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中耳内窥镜检查可疑中耳疾病46例
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
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豚鼠耳蜗核复合体的立体定位
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
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氟桂嗪对豚鼠耳蜗血后ABR和形态学变化的影响（英）
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
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庆大霉素耳毒性和脂质过氧化的相关性研究（英）
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
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豚鼠耳蜗核复合体的解剖
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
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人胚神经干细胞的分离和培养
There have been many studies on the gentamicin(GM) cochlear toxicity, however, the mechanism has notbeen understood fully.The correlation between the protection of dimethyl-sulphoxide (DMSO) against cochlear damage caused byGM and the inhibition of oxygen free radicals and lipidperoxidation were observed in guinea pigs.One hundred healthy guinea pigs, weighing (221±23) g (x±s) with normal Preyer' s reflex were equallyrandomized four groups. The normal control was not treat-ed; GM group was intramuscularly injected with GM 200mg·kg-1·d-1 for eight days; GM + DMSO group was givenGM at the same dose and intraperitoneal DMSO (2.0g·kg-1·d-1) for eight days; Normal saline (NS) group re-ceived normal saline 4.5 ml·kg-1·d-1 for eight days.
