中华耳鼻咽喉头颈外科杂志
中華耳鼻嚥喉頭頸外科雜誌
중화이비인후두경외과잡지
CHINESE JOURNAL OF OTORHINOLARYNGOLOGY HEAD AND NECK SURGERY
2008年
6期
439-442
,共4页
刘建平%戴春富%王正敏%迟放鲁%田洁%笪翠弟
劉建平%戴春富%王正敏%遲放魯%田潔%笪翠弟
류건평%대춘부%왕정민%지방로%전길%달취제
庆大霉素类%组织分布%Corti器%器官培养技术
慶大黴素類%組織分佈%Corti器%器官培養技術
경대매소류%조직분포%Corti기%기관배양기술
Gentamicins%Tissure distribution%Organ of Corti%Organ culture techniques
目的 观察庆大霉素-德州红耦联物在体外培养小鼠耳蜗Corti器的分布情况,比较不同时间庆大霉素吸收的差异.方法 分离小鼠耳蜗Corti器,体外培养,培养液中加有庆大霉素-德州红耦联物,分别于培养后3 h、6 h、12 h、24 h、48 h、3 d.4 d和7 d收集标本,荧光染色后行激光扫描共聚焦显微镜观察基底膜庆大霉素的分布情况.结果 小鼠耳蜗Corti器在培养3 h后即可见外毛细胞的纤毛和胞体两侧的胞膜有庆大霉素分布;随着培养时间的延长,庆大霉素在Corti器中的所有细胞均见分布,尤以外毛细胞明显,主要聚集在毛细胞顶端纤毛的下方;培养24 h后庆大霉素在外毛细胞的聚集达到最高峰,而在支持细胞未见明显的聚集;体外培养7 d后在毛细胞胞质中仍可见庆大霉素分布.结论 小鼠Corti器体外培养可用来动态检测庆大霉素在耳蜗细胞的吸收和聚集情况.
目的 觀察慶大黴素-德州紅耦聯物在體外培養小鼠耳蝸Corti器的分佈情況,比較不同時間慶大黴素吸收的差異.方法 分離小鼠耳蝸Corti器,體外培養,培養液中加有慶大黴素-德州紅耦聯物,分彆于培養後3 h、6 h、12 h、24 h、48 h、3 d.4 d和7 d收集標本,熒光染色後行激光掃描共聚焦顯微鏡觀察基底膜慶大黴素的分佈情況.結果 小鼠耳蝸Corti器在培養3 h後即可見外毛細胞的纖毛和胞體兩側的胞膜有慶大黴素分佈;隨著培養時間的延長,慶大黴素在Corti器中的所有細胞均見分佈,尤以外毛細胞明顯,主要聚集在毛細胞頂耑纖毛的下方;培養24 h後慶大黴素在外毛細胞的聚集達到最高峰,而在支持細胞未見明顯的聚集;體外培養7 d後在毛細胞胞質中仍可見慶大黴素分佈.結論 小鼠Corti器體外培養可用來動態檢測慶大黴素在耳蝸細胞的吸收和聚集情況.
목적 관찰경대매소-덕주홍우련물재체외배양소서이와Corti기적분포정황,비교불동시간경대매소흡수적차이.방법 분리소서이와Corti기,체외배양,배양액중가유경대매소-덕주홍우련물,분별우배양후3 h、6 h、12 h、24 h、48 h、3 d.4 d화7 d수집표본,형광염색후행격광소묘공취초현미경관찰기저막경대매소적분포정황.결과 소서이와Corti기재배양3 h후즉가견외모세포적섬모화포체량측적포막유경대매소분포;수착배양시간적연장,경대매소재Corti기중적소유세포균견분포,우이외모세포명현,주요취집재모세포정단섬모적하방;배양24 h후경대매소재외모세포적취집체도최고봉,이재지지세포미견명현적취집;체외배양7 d후재모세포포질중잉가견경대매소분포.결론 소서Corti기체외배양가용래동태검측경대매소재이와세포적흡수화취집정황.
Objective To investigate the uptaking and accumulation of gentamicin by mouse hair cells in vitro.Methods Cochlear explants were prepared from the microdissected neonatM mouse cochlea. Cochlear explants were cultured with gentamicin-Texas-red conjunction (G1TrR) for difierent time.Laser confocal microscopy was used to observe the distribution of GTYR in the cochlear sensoty ceUs after labeling with phalloidin-alexa-488.ResulIs Soon after culture,there was diffuse red staining all tissue cells in the explants.At later time the hair cells were more staining tllan other cells in the explants.There was no obviously accumulation of GTTR in the supporting cells.The peak level of fluorescent density was reached at 24 hours culture.The GTTR was seen in the infracuticular zone of the hair cells.There was still accumulation of GTTR in the hair cells of the explants after 7 days culturing.Conclusions GTTR and Cochlea explants were useful methods to investigate the pharmacokinetics and mechanisms of gentamicin accumulation over time.