Projections of the optic tectum and the mesencephalic nucleus of the trigeminal nerve in the tegu lizard (Tupinambis nigropunctatus)

Summary Fibers undergoing Wallerian degeneration following tectal lesions were demonstrated with the Nauta and Fink-Heimer methods and traced to their termination. Four of the five distinct fiber paths originating in the optic tectum appear related to vision, while one is related to the mesencephalic nucleus of the trigeminus. The latter component of the tectal efferents distributes fibers to 1) the main sensory nucleus of the trigeminus, 2) the motor nucleus of the trigeminus, 3) the nucleus of tractus solitarius, and 4) the intermediate gray of the cervical spinal cord.The principal ascending bundle projects to the nucleus rotundus, three components of the ventral geniculate nucleus and the nucleus ventromedialis anterior ipsilaterally, before it crosses in the supraoptic commissure and terminates in the contralateral nucleus rotundus, ventral geniculate nucleus and a hitherto unnamed region dorsal to the nucleus of the posterior accessory optic tract.Fibers leaving the tectum dorso-medially terminate in the posterodorsal nucleus ipsilaterally and the stratum griseum periventriculare of the contralateral tectum. The descending fiber paths terminate in medial reticular cell groups and the rostral spinal cord contralaterally and in the torus and the lateral reticular regions ipsilaterally. The ipsilateral fascicle also issues fibers to the magnocellular nucleus isthmi.     

Anatomy,neurophysiology and functional aspects of the nucleus isthmi in salamanders of the family Plethodontidae

Summary Tongue-projecting plethodontid salamanders have massive direct ipsilateral retinal afferents to the tectum opticum as well as a large and well developed nucleus isthmi. Retrograde staining revealed two subnuclei: A ventral one projecting to the contralateral tectal hemisphere and a dorsal one projecting back to the ipsilateral side. The isthmic nuclei show a retinotopic organization, which is in register with that of the tectum. Electrophysiological recordings from nucleus-isthmi neurons revealed response properties that are very similar to those found in tectal neurons. Thus, there is no substantial processing of tectal neural activity in the nucleus isthmi. Measurements of peak latencies after electrical and light stimulation suggest the continuous coexistence of 4 representations of the visual field in the tectum mediated by (1) the contralateral and (2) the ipsilateral direct retinal afferents, (3) the uncrossed and (4) the crossed isthmo-tectal projection. (1) and (2) originate at the same moment in the retina and arrive simultaneously in the tectum. It is assumed that in plethodontid salamanders with massive ipsilateral retino-tectal projections depth perception based on disparity cues is achieved by comparison of these images.Representations mediated by (3) and (4) arriving in the tectum at the same time as (1) and (2) originate 10–30 ms earlier in the retina. It is hypothesized that these time differences between (1)/(2) and (3)/(4) are used to calculate three-dimensional trajectories of fast-moving prey objects.Abbreviations EL edge length - FDA fluoresceine dextranamine - RDA tetramethylrhodamine dextranamine - RF receptive field     

Target areas innervated by PACAP-immunoreactive retinal ganglion cells

The retinohypothalamic tract (RHT) originates from a subset of retinal ganglion cells (RGCs). The cells of the RHT co-store the neurotransmitters PACAP and glutamate, which in a complex interplay mediate light information to the circadian clock located in the suprachiasmatic nuclei (SCN). These ganglion cells are intrinsically photosensitive probably due to expression of melanopsin, a putative photoreceptor involved in light entrainment. In the present study we examined PACAP-containing retinal projections to the brain using intravitreal injection of the anterograde tracer cholera toxin subunit B (ChB) and double immunostaining for PACAP and ChB. Our results show that the PACAP-containing nerve fibres not only constituted the major projections to the SCN and the intergeniculate leaflet of the thalamus but also had a large terminal field in the olivary pretectal nucleus. The contralateral projection dominated except for the SCN, which showed bilateral innervation. PACAP-containing retinal fibres were also found in the ventrolateral preoptic nucleus, the anterior and lateral hypothalamic area, the subparaventricular zone, the ventral part of the lateral geniculate nucleus and the nucleus of the optic tract. Retinal projections not previously described in the rat also contained PACAP. These new projections were found in the lateral posterior nucleus, the posterior limitans nucleus, the dorsal part of the anterior pretectal nucleus and the posterior and medial pretectal nuclei. Only a few PACAP-containing retinal fibres were found in the superior colliculus. Areas innervated by PACAP-immunoreactive fibres also expressed the PACAP-specific PAC1 receptor as shown by in situ hybridization histochemistry. The findings suggest that PACAP plays a role as neurotransmitter in non-imaging photoperception to target areas in the brain regulating circadian timing, masking, regulation of sleep-wake cycle and pupillary reflex.Abbreviations 3v Third ventricle - ac Anterior commissure - AD Anterodorsal thalamic nucleus - AH Anterior hypothalamic area - APTD Anterior pretectal nucleus, dorsal part - ChB Cholera toxin subunit B - CPu Caudate putamen - CPT Commissural pretectal nucleus - DGL Dorsal geniculate nucleus - IGL Intergeniculate leaflet - LH Lateral hypothalamic area - LP Lateral posterior thalamic nucleus - LS Lateral septum - MB Mammillary body - MPO Medial preoptic nucleus - MPT Medial pretectal nucleus - oc Optic chiasma - OPT Olivary pretectal nucleus - OT Nucleus of the optic tract - PACAP Pituitary adenylate cyclase-activating polypeptide - PAC1 PACAP receptor type 1 - PAG Periaqueductal gray - Pe Periventricular hypothalamic nucleus - PLi Posterior limitans thalamic nucleus - PPT Posterior pretectal nucleus - PVT Paraventricular thalamic nucleus - PVN Paraventricular hypothalamic nucleus - RGCs Retinal ganglion cells - RHT Retinohypothalamic tract - SCN Suprachiasmatic nucleus - SC Superior colliculus - SNR Substantia nigra, reticular part - SON Supraoptic nucleus - SPVZ Subparaventricular zone - VGL Ventral geniculate nucleus - VIP Vasoactive intestinal peptide - VPAC1 VIP/PACAP receptor type 1 - VPAC2 VIP/PACAP receptor type 2 - VLPO Ventrolateral preoptic nucleus - VTA Ventral tegmental areaThis study was supported by The Danish Biotechnology Center for Cellular Communication and The Danish Neuroscience Programme. J.H. is postdoc funded by the Danish Medical Research Council (Jr. No. 0001716)     

Efferent projections from the lateral geniculate nucleus to the pineal complex of the Mongolian gerbil (Meriones unguiculatus)

Summary The intergeniculate leaflet of the lateral geniculate nucleus is considered to modulate circadian activity rhythms probably mediated by a direct neuronal connection to the suprachiasmatic nucleus. The present study in the gerbil demonstrates, by anterograde tracing with Phaseolus vulgaris-leucoagglutinin (PHA-L), the existence of an additional neuronal projection from a subportion of the lateral geniculate nucleus, involving the intergeniculate leaflet, directly to the pineal gland. PHA-L-immunoreactive nerve fibers originating from perikarya at the injection site were located under the optic tract projecting towards the midsagittal plane. Delicate PHA-L-immunoreactive nerve fibers were observed in the posterior paraventricular thalamic nucleus, precommissural nucleus, olivary pretectal nucleus, anterior and posterior pretectal nuclei, and posterior commissure. Single fibers could be followed from the caudal part of the medial habenular nucleus and the pretectal area into the rostral part of the deep pineal gland. Other fibers continued through the posterior commissure into the contralateral hemisphere to terminate in the same structures as on the ipsilateral side. From the posterior commissure, small bundles of thick fibers entered the deep pineal gland where they arborized among the endocrine cells. A few nerve fibers were observed in the habenular commissure and the pineal stalk, but no fibers were identified in the superficial pineal. This direct geniculo-pineal connection suggests that the pineal gland is directly influenced by the optic system.     

Pretecto-tectal influences

(1)From the dorsal surface of the toad (Bufo b. spinosus, B. marinus) optic tectum (OT), field potentials (FP) were recorded at 9 reference sites in response to electrical stimulation of the optic nerve (ON). The FP showed 4 main components, besides an initial deflection attributed to axonal potentials: two negative waves N1, N2 (attributed to postsynaptic excitatory processes) and two positive waves P2, P3 (attributed to postsynaptic inhibitory processes). The responses across the reference sites were rather similar in different individuals. (2) Electrical stimulation of an area in the ipsilateral pretectal lateral posterodorsal and posterior (Lpd/P) thalamic region evoked tectal FPs showing mainly a negative and a positive wave. Regarding wave amplitudes, the FPs displayed disproportionalities across the reference sites. (3) Electrical stimulation of the contralateral Lpd/P evoked mainly a positive wave in the tectal FP whose disproportionality corresponded roughly to the one obtained to ipsilateral Lpd/P stimulation. (4) The inital negative wave of the tectal FP in response to ON stimulation was nearly abolished, if Lpd/P stimulation preceded ON stimulation at a delay of 17–25 ms. (5) Since FPs showed adaptation to repetitive stimulation, various experiments were carried out to distinguish adaptation phenomena from effects of neuronal interactions between Lpd/P and OT. (6) The results provide evidence that ON- and Lpd/P-mediated inputs interact in superficial tectal layers, whereby pretectotectal input suppresses retinotectal excitatory information transfer. Input of Lpd/P to the contralateral superficial OT suggests postsynaptic inhibition. This study provides no information about pretectal inputs to deeper tectal layers, which anatomically are known to exist.Abbreviations A-I recording sites from the dorsal tectal surface - D _t delay between Lpd/P and ON stimulation - EPSP IPSP excitatory and inhibitory postsynaptic potentials, respectively - FP field potential - L latency of FP waves - ON optic nerve - OT optic tectum - Lpd/P lateral posterodorsal and posterior pretectal thalamic region - Lpv lateral posteroventral pretectal thalamic nucleus - N, P negative and positive waves of FPs, respectively - PRE presynaptic axonal input - TH pretectal thalamic neurons     

Xenopus exhibits seasonal variation in retinotectal latency but not tecto-isthmo-tectal latency

1. The tectum of Xenopus receives visuotopic input from both eyes. The contralateral eye's projection reaches the tectum directly, via the optic nerve. The ipsilateral eye's projection reaches the tectum indirectly, via the nucleus isthmi and isthmo-tectal projection. 2. Because of the multi-synaptic nature of the ipsilateral pathway, there is an inherent delay between the time that information from the contralateral eye reaches the tectum and the time that information from the ipsilateral eye arrives at the tectum. The length of the intertectal delay is a function of the latencies of the contralateral and ipsilateral pathways. 3. The length of this intertectal delay has functional, as well as developmental, implications with regard to the role of N-methyl-D-aspartate receptors in tectal cell activity and development of orderly synaptic connections. 4. We have found that the latencies of the contralateral and ipsilateral pathways exhibit a seasonal variation, increasing during the winter months. The increases of both latencies during the winter were of similar magnitude, indicating that there were no significant changes in intertectal delay. The seasonal alteration in contralateral latency was not affected by dark-rearing and was affected to only a minor extent by a week-long alteration of ambient temperature.     

Retinal projections in the catfish,Mystus vittatus (Bloch) as revealed by tracer studies with horseradish peroxidase

Summary The retinal efferents of the catfish, Mystus vittatus, were investigated with the use of the horseradish peroxidase (HRP) technique. Most retinal fibres extended contralateral to the eye that had received HRP label, while a few fascicles projected to the ipsilateral side without decussation in the optic chiasma. The contralateral fibres projected to the suprachiasmatic nucleus, the nucleus opticus dorsolateralis, the nucleus of the posterior commissure, the nucleus geniculatus lateralis, pretectal nuclear complex, and to two layers of the optic tectum, i.e., stratum fibrosum et griseum superficiale and stratum griseum centrale. The accessory optic tract arose from the inner area of the optic tract and extended ventromedially to the accessory optic nucleus. The ipsilateral fascicles projected to almost all the above mentioned nuclei, but these projections were comparatively sparse. The ipsilateral retinal projection was restricted to the rostral tectum.     

Central projections of the pineal complex in the silver lamprey Ichthyomyzon unicuspis

Summary The central projections of the pineal complex of the silver lamprey Ichthyomyzon unicuspis were studied by injection of horseradish peroxidase. The pineal tract courses caudally along the left side of the habenular commissure, and a few fibers penetrate the brain through the caudalmost portion of this commissure. Most of the fibers, however, continue caudally and enter the brain through the posterior commissure. The pineal tract projects bilaterally to the subcomissural organ, the superficial and periventricular pretectum, the posterior tubercular nucleus, the dorsal and ventral thalamus, the dorsal hypothalamus, the optic tectum, the torus semicircularis, the midbrain tegmentum, and the oculomotor nucleus. A few fibers decussate in the tubercular commissure, but the course of these decussate fibers could not be followed owing to the bilateral nature of the projections. No retrogradely labeled cells were found in the brain. With the exception of the projections to the optic tectum and torus semicircularis, the pineal projections in the silver lamprey are similar to those reported in other anamniote vertebrates.     

Anterograde labelling from the optic nerve reveals multiple central targets in the teleost,Lethrinus chrysostomus (Perciformes)

Summary Cobaltous-lysine is transported anterogradely from the optic nerve of the teleost, Lethrinus chrysostomus (Lethrinidae, Perciformes). The marginal optic tract is labelled in longtitudinal bands of light and dark staining fibres which persists caudally within the ventral division but not in the dorsal division. This species possesses multiple central targets in the contralateral preoptic, diencephalic, pretectal, periventricular and tectal regions of the brain. In addition, a greater subdivision of the marginal optic tract is found to project to various nuclei. Ipsilateral projections are found in the suprachiasmatic nucleus and in the region of the horizontal commissure. Projections are also found in the telencephalic region of the nucleus olfactoretinalis and the thalamic region of the nucleus thalamoretinalis. The retinotopicity of some of these nuclei, found in previous studies, is discussed in relation to the possibility of specific sub-populations of retinal ganglion cells having different central targets.Abbreviations used in the Text and Figures A nucleus anteriorthalami - AO accessory optic nucleus - AOT accessory optic tract - AxOT axial optic tract - BO nucleus of the basal optic root - C cerebellum - HCv ventral division of horizontal commissure - I nucleus intermedius thalami - IL inferior lobe - MdOT medial optic tract - MO medulla oblongata - MOTd dorsal division of the marginal optic tract - MOTi intermediate division of the marginal optic tract - MOtv ventral division of the marginal optic tract - O olfactory bulb - OT optic tract - PC nucleus pretectalis centralis - PCo posterior commissure - Pd nucleus pretectalis dorsalis - PG preglomerular complex - PPd nucleus pretectalis periventricularis, pars dorsalis - PPv nucleus pretectalis periventricularis, pars ventralis - PSm nucleus pretectalis superficial pars magnocellularis - PSp nucleus pretectalis superficialis, pars parvocellularis - Sn suprachiasmatic nucleus - TEL telencephalon - TeO optic tectum - TL torus longtitudinalis - TrOlfR tractus olfactoretinalis - VCg granular layer of the valvula cerebelli - VCm molecular layer of the valvula cerebelli - VM nucleus medialis thalami - VL nucleus ventrolateralis thalami - VMdOT ventro-medial optic tract     

The organization of cholinergic neurons in the mesencephalon of the eel,Anguilla anguilla,as determined by choline acetyltransferase immunohistochemistry and acetylcholinesterase enzyme histochemistry

Cholinergic systems in the midbrain of the eel were identified by using histochemical procedures for the demonstration of the enzymes choline acetyltransferase (ChAT) and acetylcholinesterase. Neurons detected by both methods are located in the stratum periventriculare of the tectum, cranial motor nuclei III and IV, nucleus isthmi, nucleus gustatorius secundarius, nucleus reticularis superior, and nucleus lateralis valvulae. Some projections of these cell groups were studied by injecting horseradish peroxidase into selected brain regions. Cholinergic neurons make up about 10% of the neurons in the stratum periventriculare of the tectum and are a subset of the type-XIV neurons. Neurons in n. isthmi project primarily to the ipsilateral tectum; some cholinergic isthmal neurons project to n. pretectalis superficialis. A few ChAT-positive axons, perhaps belonging to the tectopetal system, were observed in the optic nerve. The cholinergic neurons of n. gustatorius secundarious project to the inferior lobes of the hypothalamus. The neurons of the superior reticular nucleus are a cholinergic subset of the superior reticular formation. Their axons project rostrally, probably to the thalamus and pretectum. The findings are discussed in relation to functional features of the mesencephalon, particularly in relation to locomotory control.     

Commissural connections mediate inhibition for the computation of interaural level difference in the barn owl

Summary In the barn owl (Tyto alba), the posterior nucleus of the ventral lateral lemniscus (VLVp) is the first site of binaural convergence in the pathway that processes interaural level difference (ILD), an important sound-localization cue. The neurons of VLVp are sensitive to ILD because of an excitatory input from the contralateral ear and an inhibitory input from the ipsilateral ear. A previously described projection from the contralateral cochlear nucleus, can account for the excitation. The present study addresses the source of the inhibitory input.We demonstrate with standard axonal transport methods that the left and right VLVps are interconnected via fibers of the commissure of Probst. We further show that the anesthetization of one VLVp renders ineffective the inhibition that is normally evoked by stimulation of the ipsilateral ear. Thus, one cochlear nucleus (driven by the ipsilateral ear) appears to provide inhibition to the ipsilateral VLVp by exciting commissurally-projecting inhibitory neurons in the contralateral VLVp.Abbreviations ABL average binaural level - CP commissure of Probst - DNLL dorsal nucleus of the lateral lemniscus - IC inferior colliculus - ILD interaural level difference - IPc nucleus isthmi, pars parvocellularis - ITD interaural time difference - LSO lateral superior olive - MNTB medial nucleus of the trapezoid body - NA nucleus angularis - SL nucleus semilunaris - VLVa nucleus ventralis lemnisci lateralis, pars anterior - VLVp nucleus ventralis lemnisci lateralis, pars posterior     

Biogene Amine im Gehirn vom Frosch (Rana esculenta)

Zusammenfassung Mit Hilfe der Methode zur fluoreszenzmikroskopischen Lokalisation von Catechol- und Tryptaminen wurde die Verteilung dieser Stoffe im ZNS von Rana esculenta untersucht. Catecholamin- und serotoninhaltige Neurone liegen im Nucleus reticularis mesencephali. Außerdem finden sich catecholaminhaltige Nervenzellen im Organon vasculosum hypothalami und in der Area praeoptica. Diese aminproduzierenden Zellen entsenden Zellfortsätze durch die Ependymschicht in den Ventrikel. Über diese Ausläufer erfolgt möglicherweise eine Sekretion biogener Amine in den Liquor cerebrospinalis. Catecholamin- und serotoninhaltige Axone erreichen voneinander verschiedene Kerngebiete und Areale. Neben dem periventrikulären Zellager im Tuber cinereum und in der Area praeoptica werden vor allem der ventrolaterale Teil des lateralen Septumkerns, Striatum ventrale und Epistriatum von Endstrecken catecholaminhaltiger Axone durchdrungen. Serotoninhaltige Varicositäten finden sich dagegen vor allem in Kerngebieten, die in sensorische Bahnen eingeschaltet sind (Nucleus isthmi, corpus geniculatum laterale, Area praetectalis, Tectum opticum, Thalamus dorsalis, Neostriatum). Weitere Ausbreitungsgebiete 5-Hydroxytryptamin-haltiger Fasern sind die Habenula und der Nucleus interpeduncularis, Kerngebiete, über die Erregungen aus dem limbischen System auf vegetative Zentren der Medulla oblongata geleitet werden.

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Biogenic amines in the brain of the frog (Rana esculenta)

Summary The distribution of biogenic amines in the central nervous system of Rana esculenta was investigated by means of the fluorescence-microscopical detection of catecholand tryptamines. The nucleus reticularis mesencephali was found to contain numerous neurones rich in catechol- and tryptamines. Apart from this nucleus nerve cells in the organon vasculosum hypothalami and in the area praeoptica were found to contain catecholamines. The clublike processes of these neurones penetrate the ependymal layer and extend into the ventricle. These structures are presumably responsible for a secretion of biogenic amines into the cerebrospinal fluid. Catecholamine- and serotonin-containing axons terminate on different nuclei and areas. Besides the periventricular cellular layer of the tuber cinereum and the area praeoptica, the pars ventrolateralis of the nucleus septalis lateralis, striatum ventrale and epistriatum are pervaded by terminals of catecholamine-containing neurons. Serotonincontaining varicosities are mainly to be found in nuclei, which are intercalated in sensory pathways (nucleus isthmi, corpus geniculatum laterale, area praetectalis, tectum opticum, thalamus dorsalis, neostriatum). Further areas of distribution of 5-hydroxytryptamine-fibers are the habenula and the nucleus interpeduncularis, nuclei which coordinate impulses from the limbic system projecting them on visceral centers of the medulla oblongata.

Mit dankenswerter Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Connectivity of the auditory forebrain nuclei in the Guinea Fowl (Numida meleagris)

Summary Injection of tritiated leucine and proline into the nucleus ovoidalis of the Guinea Fowl (Numida meleagris) produces terminal labeling in the palaeostriatum and in three adjacent zones (field L₁–L₃) of the auditory neostriatum (AN). L₂, situated between L₁ and L₃, receives the main input and corresponds to the former field L of Rose. These neuroanatomically defined zones of the auditory neostriatum are also characterized by differing properties of their neurons. Injection of radioactive material into the auditory neostriatum produces labeling of (i) a palaeostriatal, (ii) a ventral hyperstriatal, and (iii) an additional neostriatal area (Nd). Injection into the hyperstriatum ventrale reveals connections (i) to field L₂, (ii) to the palaeostriatum, (iii) to Nd, and (iv) to the archistriatum. After injection into the palaeostriatum, labeling can be observed (i) in the neostriatum dorsale, (ii) in the hyperstriatum ventrale, (iii) in the archistriatum, (iv) in the diencephalic nuclei, nucleus ansae lenticularis and nucleus spiriformis lateralis, and (v) in the mesencephalic nuclei, nucleus tegmenti pedunculo-pontinus and nucleus intercollicularis. These results show that a widespread connectivity exists among primary and presumably higher order auditory areas in the forebrain of birds. Connections also exist between these auditory areas and presumed vocal-motor areas (neostriatum dorsale, archistriatum, nucleus intercollicularis).Abbreviations A Archistriatum - AL Ansa lenticularis - AN Auditory neostriatum - Bas Nucleus basalis - CA Commissura anterior - Cb Cerebellum - CP Commissura posterior - DLP Nucleus dorsolateralis posterior thalami - DTh Dorsal thalamus - E Ectostriatum - EM Nucleus ectomamillaris - FA Tractus fronto-archistriatalis - FPL Fasciculus prosencephali lateralis - GLv Nucleus geniculatus lateralis, pars ventralis - HA Hyperstriatum accessorium - HD Hyperstriatum dorsale - HIS Hyperstriatum intercalatum superius - HV Hyperstriatum ventrale - HVc Hyperstriatum ventrale, pars caudale - I Injection site - ICo Nucleus intercollicularis - ICT Nucleus intercalatus thalami - Imc Nucleus isthmi, pars magnocellularis - Ipc Nucleus isthmi, pars parvocellularis - l₁, L₂, L₃ Auditory neostriatum: zones L₁, L₂, L₃ - LAD Lamina archistriatalis dorsalis - LH Lamina hyperstriatica - LMD Lamina medullaris dorsalis - LPO Lobus parolfactorius - M Mesencephalon - MLd Nucleus mesencephalicus lateralis, pars dorsalis - N Neostriatum - nAL Nucleus ansae lenticularis - Nc Neostriatum caudale - Nd Neostriatum dorsale - OM Tractus occipito-mesencephalicus - OMv Nucleus nervi oculomotorii, pars ventralis - Ov Nucleus ovoidalis - PA Palaeostriatum augmentatum - PP Palaeostriatum primitivum - PT Nucleus praetectalis - PVM Nucleus periventricularis magno-cellularis - RSd Nucleus reticularis superior, pars dorsalis - RSv Nucleus reticularis superior, pars ventralis - Rt Nucleus rotundus - SMe Stria medullaris - SpL Nucleus spiriformis lateralis - SpM Nucleus spiriformis medialis - SRt Nucleus subrotundus - TeO Tectum opticum - TOv Tractus ovoidalis - TPc Nucleus tegmenti pedunculo-pontinus - TrO Tractus opticus - TSM Tractus septo-mesencephalicus - Ve Ventricle The authors are indebted to Mrs. I. Röder and Mrs. M. Hansel for their aid in the preparation of the histological material and the illustrationsThis work was supported by the Deutsche Forschungsgemeinschaft, Sche 132/4     

Retinal projections in a snake, Thamnophis sirtalis

The retinofugal projections of the snake Thamnophis sirtalis were studied by the method of experimentally induced Wallerian degeneration stained by the Fink-Heimer method. The retinal ganglion cells project to all parts of the contralateral lateral geniculate complex, nucleus lentiformis mesencephali, nucleus geniculatus pretectalis, nucleus posterodorsalis, basal optic nucleus and superficial layers of the optic tectum. In addition, the retinofugal projections were observed terminating in portions of the ipsilateral lateral geniculate complex and nucleus posterodorsalis. Examination of the morphology of the retinal terminal areas stained for Nissl substance with cresyl violet led to the conclusion that these regions are well differentiated and should not be considered poorly developed when compared with other reptilian forms such as turtles.     

Central projections of the nervus terminalis in the bichir,Polypterus palmas

Summary Central pathways of the nervus terminalis (n.t.) in the bichir, Polypterus palmas, were studied with the use of tracing techniques. After application of horseradish peroxidase to the unilateral olfactory mucosa labeled n.t. fibers were traced in seven distinct bundles through the subpallium. Projection areas are found in the precommissural ventral nucleus of the area ventralis telencephali ipsilaterally, the anterior commissure and commissural parts of the periventricular preoptic nucleus bilaterally; few n.t.-fibers cross via the anterior commissure to the contralateral side; no fibers were observed to turn rostrally to the contralateral olfactory bulb. Major targets of the n.t. include a restricted ventral part of the periventricular preoptic nucleus at the level of the optic chiasma bilaterally, and the periventricular nuclei located between the thalamic nuclei and the hypothalamus bilaterally. N.t. fibers continue their course through the ipsilateral hypothalamus and are traced as far as the mesencephalic tegmentum ipsilaterally. N.t. terminations are found consistently within the boundaries of periventricular cell nuclei, suggesting axosomatic synaptic contacts. We propose a differentiation of the n.t. ganglion cells into a distal (mucosal) and proximal (bulbar) type regarding the peripheral cell processes. Our findings are compared with those of other reports on the n.t. system.     

Mapping of brain activity in mesencephalic and diencephalic structures of toads during presentation of visual key stimuli: a computer assisted analysis of (14C)2DG autoradiographs

Summary The (¹⁴C)2DG autoradiographic technique has been employed to quantitatively map glucose utilization in the mesencephalon, the diencephalon and the cerebellum, of toads in response to configurational moving visual stimuli: (i) a 0.4 cm × 2.8 cm worm-like stripe (W) which elicited prey catching responses, (ii) a 8.4 cm × 8.4 cm square (S) that released predator avoidance responses, and (iii) a 2.8 cm × 0.4 cm antiworm-like stripe (A) which elicited no motor activity.For various brain nuclei different relationships were obtained: The optic tectum showed statistical significant higher 2DG uptake during worm-stimulation (¯X _W) than during antiworm stimulation (¯X _A), i.e.¯X _W>¯X _A. The latter visual pattern led to a 2DG utilization that was statistically significant stronger than during stimulation with a square (¯X _S), i.e.¯X _A>¯X _S. Thus, in comparison between right and left hemisphere as well as between brains the following ratios were obtained:Optic tectum:¯X _W>¯X _A>¯X _S; nucleus isthmi:¯X _W>¯X _A-¯X _s; posterodorsal lateral thalamic nucleus:¯X _S>¯X _A>¯X _W; posteroventral lateral thalamic nucleus:¯X _S>¯X _A¯X _W; posterior thalamic nucleus:¯X _W>¯X _A¯X _S; anteripr division of the lateral thalamic nucleus:¯X _W>¯X _A¯X _S; anterior thalamic nucleus:¯X _A>¯X _S>¯X _W; nucleus of Bellonci and dorsal division of the ventrolateral thalamic nucleus:¯X _W¯X _A¯X _S; cerebellum:¯X _S¯X _W>¯X _A.Abbreviations A anterior thalamic nucleus - Cb cerebellum - Hyp hypothalamus - Ist nucleus isthmi - cl. Ist contralateral Ist - La lateral thalamic nucleus, anterior division - Lpd lateral thalamic nucleus, posterodorsal division - Lpv lateral thalamic nucleus, posteroventral division - MP medial pallium - NB/VLd nucleus of Bellonci and ventrolateral thalamic nucleus, dorsal division - P posterior thalamic nucleus - PO preoptic area - Sna snapping evoking area=ventrolateral tectum - Str striatum - Tec tectum opticum     

Analysis of the efferent projections of the lateral geniculate nucleus with special reference to the innervation of the subcommissural organ and related areas

In order to define central neurons projecting to the subcommissural organ (SCO) and to related areas in the postero-medial diencephalon, Phaseolus vulgaris-leucoagglutinin (PHA-L) was injected into the lateral geniculate nucleus of the rat. PHA-L-labelled neurons send axonal processes medially through the posterior thalamic nuclei and the posterior commissure to the other hemisphere. Branches of fibres originating from this projection form a plexus of nerve terminals in the underlying precommissural nucleus and in the nucleus of the posterior commissure. A small number of PHA-L-immunoreactive nerve fibres penetrate from the precommissural nucleus into the lateral part of the SCO. A few labelled fibres penetrate directly from the posterior commissure into the medial part of the caudal SCO. Most of the PHA-L-immunoreactive fibres occur in the hypendymal layer, although a few terminate near the ependymal cells of the organ. Many labelled fibres are found in the ventricular ependyma adjacent to the SCO, some fibres lying close to the ventricular lumen. These results were obtained only if the tracer was delivered into the intergeniculate leaflet of the lateral geniculate nucleus (IGL). The IGL innervates both the suprachiasmatic nucleus and the pineal organ; the connections between the IGL and the midline structures, including the SCO, suggest that these areas are influenced by the circadian system.     

Extrinsic cells, immunoreactive to Ca-binding protein, as sources of thalamic visual centres in tortoises

Extrinsic sources of calcium-binding proteins involved in immunoreactive innervation of the visual thalamic nuclei Rot and GLd in turtles (Testudo horsfieldi and Emys orbicularis) were studied using HRP tracing method and immunohistochemistry. In 1.5-4.5 months after monocular enucleation calbindin (Calb)-, parvalbumin (Parv)- and calretinin (Calr)-labeling was found in fragments of degenerated retinal fibers in the contralateral optic tract and in some retinorecipient structures (optic tectum, GLd and GLv). Changes in GLd were detected in its neuropil part. in 2.0-3.5 months after unilateral ablation of tectum and pretectum, the densities of Parv-, Calb- and Aclr-immunoreactivity terminals and fibers were diminisched in the ipsilateral n. Rot, with the maximum effect seen in Parv. Following HRP injection into the visual thalamus (Rot and GLd), retrogradely labeled cells with Parv label only, were revealed in the ventrothalamic nucleus Enta, pretectal nucleus Ptv, and in all types of Ca-binding proteins (CaBPr) in separately labeled cells of the optic tectum. Thus, it has been shown that thalamic visual centers in turtles have multiple extrinsic cells, which serve as sources of CaBPr projections. The present data suggest that organization of CaBPr inputs to visual thalamus in reptiles (turtle) and higher amniotes are fundamentally similar.     

Evolutionary evaluation of reciprocity of connections in the turtle tectofugal visual system

In two turtle species—Emys orbicularis and Testudo horsfieldi—by the method of anterograde and retrograde traicing at the light and electron microscopy level, the existence is proven of direct descending projections from the thalamic nucleus of the tectofugal visual system n. rotunds (Rot) to the optic tectum. After injection of tracers into Rot alone and into Rot with involvement of the tectothalamic tract (Trtth), occasional labeled fibers with varicosities and terminals are revealed predominantly in the deep sublayers of SGFS of the rostral optic tectum, while in the lower amount—in other tectal layers. After the tracer injections into the optic tectum, a few retrogradely labeled neurons were found mainly in the Rot ventral parts and within Trtth. Their localization coincides with that of GABA-immunoreactive cells. Electron microscopy showed the existence of many retrogradely labeled dendrites throughout the whole Rot; a few labeled cell bodies were also present there, some of them being also GABA-immunoreactive. These results allow us to conclude about the existence of reciprocal connections between the optic tectum and Rot in turtles, these connections being able to affect processing of visual information in tectum. We suggest that reciprocity of tectothalamic connections might be the ancestral feature of the vertebrate brain; in the course of amniote evolution the functional significance of this feature can be decreased and even lost in parallel with a rise of the role of direct corticotectal projections.     

Transthalamic conduction of visual impulses to the cortex and subcortical forebrain structures in turtles

The thalamic relays for the conduction of impulses arising during photic stimulation of the eyes and electrical stimulation of the tectum in the general cortex, hyperstriatum (the dorsal ventricular ridge), and the striatum proper were studied in the turtleEmys orbicularis. Acute experiments on immobilized animals showed that anodal polarization temporarily and destruction of n. rotundus irreversibly suppress the main negative wave of the responses to tectal stimulation and to flashes in the hyperstriatum, whereas the corresponding responses in the general cortex still persist. Polarization and destruction of the lateral thalamic region, including the lateral geniculate body, have the opposite effect: responses in the hyperstriatum to photic and tectal stimulation are virtually unchanged whereas those in the general cortex disappear, except their late components. Preceding single stimulation of the tectum or n. rotundus depresses responses in the hyperstriatum evoked by flashes. However, during stimulation of the lateral thalamic region, combined potentials and single unit responses appear in the hyperstriatum and interact with responses evoked by tectal stimulation. It is concluded that the main pathways in turtles which supply visual information to the general cortex and hyperstriatum differ: the former relay in the lateral thalamic region, the latter in n. rotundus, although some overlapping of their projections in the hyperstriatum and striatum is possible.I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Leningrad. Translated from Neirofiziologiya, Vol. 9, No. 5, pp. 486–494, September–October, 1977.