The distribution of NPY-like immunoreactivity in the chameleon brain.

The distribution of neuropeptide Y (NPY) immunoreactivity was studied in the brain of the chameleon. Cell bodies and fibers displaying NPY-like immunoreactivity were widely dispersed throughout the brain and at the highest density in the telencephalon and diencephalon. Immunolabeled cell bodies were numerous in the medial and dorsomedial cortex and in the dorsal ventricular ridge, while the striatum and basal telencephalon only contained sparsely scattered NPY-positive somata. Immunopositive neurons were densely distributed in the dorsal thalamus (particularly in the perirotundal belt), the area triangularis, the nucleus geniculatus lateralis pars dorsalis, the periventricular hypothalamus and the medial eminence. In the pretectum, NPY-immunoreactive cell bodies were limited to the nucleus posterodorsalis, while in the mesencephalon immunolabeled somata were found in the stratum album centrale of the optic tectum and in the substantia nigra. Immunopositive fibers and terminals were particularly dense in the dorsomedial cortex, the periventricular hypothalamus, the nuclei accumbens, suprachiasmaticus and griseus tectalis, in the substantia nigra and in the torus semicircularis. These findings show that the NPY system in the chameleon has the same basic organization as in other vertebrate species, and indicate that this peptide could be also implicated in the regulation of several aspects of cerebral functions. In addition, and of particular interest, is the observation of numerous NPY-immunoreactive neurons and fibers in several visual nuclei, suggesting an important involvement of this substance in the visual function.

Pretectal connections in turtles with special reference to the visual thalamic centers: a hodological and gamma-aminobutyric acid-immunohistochemical study.

Projections of the pretectal region to forebrain and midbrain structures were examined in two species of turtles (Testudo horsfieldi and Emys orbicularis) by axonal tracing and immunocytochemical methods. Two ascending gamma-aminobutyric acid (GABA)ergic pathways to thalamic visual centers were revealed: a weak projection from the retinorecipient nucleus lentiformis mesencephali to the ipsilateral nucleus geniculatus lateralis pars dorsalis and a considerably stronger projection from the nonretinorecipient nucleus pretectalis ventralis to the nucleus rotundus. The latter is primarily ipsilateral, with a weak contralateral component. The interstitial nucleus of the tectothalamic tract is also involved in reciprocal projections of the pretectum and nucleus rotundus. In addition, the pretectal nuclei project reciprocally to the optic tectum and possibly to the telencephalic isocortical homologues. Comparison of these findings with previous work on other species reveals striking similarities between the pretectorotundal pathway in turtles and birds and in the pretectogeniculate pathway in turtles, birds, and mammals.

Retinal projections in two crocodilian species, Caiman crocodilus and Crocodylus niloticus.

The retinal projections of Caiman crocodilus and Crocodylus niloticus were investigated by means of the orthograde axonal transport of either rhodamine beta-isothiocyanate or tritiated proline. In these two species, each tracer revealed contralateral retinal projections to three hypothalamic regions (subventricular gray matter, nucleus suprachiasmaticus, and area optica hypothalami lateralis), five thalamic regions (nuclei ovalis, dorsolateralis anterior, ventrolateralis and ventrobasalis, and lateral geniculate complex, of which six subcomponents can be distinguished), six pretectal regions (nuclei posterodorsalis, lentiformis mesencephali, griseus tectalis, geniculatus pretectalis, area optica commissurae posterior and area optica pretectalis lateroventralis), six outermost layers of the optic tectum, and the nucleus opticus tegmenti. Weak ipsilateral retinal projections have been observed in two hypothalamic nuclei and in the nucleus opticus tegmenti. Comparative analysis with other data show that the contralateral retinal projections of crocodiles are considerably more reptilian than avian. Moreover, crocodiles share with birds an extremely poor contingent of ipsilateral retinal projections.

Interspecific variation in the chelonian primary visual system.

The primary visual system of 21 species of turtles, distributed among nine of the existing 12 families, were studied by autoradiography. In all species, contralateral visual projections exist to 15 targets: two hypothalamic structures (nucleus suprachiasmaticus and n. periventricularis), three major thalamic visual centres (nucleus ovalis, n. geniculatus lateralis ventralis and n. geniculatus lateralis dorsalis) and two minor thalamic targets (nucleus dorsolateralis anterior and n. ventrolateralis), five pretectal sites (nucleus geniculatus pretectalis, n. opticus pretectalis ventrolateralis, n. lentiformis mesencephali, n. posterodorsalis and n. griseus tectalis), two strata of the optic tectum (stratum opticum and s. fibrosum et griseum superficiale), and a single tegmental target (nucleus opticus tegmenti). In contrast to the stability of contralateral visual projections, their ipsilateral counterparts varied considerably between species, being limited to the hypothalamus in some species, and involving the majority of the primary visual centres in others. This variation is not readily explainable in terms of taxonomic position or of differences in mode of life.

An experimental re-evaluation of the primary visual system of the European chameleon, Chamaeleo chameleon.

The retinofugal projections of the chameleon were investigated by means of autoradiography, horseradish peroxidase and fluorescent techniques after intraocular injection of tracers. An ipsilateral contingent of visual fibers and projections is absent. The retinal fibers decussate completely in alternating fascicles at the optic chiasma and course to terminate in two hypothalamic nuclei (nucleus suprachiasmaticus and nucleus opticus periventricularis hypothalami posterior), six thalamic nuclei (nucleus ovalis, nucleus geniculatus lateralis dorsalis partes lateralis and medialis, nucleus geniculatus lateralis ventralis, lateral part of nucleus dorsolateralis anterior, and nucleus ventrobasalis), four pretectal nuclei (nucleus griseus tectalis, nucleus lentiformis mesencephali, nucleus geniculatus pretectalis and nucleus posterodorsalis), the optic tectum (stratum griseum et fibrosum superficiale) and the tegmental nucleus opticus tegmenti. Our findings are, in general, compatible with previous descriptions of the primary visual system in other species of lizards. However, they indicate three features particular to chameleons: first, the total absence of an ipsilateral retinofugal projection; second, the existence of an additional hypothalamic visual center located in the posterior mediodorsal hypothalamus; and third, the large size of nucleus opticus tegmenti. These features are discussed in terms of the taxonomic position of chameleons with respect to other lizards.

A reconsideration of the primary visual system of the turtle Emys orbicularis.

The retinocerebral projections of Emys orbicularis were investigated by means of [3H]-proline or HRP, administered by intraocular injection. Two newly-hatched, two juvenile and seven adult specimens were examined. The results reveal contralateral retinal projections to fifteen sites: two in the hypothalamus (the nuclei suprachiasmaticus and periventricularis), five in the thalamus (the nuclei ovalis, geniculatus lateralis ventralis, geniculatus laleralis dorsalis, dorsolateralis anterior and ventrolateralis), five in the pretectal region (the nuclei geniculatus pretectalis, opticus pretectalis ventrolateralis, lentiformis mesencephali, posterodorsalis and griseus tectalis), two in the optic tectum (the stratum opticum and the stratum fibrosum et griseum superficiale), and one in the tegmentum (the nucleus opticus tegmenti). Ipsilateral projections to nine of these sites at thalamic, pretectal, tectal and tegmental levels, while weak, could be clearly demonstrated. These results differ considerably from those obtained in a previous investigation using a Nauta-paraffin technique; it is suggested that the differences are due to limitations of the latter technique. A review of the existing literature on the Chelonian primary visual system reveals considerable terminological diversity, and a standard nomenclature for the primary visual centres of turtles is proposed.

Projections of the dorsolateral anterior complex and adjacent thalamic nuclei upon the visual Wulst in the pigeon.

The distinctive patterns of thalamic input to the rostral (R), intermediate (I) and caudal (C) divisions of the pigeon Wulst were determined using the retrograde multiple label technique following concomitant injections of various fluorescent tracers into different Wulst loci. The results showed topographical projections from components of the visual thalamic n. dorsolateralis anterior complex. Major ipsilateral and contralateral projections upon the R and I Wulst stem from the pars lateralis ventralis and dorsalis nuclei, respectively. The nuclei pars lateralis rostralis, pars magnocellularis and n. suprarotundus provide weak bilateral projections to all of the Wulst divisions sampled. Lastly, bilateral connections from the n. superficialis parvocellularis upon I and C, and from n. dorsolateralis posterior upon the posterior C Wulst were also demonstrated. Based upon their patterns of terminal distribution upon the Wulst, some of these thalamic nuclei are compared to specific components of the mammalian geniculate and extrageniculate visual systems.

Visual system degeneration in the glaucomatous albino quail.

The peripheral (eye, retina, optic nerve) and central (primary optic tracti and centers, centrifugal visual tractus and nucleus) visual system of an imperfect albino quail mutant with a sex linked recessive gene was examined in 32 specimens ages 1 week - 16 months-hatch using various histological techniques. During the first weeks the visual system was normal and comparable in its overall organization to that found in the pigmented quail. However, the ipsilateral retinal projections were observed to be weaker in the young mutant, then completely disappeared two months after birth. Initial signs of the bupthalmos, a form of spontaneous glaucoma, appeared between the 3rd and 5th months. This was characterized by a distention of the eye linked to an increase in intraocular pressure. The pathological process was progressive and at 16 months the eye was very prominent, the anterior chamber deep and a large and globular cornea was noted. The glaucoma progressively induced different histopathological changes in the visual system including: cupping of the optic disc, degeneration of optic axons and their parent ganglion and centrifugal cells and cavernous degeneration. All of these phenomena were identifiable at about the 10th post-natal month and progressed in a relatively constant and orderly manner. The retinal projections to the nucleus ectomamillaris, ventral and lateral optic tectum and ventral pretectum were the first to degenerate. The degeneration of optic fibers attaining the dorsal pretectum and dorsal thalamus occurred later. Furthermore the retrograde degeneration in the centrifugal isthmo-optic nucleus progressed from the external to the internal pole. The mechanisms involved in the selective degeneration of centrifugal and centripetal optic fibers is discussed.

The anatomical organization of retinal projections in the shark Scyliorhinus canicula with special reference to the evolution of the selachian primary visual system.

The retinal projections of the shark Scyliorhinus canicula were investigated using both the degeneration technique after eye removal and the radioautographic method following the intraocular injection of various tritiated tracers (proline, leucine, fucose, adenosine). The results showed contralateral projection via different optic tract components (TOM, AOT, TOm, TOl, ROVm, RODm) to various areas and nuclei of the hypothalamus (NSC), thalamus (NODLAT, NODMAT, NTTOM, NOVT, NODPT), pretectum (NOPC, NOCPd, NOCPv), tectum (SFGS, SGI) and mesencephalic tegmentum (AOTMd, NOTMv). Ipsilateral retinal projections were found to arborize within 7 distinct zones at the hypothalamic (NSC), thalamo-pretectal (NODLAT, NTTOM, NOVT, NOPC, NOCpd) and tectal (SFGS) levels. A comparison of the data with those previously obtained in different species of elasmobranchs and batoids indicate the existence of a common and consistent pattern of organization of the primary visual system in all selachians. Many of the discrepancies reported in studies on the organization of selachian retinal projection may be listed to methodological differences and/or interspecies variations in the cytoarchitecture of the different visual centers. Moreover, a comparison of the primary visual system of more primitive squalomorph sharks with that of the more advanced galeomorph sharks and batoids suggests that this system evolved through an increase in the neuronal density of the target structures and transformations in the dendritic configurations of the postsynaptic neurons rather than through an increase in the total number of projection zones.

The retinofugal pathways in a primitive actinopterygian, the chondrostean Acipenser güldenstädti. An experimental study using degeneration, radioautographic and HRP methods.

Experimental study of the retinofugal pathways in Acipenser güldenstädti was carried out on 109 specimens using 3 experimental tracing methods: Fink-Heimer (after retinal ablation), radioautography (after intraocular injection of tritiated markers) and HRP (after intraocular injection of HRP or iontophoretic deposit of HRP on the optic nerve). The optic fiber was found to partially decussate at the chiasm and to project to 5 contralateral regions: (1) hypothalamus (area optica hypothalami); (2) thalamus (area optica dorsalis thalami, area optica mediale thalami, nucleus thalamicus tractus optici marginalis, nucleus laminaris ventralis); (3) pretectum (nucleus pretectalis ventralis, nucleus commissurae posterioris, nucleus intercalaris lateralis); (4) optic tectum (superficial layers); and (5) mesencephalic tegmentum (area optica accessoria). The ipsilateral component was well developed and innervated the same regions mentioned above. A few contralateral optic fibers crossed again in the posterior commissure and terminated within ipsilateral visual pretectal structures. Although the architecture of the visual centers was less elaborated in this paleopterygian than in neopterygians (holosteans, teleosteans), we observed that the general organization of the retinal contralateral projections in this fish was comparable to that of more advanced actinopterygians. Our results indicate that this pattern was probably set at a very early date, perhaps as soon as the emergence of the chondrostean grade at the beginning of the Devonian.

The retinofugal pathways in the primitive African bony fish Polypterus senegalus (Cuvier, 1829).

Retinal projections were studied using Fink-Heimer and radioautographic methods in Polypterus senegalus, a species which is representative of a small group of African fresh-water bony fish often considered to be very primitive. The large optic nerve showed partial decussation at the chiasm. Two major contralateral tracts were observed: the axillary and marginal optic tracts, with the latter being subdivided posteriorly into the tractus opticus medialis and tractus opticus lateralis. The retina projected onto the: (1) hypothalamus (area optica postoptica); (2) thalamus (nucleus opticus dorsolateralis thalimi, nucleus dorsomedialis thalami, corpus geniculatum laterale, area optica dorsolateralis thalami, area optica ventrolateralis thalami); (3) pretectum (nuclei commissurae posterioris, pretectalis ventralis, pretectalis dorsalis); and (4) optic tectum (stratum marginale, stratum opticum, stratum griseum et fibrosum superficiale, stratum griseum et album centrale, stratum griseum et fibrosum periventriculare). Ipsilateral retinal projections were demonstrated to the same 4 levels and more precisely to the nucleus opticus dorsolateralis thalami, area optica dorsolaterale thalami, nucleus commissurae posterioris, stratum marginale and stratum griseum et album centrale. The existence of a retinal projection to the mesencephalic tegmentum is discussed. Comparing the primary optic system of Polypterus with that of other jawed vertebrates, and particularly with that of other bony fish, indicated that this species possesses a combination of characteristics which are both actinopterygian and sarcopterygian. The phylogenetic significance of this mozaic anatomical arrangement is discussed.

[Radioautographic analysis of retinofugal projections in the primitive bony fish Polypterus senegalus C]. / Analyse radioautographique des projections rétiniennes chez le poisson osseux primitif Polypterus sengalus C.

Retinofugal pathways of Polypterus senegalus C. have been examined by means of the radioautographic method. Contralaterally the retina projects to the hypothalamus, thalamus, pretectum and tectum. An important ipsilateral component has been observed. No retinal projection to the mesencephalic tegmentum has been identified. Comparing the primary optic system of Polypterus with that of other body Fish, indicates that this species possesses a combination of characteristics which are both actinopterygian and sarcopterygian. The significance of this mozaic arrangement is discussed.

A radioautographic study of retinal projections in type I and type II lizards.

The retinofugal projections of 5 species (Acanthodactylus boskianus, Scincus scincus, Tarentola mauritanica, Uromastix acanthinurus and Zonosaurus ornatus) belonging to 5 different families of Type I and Type II lizards have been examined by means of the radioautographic method. In the 5 species the retinal ganglion cells project to the contralateral hypothalamus (nucleus suprachiasmaticus), thalamus (nucleus geniculatus lateralis pars ventralis, nucleus geniculatus lateralis pars dorsalis), pretectum (nuclei lentiformis mesencephali, geniculatus pretectalis, postero-dorsalis griseus tectalis), tectum opticum (layer 2 to layer 6 of the stratum griseum et fibrosum superficiale) and tegmentum mesencephali (nucleus opticus tegmenti). Ipsilateral optic fibers were never observed in Uromastix acanthinurus, whereas an uncrossed quota was visible in both nucleus geniculatus lateralis pars dorsalis and nucleus postero-dorsalis in the other species. An ipsilateral retinotectal projection was observed only in Tarentola mauritanica. With the exception of the nucleus griseus tectalis the contralateral optic centers identified in this material have to a large extent been observed in other reptiles belonging to the different orders. The presence in reptiles of a general pattern of contralateral visual projections indicates that these were established very clearly in the course of evolution. Similarities become apparent when this plan is compared with that observed in birds. In marked contrast the ipsilateral component in reptiles is unstable and mutable in nature. This ipsilateral retinotectal projections do not appear to be a feature restricted to Type I lizards. On the other hand, the presence of this optic component cannot be linked solely to nocturnal habits.