Rat posterior parietal cortex: topography of corticocortical and thalamic connections

Anatomical and functional findings support the contention that there is a distinct posterior parietal cortical area (PPC) in the rat, situated between the rostrally adjacent hindlimb sensorimotor area and the caudally adjacent secondary visual areas. The PPC is distinguished from these areas by receiving thalamic afferents from the lateral dorsal (LD), lateral posterior (LP), and posterior (Po) nuclei, in the absence of input from the ventrobasal complex (VB) or dorsal lateral geniculate (DLG) nuclei. Behavioral studies have demonstrated that PPC is involved in spatial orientation and directed attention. In the present study we used fluorescent retrograde axonal tracers primarily to investigate the cortical connections of PPC, in order to determine the organization of the circuitry by which PPC is likely to participate in these functions, and also to determine how the topography of its thalamic connections differs from that of neighboring cortical areas. The cortical connections of PPC involve the ventrolateral (VLO) and medial (MO) orbital areas, medial agranular cortex (area Fr2), portions of somatic sensory areas Par1 and Par2, secondary visual areas Oc2M and Oc2L, auditory area Tel, and retrosplenial cortex. The secondary visual areas Oc2L and Oc2M have cortical connections which are similar to those of PPC, but are restricted within orbital cortex to area VLO, and within area Fr2 to its caudal portion, and do not involve auditory area Te1. The cortical connections of hindlimb cortex are largely restricted to somatic sensory and motor areas. Retrosplenial cortex, which is medially adjacent to PPC, has cortical connections that are prominent with visual cortex, do not involve somatic sensory or auditory cortex, and include the presubiculum. We conclude that PPC is distinguished by its pattern of cortical connections with the somatic sensory, auditory and visual areas, and with areas Fr2, and VLO/MO, in addition to its exclusive thalamic connectivity with LD, LP and Po. Because recent behavioral studies indicate that PPC, Fr2 and VLO are involved in directed attention and spatial learning, we suggest that the interconnections among these three cortical areas represent a major component of the circuitry for these functions in rats.     

Afferent connections of dorsal and ventral agranular insular cortex in the hamsterMesocricetus auratus

The agranular insular cortex is transitional in location and structure between the ventrally adjacent olfactory allocortex primutivus and dorsally adjacent sensory-motor isocortex. Its ventral anterior division receives major afferent projections from olfactory areas of the limbic system (posterior primary olfactory cortex, posterolateral cortical amygdaloid nucleus and lateral entorhinal cortex) while its dorsal anterior division does so from non-olfactory limbic areas (lateral and basolateral amygdaloid nuclei).The medial segment of the mediodorsal thalamic nucleus projects to both the ventral and dorsal divisions of the agranular insular cortex, to the former from its anterior portion and to the latter from its posterior portion. Other thalamic inputs to the two divisions arise from the gelatinosus, central medial, rhomboid and parafascicular nuclei. The dorsal division, but not the ventral division, receives input from neurons in the lateral hypothalamus and posterior hypothalamus.The medial frontal cortex projects topographically and bilaterally upon both ventral and dorsal anterior insular cortex, to the former from the ventrally located medial orbital and infralimbic areas, to the latter from the dorsally-located anterior cingulate and medial precentral areas, and to both from the intermediately located prelimbic area. Similarly, the ipsilateral posterior agranular insular cortex and perirhinal cortex project in a topographic manner upon the two divisions of the agranular insular cortex.Commissural input to both divisions originates from pyramidal neurons in the respective contralateral homotopical cortical area. In each case, pyramidal neurons in layer V contribute 90% of this projection and 10% arises from layer III pyramidals.In the brainstem, the dorsal raphe nucleus projects to the ventral and dorsal divisions of the agranular insular cortex and the parabrachial nucleus projects to the dorsal division.Based on their cytoarchitecture, pattern of afferent connections and known functional properties, we consider the ventral and dorsal divisions of the agranular insular cortex to be, respectively, periallocortical and proisocortical portions of the limbic cortex.     

Efferent connections of dorsal and ventral agranular insular cortex in the hamster, Mesocricetus auratus

The anterior portion of rodent agranular insular cortex consists of a ventral periallocortical region (AIv) and a dorsal proisocortical region (AId). Each of these two cortical areas has distinct efferent connections, but in certain brain areas their projection fields are partially or wholly overlapping. Bilateral projections to layers I, III and VI of medial frontal cortex originate in the dorsal agranular insular cortex and terminate in the prelimbic, anterior cingulate and medial precentral areas; those originating in ventral agranular insular cortex terminate in the medial orbital, infralimbic and prelimbic areas. The dorsal and ventral regions of the agranular insular cortex project topographically to the ipsilateral cortex bordering the rhinal fissure, which includes the posterior primary olfactory, posterior agranular insular, perirhinal and lateral entorhinal areas. Fibers to these lateral cortical areas were found to travel in a cell-free zone, between cortical layer VI and the claustrum, which corresponds to the extreme capsule. The dorsal and ventral regions send commissural projections to layer I, lamina dissecans and outer layer V, and layer VI of the contralateral homotopical cortex, via the corpus callosum. Projections from the ventral and dorsal regions of the agranular insular cortex to the caudatoputamen are topographically arranged and terminate in finger-like patches. The ventral, but not the dorsal region, projects to the ventral striatum and ventral pallidum. The thalamic projections of the ventral and dorsal regions are largely overlapping, with projections from both to the ipsilateral reticular nucleus and bilaterally to the rhomboid, mediodorsal, gelatinosus and ventromedial nuclei. The heaviest projection is that to the full anteroposterior extent of the medial segment of the mediodorsal nucleus. Brainstem areas receiving projections from the ventral and dorsal regions include the lateral hypothalamus, substantia nigra pars compacta, ventral tegmental area and dorsal raphe nucleus. In addition, the ventral region projects to the periaqueductal gray and the dorsal region projects to the parabrachial and ventral pontine nuclei.These efferent connections largely reciprocate the afferent connections of the ventral and dorsal agranular insular cortex, and provide further support for the concept that these regions are portions of an outer ring of limbic cortex which plays a critical role in the expression of motivated, species-typical behaviors.     

Connections of the medial posterior parietal cortex (area 7m) in the monkey

The afferent and efferent cortical and subcortical connections of the medial posterior parietal cortex (area 7m) were studied in cebus (Cebus apella) and macaque (Macaca fascicularis) monkeys using the retrograde and anterograde capabilities of the horseradish peroxidase (HRP) technique. The principal intraparietal corticocortical connections of area 7m in both cebus and macaque cases were with the ipsilateral medial bank of the intraparietal sulcus (MIP) and adjacent superior parietal lobule (area 5), inferior parietal lobule (area 7a), lateral bank of the IPS (area 7ip), caudal parietal operculum (PGop), dorsal bank of the caudal superior temporal sulcus (visual area MST), and medial prestriate cortex (including visual area PO and caudal medial lobule). Its principal frontal corticocortical connections were with the prefrontal cortex in the shoulder above the principal sulcus and the cortex in the shoulder above the superior ramus of the arcuate sulcus (SAS), the area purported to contain the smooth eye movement-related frontal eye field (FEFsem) in the cebus monkey by other investigators. There were moderate connections with the cortex in the rostral bank of the arcuate sulcus (purported to contain the saccade-related frontal eye field; FEFsac), supplementary eye field (SEF), and rostral dorsal premotor area (PMDr). Area 7m also had major connections with the cingulate cortex (area 23), particularly the ventral bank of the cingulate sulcus. The principal subcortical connections of area 7m were with the dorsal portion of the ventrolateral thalamic (VLc) nucleus, lateral posterior thalamic nucleus, lateral pulvinar, caudal mediodorsal thalamic nucleus and medial pulvinar, central lateral, central superior lateral, and central inferior intralaminar thalamic nuclei, dorsolateral caudate nucleus and putamen, middle region of the claustrum, nucleus of the diagonal band, zona incerta, pregeniculate nucleus, anterior and posterior pretectal nuclei, intermediate layer of the superior colliculus, nucleus of Darkschewitsch and dorsomedial parvicellular red nucleus (macaque cases only), dorsal, dorsolateral and lateral basilar pontine nuclei, nucleus reticularis tegmenti pontis, locus ceruleus, and superior central nucleus. The findings are discussed in terms of the possibility that area 7m contains a "medial parietal eye field" and belongs to a neural network of oculomotor-related structures that plays a role in the control of eye movement.     

Dorsal thalamic connections of the ventral lateral geniculate nucleus of rats

In order to understand better the organisation of the ventral lateral geniculate nucleus of the ventral thalamus, this paper has examined the patterns of connections that this nucleus has with various nuclei of the dorsal thalamus in rats. Injections of biotinylated dextran or cholera toxin subunit B were made into the parafascicular, central lateral, posterior thalamic, medial dorsal, lateral dorsal, lateral posterior, dorsal lateral geniculate, anterior, ventral lateral, ventrobasal and medial geniculate nuclei of Sprague-Dawley rats and their brains were processed using standard tracer detection methods. Three general patterns of ventral lateral geniculate connectivity were seen. First, the parafascicular, central lateral, medial dorsal, posterior thalamic and lateral dorsal nuclei had heavy connections with the parvocellular (internal) lamina of the ventral lateral geniculate nucleus. This geniculate lamina has been shown previously to receive heavy inputs from many functionally diverse brainstem nuclei. Second, the visually related dorsal lateral geniculate and lateral posterior nuclei had heavy connections with the magnocellular (external) lamina of the ventral lateral geniculate nucleus. This geniculate lamina has been shown by previous studies to receive heavy inputs from the visual cortex and the retina. Finally, the anterior, ventral lateral, ventrobasal and medial geniculate nuclei had very sparse, if any, connections with the ventral lateral geniculate nucleus. Overall, our results strengthen the notion that one can package the ventral lateral geniculate nucleus into distinct visual (magnocellular) and non-visual (parvocellular) components.     

Sagittal organization of the olivocerebellonuclear pathway in the rat. II. Connections with the nucleus interpositus

The organization of the sagittal Zone C of the cerebellar cortex of the rat was studied with respect to its efferent projections and to its inferior olive (IO) afferent connections. Wheat-germ agglutinin conjugated to horseradish peroxidase was used as a tracer. Zone C has been defined as the cortical region projecting to the nucleus interpositus anterior (NIA) and posterior (NIP). The results show that, in spite of some differences, Zone C of the rat is homologous to that of the cat. Three subzones, C1, C2 and C3, were clearly identified. Subzone C1 appears as a longitudinal band of the cerebellar cortex interrupted at the level of lobules VIb,c and part of lobule VII. It is therefore divided into two sagittal segments, one anterior to lobules I to VIa adjacent to Zone B; and one posterior to lobules VII to VIII adjacent to Zone A. Both segments receive climbing fibres from the lateral aspect of the rostral two-thirds and the medial aspect of the caudal one-third of the dorsal accessory olive (DAO). The Purkinje cell axons from subzone C1 project to both the NIA and the NIP where they occupy the medial one-third of the nucleus. Subzone C2 consists of a continuous sagittal band of the cerebellar cortex and lies between Subzones C1 and C3. It receives climbing fibres from the rostral aspect of the medial accessory olive (MAO) and projects to the central aspect of the NIA and to the lateral half of the NIP. Subzone C3, which is lateral to Subzone C2 and medial to Zone D, appears as a sagittal band of cortex interrupted at the level of lobule VI. It receives climbing fibres from the medial aspect of the DAO and projects to the lateral aspect of the NIA. The orientation of the olivocerebellonuclear circuit is fundamentally sagittal not only in the cerebellar cortex but also in the nuclei and, although less sharply, in the inferior olive.     

Forebrain connections of medial agranular cortex in the prairie vole, Microtus ochrogaster

 Fluorescent axonal tracers were used to investigate the connections of medial agranular cortex (frontal area 2, Fr2) in male prairie voles. The rostral and caudal portions of Fr2 (rFr2 and cFr2) have distinct but partially overlapping patterns of connections. Thalamic labeling after cFr2 injections was present in anteromedial nucleus (AM), ventrolateral nucleus (VL), lateral segment, mediodorsal nucleus (MDl), centrolateral nucleus (CL), ventromedial nucleus (VM), posterior nucleus (Po) and lateral posterior nucleus (LP). A band of labeled cells involving CL, central medial nucleus (CM) and rhomboid nucleus (Rh) formed a halo around the periphery of submedial (gelatinosus) nucleus (Sm). Within cFr2 there is a rostrocaudal gradient whereby projections from VL and MDl become progressively sparser caudally, whereas those from LP and Po become denser. Rostral Fr2 receives afferents from a similar group of thalamic nuclei, but has denser innervation from VL and MDl, lacks afferents from LP, and receives less input from nuclei around the periphery of Sm. Caudal Fr2 has extensive cortical connections including orbital cortex, rostral Fr2, Fr1, caudal parietal area 1 (Par1), parietal area 2 (Par2), and posterior parietal, retrosplenial and visual areas. Rostral Fr2 has similar connections with areas Fr1, Par1 and Par2; orbital connections focused in ventrolateral orbital cortex (VLO); connections with caudal Fr2; greatly reduced connections with posterior parietal cortex and the visual areas; and no connections with retrosplenial cortex. The axons linking rFr2 and cFr2 with each other and with other cortical areas travel predominately in the deep gray matter of layers VI and VII rather than in the white matter. Projections to the dorsal striatum from rFr2 are widespread in the head of the caudate, become progressively restricted to a dorsocentral focus more caudally, and disappear by the level of the anterior commissure. The projections from cFr2 are largely restricted to a focal dorsocentral region of the striatum and to the dorsolateral margin of the caudatoputamen. In comparison to area Fr2, the laterally adjacent area Fr1 has thalamic and cortical connections which are markedly restricted. Area Fr1 receives thalamic input from nuclei VL, anteroventral nucleus (AV), CL and Po, but none from mediodorsal nucleus (MD) or LP, and its input from VM is reduced. Cortical afferents to Fr1 originate from areas Fr2, caudal Par1 and Par2. Medial agranular cortex of prairie voles has a pattern of connections largely similar to that seen in rats, suggesting that area Fr2 in prairie voles is part of a cortical network that may mediate complex behaviors involving spatial orientation. Received: 20 May 1998 / Accepted: 14 October 1998     

Neuronal connections of orbital cortex in rats: topography of cortical and thalamic afferents

The cortical and thalamic afferent connections of rat orbital cortex were investigated using fluorescent retrograde axonal tracers. Each of the four orbital areas has a distinct pattern of connections. Corticocortical connections involving the ventral and ventrolateral orbital areas are more extensive than those of the medial and lateral orbital areas. The medial orbital area has cortical connections with the cingulate, medial agranular (Fr2) and posterior parietal (PPC) cortices. The ventral orbital area has connections with the cingulate area, area Fr2, secondary somatic sensory area Par2, PPC, and visual areas Oc2M and Oc2L. The ventrolateral orbital area (VLO) receives cortical input from insular cortex, area Fr2, somatic sensory areas Par1 and Par2, PPC and Oc2L. The lateral orbital area has cortical connections limited to the agranular and granular insular areas, and Par2. Thalamic afferents to the four orbital fields are also topographically organized, and are focused in the submedial and mediodorsal nuclei. The ventrolateral orbital area receives input from the entirety of the submedial nucleus, whereas the other orbital areas receive input from its periphery only. Each orbital area is connected with a particular segment of the mediodorsal nucleus. The medial orbital area receives its principal thalamic afferents from the parataenial nucleus, the dorsocentral portion of the mediodorsal nucleus, and the ventromedial portion of the submedial nucleus. The ventral orbital area receives input from the lateral segment of the mediodorsal nucleus, the rostromedial portion of the submedial nucleus and the central lateral nucleus. Thalamic afferents to the ventrolateral orbital area arise from the entirety of the submedial nucleus and from the lateral segment of the mediodorsal nucleus. The lateral orbital area receives thalamic afferents from the central segment of the mediodorsal nucleus, the ventral portion of the submedial nucleus and the ventromedial nucleus. The paraventricular, ventromedial, rhomboid and reuniens nuclei also provide additional input to the four orbital areas. The connections of the ventrolateral orbital area are interpreted in the context of its role in directed attention and allocentric spatial localization. The present findings provide anatomical support for the view that areas Fr2, PPC and VLO comprise a cortical network mediating such functions.     

The thalamic connections of motor, premotor, and prefrontal areas of cortex in a prosimian primate (Otolemur garnetti)

Connections of motor areas in the frontal cortex of prosimian galagos (Otolemur garnetti) were determined by injecting tracers into sites identified by microstimulation in the primary motor area (M1), dorsal premotor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), frontal eye field (FEF), and granular frontal cortex. Retrogradely labeled neurons for each injection were related to architectonically defined thalamic nuclei. Nissl, acetylcholinesterase, cytochrome oxidase, myelin, parvalbumin, calbindin, and Cat 301 preparations allowed the ventral anterior and ventral lateral thalamic regions, parvocellular and magnocellular subdivisions of ventral anterior nucleus, and anterior and posterior subdivisions of ventral lateral nucleus of monkeys to be identified. The results indicate that each cortical area receives inputs from several thalamic nuclei, but the proportions differ. M1 receives major inputs from the posterior subdivision of ventral lateral nucleus while premotor areas receive major inputs from anterior parts of ventral lateral nucleus (the anterior subdivision of ventral lateral nucleus and the anterior portion of posterior subdivision of ventral lateral nucleus). PMD and SMA have connections with more dorsal parts of the ventral lateral nucleus than PMV. The results suggest that galagos share many subdivisions of the motor thalamus and thalamocortical connection patterns with simian primates, while having less clearly differentiated subdivisions of the motor thalamus.     

The laminar distribution of cortical connections with the tecto- and cortico-recipient zones in the cat's lateral posterior nucleus

The anterograde and retrograde transport of wheat germ agglutinin congugated to horseradish peroxidase was used to examine the laminar organization of cortical connections with the two visual zones that comprise the cat's lateral posterior nucleus. Microelectrophoretic deposits of the tracer into the principal tecto-recipient zone in the medial division of the lateral posterior nucleus revealed reciprocal connections with the following cortical fields: areas 19 and 21a, the medial and lateral banks of the middle suprasylvian sulcus, and the dorsal and ventral banks of the lateral suprasylvian sulcus, which correspond to the dorsal lateral suprasylvian and ventral lateral suprasylvian visual areas of Palmer et al. [(1978) Brain Res. 177, 237-256] and an area in the fundus of the posterior suprasylvian sulcus. In each of these cortical areas two distinct populations of cells were labeled, small pyramidal neurons in layer VI and large pyramidal cells in layer V. Overlying these backfilled cells were two bands of anterograde label, a narrow strip in layer I and a wide band centered in layer IV. Deposits of wheat germ agglutinin conjugated to horseradish peroxidase confined to the striate-recipient zone in the lateral portion of the lateral posterior nucleus resulted in cortical label in areas 17, 18, 19, 20a and b, 21a, the medial and lateral banks of the middle suprasylvian sulcus, the posterior suprasylvian sulcus and in the fundus of the splenial sulcus. In all cortical areas other than 17 and 18, the laminar distribution of label was the same as that found after deposits of the tracer into the medial division of the lateral posterior nucleus. In contrast, areas 17 and 18 contained backfilled cells that were confined to layer V and anterograde label that was restricted to layer I. These findings indicate that the cortical areas that receive a direct projection from the A laminae of the dorsal lateral geniculate nucleus maintain a distinct laminar organization of reciprocal connections with the extrageniculate visual thalamus. Conversely, all other visual areas of the cortex share a common pattern of reciprocal connections with both the tecto- and striate-recipient zones of the lateral posterior nucleus.     

Cortical and subcortical connections of the pars compacta of the anterior pretectal nucleus in the rat.

The efferent and afferent connections of the dorsal part of the anterior pretectal nucleus, pars compacta (APc), were studied experimentally in the rat by using neurotracers. A restricted number of structures supply afferents to the anterior pretectal nucleus: the visual cortex (areas 17, 18 and 18a), ventral lateral geniculate nucleus and superficial layers of the superior colliculus. Additional afferents have been demonstrated originating from the Darkschewitsch nucleus, periaqueductal gray, zona incerta and anterior cingulate cortex. Efferent fibers are distributed to a sector of the deep mesencephalic nucleus just dorsolateral to the red nucleus, the basilar pontine gray, posterior and olivary pretectal nuclei, superficial layers of the superior colliculus, lateral posterior thalamic nucleus, ventral lateral geniculate nucleus and zona incerta. These anatomical observations indicate that the pars compacta of the anterior pretectal nucleus is closely related to visual centers, suggesting an involvement of this nucleus in visually mediated behavior.     

Corticothalamic connections of the superior temporal sulcus in rhesus monkeys

Summary The corticothalamic connections of the superior temporal sulcus (STS) were studied by means of the autoradiographic technique. The results indicate that corticothalamic connections of the STS in general reciprocate thalamocortical connections. The cortex of the upper bank of the STS-multimodal areas TPO and PGa-projects to four major thalamic targets: the pulvinar complex, the mediodorsal nucleus, the limitanssuprageniculate nucleus, as well as intralaminar nuclei. Within the pulvinar complex, the main projections of the upper bank of the STS are directed to the medial pulvinar (PM) nucleus. Rostral upper bank regions tend to project caudally and medially within the PM nucleus, caudal upper bank regions, more laterally and ventrally. The mid-portion of the upper bank tends to occupy the central sector of the PM nucleus. There are also relatively minor projections from upper bank regions to the lateral pulvinar (PL) and oral pulvinar (PO) nuclei. In contrast to the upper bank, the projections from the lower bank are directed primarily to the pulvinar complex, with only minor projections to intralaminar nuclei. The rostral portion of the lower bank projects mainly to caudal and medial regions of the PM nucleus, whereas the caudal lower bank projects predominantly to the lateral PM nucleus, and also to the PL, PO, and inferior pulvinar (PI) nuclei. The mid-portion of the lower bank projects mainly to central and lateral portions of the PM nucleus, and also to the PI and PL nuclei. The rostral depth of the STS projects mainly to the PM nucleus, with only minor connections to the PO, PI, and PL nuclei. The midportion of multimodal area TPO of the upper bank, areas TPO₂ and TPO₃, projects preferentially to the central sector of the PM nucleus. It is possible that this STS-thalamic connectivity has a role in behavior that is dependent upon more than one sensory modality.Abbreviations AM anterior medial nucleus - AS arcuate sulcus - AV anterior ventral nucleus - BSC brachium of the superior colliculus - Cd caudate nucleus - Cif nucleus centralis inferior - Cim nucleus centralis intermedialis - CL central lateral nucleus - CM centromedian nucleus - CM-Pf centromedian-parafascicular nucleus - Cs nucleus centralis superior - CS central sulcus - CSL nucleus centralis lateralis superior - GLd dorsal lateral geniculate nucleus - GM medial geniculate nucleus - Hb habenula - IOS inferior occipital sulcus - IPS intraparietal sulcus - LD lateral dorsal nucleus - LF lateral fissure - Li limitans nucleus - LP lateral posterior nucleus - LS lunate sulcus - MD mediodorsal nucleus - Pa paraventricular nucleus - Pen paracentral nucleus - Pf parafascicular nucleus - PI inferior pulvinar nucleus - PL lateral pulvinar nucleus - PM medial pulvinar nucleus - PO oral pulvinar nucleus - PS principal sulcus - Pt parataenial nucleus - R reticular nucleus - Re reuniens nucleus - SG suprageniculate nucleus - STN subthalamic nucleus - STS superior temporal sulcus - THI habenulo-interpeduncular tract - VLc nucleus ventralis lateralis, pars caudalis - VLm nucleus ventralis lateralis, pars medialis - VLo nucleus ventralis lateralis, pars oralis - VLps nucleus ventralis lateralis, pars postrema - VPI ventroposteroinferior nucleus - VPLc nucleus ventralis posterior lateralis, pars caudalis - VPLo nucleus ventralis posterior lateralis, pars oralis - VPM ventroposteromedial nucleus - VPMpc ventroposteromedial nucleus, parvocellular portion - X nucleus X     

大鼠间脑和皮质下端脑到前额叶皮质的传入投射——WGA-HRP法研究

本研究将 WGA-HRP 注射于25只大鼠前额叶皮质的前扣带回背部、前边缘区及岛叶无颗粒皮质背部,观察其间脑和皮质下端脑的传入联系。间脑的传入主要来自丘脑背内侧核,并有一定的局部定位。此外,丘脑的板内核群(中央外侧核、旁中央核、中央内侧核及束旁核)、腹侧核群(腹外侧核、腹内侧核、腹前核及腹后核)、中线核群(菱形核、连合核、带旁核及室旁核)、前内侧核、外侧缰核、后核及外侧核亦有到前额叶皮质的传入投射,且投射到前额叶皮质不同部位的数量不同。丘脑下部的传入主要来自外侧区、外侧视前区、尾侧大细胞核及乳头体上核,少量传入也可见于丘脑下部后区、背内侧核、腹内侧核及未定带。皮质下端脑的传入主要来自苍白球,其次为斜角带核、隔核、杏仁核及屏状核。在隔核中,除内侧隔核外还观察到外侧隔核,繖隔核及三角隔核亦投射到前额叶皮质。杏仁核中除杏仁外侧核、杏仁基底核外侧部及内侧部外,还观察到杏仁内侧核及杏仁皮质核亦有少量到前额叶皮质的传入。     

Connections of the anterior ectosylvian visual area (AEV)

Summary We have previously described a visual area situated in the cortex surrounding the deep infolding of the anterior ectosylvian sulcus of the cat (Mucke et al. 1982). Using orthograde and retrograde transport methods we now report anatomical evidence that this anterior ectosylvian visual area (AEV) is connected with a substantial number of both cortical and subcortical regions. The connections between AEV and other cortical areas are reciprocal and, at least in part, topographically organized: the rostral AEV is connected with the bottom region of the presylvian sulcus, the lower bank of the cruciate sulcus, the rostral part of the ventral bank of the splenial sulcus, the rostral portion of the lateral suprasylvian visual area (LS) and the lateral bank of the posterior rhinal sulcus; the caudal AEV is connected with the bottom region of the presylvian sulcus, the caudal part of LS, the ventral part of area 20 and the lateral bank of the posterior rhinal sulcus. Subcortically, AEV has reciprocal connections with the ventral medial thalamic nucleus (VM), with the medial part of the lateralis posterior nucleus (LPm), as well as with the lateralis medialis-suprageniculate nuclear (LM-Sg) complex. These connections are also topographically organized with more rostral parts of AEV being related to more ventral portions of the LPm and LM-Sg complex. AEV also projects to the caudate nucleus, the putamen, the lateral amygdaloid nucleus, the superior colliculus, and the pontine nuclei. It is concluded that AEV is a visual association area which functionally relates the visual with both the motor and the limbic system and that it might play a role in the animal's orienting and alerting behavior.Abbreviations Ac aqueductus cerebri - AEs anterior ectosylvian sulcus - ALLS anterolateral lateral suprasylvian area - AMLS anteromedial lateral suprasylvian area - ASs anterior suprasylvian sulcus - Cd caudate nucleus - CL central lateral nucleus - Cl claustrum - Cos coronal sulcus - Crs cruciate sulcus - DLS dorsal lateral suprasylvian area - GI stratum griseum intermediale - GP stratum griseum profundum - IC inferior colliculus - LAm lateral amygdaloid nucleus - LGNd dorsal nucleus of lateral geniculate body - LGNv ventral nucleus of lateral geniculate body - Llc nucleus lateralis intermedius, pars caudalis - LM nucleus lateralis medialis - LPl nucleus lateralis posterior, pars lateralis - LPm nucleus lateralis posterior, pars medialis - Ls lateral sulcus - MD nucleus mediodorsalis - MG medial geniculate body - MSs middle suprasylvian sulcus - Ndl nucleus dorsolateralis pontis - Nl nucleus lateralis pontis - Np nucleus peduncularis pontis - Npm nucleus paramedianus pontis - Nrt nucleus reticularis tegmenti pontis - Nv nucleus ventralis pontis - Ped cerebral peduncle - PEs posterior ectosylvian sulcus - Pg periaqueductal gray - PLLS posterolateral lateral suprasylvian area - PMLS posteromedial lateral suprasylvian area - PSs presylvian sulcus - Pul pulvinar - Put putamen - R red nucleus - Sg suprageniculate nucleus - SN substantia nigra - Sps splenial sulcus - Syls sylvian sulcus - T trapezoid body - VA ventral anterior nucleus - VL ventral lateral nucleus - VLS ventral lateral suprasylvian area - VM ventral medial nucleus - VPL ventral posterolateral nucleus - VPM ventral posteromedial nucleus Sponsored by Max-Planck-Society during part of the studySponsored by Thyssen FoundationSponsored by Alexander von Humboldt-Foundation     

Efferent connections of the "olfactostriatum": a specialized vomeronasal structure within the basal ganglia of snakes

The olfactostriatum is a portion of the basal ganglia of snakes that receives substantial vomeronasal afferents through projections from the nucleus sphericus. In a preceding article, the olfactostriatum of garter snakes (Thamnophis sirtalis) was characterized on the basis of chemoarchitecture (distribution of serotonin, neuropeptide Y and tyrosine hydroxylase) and pattern of afferent connections [Martinez-Marcos, A., Ubeda-Banon, I., Lanuza, E., Halpern, M., 2005. Chemoarchitecture and afferent connections of the "olfactostriatum": a specialized vomeronasal structure within the basal ganglia of snakes. J. Chem. Neuroanat. 29, 49-69]. In the present study, its efferent connections have been investigated. The olfactostriatum projects to the main and accessory olfactory bulbs, lateral cortex, septal complex, ventral pallidum, external, ventral anterior and dorsolateral amygdalae, bed nucleus of the stria terminalis, preoptic area, lateral posterior hypothalamic nucleus, ventral tegmental area, substantia nigra and raphe nuclei. Tracer injections in the nucleus accumbens proper, a structure closely associated with the olfactostriatum, result in a similar pattern of efferent connections with the exception of those reaching the main and accessory olfactory bulbs, lateral cortex, external, ventral anterior and dorsolateral amygdalae and bed nucleus of the stria terminalis. These data, therefore, help to characterize the olfactostriatum, an apparently specialized area of the nucleus accumbens. Double labeling experiments after tracer injections in the nucleus sphericus and the lateral posterior hypothalamic nucleus demonstrate a pathway between these two structures through the olfactostriatum. Injections in the olfactostriatum and in the medial amygdala show parallel projections to the lateral posterior hypothalamic nucleus. Since this hypothalamic nucleus has been previously described as projecting to the hypoglossal nucleus, both, the medial amygdala and the olfactostriatum may mediate vomeronasal influence on tongue-flick behavior.     

Insular interconnections with the amygdala in the rhesus monkey

Connections between the insular cortex and the amygdala were investigated with tritiated amino acid autoradiography and horseradish peroxidase histochemistry in the rhesus monkey. Our findings revealed widespread reciprocal connections between the insular cortex and almost all subnuclei of the amygdaloid complex. The posterior insula projects predominantly to the dorsal aspect of the lateral and to the central amygdaloid nuclei. In contrast, the anterior insula projects to the anterior amygdaloid area as well as the medial, the cortical, the accessory basal magnocellular, the medial basal and the lateral amygdaloid nuclei. Approximately 90% of the cells of origin of the insulo-amygdala projections are located in layers 2 and 3 with fewer labeled cells in layer 5. Amygdalo-insular projections arise predominantly from medial and anterior parts of the amygdala and reach mostly layers 2 and 5 of the insula.The results demonstrate that the insula and the amygdala have widespread reciprocal connections, which may explain their functional similarities.     

Subcortical projections to layer I of the visual cortex,area 17, of the rat

Summary The afferent connections to layer I of the visual cortex, area 17, of the albino rat were studied using the retrograde transport of horseradish peroxidase (HRP). In all animals examined, the majority of labeled cells were observed in the dorsal lateral geniculate nucleus and in the lateral posterior nucleus. In addition, in one-half of the animals examined labeled cells were also present in the posterior complex of the thalamus and in the ventromedial nucleus. Finally, in three cases a few HRP-positive neurons were observed in the locus coeruleus and in the dorsal raphe nucleus.This work was supported by USPHS grant EY029464 and by an Alfred P. Sloan Foundation Research Fellowship to John G. Parnavelas     

Sagittal organization of the olivocerebellonuclear pathway in the rat. I. Connections with the nucleus fastigii and the nucleus vestibularis lateralis

The organization of the afferent and efferent connections of the sagittal Zones A and B of the cerebellar cortex of the rat have been studied using wheat-germ agglutinin conjugated to horseradish peroxidase as a tracer. A single injection of this tracer into the cerebellar cortex allowed us to study, simultaneously, the crossed olivocortical connections (revealed by the retrograde transport) and the direct corticonuclear connections (revealed by the anterograde transport). The results demonstrate that the olivocerebellonuclear pathway is organized in a longitudinal direction so that for a given small injection of the tracer in one lobule of the cortex, a long sagittal band of the retrograde-labelled cells is obtained in the inferior olive, and a long sagittal band of the labelled terminals is obtained in the cerebellar nuclei. Zone A and Zone B have been arbitrarily defined as the cortical regions projecting, respectively, to the nucleus fastigii (NF) and the nucleus vestibularis lateralis (NVL). Zone A of the rat runs parasagitally from lobules I to IX as described in the cat, but in the posterior lobe it extends much more laterally than in the other mammals to include the lobulus paramedianus and crus I regions. The projections of Zone A to the NF recognize a mediolateral as well as a dorsoventral organization. Zone A receives climbing fibres exclusively from the caudal half of the medial accessory olive (MAO) with a further topographical organization in 4 distinct connections. Zone B of the rat is a narrow strip of the cortex lying adjacent to Zone A and extending from lobule I to VI. It receives climbing fibres from the caudolateral half of the dorsal accessory olive (DAO) and projects to the ipsilateral NVL with no other detectable organization. The majority of the labelled terminals end in the dorsal aspect of the NVL, but a non-negligible quantity also end in the ventral aspect.     

Subcortical afferent and efferent connections of the superior colliculus in the rat and comparisons between albino and pigmented strains

Summary Subcortical connections of the superior colliculus were investigated in albino and pigmented rats using retrograde and anterograde tracing with horseradish peroxidase (HRP), following unilateral injection of HRP into the superior colliculus. Afferents project bilaterally from the parabigeminal nuclei, the nucleus of the optic tract, the posterior pretectal region, the dorsal part of the lateral posterior-pulvinar complex and the ventral nucleus of the lateral lemniscus; and ipsilaterally from the substantia nigra pars reticulata, the pars lateralis of the ventral lateral geniculate nucleus, the intergeniculate leaflet, the zona incerta, the olivary pretectal nucleus, the nucleus of the posterior commissure, the lateral thalamus, Forel's field H₂, and the ventromedial hypothalamus. Collicular efferents terminate ipsilaterally in the anterior, posterior and olivary pretectal nuclei, the nuclei of the optic tract and posterior commissure, the ventrolateral part of the dorsal lateral geniculate nucleus, the pars lateralis of the ventral lateral geniculate nucleus, the intergeniculate leaflet, and the zona incerta; and bilaterally in the parabigeminal nuclei and lateral posterior-pulvinar complex (chiefly its dorsal part). The general topographical patterns of some of the afferent and efferent projections were also determined: the caudal and rostral parts of the parabigeminal nucleus project to the caudal and rostral regions, respectively, of the superior colliculus; caudal superior colliculus projects to the most lateral, and lateral superior colliculus to the most caudal part of the terminal field in the dorsal lateral geniculate nucleus; caudolateral superior colliculus projects to the caudal ventrolateral part of the ventral lateral geniculate nucleus, while rostromedial parts of the colliculus project more rostrally and dorsomedially. Following comparable injections in pigmented and albino animals, fewer retrogradely labelled cells were found in subcortical structures in the albino than in the pigmented rats. The difference was most marked in nuclei contralateral to the injected colliculus. Thus, the effects of albinism on the nervous system may be more widespread than previously thought.M. R. C. Scholar     

Evidence for a projection from the perireticular thalamic nucleus to the dorsal thalamus in the adult rat and ferret

Summary During early development, the perireticular thalamic nucleus is very large (i.e. has many cells) and has a strong projection to the dorsal thalamus and to the cerebral neocortex. By adulthood, the nucleus has much reduced in size and only a few cells remain. It is not clear whether these perireticular cells that remain into adulthood maintain their connections with the dorsal thalamus and with the neocortex. This study examines this issue by injecting neuronal tracers into various nuclei of the dorsal thalamus (dorsal lateral geniculate nucleus, medial geniculate complex, ventroposteromedial nucleus, lateral posterior nucleus, posterior thalamic nucleus) and into different areas of the neocortex (somatosensory, visual, auditory). After injections of tracer into the individual nuclei of the rat and ferret dorsal thalamus, retrogradely-labelled perireticular cells are seen. In general, after each injection, the retrogradely-labelled perireticular cells lie immediately adjacent to a group of retrogradely-labelled reticular cells. For instance, after injections into the medial geniculate complex, perireticular cells adjacent to the auditory reticular sector are retrogradely-labelled, whilst after an injection into the dorsal lateral geniculate nucleus, retrogradely-labelled perireticular cells adjacent to the visual reticular sector are seen. By contrast, injections of tracer into various areas of the rat and ferret neocortex result in no retrogradely-labelled cells in the perireticular nucleus. Thus, unlike during perinatal development when perireticular cells project to both neocortex and dorsal thalamus, perireticular cells in the adult seem to project to the dorsal thalamus only: the perireticular projection to the neocortex appears to be entirely transient.