中华耳科学杂志
中華耳科學雜誌
중화이과학잡지
CHINESE JOURNAL OF OTOLOGY
2013年
4期
593-596
,共4页
王建军%毛华杰%董吕华%翟所强%马龙
王建軍%毛華傑%董呂華%翟所彊%馬龍
왕건군%모화걸%동려화%적소강%마룡
卡那霉素%速尿%毛细胞%螺旋神经节细胞
卡那黴素%速尿%毛細胞%螺鏇神經節細胞
잡나매소%속뇨%모세포%라선신경절세포
kanamycin%furosemide%hair cells%spiral ganglion cells
目的:观察耳蜗毛细胞严重损伤后螺旋神经节细胞的病变过程。方法豚鼠肌肉注射硫酸卡那霉素(1000mg/kg)2小时后给予速尿(100mg/kg)静脉注射,分别于用药3天、7天、1月及2月行听觉脑干诱发电位(auditory brainstem response ABR)及耳蜗形态学检测。结果联合应用速尿和硫酸卡那霉素后,豚鼠鼠ABR阈值出现很大程度提高,给药3天、7天、1月、2个月组各频率ABR阈值比较无差别;对药物损伤致聋豚鼠进行耳蜗切片、扫描电镜观察,发现用药7天后耳蜗毛细胞严重受损,以外毛细胞(OHCs)缺失为主,严重致聋的豚鼠内毛细胞(IHCs)也广泛缺失,但是切片显示柯替氏器的支持细胞存在;螺旋神经节细胞正常。联合用药1月后螺旋神经节细胞大量缺失,Corti’s器塌陷。结论药物性耳聋首先损伤毛细胞,螺旋神经节细胞的损伤延后发生,螺旋神经节细胞缺失程度取决于致聋后的时间长短,致聋后螺旋神经节细胞变性可以持续数年。这为我们植入电子耳蜗提够了宝贵的时间窗。
目的:觀察耳蝸毛細胞嚴重損傷後螺鏇神經節細胞的病變過程。方法豚鼠肌肉註射硫痠卡那黴素(1000mg/kg)2小時後給予速尿(100mg/kg)靜脈註射,分彆于用藥3天、7天、1月及2月行聽覺腦榦誘髮電位(auditory brainstem response ABR)及耳蝸形態學檢測。結果聯閤應用速尿和硫痠卡那黴素後,豚鼠鼠ABR閾值齣現很大程度提高,給藥3天、7天、1月、2箇月組各頻率ABR閾值比較無差彆;對藥物損傷緻聾豚鼠進行耳蝸切片、掃描電鏡觀察,髮現用藥7天後耳蝸毛細胞嚴重受損,以外毛細胞(OHCs)缺失為主,嚴重緻聾的豚鼠內毛細胞(IHCs)也廣汎缺失,但是切片顯示柯替氏器的支持細胞存在;螺鏇神經節細胞正常。聯閤用藥1月後螺鏇神經節細胞大量缺失,Corti’s器塌陷。結論藥物性耳聾首先損傷毛細胞,螺鏇神經節細胞的損傷延後髮生,螺鏇神經節細胞缺失程度取決于緻聾後的時間長短,緻聾後螺鏇神經節細胞變性可以持續數年。這為我們植入電子耳蝸提夠瞭寶貴的時間窗。
목적:관찰이와모세포엄중손상후라선신경절세포적병변과정。방법돈서기육주사류산잡나매소(1000mg/kg)2소시후급여속뇨(100mg/kg)정맥주사,분별우용약3천、7천、1월급2월행은각뇌간유발전위(auditory brainstem response ABR)급이와형태학검측。결과연합응용속뇨화류산잡나매소후,돈서서ABR역치출현흔대정도제고,급약3천、7천、1월、2개월조각빈솔ABR역치비교무차별;대약물손상치롱돈서진행이와절편、소묘전경관찰,발현용약7천후이와모세포엄중수손,이외모세포(OHCs)결실위주,엄중치롱적돈서내모세포(IHCs)야엄범결실,단시절편현시가체씨기적지지세포존재;라선신경절세포정상。연합용약1월후라선신경절세포대량결실,Corti’s기탑함。결론약물성이롱수선손상모세포,라선신경절세포적손상연후발생,라선신경절세포결실정도취결우치롱후적시간장단,치롱후라선신경절세포변성가이지속수년。저위아문식입전자이와제구료보귀적시간창。
Objective To study morphological changes of spiral ganglion cells (SGN) following severe cochlear hair cells injury. Methods Guinea pigs were given kanamycin sulfate (1000 mg/kg) intramuscularly followed by furosemide (100 mg/kg) intravenously 2 hours later. Auditory brainstem responses (ABRs) and cochlear morphology were examined at 3 days, 7 days, 1 month and 2 months respectively after the treatment. Results ABR thresholds were greatly elevated after the treatment, with no significant difference among the different time groups. Scanning electron microscopy revealed severe damage to cochlear hair cells, especially out hair cells (OHC) after 7 days. There was also extensive loss of inner hair cells in animals with severe auditory function damage while supporting cells in the organ of Corti were preserved. The SGN showed no change on Day 7, al-though severe SGN loss was seen after 1 month, with total collapse of the organ of Corti. Conclusion Drug-induced hearing loss starts with hair cell loss, followed by SGN loss. In addition, the extent of SGN damage seems to correlate to time lapse after drug administration and can take years to develop, which may provide a time window for cochlear implant.