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The cells of origin and terminal fields of the amygdalo-hypothalamic projections in the lizard Podarcis hispanica were determined by using the anterograde and retrograde transport of the tracers, biotinylated dextran amine and horseradish peroxidase. The resulting labeling indicated that there was a small projection to the preoptic hypothalamus, that arose from the vomeronasal amygdaloid nuclei (nucleus sphericus and nucleus of the accessory olfactory tract), and an important projection to the rest of the hypothalamus, that was formed by three components: medial, lateral, and ventral. The medial projection originated mainly in the dorsal amygdaloid division (posterior dorsal ventricular ridge and lateral amygdala) and also in the centromedial amygdaloid division (medial amygdala and bed nucleus of the stria terminalis). It coursed through the stria terminalis and reached mainly the retrochiasmatic area and the ventromedial hypothalamic nucleus. The lateral projection originated in the cortical amygdaloid division (ventral anterior and ventral posterior amygdala). It coursed via the lateral amygdalofugal tract and terminated in the lateral hypothalamic area and the lateral tuberomammillary area. The ventral projection originated in the centromedial amygdaloid division (in the striato-amygdaloid transition area), coursed through the ventral peduncle of the lateral forebrain bundle, and reached the lateral posterior hypothalamic nucleus, continuing caudally to the hindbrain. Such a pattern of the amygdalo-hypothalamic projections has not been described before, and its functional implications in the transfer of multisensory information to the hypothalamus are discussed. The possible homologies with the amygdalo-hypothalamic projections in mammals and other vertebrates are also considered.

The ascending projections of the optic tectum, including their cells of origin, have been studied in the lizard Podarcis hispanica by means of a two-step experimental procedure. First, tracers were injected in the tectum to study the anterograde labeling in the forebrain. Second, the cells of origin of these projections have been identified by analyzing the retrograde labeling after tracer injections in the thalamus, hypothalamus, and pretectum. Three main tectal ascending pathways have been described: the dorsal tecto-thalamic tract (dtt), the medial tecto-thalamic tract (mtt), and the ventral tecto-thalamic tract (vtt). The dtt originates in radial cells of layers 5 and 7 and bipolar cells of layers 8 and 10 that project to the lateral neuropile of the dorsal lateral geniculate nucleus (GLD), to the intergeniculate leaflet (IGL), and to the ventral lateral geniculate nucleus (GLV). The mtt arises from radial neurons of layers 3 and 5 and bilaterally reaches the putative reticular thalamus and its boundary with the hypothalamus, the rostral IGL, and the area triangularis (AT). The vtt is composed of fibers from ganglion and multipolar cells of the layer 7 that project bilaterally to the nucleus of the vtt, the ventrolateral thalamic nucleus, the medial posterior thalamic nucleus (MP), the nucleus rotundus (Rot), the IGL, and the cell plate of the GLD. Therefore, the GLD receives not only direct retinal afferents but also two different tectal inputs, thus constituting a convergence point in the two visual pathways to the telencephalon. Moreover, different tectal cells specifically project to the ventrolateral thalamus and to pretectal nuclei. These results are discussed from comparative and functional viewpoints.

In this paper we study the septal complex architecture in the lizard Podarcis hispanica (Lacertidae). Histochemical and immunohistochemical techniques were used to define the distribution of zinc (Timm stain), acetyl cholinesterase (AChase), gamma-aminobutyric acid (GABA), tyrosine hydroxylase (TH), dopamine (DA), serotonin (5-HT), and two neuropeptides: leu-enkephalin (L-ENK) and substance P (SP). These reactions delineate a coherent map of nine septal nuclei that are named with a topographical nomenclature: anterior, lateral, ventromedial, medial, dorsolateral, ventrolateral, and dorsal septal nuclei, nucleus septalis impar, and nucleus of the posterior pallial commissure. The anterior septal nucleus is characterized by intense reaction for zinc and the presence of fibers immunoreactive for GABA, 5-HT, and L-ENK, which form pericellular nests. The lateral septal nucelus shows intense reaction for zinc, a high density of GABA-immunoreactive cells, and L-ENK-immunoreactive fibers forming basketlike figures around unstained somata. The ventromedial septal nucleus shows intense AChase reactivity, a dense network of 5-HT-immunoreactive fibers, and virtually no labeling for the other histochemical stains. The medial septal nucleus is defined by heavy reactivity for zinc, dense DA/TH and L-ENK innervations, and the presence of L-ENK-immunoreactive cells. The dorsolateral septal nucleus shows intense AChase staining in the neuropile and a dense network of fibers immunoreactive for 5-HT and DA/TH, but it shows low staining for zinc. The ventrolateral septal nucleus shows L-ENK-immunoreactive cells and a dense L-ENK innervation, but low reactivity for zinc. The dorsal septal nucleus, intermingled with the fimbrial fibers, shows a dense population of GABA-immunoreactive cells and terminals, but it is unreactive for zinc. Two subdivisions can be established in this dorsal septal nucleus: the dorsal part, intensely reactive for AChase and innervated by 5-HT fibers, and the central part, which shows L-ENK-immunoreactive neurons and fibers without reactivity for either AChase or 5-HT. The nucleus septalis impar, traversed by the fibers of the anterior pallial commissure (mildly reactive for zinc), shows reaction for AChase but low (if present) reactivity for the remaining markers. The nucleus of the posterior pallial commissure shows a generally low reactivity for the histochemical reactions employed. The distribution of these markers is similar to that found in other squamate reptiles and allows for a direct comparison with the septal formation of mammals. Such a comparison reinforces the view that the limbic system has undergone a conservative evolution within vertebrates.

The aim of this work is to delineate the retinorecipient cell groups of the dorsal thalamus of lizards and to study some of the differential connections in order to help to understand the evolution of the visual system in tetrapods. Tract-tracing and immunohistochemical techniques were applied to the retinorecipient dorsal thalamus of the lizard Podarcis hispanica. The retina of Podarcis projects to four areas of the dorsal thalamus: nucleus ovalis (Ov), intergeniculate leaflet (IGL), dorsal lateral geniculate nucleus (GLD) and dorsolateral anterior nucleus (DLA). Nucleus ovalis shows a clear cell plate/neuropile organization and projects to the ventral thalamus. Thus, it seems to belong to the ventral rather than to the dorsal thalamus. The IGL contains large cells reactive for GABA and/or NPY immunohistochemistry. It is interconnected with the supra/retrochiasmatic hypothalamus and projects to the opposite thalamus and to the ipsilateral tectum. The caudal DLA, which lacks both GABA- and NPY-like immunoreactive cells is reached by a few thin retinal fibers, although distal dendrites of DLA cells enter the GLD, suggesting an important retinal input. The DLA projects to the medial and dorsal telencephalic cortices. The GLD is the main retinorecipient thalamic structure that projects to the telencephalon. It shows a crude laminar organization in which cell plate neurons project to the ipsilateral pallial thickening, but it does not receive a descending projection from the visual telencephalon and thus differs from the GLD of other amniotic vertebrates. In the context of present knowledge, these results suggest that an IGL homologue is present in all tetrapods studied, whereas Ov seems to be restricted to diapsid vertebrates. Moreover, our data suggest that a unimodal visual projection to the telencephalon (arising from the GLD) first appeared in reptiles by segregation from a limbic (multimodal) thalamo-telencephalic pathway.