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Superior colliculus lesions preferentially disrupt multisensory orientation.

The general involvement of the superior colliculus (SC) in orientation behavior and the striking parallels between the multisensory responses of SC neurons and overt orientation behaviors have led to assumptions that these neural and behavioral changes are directly linked. However, deactivation of two areas of cortex which also contain multisensory neurons, the anterior ectosylvian sulcus and rostral lateral suprasylvian sulcus have been shown to eliminate multisensory orientation behaviors, suggesting that this behavior may not involve the SC. To determine whether the SC contributes to this behavior, cats were tested in a multisensory (i.e. visual-auditory) orientation task before and after excitotoxic lesions of the SC. For unilateral SC lesions, modality-specific (i.e. visual or auditory) orientation behaviors had returned to pre-lesion levels after several weeks of recovery. In contrast, the enhancements and depressions in behavior normally seen with multisensory stimuli were severely compromised in the contralesional hemifield. No recovery of these behaviors was observed within the 6 month testing period. Immunohistochemical labeling of the SC revealed a preferential loss of parvalbumin-immunoreactive pyramidal neurons in the intermediate layers, a presumptive multisensory population that targets premotor areas of the brainstem and spinal cord. These results highlight the importance of the SC for multisensory behaviors, and suggest that the multisensory orientation deficits produced by cortical lesions are a result of the loss of cortical influences on multisensory SC neurons.

Animals↗

Audition.

Explore the source record for details and available documents.

Acoustic Stimulation↗

Multisensory orientation behavior is disrupted by neonatal cortical ablation.

The integration of visual and auditory information can significantly amplify the sensory responses of superior colliculus (SC) neurons and the behaviors that depend on them. This response amplification depends on the development of SC inputs that are derived from two regions of cortex: the anterior ectosylvian sulcus (AES) and the rostral lateral suprasylvian sulcus (rLS). Neonatal ablation of these cortico-collicular areas has been shown to disrupt the development of the multisensory enhancement capabilities of SC neurons and the present results demonstrate that it also precludes the development of the normal multisensory enhancements in orientation behavior. Animals with neonatal ablation of AES and rLS were tested at maturity and found unable to benefit from the combination of visual and auditory cues in their efforts to localize targets in contralesional space. In contrast, their ipsilesional multisensory orientation capabilities were indistinguishable from those of normal animals. However, when only one of these cortical areas was removed during early life, later behavioral consequences were negligible. Whether similar compensatory processes would occur in adult animals remains to be determined. These observations, coupled with those from previous studies, also suggest that a surprisingly high proportion of SC neurons capable of multisensory integration must be present for orientation behavior benefits to be realized. Compensatory mechanisms can achieve this if early lesions spare either AES or rLS, but even the impressive plasticity of the neonatal brain cannot compensate for the early loss of both of them.

Adaptation, Physiological↗

Brainstem auditory evoked potentials.

Brainstem auditory evoked potentials (BAEPs) have obtained widespread clinical application in assessing neurologic and audiologic problems. Seven waves (I-VII) are usually recorded in the first 10 ms following broad-band and high-intensity clicks. Latencies of waves I, III, and V, interpeak latencies of I-III, III-V, and I-V, and the amplitude ratio of wave V to wave I are common parameters evaluated for assessing clinically relevant abnormalities of BAEPs. Usually two-channel recordings are obtained: vertex (Cz) to ipsilateral ear and Cz to contralateral earlobe derivation. Evaluating different components in the two derivations helps their identification, particularly when the BAEPs are abnormal. Several technical and subject-related factors affect the amplitude and latencies of BAEP components besides lesions and dysfunctions involving the peripheral auditory structures and brainstem auditory pathways. BAEPs have maximal clinical utility in evaluating comatose patients, in patients with suspected demyelinating disorders, posterior fossa tumors, or in audiologic evaluation, especially in infants. They are also used for intraoperative monitoring of eighth-nerve and brainstem function during different types of posterior fossa surgery.

Brain Stem↗

The acute deafness of definite multiple sclerosis: BAEP patterns.

Of 705 patients with or suspected of multiple sclerosis who underwent evoked potential recording during a 5 year period, 12 patients with definite multiple sclerosis experienced an acute hearing loss during a relapse of the demyelinating disease. Hearing loss was unilateral in all of the 12 cases but one; tinnitus was associated with hearing loss in 9 of the 12 patients. Deafness is an unfrequent symptom in the course of multiple sclerosis, being estimated to be no more than 3% in large series of multiple sclerosis. Brain-stem auditory evoked potentials were recorded in all 12 patients, during the relapse with acute hearing loss in 4 of them, after the relapse with hearing loss in the 8 others. During the relapse with hearing loss, BAEP abnormalities were present ipsilateral to the hearing loss in all 4 patients, wave I being absent in 2 of them. BAEPs were drastically improved when recorded after the relapse with hearing loss in 2 of the 3 patients in whom repeated records were made. BAEPs were abnormal on the side of the previous hearing loss in 5 out of the 8 patients recorded after the relapse with hearing loss. Clinical and BAEP data suggest that, in accordance with the anatomical organization of the auditory pathways, the lesion causing unilateral hearing loss in multiple sclerosis could be situated in the cochlear nerve or close to its entry zone in the brain-stem. However, dissociation between unilateral hearing loss and a normal peak I and I-III interval may occur.

Acoustic Stimulation↗

Imaging and cochlear implant.

The auditory pathway imaging may be morphologic and/or functional. The high resolution computed tomography and the magnetic resonance imaging (MRI) provide an evaluation of the anatomical and structural landmarks useful for a safe and successful cochlear implantation. The electrical stimulations supplied by the cochlear implant give rise to ascending electrochemical activities reaching the cortex. These activities can be recorded with scalp electrodes by Evoked Potentials (EP) or fields techniques and eventually translated in isochronic or isopotential brain mapping. These techniques provide a very sharp temporal resolution with an imprecise spatial resolution. The late auditory EP of implantees are closely comparable to the responses of normal hearing people. The neuronal metabolism's increase is associated with a cerebral blood flow increase. Comparing regional cerebral blood flow (rCBF) between two or more conditions allows the localisation of brain areas involved in a fixed task. Single photon or positron emission tomography and functional MRI (fMRI) demonstrate cBF changes associated with an auditory stimulation. (f)MRI is contraindicated in cochlear implantees.

Brain↗

Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patients.

A multimodal electrophysiological study was performed on 41 patients from 24 families with autosomal dominant cerebellar ataxia type I (ADCA I). Upper- and lower-limb motor evoked potentials (MEPs) to transcranial magnetic stimulation, median and tibial nerve somatosensory evoked potentials (Mn and Tn-SSEPs), orthodromic sensory (SCV) and motor conduction (MCV) velocity along median and tibial nerve, brainstem auditory evoked potentials (BAEPs), and visual evoked potentials (VEPs) were examined. Molecular analysis showed 2 SCA1 families and 2 families linked to the SCA2 locus. A sural nerve biopsy was performed in 5 patients. Brainstem damage of the auditory pathway was observed in 79% of patients examined. VEP abnormalities possibly of central origin were found in 52% of patients. MEP and SSEP abnormalities were differently distributed along the pathways examined: the longer the pathway, the higher the occurrence and severity of impairment. Peripheral dying-back neuropathy (confirmed by nerve bioptic data) was a frequent finding (56%). A progressive degenerative process involving first the longest tracts of the central motor and central and peripheral branches of somatosensory pathways is hypothesized in ADCA I. MEP abnormalities were more frequent in SCA1, and the sensory-motor neuropathy was more severe in SCA2.

Adolescent↗

Expression of the mouse Macf2 gene during inner ear development.

Plakins, a family of linker proteins that connect cytoskeletal elements to cellular junctions and the extracellular matrix, are primarily responsible for the mechanical properties of cells and tissues. They include desmoplakin, envoplakin, plectin, dystonin/BPAG1, and Kakapo. Mutations in plakins cause several skin, muscular and neurological disorders. Macrophins are a recently discovered subfamily of plakins with binding domains for actin, intermediate filaments and microtubules. Characteristic features of macrophins include variable actin binding domains, a central rod domain containing both plectin and spectrin repeats, and a C-terminus containing EF hands and GAS2/GAR22 domain. We have examined expression of mouse Macf2, encoding macrophin-2, in adult tissues and in the developing, neonatal, and mature inner ear by in situ hybridization. Northern blot analysis identified three large tissue-specific Macf2 transcripts: a 16-kb mRNA in skeletal muscle and heart, a 15-kb mRNA in brain, and a 9-kb mRNA in RNA from ovary plus uterus. In situ hybridization of the developing mouse inner ear indicated that Macf2 is expressed in the otocyst at day 12.5, in the sensory epithelium by embryonic day 16.5, and in both inner and outer hair cells by day 16.5. Macf2 is expressed in the bodies of both sensory and motor neurons in the central and peripheral nervous system, including the auditory pathway. The Macf2 protein could be involved in the regulation of cytoskeletal connections to cellular junctions and play an important structural role in organs, such as the inner ear, that are subjected to strong mechanical forces.

Animals↗

Neural correlates of sensory gating in the rat: decreased Fos induction in the lateral septum.

In the P(50) gating or conditioning-testing paradigm in the rat, two identical click stimuli are presented with an inter-click interval of 500 ms. The reaction towards the second click, as measured with evoked potentials, is reduced in respect to that towards the first click; this phenomenon is called sensory gating. In the present experiments, the inter-click interval was varied systematically and auditory evoked potentials were measured. Sensory gating was found to occur only at intervals between 500 and 1000 ms, but not at longer intervals. Fos immunohistochemistry was then performed using two groups of rats exposed to double clicks: the inter-click interval was 500 ms in the experimental group and 2500 ms in the control group. Fos induction was analyzed in selected brain structures. In the auditory pathways, Fos-immunoreactive neurons were found in both groups of rats in the inferior colliculus and medial geniculate body. Fos-immunoreactive cells were also examined in the septum and hippocampus. In the ventral part of the lateral septal nucleus, the labeled neurons were significantly fewer in the experimental animals compared to the control group. Smaller and non-significant quantitative differences of Fos-positive neurons were documented in the medial septum and hippocampal CA1 region. These data point out a selective decrease in the lateral septum of Fos induced by auditory sensory gating, and suggest an involvement of this structure, and possibly of other parts of the septo-hippocampal system, in sensory gating mechanisms. The results might be relevant for theories on sensory gating deficits in schizophrenia.

Acoustic Stimulation↗

Normalization of middle latency auditory P1 potential following posterior ansa-pallidotomy in idiopathic Parkinson's disease.

The P1 potential (50 msec) of middle latency auditory evoked potential was evaluated in seven patients with advanced idiopathic Parkinson's disease before and after contemporaneous bilateral posterior ansa-pallidotomy. P1 potential was lacking in two patients preoperatively and was prolonged in the remainder of the patients when examined in a best medicated 'on' state. All patients showed varying degrees of dementia preoperatively on clinical examination. Remarkable improvement in their Unified Parkinson's Disease Rating Scale (UPDRS) scores during 'on' states from a mean of 45.85 to 14.28 post-operatively was achieved. Subsidence of akinetic symptoms, abolishment of dyskinesia, improvement in gait freezing, rigidity, and tremors represented main areas of improvement. P1 latencies and amplitudes reverted back to normal values in six patients including the two patients who lacked P1 wave preoperatively. One patient showed mild worsening of both Pa and P1 values post-operatively attributed to sleepiness during testing, a transient phenomenon commonly encountered following posterior ansa-pallidotomy. The post-operative P1 changes were statistically significant for both latencies and amplitudes at p = 0.078 and p = 0.073, respectively, for all seven patients using one tailed paired t-test. The change in UPDRS post-operatively best correlated with the post-operative difference in P1; specifically, UPDRS subscore II with P1 amplitude (r = -0.068, p = 0.09), and UPDRS subscore IV with Pa: P1 ratio (r = +0.77, p = 0.04). Earlier clinical and experimental work support the tegmental pedunculopontine nucleus (PPN) as the site of origin of P1 wave. In addition, its presence reflects the integrity of output cholinergic projection from PPN to both ascending reticular activating system ARAS and auditory pathway. We believe this is the first report of restoring the integrity of P1 wave following posterior ansa-pallidotomy in patients with advanced idiopathic Parkinson's disease. Disinhibition of the PPN by posterior ansa-pallidotomy can explain improvements in motor symptoms in view of reemergence and normalization of P1 wave form.

Evoked Potentials, Auditory↗

Complex auditory behaviour emerges from simple reactive steering.

The recognition and localization of sound signals is fundamental to acoustic communication. Complex neural mechanisms are thought to underlie the processing of species-specific sound patterns even in animals with simple auditory pathways. In female crickets, which orient towards the male's calling song, current models propose pattern recognition mechanisms based on the temporal structure of the song. Furthermore, it is thought that localization is achieved by comparing the output of the left and right recognition networks, which then directs the female to the pattern that most closely resembles the species-specific song. Here we show, using a highly sensitive method for measuring the movements of female crickets, that when walking and flying each sound pulse of the communication signal releases a rapid steering response. Thus auditory orientation emerges from reactive motor responses to individual sound pulses. Although the reactive motor responses are not based on the song structure, a pattern recognition process may modulate the gain of the responses on a longer timescale. These findings are relevant to concepts of insect auditory behaviour and to the development of biologically inspired robots performing cricket-like auditory orientation.

Acoustic Stimulation↗

Mismatch negativity on the cone of confusion.

Localization of sounds by the auditory system is based on the analysis of three sources of information: interaural level differences (ILD, caused by an attenuation of the sound as it travels to the more distant ear), interaural time differences (ITD, caused by the additional amount of time it takes for the sound to arrive at the more distant ear), and spectral cues (caused by direction-specific spectral filter properties of the pinnae). Although in a number of psychophysiological studies cortical processes of ITD and ILD analysis were investigated, there is hitherto no evidence on the cortical processing of spectral cues for sound localization. The objective of the present experiment was to test whether it is possible to observe electrophysiological correlates of sound localization based on spectral cues. In an auditory oddball experiment, 80 ms of broadband noise from varying free field locations were presented to inattentive participants. Mismatch negativities (MMNs) were observed for pairs of standards and location deviants located symmetrically with respect to the interaural axis. As interaural time and level differences are identical for such pairs of sounds, the observed MMNs most likely reflect cognitive processes of sound localization utilizing the spectral filter properties of the pinnae. MMN latencies suggest that sound localization based on spectral cues is slower than ITD- or ILD-based localization.

Acoustic Stimulation↗

Temporal codes and computations for sensory representation and scene analysis.

This paper considers a space of possible temporal codes, surveys neurophysiological and psychological evidence for their use in nervous systems, and presents examples of neural timing networks that operate in the time-domain. Sensory qualities can be encoded temporally by means of two broad strategies: stimulus-driven temporal correlations (phase-locking) and stimulus-triggering of endogenous temporal response patterns. Evidence for stimulus-related spike timing patterns exists in nearly every sensory modality, and such information can be potentially utilized for representation of stimulus qualities, localization of sources, and perceptual grouping. Multiple strategies for temporal (time, frequency, and code-division) multiplexing of information for transmission and grouping are outlined. Using delays and multiplications (coincidences), neural timing networks perform time-domain signal processing operations to compare, extract and separate temporal patterns. Separation of synthetic double vowels by a recurrent neural timing network is used to illustrate how coherences in temporal fine structure can be exploited to build up and separate periodic signals with different fundamentals. Timing nets constitute a time-domain scene analysis strategy based on temporal pattern invariance rather than feature-based labeling, segregation and binding of channels. Further potential implications of temporal codes and computations for new kinds of neural networks are explored.

Action Potentials↗

Auditory brainstem response, middle-latency response, and slow cortical potential in patients with partial epilepsy.

Auditory brainstem responses (ABRs), middle-latency responses (MLRs), and slow cortical potentials (SCPs) have been recorded in patients with partial epilepsy previously untreated by anticonvulsants. Peak latencies, interpeak intervals, and amplitudes were estimated and the mean group values were compared with the respective data in age- and gender-matched healthy individuals. Neither ABRs nor MLRs in the patients differed significantly from those in the control group. Conversely, the SCP characteristics demonstrated regular differences: the P2 peak latency in the patients was prolonged and both the P1N1 and N1P2 amplitudes were increased. Considering the mechanisms of the ABR and MLR, it has been suggested that the specific structures of central auditory pathway up to the primary cortex do not play any essential role in the pathogenesis of partial epilepsy. Furthermore, it is speculated that the SCP-generating cortical areas, being primarily of non-specific qualities, are intimately involved in the mechanisms of epilepsy.

Adolescent↗

Arecoline-induced elevations of regional cerebral metabolism in the conscious rat.

Local cerebral glucose utilization (LCGU) was measured, using the quantitative [14C]2-deoxy-D-glucose ([14C]DG) method, at 3 min after administration to 3-month-old, awake Fischer rats of the muscarinic agonist arecoline (AREC) 0.05, 0.5, 5, 15 or 50 mg/kg or saline i.p. Animals were pretreated with methylatropine (a cholinergic antagonist which does not enter the brain and has no effect on cerebral metabolism) 4 mg/kg s.c. to prevent parasympathomimetic side-effects of AREC. Tremor produced by AREC was rated subjectively. Intensity of tremor was dose-related, peaked at 2-5 min after AREC, and abated within 30 min. Elevations in LCGU (measured after [14C]DG injection during peak behavior) in extrapyramidal regions, which mediate tremor, were related to the intensity of tremor. The lowest dose of AREC selectively increased LCGU in the hippocampus and median raphe; higher doses produced more generalized metabolic enhancement. In the hippocampus and cortex, LCGU rose in layers in which cholinoceptive cells are located. Regions of the auditory pathway and superficial neocortical layers (I-III) were generally unaffected by AREC, but LCGU did not decrease in any region. The selective increase in LCGU produced by low doses of AREC in the hippocampus presumably is due to a specific action of AREC, and demonstrates the high sensitivity of this region to cholinomimetic stimulation.

Animals↗

Emerging auditory response interactions to harmonic complexes in field L of the zebra finch.

Auditory responses of single units to harmonic complexes were studied in field L of the adult male zebra finch (Poephila guttata) to understand the origin of song selectivity in HVc. One of the attributes in this song selectivity is a large increase in response interactions when tones are presented simultaneously. Single units in the subdivisions of field L-L1, L2 and L3, were examined to see where these response interactions to harmonic complexes begin to develop along the auditory pathway towards HVc. Results showed relatively simple stereotyped response in L2 and widely varying ones in L1 and L3. The responses of some neurons in L1 and L3 to signals composed of the simultaneous sum of two harmonic complexes significantly differed from the linear sum of their responses to individual harmonic complexes whereas the neurons of L2 showed relatively weak response interactions. These neurons in L1 and L3 exhibited strong response interactions to harmonic complexes comparable to those of song-selective neurons in HVc. Thus, L1 and L3 are suggested to have emerging selective response properties and to provide auditory inputs relevant to the song selective HVc neurons.

Animal Communication↗