Biology subjects

Greene, N. T.

Publications and source records attributed to Greene, N. T..

3 recordsLinked to original sources

bioRxiv2019

Auditory binaural and spatial hearing impairments in a Fragile X Syndrome mouse model

The auditory brainstem compares sound-evoked excitation and inhibition from both ears to compute sound source location. Although alterations to the anatomy and physiology of the auditory brainstem have been demonstrated in Fragile X Syndrome (FXS) it is not known whether these changes cause sound localization impairments in FXS. To test the hypothesis that FXS-related alterations to brainstem circuits impair spatial hearing abilities, a reflexive prepulse inhibition (PPI) task, with sound source location as the prepulse stimulus, was used to show that Fmr1 knockout mice have decreased inhibition of their startle responses. Specifically, Fmr1 mice show decreased PPI compared to wildtype during gap detection, changes in sound source location, and spatial release from masking with no alteration to their overall startle thresholds compared to wildtype. Lastly, Fmr1 mice have increased latency to respond in these tasks suggesting additional impairments in the pathway responsible for reacting to a startling sound.

neuroscience↗

bioRxiv2019

Sensitivity of single units in the LSO of decerebrate cat to sinusoidally amplitude modulated tones

Fluctuations in amplitude are a common component of behaviorally important sound stimuli. Amplitude modulation (AM) is encoded by the peripheral auditory system in the timing of discharge spikes, and, more centrally, in the discharge rate. The mechanism producing this transformation from a time- to rate-based code is not known, but recent modeling efforts have suggested a role for neurons with response characteristics consistent with cells in the lateral superior olive (LSO). The responses of single units in the LSO of unanesthetized decerebrate cat were recorded to monaural sinusoidally amplitude modulated (SAM) tones by systematically varying sound level and modulation frequency (fm), and are described in terms of synchronization to the envelope and average discharge rate as a function of fm. LSO units typically synchronize strongly to low fm, and discharge preferentially (i.e. more strongly) over a small range of fm in response to low level SAM tones. At higher sound levels synchronization decreases and response rate increases until most or all modulation in the response is lost. These results contrast with responses recorded in the barbiturate-anesthetized cat, which tend to respond to most low-frequency modulations, and are consistent with LSO as an intermediate processing stage between the peripheral temporal- and central rate-based code for AM sounds.

neuroscience↗

bioRxiv2019

Evidence of a Functionally Segregated Pathway from Lateral Superior Olive to Inferior Colliculus

Neurons in the central nucleus of the inferior colliculus (ICC) of decerebrate cats show three major response patterns when tones of different frequencies and levels are presented to the contralateral ear. The frequency response maps of type I units uniquely exhibit a narrowly tuned I-shaped area of excitation around best frequency (the most sensitive frequency) and flanking regions of inhibition at lower and higher frequencies. Type I units receive ipsilateral inhibition, and show binaural excitatory/inhibitory interactions. Lateral superior olive (LSO) principal cells display a similar receptive field organization and sensitivity to interaural level differences (ILDs) and project directly to the ICC, therefore are supposed to be the dominant source of excitatory input for type I units. To test this hypothesis, the responses of ICC units were compared before and after reversible inactivation of the LSO by injection of the non-specific excitatory amino-acid antagonist kynurenic acid. When excitatory activity within the LSO was blocked, many ICC type I units (~50%) were silenced or showed substantially decreased activitycomparable. By contrast, the responses of the other two ICC unit types were largely unaffected. With regard to the origins of unaffected ICC type I units, evidence indicates that the LSO was inactivated in an incomplete, anisotropic manner, and the monaural and binaural responses of such units are similar to those of affected type I units. Taken together, these results support the interpretation that most type I units are the midbrain components of a functionally segregated ILD processing pathway initiated by the LSO.

neuroscience↗