纹毒性作用的观察[J]. 听力学及言语疾病杂志, 2002, 10(3): 174-176,T002
作者姓名:张运东  孔维佳
作者单位:1. 随州市中心医院耳鼻咽喉科
2. 华中科技大学同济医学院附属协和医院耳鼻咽喉科,武汉,430022
摘    要:目的:观察速尿对离体培养的豚鼠血管纹组织的影响,探讨速尿耳毒性的作用机制。方法:20只花色豚鼠随机分成二组:速尿组(n=16),正常对照组(n=4)。应用组织块培养的方法,将血管纹组织培养24小时,随即对不同的实验组分别应用不同终浓度的的速尿(60、300、600、1250、2500μg/ml),分别继续培养30分钟和90分钟,观察培养的血管纹组织学结构。结果:速尿组在组织学方面均未出现血管纹水肿、缘细胞胞浆肿胀、细胞间隙扩大和中间细胞皱缩等病理改变,与对照组相比较血管纹结构无显著性差异。结论:速尿对体外培养的豚鼠血管纹组织无明显诱导水肿的作用,提示速尿耳毒性的产生,可能是间接的作用机制。

关 键 词:速尿 耳毒性 血管纹 组织块培养 FUR
文章编号:1006-7299(2002)03-0174-03

Observation of In Vitro Interaction of Furosemide On Stria Vascularis Cultureds From Guinea Pig
Zhang Yundong,Kong Weijia. Observation of In Vitro Interaction of Furosemide On Stria Vascularis Cultureds From Guinea Pig[J]. Journal of Audiology and Speech Pathology, 2002, 10(3): 174-176,T002
Authors:Zhang Yundong  Kong Weijia
Abstract:Objective To observe the effect of furosemide on stria vascularis cultivated in vitro from guinea pig, to explore the probable mechanism of furosemide ototoxicity.Methods 20 healthy pigmented guinea pigs was randomly divided into two groups: Furosemide group (n=16), control group (n=4). The stria vascularis explant were cultured for 24 hours using the explant-culture technique. Experimental groups were added into imediately different final concentration of Furosemide (60ug/ml?300ug/ml?600ug/ml?1250ug/ml?2500ug/ml) differently, and continuously cultivated 30 minutes or 90 minutes , then observed structure feature of the cultivated stria vascularis .Results Furosemide group did not show pathological changes such as edema of stria vascularis,shrinkage of the intermediate cells and enlargement of intercellular spaces. No significant changes were found in the stria vascularis structure features between furosemide group and control group. Conclusion Furosemide did not induce remarkable edema on cultivated stria vascularis from guinea pig.These findings suggested that furosemide might induce ototoxicity by indirect mechanism.
Keywords:Furosemide Ototoxicity Stria vascularis Explant culture technique
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