Literature DB >> 3171636

Modality specificity of neuronal responses within the cat's insula.

T P Hicks1, G Benedek, G A Thurlow.   

Abstract

1. Electrophysiological recordings of single-unit responses, multiunit responses, and electrically evoked field potentials have been made using carbon fiber-containing micropipettes in cats anesthetized with barbiturate and immobilized with gallamine triethiodide. Recording sites sampled cortical regions throughout the insula, including zones more ventrally situated and more rostral and caudal than those described in the preceding, companion paper. One-hundred eleven cells in total were tested with a battery of different types of stimuli. 2. Stimuli were divided into two classes, according to either the intensity of the stimulus or its form. These are called physiological forms, or levels of stimulation, and nonphysiological forms or levels. The nonphysiological forms of stimuli for visual, somatosensory, and auditory modalities consisted of (for visual stimuli): 1) electrical stimulation of the optic nerve or 2) bright flashes light at 100% contrast; for somatosensory, electrical stimulation of the radial nerve by implanted cuff electrodes; and for auditory, stimulation with bursts of white noise generated at high intensities (80-100 dB) or with a loud click stimulus. Physiologically relevant levels of stimuli for these same modalities were: moving bars of light projected onto a tangent screen in front of the animal (visual); light cutaneous deformation, hair displacement, and light pressure delivered to various regions on the surface of the cat's body with hand-held probes, or delivered manually (somatosensory); and white noise generated at low intensities (ca. 40 dB) (auditory). 3. Cells situated in dorsal insular regions responded to visual stimuli when levels of sensory activation were employed using natural means, within normal, physiologically relevant limits. Responses to auditory or somatosensory stimulation were observed in this region only when very intense forms of "natural" stimulation, or when electrical stimulation (nonphysiologically relevant levels of stimulation) was delivered. In this latter case, the same cells in several instances could be made to appear polymodally responsive. With cells situated in ventral insular regions, some polymodal responses to physiologically relevant levels of stimulation were noted, although it was considerably more common to obtain unimodal responses. Nonphysiological levels of activation yielded evidence for a polymodal convergence onto the greater proportion of cells recorded. 4. Field potential recordings with microelectrodes revealed widely overlapping representations of all modalities in both dorsal and ventral regions of the insula, irrespective of the sensitivity displayed by the local neuronal r

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Year:  1988        PMID: 3171636     DOI: 10.1152/jn.1988.60.2.422

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  5 in total

1.  Brain responses to auditory and visual stimulus offset: shared representations of temporal edges.

Authors:  Marcus Herdener; Christoph Lehmann; Fabrizio Esposito; Francesco di Salle; Andrea Federspiel; Dominik R Bach; Klaus Scheffler; Erich Seifritz
Journal:  Hum Brain Mapp       Date:  2009-03       Impact factor: 5.038

2.  Neural correlates of auditory-visual stimulus onset asynchrony detection.

Authors:  K O Bushara; J Grafman; M Hallett
Journal:  J Neurosci       Date:  2001-01-01       Impact factor: 6.167

3.  Sensory modality distribution in the anterior ectosylvian cortex (AEC) of cats.

Authors:  H Jiang; F Lepore; M Ptito; J P Guillemot
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

4.  The sensory insular cortex mediates the stress-buffering effects of safety signals but not behavioral control.

Authors:  John P Christianson; Alexander M Benison; Joshua Jennings; Emilee K Sandsmark; Jose Amat; Richard D Kaufman; Michael V Baratta; Evan D Paul; Serge Campeau; Linda R Watkins; Daniel S Barth; Steven F Maier
Journal:  J Neurosci       Date:  2008-12-10       Impact factor: 6.167

5.  Effects of top-down influence suppression on behavioral and V1 neuronal contrast sensitivity functions in cats.

Authors:  Jian Ding; Zheng Ye; Fei Xu; Xiangmei Hu; Hao Yu; Shen Zhang; Yanni Tu; Qiuyu Zhang; Qingyan Sun; Tianmiao Hua; Zhong-Lin Lu
Journal:  iScience       Date:  2021-12-24
  5 in total

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