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A METHOD FOR ESTABLISHING AN ANIMAL MODEL OF LIKE-AUDITARY NEUROPATHY

A METHOD FOR ESTABLISHING AN ANIMAL MODEL OF LIKE-AUDITARY NEUROPATHY
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摘要 Objective: To establish an animal model of like-auditory neuropathy in neonatal rat. Methods The ani-mals were injected with phenylhydrazine hydrochloride or saline at 7-day of age. ABR and DPOAE were performed to assess the auditory function. The cochlea basilar membrane stretched preparation and cochlear frozen sections were prepared for immunohistochemical staining to examine the morphological change of hair cells and spiral ganglion cells (SGNs). Results At 7-day age the ABR waveI, III, V, latencies andI-III,I-V IWIs in the experimental group were significantly prolonged compared with those in the control group. The ABR thresholds were also elevated in the experimental group. We found there is no significant differ-ence in DPOAE in phenylhydrazine hydrochloride exposure group compare to control group. The cochlear hair cells showed no signs of loss in both group, but the total number of neurofilaments positive cells in SGNs were significantly reduced in the phenylhydrazine treated animals. Conclusion Our study suggests that phenylhydrazine hydrochloride can change the auditory function and induce peripheral nerve pathology by targeted mainly the SGNs in neonatal rat. Objective: To establish an animal model of like-auditory neuropathy in neonatal rat. Methods The ani-mals were injected with phenylhydrazine hydrochloride or saline at 7-day of age. ABR and DPOAE were performed to assess the auditory function. The cochlea basilar membrane stretched preparation and cochlear frozen sections were prepared for immunohistochemical staining to examine the morphological change of hair cells and spiral ganglion cells (SGNs). Results At 7-day age the ABR waveI, III, V, latencies andI-III,I-V IWIs in the experimental group were significantly prolonged compared with those in the control group. The ABR thresholds were also elevated in the experimental group. We found there is no significant differ-ence in DPOAE in phenylhydrazine hydrochloride exposure group compare to control group. The cochlear hair cells showed no signs of loss in both group, but the total number of neurofilaments positive cells in SGNs were significantly reduced in the phenylhydrazine treated animals. Conclusion Our study suggests that phenylhydrazine hydrochloride can change the auditory function and induce peripheral nerve pathology by targeted mainly the SGNs in neonatal rat.
出处 《Journal of Otology》 2014年第1期48-51,共4页 中华耳科学杂志(英文版)
基金 supported by grants from the National Basic Research Program of China(973Program) And the National Natural Science Foundation of China(NSFC)(#81271082)
关键词 Animal model Auditory brainstem response Distortion-product otoacoustic emission auditory neuropathy Animal model Auditory brainstem response Distortion-product otoacoustic emission auditory neuropathy
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  • 1Jiang ZD,Chen C,Wilkinson AR. Changes in brainstem audito-ry evoked response latencies in term neonates with hyperbilirubi-nemia[J].Pediatric Neurology,2007.35.
  • 2Gerardo Barragàn Mejia. Experimental hemolysis mod-el to study bilirubin encephalopathy in rat brain[J].Journal of Neu-roscience Methods,2008.35-41.
  • 3Harrison RV. An animal model of auditory neuropathy[J].Ear and Hearing,1998.355.
  • 4Raveh E,Bul1er N,Badrana O. Auditory neuropathy:clinical characteristics and therapeutic approach[J].Am J Otolaryn-gol,2007.302.
  • 5Trautwein PG,Sininger YS,Nelson R. Cochlear implantation of auditory neuropathy[J].J Am Audiol,2000.309.
  • 6Spencer RF,Shaia WT,Gleason AT. Changes in calcium-bind-ing protein expression in the auditory brainstem nuclei of the jaun-diced Gunn rat[J].Hearing Research,2002.l29.
  • 7Shi HB,Kakazu Y,Shibata S. Bilirubin potentiates inhibito-ry synaptic transmission in lateral superior olive neurons of the rat[J].Neuroscience Research,2006.161-170.
  • 8Sano M,Kaga K,Kitazumi E,et a1. Sensorineural hearing loss in patients with cerebral palsy after asphyxia and hyperbilirubine-mia[J].Int J Pediatr Otorhinolaryngol,2005.l211.
  • 9Naito R,Murofushi T,Mizutani M. Auditory brainstem responses,electrocochleograms,and cochlear microphonics in the myelin deficient mutant hamster‘bt’[J].Hearing Research,1999.44.
  • 10Schmiedt RA,Okamura HO,Lang H. Ouabain application to the round window of the gerbil cochlea:a model of auditory neu-ropathy and apoptosis[J].Journal of the Association for Research in Otolaryngology,2002.223.

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