CD1 hearing-impaired mice. I: Distortion product otoacoustic emission levels, cochlear function and morphology

• Published in: Hearing research 1998-06, Vol.120 (1), p.37-50
• Main Authors: Le Calvez, S, Avan, P, Gilain, L, Romand, R
• Format: Article
• Language: English
• Subjects: Acoustic Stimulation; Actins; Animals; Auditory Threshold - physiology; Biological and medical sciences; Cochlea; Cochlea - anatomy & histology; Cochlea - physiology; Cochlear microphonic; Cochlear Microphonic Potentials - physiology; Distortion product otoacoustic emission; Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology; Evoked Potentials, Auditory, Brain Stem - physiology; Hearing Loss, Sensorineural - genetics; Hearing Loss, Sensorineural - physiopathology; Intermediate Filaments - physiology; Medical sciences; Mice; Mice, Inbred CBA; Mice, Mutant Strains; Mutant mouse; Non tumoral diseases; Otoacoustic Emissions, Spontaneous - physiology; Otorhinolaryngology. Stomatology; Phalloidin staining; Phalloidine; Summating potential
• ISSN: 0378-5955; 1878-5891
• DOI: 10.1016/S0378-5955(98)00050-1

The levels of distortion product otoacoustic emissions (DPOAEs) were measured in a strain of hearing-impaired mutant mice (CD1) at various stages of outer hair cell impairment and compared to those of a control inbred strain (CBA/J). Parallel measurements of cochlear potentials and auditory brainstem evoked responses (ABRs) were performed and surface preparations of organs of Corti were observed using phalloidin staining of filamentous actin. Comparison of DPOAEs (elicited by stimulus levels of 60 and 70 dB SPL) with standard functional tests allowed the categorization of CD1 ears into two groups on the basis of the presence or absence of DPOAE, which corresponded to mean ABR thresholds greater or less than 40 dB nHL respectively. When adopting ABR threshold as the gold standard, this procedure yielded rates of false-positives and -negatives ranging from 5 to 16%. However, individual predictions of electrophysiological function from DPOAE levels were not accurate, owing to their large variance, and attempts to optimize stimulus levels did not reduce this variance. In contrast, the profiles of DPOAE level vs. f 2 exhibited large correlations with ABR threshold profiles as a function of f 2. It was also noteworthy that the mean levels of DPOAEs in CD1 mice recorded in frequency intervals with normal ABR thresholds were significantly smaller than those of CBA/J mice. Although hearing loss was revealed early both by DPOAEs and by other functional tests, surface preparations often remained normal until about 3–4 months of age.