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
2014年
10期
848-853
,共6页
张少华%黄文钦%林晨希%陈瑾%农东晓%唐安洲
張少華%黃文欽%林晨希%陳瑾%農東曉%唐安洲
장소화%황문흠%림신희%진근%농동효%당안주
诱发电位,听觉%前庭神经核%蜗神经核%豚鼠
誘髮電位,聽覺%前庭神經覈%蝸神經覈%豚鼠
유발전위,은각%전정신경핵%와신경핵%돈서
Evoked potentials,auditory%Vestibular nucleus%Cochlear nucleus%Guinea pigs
目的 通过建立声诱发短潜伏期负电位(acoustically evoked short latency negative response,ASNR)豚鼠模型,直流电损毁前庭神经核或蜗神经核,验证ASNR的神经来源.方法 24只健康豚鼠采用随机数字表法分为两组,正常对照组8只(16耳),致聋组16只(32耳).致聋组应用卡那霉素和利尿酸联合致聋,根据ASNR引出与否又分为ASNR组和非ASNR组.对照组、ASNR组及非ASNR组按损毁核团不同又分为前庭神经核损毁组及蜗神经核损毁组.所有动物均分别进行前庭神经核及蜗神经核定位,直流电损毁神经核团,24 h后观察声诱发脑干电位的改变.处死动物后脑干标本经冰冻切片及染色,显微镜下验证损毁部位.结果 致聋组16只豚鼠(32耳)中10耳出现ASNR(31.3%).正常对照组豚鼠前庭神经核损毁后听性脑干反应(ABR)波形无明显改变,蜗神经核损毁后ABR仅余Ⅰ波.ASNR组中前庭神经核损毁组(7耳)ASNR均消失,而蜗神经核损毁组(3耳)ASNR均未消失;非ASNR组前庭神经核或蜗神经核损毁后ABR波形均无明显改变.脑干切片证实直流电破坏部位准确.结论 ASNR的责任神经核是前庭神经核,与蜗神经核无关.
目的 通過建立聲誘髮短潛伏期負電位(acoustically evoked short latency negative response,ASNR)豚鼠模型,直流電損燬前庭神經覈或蝸神經覈,驗證ASNR的神經來源.方法 24隻健康豚鼠採用隨機數字錶法分為兩組,正常對照組8隻(16耳),緻聾組16隻(32耳).緻聾組應用卡那黴素和利尿痠聯閤緻聾,根據ASNR引齣與否又分為ASNR組和非ASNR組.對照組、ASNR組及非ASNR組按損燬覈糰不同又分為前庭神經覈損燬組及蝸神經覈損燬組.所有動物均分彆進行前庭神經覈及蝸神經覈定位,直流電損燬神經覈糰,24 h後觀察聲誘髮腦榦電位的改變.處死動物後腦榦標本經冰凍切片及染色,顯微鏡下驗證損燬部位.結果 緻聾組16隻豚鼠(32耳)中10耳齣現ASNR(31.3%).正常對照組豚鼠前庭神經覈損燬後聽性腦榦反應(ABR)波形無明顯改變,蝸神經覈損燬後ABR僅餘Ⅰ波.ASNR組中前庭神經覈損燬組(7耳)ASNR均消失,而蝸神經覈損燬組(3耳)ASNR均未消失;非ASNR組前庭神經覈或蝸神經覈損燬後ABR波形均無明顯改變.腦榦切片證實直流電破壞部位準確.結論 ASNR的責任神經覈是前庭神經覈,與蝸神經覈無關.
목적 통과건립성유발단잠복기부전위(acoustically evoked short latency negative response,ASNR)돈서모형,직류전손훼전정신경핵혹와신경핵,험증ASNR적신경래원.방법 24지건강돈서채용수궤수자표법분위량조,정상대조조8지(16이),치롱조16지(32이).치롱조응용잡나매소화이뇨산연합치롱,근거ASNR인출여부우분위ASNR조화비ASNR조.대조조、ASNR조급비ASNR조안손훼핵단불동우분위전정신경핵손훼조급와신경핵손훼조.소유동물균분별진행전정신경핵급와신경핵정위,직류전손훼신경핵단,24 h후관찰성유발뇌간전위적개변.처사동물후뇌간표본경빙동절편급염색,현미경하험증손훼부위.결과 치롱조16지돈서(32이)중10이출현ASNR(31.3%).정상대조조돈서전정신경핵손훼후은성뇌간반응(ABR)파형무명현개변,와신경핵손훼후ABR부여Ⅰ파.ASNR조중전정신경핵손훼조(7이)ASNR균소실,이와신경핵손훼조(3이)ASNR균미소실;비ASNR조전정신경핵혹와신경핵손훼후ABR파형균무명현개변.뇌간절편증실직류전파배부위준학.결론 ASNR적책임신경핵시전정신경핵,여와신경핵무관.
Objective This study established a model of acoustically evoked short latency negative response (ASNR) in guinea pigs.Stereotaxic coordinate guided electrolytic lesion was applied to animal brainstem nuclei,the vestibular nucleus and the cochlear nucleus,to define the neural origin of ASNR.Methods Twenty four guinea pigs with normal hearing were randomly divided into the control group (8 subjects,16 ears) and the deafened group (16 subjects,32 ears).Each animal experienced the auditory brainstem response (ABR) test.According to the presence of ASNR,the deafened group was further divided into ASNR group and non-ASNR group.Electrolytic lesion was conducted to the vestibular nucleus and cochlear nucleus respectively,followed by ABR test.The lesion structures were verified by brainstem slice and microscope.Results In deafened group,the ASNR was elicited in 10 ears (31.3%).The ASNR was eliminated due to the electrolytic destruction to the vestibular nucleus,but it remained unchanged after the same procedure to the cochlear nucleus.Conclusion It is clear that the ASNR is originated from the vestibular nucleus,but not the cochlear nucleus.