Distribution of vesicular glutamate transporters in the brain of the turtle (Pseudemys scripta elegans)

The distribution of glutamatergic neurons has been extensively studied in mammalian and avian brains, but its distribution in a reptilian brain remains unknown. In the present study, the distribution of subpopulations of glutamatergic neurons in the turtle brain was examined by in situ hybridization using probes for vesicular glutamate transporter (VGLUT) 1–3. Strong VGLUT1 expression was observed in the telencephalic pallium; the mitral cells of the olfactory bulb, the medial, dorsomedial, dorsal, and lateral parts of the cerebral cortex, pallial thickening, and dorsal ventricular ridge; and also, in granule cells of the cerebellar cortex. Moderate to weak expression was found in the lateral and medial amygdaloid nuclei, the periventricular cellular layer of the optic tectum, and in some brainstem nuclei. VGLUT2 was weakly expressed in the telencephalon but was intensely expressed in the dorsal thalamic nuclei, magnocellular part of the isthmic nucleus, brainstem nuclei, and the rostral cervical segment of the spinal cord. The cerebellar cortex was devoid of VGLUT2 expression. The central amygdaloid nucleus did not express VGLUT1 or VGLUT2. VGLUT3 was localized in the parvocellular part of the isthmic nucleus, superior and inferior raphe nuclei, and cochlear nucleus. Our results indicate that the distribution of VGLUTs in the turtle brain is similar to that in the mammalian brain rather than that in the avian brain.     

Afferents of the lamprey optic tectum with special reference to the GABA input: combined tracing and immunohistochemical study

The optic tectum in the lamprey midbrain, homologue of the superior colliculus in mammals, is important for eye movement control and orienting responses. There is, however, only limited information regarding the afferent input to the optic tectum except for that from the eyes. The objective of this study was to define specifically the gamma-aminobutyric acid (GABA)-ergic projections to the optic tectum in the river lamprey (Lampetra fluviatilis) and also to describe the tectal afferent input in general. The origin of afferents to the optic tectum was studied by using the neuronal tracer neurobiotin. Injection of neurobiotin into the optic tectum resulted in retrograde labelling of cell groups in all major subdivisions of the brain. The main areas shown to project to the optic tectum were the following: the caudoventral part of the medial pallium, the area of the ventral thalamus and dorsal thalamus, the nucleus of the posterior commissure, the torus semicircularis, the mesencephalic M5 nucleus of Schober, the mesencephalic reticular area, the ishtmic area, and the octavolateral nuclei. GABAergic projections to the optic tectum were identified by combining neurobiotin tracing and GABA immunohistochemistry. On the basis of these double-labelling experiments, it was shown that the optic tectum receives a GABAergic input from the caudoventral part of the medial pallium, the dorsal and ventral thalamus, the nucleus of M5, and the torus semicircularis. The afferent input to the optic tectum in the lamprey brain is similar to that described for other vertebrate species, which is of particular interest considering its position in phylogeny.     

Noradrenaline decreases spike voltage threshold and induces electrographic sharp waves in turtle medial cortex in vitro

The noradrenergic modulation of neuronal properties has been described at different levels of the mammalian brain. Although the anatomical characteristics of the noradrenergic system are well known in reptiles, functional data are scarce. In our study the noradrenergic modulation of cortical electrogenesis in the turtle medial cortex was studied in vitro using a combination of field and intracellular recordings. Turtle EEG consists of a low voltage background interspersed by spontaneous large sharp waves (LSWs). Noradrenaline (NA, 5-40 microM) induced (or enhanced) the generation of LSWs in a dose-dependent manner. Pharmacological experiments suggest the participation of alpha and beta receptors in this effect. In medial cortex neurons NA induced a hyperpolarization of the resting potential and a decrease of input resistance. Both effects were observed also after TTX treatment. Noradrenaline increased the response of the cells to depolarizing pulses, resulting in an upward shift of the frequency/current relation. In most cells the excitability change was mediated by a decrease of the spike voltage threshold resulting in the reduction of the amount of depolarization needed to fire the cell (voltage threshold minus resting potential). As opposed to the mechanisms reported in mammalian neurons, no changes in the frequency adaptation or the post-train afterhyperpolarization were observed. The NA effects at the cellular level were not reproduced by noradrenergic agonists. Age- and species-dependent properties in the pharmacology of adrenergic receptors could be involved in this result. Cellular effects of NA in turtle cortex are similar to those described in mammals, although the increase in cellular excitability seems to be mediated by a different mechanism.     

Morphology, axonal projection pattern, and responses to optic nerve stimulation of thalamic neurons in the salamander Plethodon jordani

In the salamander Plethodon jordani, the morphology and axonal projections of thalamic (TH) neurons and their responses to electrical optic nerve stimulation were determined by intracellular recording and biocytin labeling under in vitro, whole-brain conditions. Based on their axonal projections, labeled neurons (n = 76) were divided into the following groups: TH1 neurons, with mostly ipsilateral projections to the striatum; TH2 neurons, with ipsilateral or bilateral projections to the medial amygdala and nucleus accumbens; TH3 neurons, with bilateral projections to the medial and dorsal pallium; TH4 neurons, with mostly ipsilateral projections to the striatum and ipsilateral projections to the tectum opticum, tegmentum, and rostral medulla oblongata; and TH5 neurons, with ipsilateral projections to the tegmentum, medulla oblongata, and rostral spinal cord without (TH5.1) or with (TH5.2) additional projections to the optic tectum. TH1-TH4 neurons are found in the dorsal thalamus and around the sulcus medialis, and TH5 neurons are found in the ventral thalamus. Labeled neurons with ascending projections, i.e., the more dorsally situated TH1-TH4 neurons, are mostly inhibited by electrical stimulation of the optic nerve and have significantly longer latencies (mean +/- S.D., 42.1 +/- 11.6 msec) than neurons with exclusively descending projections, i.e., the ventrally located TH5 neurons (8.5 +/- 6.1 msec), which receive the bulk of retinal afferents and show excitation at electrical optic nerve stimulation. Neurons recorded without labeling in the dorsal thalamus likewise exhibit mostly inhibition and have significantly longer latencies (35.7 +/- 18.9 msec) than those recorded in the ventral thalamus (10.9 +/- 7.7 msec), which mostly show excitation. None of the neurons recorded in the dorsal thalamus followed repetitive stimulation of the optic nerve. Thus, neurons situated in the dorsal thalamus and projecting to pallial or subpallial telencephalic targets are unlikely to receive monosynaptic or oligosynaptic, excitatory retinal input. Accordingly, no retino-thalamo-telencephalic pathway homologous to that found in amniotes appears to exist in salamanders.     

Visual system development in the duck embryo

This research investigated the ontogeny of evoked activity in the visual system of the duck embryo. Field potentials were recorded from the optic tectum of Peking ducks (Anas platyrhynchos) after electrical stimulation of the contralateral optic nerve head or photic stimulation of the contralateral eye. Recordings were made in embryos on Day 10 of incubation through hatching. Electrical stimulation elicited negative potentials at the dorsal and ventral surfaces and positive potentials in the depths of the tectum in embryos on Day 11 and later. Polarity reversals occurred within 0.5 mm of the respective surfaces. Potentials were reduced or obliterated when stimulus frequencies were increased to 15 Hz. In older embryos, potentials were more widespread, more complex, larger in amplitude, shorter in latency, and of lower threshold than in younger embryos. These results are consistent with the generation of postsynaptic activity in the optic tectum of ducks on Day 11 of incubation. Responses to photic stimuli appeared much later in development: optic tectum responses on the 21st or 22nd day and electroretinogram on the 23rd day.     

Retinal recipient nuclei in the painted turtle,Chrysemys picta: An autoradiographic and HRP study

Retinofugal pathways in the painted turtle were examined with autoradiographic and HRP methods. The majority of the retinal fibers decussate at the optic chiasm and course caudally to terminate in 12 regions of the diencephalon and mesencephalon. The pars dorsalis of the lateral geniculate nucleus is the densest target in the thalamus. Two nuclei dorsal to pars dorsalis—the dorsal optic and dorsal central nuclei—receive optic input. Three nuclei ventral to pars dorsalis are retinal targets—the ventral geniculate nucleus, nucleus ventrolateralis pars dorsalis, and nucleus ventrolateralis pars ventralis. Contralateral fibers course through the pretectum where they terminate in nucleus geniculatis pretectalis, nucleus lentiformis mesencephali, nucleus posterodorsalis, and the external pretectal nucleus. Retinal fibers also terminate within the superficial zone of the optic tectum. HRP material demonstrates three optic fiber layers—laminae 9, 12, and 14. Optic fibers leave the main optic tract as a distinct accessory tegmental optic pathway and terminate in the basal optic nucleus. Ipsilateral retinal terminals occur in a pars dorsalis and a pars ventralis of the lateral geniculate nucleus, the dorsal optic nucleus, nucleus posterodorsalis, the basal optic nucleus, and in laminae 9 and 12 of the optic tectum. Rostrally, the ipsilateral tectal fibers occupy two zones along the medial and lateral tectal roof; these zones converge caudally and are continuous along the caudal wall of the tectum.     

Retinotopic organization in the development of the young trout Salmo gairdneri Rich

The progression of the retinotopic organization in the optic nerve projections to the contralateral thalamus and tectum was studied in Salmo gairdneri from hatching stage to 3 month old stage. After quadratic lesions of the temporal, dorsal, nasal, or ventral retina, the animals were separated in two groups: one used for Fink and Heimer method or electron microscopic observation and the other one for radioautography after injection in the operated eye of 14C or 3H proline. The analysis of the projections of each retinal quadrant shows that: Projections to thalamus and pretectum are ignorganized and appear progressively during development. On the contrary in tectum and corpus geniculatum, the visual projections are retinotopically organized since hatching. In the whole retino-tectal system, two subsystems develop differently: the naso-ventral retina reaches precociously its permanent target (the posterior tectum), the temporo-dorsal part of the retina links to the anterior tectum and shifts laterally during the first month after hatching, from medial to antero-lateral tectum for temporal projections. The shifting of projections is correlated with development of the medial fascicle of the optic tract. So it appears that the pathways play an important role in the spatio-temporal ordered pattern of terminations of retinal fibers on the tectal surface during development.     

Experimental reorganization of the cerebellar cortex. 3. Regeneration of the external germinal layer and granule cell ectopia

The distribution of monoamine (catecholamines and 5-hydroxytryptamine)-containing nerve terminals in the brain of the painted turtle (Chrysemys picta) was studied by means of the histofluorescence technique of Falck and Hillarp. The highest concentration of monoamine terminals in this reptilian brain occurs within the ventral region of the strio-amygdaloid complex which on this basis may be related to the mammalian neostriatum (caudate nucleus and putamen). Numerous catecholamine type nerve endings are also present in several other regions of the turtle brain, namely: the dorsal cortical layer, the dorsolateral portion of the septum, the habenula, the nuclei dorsomedialis and dorsolateralis of the thalamus, the lateral part and median eminence of the hypothalamus, the tectum and the brain stem reticular formation (more especially its lateral edge). The greatest concentration of 5-hydroxytryptamine (serotonin) type nerve endings is found in the dorsomedial portion of the septum, nucleus geniculatus lateralis, nuclei pretectalis, interpeduncularis and isthmi, the tectum and the reticular formation of the brain stem (more especially its medial portion). These monoamine nerve terminals belong to several groups of neurons whose cell bodies are located in the brain stem and, to a lesser degree, in the hypothalamus of the turtle.     

Periaqueductal gray and cerebral cortex modulate responses of medial thalamic neurons to noxious stimulation

The response of medial thalamic neurons to noxious peripheral stimulation were studied with intracellular recording methods in the cat. Electrical stimulation of the contralateral forepaw produced an EPSP-IPSP sequence followed by rebound excitation in these medial thalamic neurons. Action potentials appeared with the initial EPSP or with the rebound excitation. The mean latency to onset was 15 ms for the EPSP and 33 ms for IPSP. In contrast, electrical stimulation of the PAG or of the pericruciate cerebral cortex produced large IPSPs in the medial thalamic neurons. When PAG or cortex stimulation were paired with noxious stimulation, both the PAG and cortex responses predominated over the noxious response. This shows that the PAG and the cerebral cortex have the capabilities of influencing the responses of the medial thalamus to noxious stimulation. The medial thalamus is part of the relay system which sends information about noxious stimulation to the cerebral cortex where the noxious information reaches conscious awareness, so influencing the message at the level of the medial thalamus would probably alter the conscious perception of pain. The data suggest the existence of an ascending pain modulation system from the midbrain to the thalamus and also suggests a mechanism of cortical control over pain perception.     

Projection of optic fibers to visual centers in a turtle (Emys orbicularis)

Studies of retinal projections to the thalamus and midbrain of the turtle were based on a personal modification of the Nauta-Laidlaw technique (modified Nauta method) after unilateral enucleation. Decussation of optic fibers in the chiasma is incomplete. In the thalamus, optic fibers are found to terminate in three nuclei – with greater density in the corpus geniculatum laterale (lateral geniculate body) (LGB) and more sparsely in the nucleus suprapeduncular and nucleus ovalis. Retinal projections to the LGB assume a focal pattern, being somewhat more compact in the lateral neuropil region. Optic fibers are also shown to end in a group of pretectal nuclei: n. pretectalis dorsalis, n. lentiformis mesencephalis, n. comissurae posterior. In addition, terminations of optic fibers have been revealed in the three upper layers of the tectum. Peculiarities of preterminal and terminal degeneration of retinal fibers have been distinguished in the different tectal layers. In the second stratum, terminations of large fibers are mostly seen with a characteristic appearance of lumpy pericellular (preterminal) degeneration. In the third stratum, both large and finer fibers degenerate, showing fine debris of preterminal degeneration. Different patterns of terminal degeneration have been revealed in tectum and thalamus. The maximal size of optic fibers in the tectum proves to be larger than in thalamus. Available evidence is discussed with particular reference to comparison of the phylogenetically more recent retinothalamic system and more ancient retinotectal system.     

Organization of the sensory input to the telencephalon in the fire-bellied toad, Bombina orientalis

The functional organization of sensory activity in the amphibian telencephalon is poorly understood. We used an in vitro brain preparation to compare the anatomy of afferent pathways with the localization of electrically evoked sensory potentials and single neuron intracellular responses in the telencephalon of the toad Bombina orientalis. Anatomical tracing showed that the anterior thalamic nucleus innervates the anterior parts of the medial, dorsal, and lateral pallia and the rostralmost part of the pallium in addition to the subpallial amygdala/ventral pallidum region. Additional afferents to the medial telencephalon originate from the thalamic eminence. Electrical stimulation of diverse sensory nerves and brain regions generated evoked potentials with distinct characteristics in the pallium, subpallial amygdala/ventral pallidum, and dorsal striatopallidum. In the pallium, this sensory activity is generated in the anterior medial region. In the case of olfaction, evoked potentials were recorded at all sites, but displayed different characteristics across telencephalic regions. Stimulation of the anterior dorsal thalamus generated a pattern of activity comparable to olfactory evoked potentials, but it became similar to stimulation of the optic nerve or brainstem after bilateral lesion of the lateral olfactory tract, which interrupted the antidromic activation of the olfactohabenular tract. Intracellular bimodal sensory responses were obtained in the anterior pallium, medial amygdala, ventral pallidum, and dorsal striatopallidum. Our results demonstrate that the amphibian anterior pallium, medial amygdala/ventral pallidum, and dorsal striatopallidum are multimodal sensory centers. The organization of the amphibian telencephalon displays striking similarities with the brain pathways recently implicated in mammalian goal-directed behavior.     

Thalamic components of the ascending vestibular system

A combined anatomical and physiological approach was used to identify the thalamic nuclei that relay vestibular activity to the cerebral cortex at short latency in the cat. For the anatomical experiments, electrical stimulation was applied to the vestibular nerve, the cortical sites showing maximal amplitude responses were defined, and horseradish peroxidase was injected in these sites. Two days later, the animals were killed and brain sections were processed to localize enzyme reaction products in thalamic neurons. After either anterior suprasylvian injection or posterior cruciate region injection, most labeled neurons were in the ventral posterolateral nucleus. A few labeled neurons were found in the intralaminar and posterior groups of nuclei. In separate physiological experiments, responses to vestibular nerve stimulation and cerebral cortical stimulation were recorded from the thalamus. Short-latency (<3.5 ms), large-amplitude evoked potentials from vestibular nerve stimulation and antidromic field potentials from cortical stimulation were recorded within the ventral basal complex and the most rostral portions of the posterior group of thalamic nuclei. These data indicate that neurons in the ventral basal complex and the region between the ventral basal complex and the posterior group relay vestibular activity to both the anterior suprasylvian and posterior cruciate regions of the cerebral cortex.     

Changes in short latency SEPs (S-SEPs) to median nerve stimulation in brain dead patients

Short latency SEPs (S-SEPs) to median nerve stimulation consist of positive waves of P1, P2, P3 and P4, followed by negative waves of N 16 and N 19. These potential reflect activities of peripheral nerve, dorsal column of the cervical cord and medial lemniscus. The origins of these waves are considered as follows, P1--peripheral part of the brachial plexus, P2--the entry into the spinal cord or the dorsal column, P3--dorsal column nucleus or upper cervical cord, P4--the medial lemniscus, N 16--rostral brain stem or the thalamus, and N 19--thalamocortical projection or the cortex. The purpose of the present study is to elucidate changes of S-SEPs in brain dead patients. Fifteen brain dead patients were examined with S-SEPs. In addition to that, thirteen cases with lesions of subcortical or the brain stem but not in the state of brain death were studied for the controls. S-SEPs with non-cephalic references, conventional SEPs with earlobe reference and the evoked potentials at the Erb's point were recorded in all these cases. Serial recordings were performed in six brain dead cases during the process of rostro-caudal deterioration of the brain stem functions due to cerebral herniation. In the state of brain death, only P1 and P2 were recorded in eleven cases, and in three cases, only P1 was recorded. The other case with anoxic brain damage showed flat S-SEPs and the evoked potentials at the Erb's point could merely be obtained by the supramaximal stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)     

Changes in somatosensory evoked potentials following an experimental focal ischaemic lesion in thalamus

Experiments have been performed to produce localized thalamic ischaemia in baboons anaesthetised with alpha-chloralose. Somatosensory evoked potentials to median nerve stimulation were recorded in the medial lemniscus, VPL of thalamus and the primary somatosensory cortex. Local blood flow was also recorded by the hydrogen clearance technique in these regions. The early potential recorded in thalamus has been shown to be generated from 3 sources: (i) a positivity generated outside the VPL, (ii) local wavelets, most likely from synaptic activity close to the recording electrode, and (iii) a local overall negativity. The first of these potentials alone remains after thalamic ischaemia. It arises below the level of the thalamus, being very likely generated by the afferent volley in the medial lemniscus, and is seen in the surface-recorded response as the early component P8 (corresponding to P15 in the human).     

Tectal fiber connections in a non-teleost actinopterygian fish, the sturgeon Acipenser

Tectal fiber connections were studied in members of an early branch of the actinopterygian lineage, the sturgeons Acipenser transmontanus and A. schrenkii, by means of biocytin, HRP, biotinylated dextran amine, and DiI tract tracing methods. The aim of this study is to elucidate the visual pathway via the optic tectum to the thalamus as a part of a series of studies on the visual pathways in sturgeons. After biocytin or biotinylated dextran amine injections to the optic tectum terminals are found bilaterally in the medial and lateral portions of both the dorsal thalamus and ventral thalamus. Ipsilateral projections are much more abundant. Tectal recipient areas in the thalamus overlap in part with the retinal recipient areas. After HRP or DiI injections to the dorsal or ventral thalamus, tectal neurons projecting to the thalamus were labeled in the ipsilateral or bilateral stratum periventriculare. Dendritic morphology of tectothalamic neurons suggests that they receive direct retinal input. These results suggest that visual information passes through the tectum to the thalamic areas which also receive direct retinal projections. In this regard, the visual system of Acipenser resembles that of chondrichthyans (sharks). Other fiber connections of the tectum are also described, which have not previously been studied by tracer methods in a sturgeon.     

Comparison of ongoing compound field potentials in the brains of invertebrates and vertebrates

(1) Ongoing compound field potential fluctuations of higher brain centers (the micro-EEG of some authors) are considered as a biological phenomenon, a sign of the activity in the organized assemblage of cells. Such activity has been compared in several taxa with quite different brain structure to look for possible evolution in the form of the field potentials and for possible explanations of differences and similarities. (2) Recordings were made with semimicroelectrodes in the neuropile of the cerebral ganglion of the mollusc, Aplysia, with comparative observations on Helix, and the arthropods Limulus, Melanoplus, and Cambarus, and in or on the cerebral cortex and optic tectum of rays, cats and rabbits, with comparative observations on sharks, bony fish, turtles and geckos in unstimulated resting or generalized arousal states. Manipulations of state did not alter the main findings. (3) Power spectra in the cerebral ganglia of various higher invertebrates are similar; activity is fast and spikey (with the exception of Octopus). Integrated energy above 50 Hz exceeds that from 2-50 Hz and falls slowly with frequency; in Aplysia the power spectrum falls less than 10 dB between 10 and 300 Hz. In vertebrates from fish to mammals activity is similar in being mainly slow (less than 40 Hz); it commonly falls greater than 20 dB between 10 and 50 Hz. (4) Amplitude is low in invertebrates and lower vertebrates. RMS voltage in Aplysia (3-300 Hz, reference electrode remote) is typically less than 10 microV; in the ray optic tectum less than 25 microV (2-50 Hz); in the dorsal cortex of the gecko less than 30 microV, in the cat cortex greater than 85 microV. In the vertebrates amplitude does not change greatly with small shifts in electrode position, as it does in invertebrates. (5) Coherence decline with distance, measured tangentially at different electrode separations in the millimeter range, is used as an estimator of synchrony. Averaged coherence between loci 1 mm apart is negligible in Aplysia in any band from 3 to 100 Hz; in the ray tectum it is low, 0.25-0.5 between 3 and 16 Hz. In the turtle dorsal pallium it is higher, at 2 mm, 0.6-0.75 in this band. In the rabbit cortex coherence is even higher, typically greater than 0.7 at 1 mm, and greater than 0.3 at 4 mm in this band. (6) Band-pass filtered electrograms, ca. one octave wide, in all species show constant waxing and waning in each band; amplitude is not maintained even for a second. (ABSTRACT TRUNCATED AT 400 WORDS)     

Kindling induces a lasting, regionally selective increase of kynurenic acid in the nucleus accumbens

We determined endogenous kynurenic acid in nine brain regions and plasma of amygdala-kindled rats at different intervals (24 h or 50 days) after the last fully kindled seizure. Data obtained were compared with age-matched electrode-implanted and non-implanted control groups. Kindling induced a lasting increase in kynurenate in nucleus accumbens, whereas no significant alterations were seen in hippocampus, cerebral cortex, olfactory bulb, striatum, thalamus, tectum, cerebellum, pons/medulla, or plasma. The regionally selective alteration in the nucleus accumbens is in line with previous studies indicating that this brain region functions as a modulatory interface between the limbic and motor systems and may be critically involved in seizure propagation in the kindling model of temporal lobe epilepsy. The increased levels of the endogenous glutamate antagonist kynurenate in nucleus accumbens may be interpreted as a compensatory change to reduce enhanced excitation in this brain region.     

Major difference in the expression of delta- and mu-opioid receptors between turtle and rat brain.

The reptilian turtle brain has a remarkably higher endurance for anoxia than mammalian brains. Since the response to O(2) deprivation is dependent in a major way on the expression and regulation of membrane proteins, differences in such proteins may play a role in the species-related differences in hypoxic responses. Because opioid system is involved in the regulation of hypoxic responses, we asked whether there are differences between rat and turtle brains in terms of opioid receptor expression. In this work, we compared the expression and distribution of delta-and mu-opioid receptors in the turtle and rat brains. Our results show that (1) the dissociation constant (K(d)) for delta-receptor binding was approximately four times lower and B(max) was more than double in the turtle brain homogenates than in rat ones; (2) the delta-receptor binding density was heterogeneously distributed in the turtle brain, with a higher density in the rostral regions than in the brainstem and spinal cord, and was generally much higher than in rat brains from the cortex to spinal cord; (3) the delta-opioid receptors in the rat brains were mostly located in the cortex, caudate putamen, and amygdala with an extremely low density in most subcortical (e.g., hippocampus and thalamus) and almost all brainstem regions; and (4) in sharp contrast to delta-opioid receptors, mu-opioid receptor density was much lower in all turtle brain regions compared with the rat ones. Our results demonstrate that the turtle brain is actually an organ of delta-opioid receptors, whereas the rat brain has predominantly mu-opioid receptors. Because we have recently found that delta-opioid receptors protect neurons against glutamate and hypoxic stress, we speculate that the unique pattern of delta-receptor receptor expression and distribution plays a critical role in the tolerance of turtle brain to stressful situations characterized by glutamate excitotoxicity.     

Electrical signs of an oligosynaptic visual projection to the rat hippocampus

In rats with pons transection photic or optic nerve stimulation elicits a response in dorsal hippocampus with approximately with same latency, amplitude and time course as the response in striate cortex. After optic nerve stimulation a positive polyphasic deflection with the last peak at 10 ms is followed by a larger biphasic major deflection with peaks at 15 and 25 ms and later, slower deflections at intervals of 125 ms. The polyphasic deflection is maximal in the inferior part of the hippocampus but does not reverse polarity; the other deflections reverse above and below an isoelectric point in the hilum of the dentate gyrus, a distribution attributable to depolarization in the molecular layers, perhaps also cell bodies, of that structure. The major deflection is more sensitive to changes in optic nerve stimulus strength than the response in striate cortex and is more resistant to reduction in amplitude during repetitive stimulation, following frequencies up to 50/s. The pathway between retina and hippocampus for all parts of the response is interrupted by lesions in the tectum. The major deflection is abolished by lesions in the posterior cingulum. In the posterior cingulum the pathway has fast and slow components in the lower and upper portions, respectively, associated with the first and second parts, respectively, of the major deflection. The pathway is not interrupted by lesions in the fornix, septal nuclei, anterior cingulum, anterior medial thalamus or medial midbrain ventral to the superficial tectum. There are complex interactions, up to several hundred milliseconds in duration, between the response to optic nerve stimulation and those elicited by stimulation in the cingulum, midbrain and thalamus. Tonic influences on the dentate gyrus from cingulum and tectum are described.     

Androgen receptor-immunoreactivity in the forebrain of the Eastern Fence lizard (Sceloporus undulatus)

Androgen receptor (AR) distribution in the lizard forebrain and optic tectum was examined using PG21 immunohistochemistry. In the male Eastern Fence lizard, AR-immunoreactive (-ir) nuclei were observed in the medial preoptic area, ventromedial and arcuate hypothalamic nuclei, periventricular hypothalamus, premammillary nucleus, bed nucleus of the stria terminalis, and ventral posterior amygdala. Punctate immunostaining of neuronal processes (axons and/or dendrites) was concentrated in the cortex, hypothalamus, and optic tectum. AR-ir nuclei in the female brain were confined to the ventral posterior amygdala and ventromedial hypothalamic nucleus. The AR distribution in the lizard brain is similar to that reported for other vertebrate classes. Sex differences in AR-immunoreactivity may contribute to sex-specific behaviors in the Eastern Fence lizard.