The anterior ectoylvian sulcal auditory field in the cat: II. A horseradisha peroxidase study of its thalamic and cortical connections (original) (raw)
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Experimental Brain Research, 1985
The cortical afferents to the cortex of the anterior ectosylvian sulcus (SEsA) were studied in the cat, using the retrograde axonal transport of horseradish peroxidase technique. Following injections of the enzyme in the cortex of both banks, fundus and both ends (postero-dorsal and anteroventral) of the anterior ectosylvian sulcus, retrograde labeling was found in: the primary, secondary, and tertiary somatosensory areas (SI, SII and SIII); the motor and premotor cortices; the primary, secondary, anterior and suprasylvian fringe auditory areas; the lateral suprasylvian (LS) area, area 20 and posterior suprasylvian visual area; the insular cortex and cortex of posterior half of the sulcus sylvius; in area 36 of the perirhinal cortex; and in the medial bank of the presylvian sulcus in the prefrontal cortex. Moreover, these connections are topographically organized. Considering the topographical distribution of the cortical afferents, three sectors may be distinguished in the cortex of the SEsA. 1) The cortex of the rostral two-thirds of the dorsal bank. This sector receives cortical projections from areas SI, SII and SIII, and from the motor cortex. It also receives projections from the anterolateral subdivision of LS, and area 36. 2) The cortex of the posterior third of the dorsal bank and of the posterodorsal end. It receives cortical afferents principally from the primary, secondary and anterior auditory areas, from SI, SII and fourth somatosensory area, from the anterolateral subdivision of LS, vestibular cortex and area 36. 3) The cortex of the ventral bank and fundus. This sulcal sector receives abundant connections from visual areas (LS, 20, posterior suprasylvian, 21 and 19), principally from the lateral posterior and dorsal subdivisions of LS. It also receives abundant connections from the granular insular cortex, caudal part of the cortex of the sylvian sulcus and suprasylvian fringe. Less abundant cortical afferents were found to arise in area 36, second auditory area and prefrontal cortex. The abundant sensory input of different modalities which appears to converge in the cortex of the anterior ectosylvian sulcus, and the consistent projection from this cortex to the deep layers of the superior colliculus, make this cortical region well suited to play a role in the control of the orientation movements of the eyes and head toward different sensory stimuli.
The Journal of Comparative Neurology, 1990
The extent of a region containing acoustically responsive neurons within the anterior ectosylvian sulcus and its relationship to surrounding gyral auditory cortical fields was examined in chloralose-anaesthetized cats. Multiple microelectrode penetrations were made orthogonal to the middle and anterior ectosylvian gyral surfaces, and longer penetrations were made into the dorsal and ventral banks and fundus of the anterior ectosylvian sulcus. The quantitative and qualitative auditory response characteristics of neurons and neuron clusters in the sulcal banks and surrounding regions were mapped in detail, and the degree of overlap of auditory and visual neurons within the sulcus was determined by routinely testing for responsiveness to a gross light flash.
Exp Brain Res., 2006
To date, evaluation of the neuronal basis for multisensory processing has focused on the convergence pattern that provides excitation from more than one sensory modality. However, a recent study (Dehner et al. in Cereb Cortex 14:387-401, 2004) has demonstrated excitatory-inhibitory multisensory effects that do not follow this conventional pattern and the present investigation documented a similar example of subthreshold cross-modal effects. Neuroanatomical tracers revealed that pyramidal neurons of the somatosensory area SIV project to the auditory field of the anterior ectosylvian sulcus (FAES), but subsequent electrophysiological tests showed that stimulation of SIV failed to elicit the expected orthodromic responses in FAES. Instead, combined auditory-SIV stimulation significantly suppressed FAES responses to auditory cues in approximately 25% of the neurons tested, and facilitated responses in another 5%. These modulatory responses in auditory FAES were similar in kind to those observed in somatosensory SIV and, as such, comprise further evidence for subthreshold forms of multisensory processing in cortex. Consequently, it seems likely that subthresh-old cross-modal effects may impact other apparently 'unimodal' areas of the brain.
Experimental Brain Research, 1987
We report electrophysiological data regarding the contribution of the corpus callosum to visual responses in the cortex around the anterior ectosylvian sulcus (AES). The experiments were performed in cats in which the optic input from each eye was surgically restricted to the ipsilateral hemisphere (split-chiasm cats), and where neuronal responses to stimulation of the contralateral eye were mediated by interhemispheric connections. A very high proportion of cells were driven by stimuli presented to either eye indicating that they were activated not only through an intrahemispheric pathway from the ipsilateral eye, but also through an interhemispheric pathway from the contralateral eye. With few exceptions, both receptive fields (RFs) of each binocular neuron abutted or were in the vicinity of the vertical meridian. All neurons responded well to moving stimuli and most of them showed directional selectivity. A few cells were activated by stimuli moving in depth. Following an additional section of the posterior half of the corpus callosum, cells in AES responded only to stimulation of the ipsilateral eye, demonstrating thus that the input from the contralateral eye was conveyed by this part of the corpus callosum. By contrast following a section of the anterior half of the corpus callosum, all visually responsive AES neurons were binocularly activated. These results suggest that the interhemispheric visual input to this ectosylvian region is conveyed via a polysynaptic loop involving visual cortical areas that are connected through the posterior portion of the corpus callosum.
Auditory response properties of neurons in the anterior ectosylvian sulcus of the cat
Brain Research, 1986
The auditory response properties of single neurons in the fundus and banks of the anterior ectosylvian sulcus (AES) were studied with simple dichotic stimuli (viz. noise-and tone-bursts) in cats anaesthetized with a-chloralose. Neurons within AES showed simple onset responses, were most commonly excited by stimulation of both ears, and showed either broad tuning or multiple high best frequencies. Some neurons were also tested for visual responsiveness and it was found that auditory cells and visual cells were intermingled within the sulcus. A small percentage of cells responded to both auditory and visual stimulation. Overall, the response properties of AES neurons differed from those of nearby auditory cortical fields. The region of AES studied appears to be outside the recently defined fourth somatosensory area (SIV), but overlaps para-SIV found deeper in the sulcus. It appears that deep within the sulcus and along most of its length there is a population of auditory, somatosensory and visual cells; to delineate this auditory population from the surrounding auditory cortical fields this region has been designated Field AES.
Brain Research Bulletin, 1984
RAMfREZ-CAMACHO, R., C. AVENDANO AND F. REINOSO-SUAREZ. Thalamic projections to the anterior suprasylvian and posterior sigmoid coretx: An HRP study of the "vestibular areas" of the cerebral cortex in the cat. BRAIN RES BULL 12(3) 245-252, 1!%4.-We have confirmed electrophysiologically the existence of an oligosynaptic vestibufar projection to the cortex surrounding the rostral end of the anterior suprasylvian sulcus (ASsS). However, we failed to confii a similar projection to area 3a in the posterior sigmoid gyrus. We studied the thrdamic projections to each of these cortical regions by injecting small amounts of HRP in the cortex and looking for neurons retrogradely labeled throughout the thalamus. The exact location of the cortical injections was assessed cytoarchitectonically. The heaviest neuronal labeling after injections in the banks of ASsS was obtained in PO (including in this complex GMmc). A moderate number of projections was found from VPi, VPm and VP1 (the labeling in the latter being particularly prominent in a case injected in the lower bank of ASsS), and also from VL. Occasional labeled neurons were found in the rostro-ventral part of LP. After injections in area 3a in the posterior sigmoid gyrus, which affected to a minor degree either area 3b or 4, many labeled cells appeared in the rostral and dorsal part of VPl, and in the central and lateral parts of VL. Fewer labeled cells were found in VPi, PO and LP. In most cases some occasional labeled cell was observed also in the intralaminar nuclei and in Vm. Vestibular cortex Thalamus Vestibular projections HRP Cat
Experimental Brain Research, 1990
The interconnections of the auditory cortex with the parahippocampal and cingulate cortices were studied in the cat. Injections of the anterograde and retrograde tracer WGA-HRP were performed, in different cats (n = 9), in electrophysiologically identified auditory cortical fields. Injections in the posterior zone of the auditory cortex (PAF or at the PAF/AI border) labeled neurons and axonal terminal fields in the cingulate gyrus, mainly in the ventral bank of the splenial sulcus (a region that can be considered as an extension of the cytoarchitectonic area Cg), and posteriorly in the retrosplenial area. Labeling was also present in area 35 of the perirhinal cortex, but it was sparser than in the cingulate gyrus. Following WGA-HRP injection in AII, no labeling was found in the cingulate gyrus, but a few neurons and terminals were labeled in area 35. In contrast, no or very sparse labeling was observed in the cingulate and perirhinal cortices after WGA-HRP injections in the anterior zone of the auditory cortex (AI or AAF). A WGA-HRP injection in the cingulate gyrus Abbreviations: AAF = anterior auditory cortical field; aes = anterior ectosylvian sulcus; AI = primary auditory cortical field; AII= secondary auditory cortical field; ALLS=anterior-lateral lateral suprasylvian visual area; BF = best frequency; C = cerebral cortex; CC = corpus callosum; CIN = cingulate cortex; CL = claustrum; DLS = dorsal lateral suprasylvian visual area; DP = dorsoposterior auditory area; E=entorhinal cortex; IC=inferior colliculus; LGN = lateral geniculate nucleus; LV = pars lateralis of the ventral division of the MGB; LVe = lateral ventricule; MGB = medial geniculate body; OT = optic tract; OV = pars ovoidea of the ventral division of the MGB; PAF=posterior auditory cortical field; pes=posterio r ectosylvian sulcus; PLLS=posterior-lateral lateral suprasylvian visual area; PS = posterior suprasylvian visual area; PU = putamen; RE = reticular complex of thalamus; rs = rhinal sulcus; SC = superior colliculus; SS = suprasylvian sulcus; T = temporal auditory cortical field; TMB = tetramethylbenzidine; VBX=vent~:obasal complex of thalamus, external nucleus; VL=pars ventrolateralis of the ventral division of the MGB; VLS=ventrolateral suprasylvian visual area; VPAF=ventroposterior auditory cortical field; WGA-HRP = wheat germ agglutinin labeled with horseradish peroxidase; wm= white matter. Offprint requests to: E.M. Rouiller labeled neurons in the posterior zone of the auditory cortex, between the posterior ectosylvian and the posterior suprasylvian sulci, but none was found more anteriorly in regions corresponding to AI, AAF and AII. The present data indicate the existence of preferential interconnections between the posterior auditory cortex and the limbic system (cingulate and parahippocampal cortices). This specialization of posterior auditory cortical areas can be related to previous observations indicating that the anterior and posterior regions of the auditory cortex differ from each other by their response properties to sounds and their pattern of connectivity with the auditory thalamus and the claustrum.
Hearing Research, 1989
The response properties to clicks, noise and tone bursts of 2152 single units located in the ventral division of the medial geniculate body were analysed as a function of their anatomical position. A particular spatial dist~bution of these properties was observed in the pars lateralis (LV) and ovoidea (0%'). The distribution of different response characteristics changed along the rostra-caudal axis. Units located posteriorly were in majority either insensitive to simple acoustical stimuli or responded exclusively to pure tones, presenting generally a broad tuning and a loose tonotopic arrangement. Inhibitory response patterns were about as frequent as excitatory ones, response latencies were long on the average and widely distributed. Only a few units showed time-locking of their discharges in response to repetitive clicks. Most units had non-monotonic intensity functions. Going anteriorly, the distribution of response properties progressively changed: the number of units sensitive to various simple acoustical stimuli (pure tones and broad band stimuli together) increased, the tonotopic arrangement was more precise and more units were sharply tuned. Response patterns were in majority of the excitatory type, and latencies were shorter on the average and less dispersed. More units were precisely time-locked to repetitive clicks. The proportion of units with monoto~c intensity fictions increased. The origin of th~~~corti~ projections was studied with focal injections of wheat-germ agglutinin labeled with horseradish peroxidase in fun~tion~ly defined loci of the various auditory cortical fields. An evolution of the density of labeled cells in LV and OV was observed along the same rostro-caudal axis for which a gradient of functional properties is described above. Thalamo-cortical projections to the primary auditory area and the anterior auditory field originated predominantly from the anterior half of LV, whereas the posterior auditory field received inputs from a wider rostro-caudal extend of LV including its posterior half.
Thalamic projections to fields A, AI, P, and VP in the cat auditory cortex
The Journal of Comparative Neurology, 1987
Thalamocortical projections to four tonotopic fields (A, AI, P, and VP) of the cat auditory cortex were studied by using combined microelectrode mapping and retrograde axonal transport techniques. Horseradish peroxidase (HRP) or HRP combined with either tritiated bovine serum albumin or nuclear yellow was injected into identified best-frequency sites of one or two different fields in the same brain. Arrays of labeled neurons were related to thalamic nuclei defined on the basis of their cytoarchitecture and physiology. In some cases, patterns of labeling were directly compared with thalamic best-frequency maps obtained in the same brain. We compared only patterns of labeling resulting from injections into similar parts of the frequency representation in different fields to insure that observed differences in patterns of labeling did not simply reflect differences in the frequency representation at the injection sites.