Sensitive hearing organs often employ nonlinear mechanical sound processing which produces distortion-product otoacoustic emissions. Such emissions are also recorded from insect tympanal organs. Here we report high frequency distortion-product emissions, evoked by stimulus frequencies up to 95 kHz, from the tympanal organ of a notodontid moth, Ptilodon cucullina, which contains only a single auditory receptor neuron. The 2f1-f2 distortion-product emission reaches sound levels above 40 dB SPL. Most emission growth functions show a prominent notch of 20 dB depth (n = 20 trials), accompanied by an average phase shift of 119 degrees , at stimulus levels between 60 and 70 dB SPL, which separates a low- and a high-level component. The emissions are vulnerable to topical application of ethyl ether which shifts growth functions by about 20 dB towards higher stimulus levels. For the mammalian cochlea, Lukashkin and colleagues have proposed that distinct level-dependent components of nonlinear amplification do not necessarily require interaction of several cellular sources but could be due to a single nonlinear source. In notodontids, such a physiologically vulnerable source could be the single receptor cell. Potential contributions from accessory cells to the nonlinear properties of the scolopidial hearing organ are still unclear.
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http://dx.doi.org/10.1007/s00359-007-0244-8 | DOI Listing |
Am J Otolaryngol
December 2024
Department of Clinical Laboratory, Wenzhou People's Hospital, Wenzhou Women and Children's Hospital, Zhejiang, China. Electronic address:
Background: The purpose of the research was to examine the prevalence rates of screening for genetics and hearing simultaneously in neonates and provide scientific evidence for the beneficial application of newborn screening in the Southeast China population.
Methods: Between June 2015 and March 2023, 27,843 newborns were enrolled in the study. All participants were screened by otoacoustic emissions at 2 days of age.
J Am Acad Audiol
December 2024
Department of Audiology, Monash Health Melbourne, Victoria, Australia.
Objective: The objectives of the study were to (i) evaluate the effectiveness of wideband absorbance (WBA) at ambient pressure (WBA), tympanic peak pressure (WBA), and 0 daPa (WBA) to identify conductive hearing loss (CHL) in infants and (ii) compare the sensitivity and specificity of the three WBA tests with that of high-frequency tympanometry (HFT) and transient-evoked otoacoustic emissions (TEOAE).
Method: A total of 31 ears with hearing thresholds no greater than 20 dB HL (reference group from 20 infants [mean age: 3.1 weeks]) and 47 ears with CHL from 31 infants (mean age: 3.
Isr Med Assoc J
December 2024
Department of Dermatology, Emek Medical Center, Afula, Israel.
Background: Little is known about audiovestibular function in psoriasis, a chronic systemic inflammatory disease that affects 2% of the world's population.
Objectives: To investigate audiovestibular function in patients with psoriasis.
Methods: In this prospective case-control trial, we enrolled 33 patients with psoriasis and 30 healthy controls.
Front Psychol
December 2024
Department of Speech, Language and Hearing Sciences, Indiana University, Bloomington, IN, United States.
The Test of Basic Auditory Capabilities (TBAC) consists of 19 discrimination and identification tasks selected to study individual differences in audition. In one TBAC study, performance was measured for 340 normal-hearing subjects, but no investigation into possible sex differences was undertaken. That dataset now has been re-analyzed by sex.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
The Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, 117513 Moscow, Russia.
Auditory neuropathy spectrum disorder (ANSD) is often missed by standard hearing tests, accounting for up to 10% of hearing impairments (HI) and commonly linked to variants in 23 genes. We assessed 122 children with HI, including 102 with sensorineural hearing loss (SNHL) and 20 with ANSD. SNHL patients were genotyped for common variants using qPCR, while ANSD patients underwent whole exome sequencing, with variants analyzed across 249 genes.
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