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Role of primate flocculus during rapid behavioral modification of vestibuloocular reflex. I. Purkinje cell activity during visually guided horizontal smooth-pursuit eye movements and passive head rotation.

1. Extracellular recordings were obtained from 124 Purkinje cells (P-cells) in the flocculus of alert monkeys. P-cell simple spike-firing rate was analyzed quantitatively during various combinations of smooth-pursuit eye movement and passive head rotation. 2. During sinusoidal smooth eye movements, 80% of the P-cells displayed increased firing rate during ipsilateral and 20% during contralateral eye movement. Over the frequency range 0.3--1.4 Hz, firing-rate modulation was proportional to and in phase with maximum eye velocity. During the steady state of triangle-wave tracking, firing rate increased monotonically as a function of eye velocity. Since firing rate was uncorrelated with retinal-error velocity, one component of P-cell firing rate was related to eye velocity. 3. During the transient phase of triangle-wave tracking, when an instantaneous change in the direction of target movement caused a large retinal-error velocity, 40% of the P-cells were related only to eye velocity. Sixty percent of the P-cells displayed an overshoot or undershoot in firing rate, indicating a relationship to either retinal-error velocity or eye acceleration as well as to eye velocity. 4. During the vestibuloocular reflex (VOR), evoked by head rotation in the dark, P-cell firing rate was only weakly modulated. In contrast, when the monkey suppressed the VOR by fixating a target that rotated with him, P-cell rate was deeply modulated. Since the modulation was proportional to and in phase with maximum head velocity, another component of P-cell firing rate was related to head velocity. 5. Of 36 P-cells tested, 35 displayed firing-rate modulation during both suppression of the VOR and smooth-pursuit eye movement. P-cells that reached peak firing rate during ipsilateral head rotation also reached peak firing rate during ipsilateral smooth eye rotation. Average population sensitivitites to head velocity and eye velocity were equal. In three conditions in which eye and head velocity were elicited simultaneously, P-cell firing rate could be predicted by the linear, vector addition of the separate eye and head velocity components of firing rate. Therefore, the relatively weak modulation of P-cell firing rate during the VOR in the dark can be accounted for by the cancellation of equal but opposite head and eye velocity components. 6. The connections of flocculus P-cells to interneurons in the brain stem VOR pathways have been established in other mammals. In the context of those connections, P-cell firing patterns were appropriate to facilitate the eye movements the monkey was required to make. We conclude that the flocculus is important for sustaining any smooth eye movements that are different from those evoked by head rotation in the dark. The eye velocity component may represent an efference copy signal that sustains ongoing eye velocity during smooth pursuit.

Animals↗

Effects of light adaptation on contrast processing in bipolar cells in the retina.

Effects of light adaptation on contrast processing in the outer retina were investigated over nearly four decades of background illumination by analyzing the intracellular responses of 111 bipolar cells, 66 horizontal cells, and 22 cone photoreceptors in the superfused eyecup of the tiger salamander (Ambystoma tigrinum). Light adaptation had striking and similar effects on the average contrast responses of the hyperpolarizing (Bh) and depolarizing (Bd) classes of bipolar cells: Over the lower two decades of background illumination, the contrast gain increased 7-fold to reach values as high as 20-30, the dynamic range and the half-maximum contrast decreased by about 60%, the total voltage range increased some 40%, and contrast dominance changed from highly positive to more balanced. At higher levels of background, most aspects of the contrast response stabilized and Weber's Law then held closely. In this background range, the contrast gain of bipolar cells was amplified some 20X relative to that of cones whereas the corresponding amplification in horizontal cells was about 6X. Differences in the growth of contrast gain with the intensity of the background illumination for cones versus bipolar cells suggest that there are at least two adaptation-dependent mechanisms regulating contrast gain. One is evident in the cone photoresponse such that an approximately linear relation holds between the steady-state hyperpolarization and contrast gain. The other arises between the voltage responses of the cones and bipolar cells. It could be presynaptic (modulation of cone transmitter release by horizontal cell feedback or other mechanisms) and/or postsynaptic, that is, intrinsic to bipolar cells. Contrast gain grew with the background intensity by a larger factor in horizontal than in bipolar cells. This provides a basis for the widely held view that light adaptation increases the strength of surround antagonism in bipolar cells. On average, the effects of light adaptation and most quantitative indices of contrast processing were remarkably similar for Bd and Bh cells, implying that both classes of bipolar cells, despite possible differences in underlying mechanisms, are about equally capable of encoding all primary aspects of contrast at all levels of light adaptation.

Adaptation, Ocular↗

Cultured ocular cells and extracellular matrices: role of growth factors, retinoic acid and cell polarity.

Culture of various types of cells on gelled, reconstituted extracellular matrices results in decreased cellular proliferation. In the present study, we evaluated several possible mechanisms for this inhibition, as applied to cultured bovine retinal microvascular endothelial cells (EC) or to retinal pigment epithelial (RPE) cells: whether the inhibition might be related to (a) inactivation of fibroblast growth factor (FGF) by binding of the molecules present in the medium to a matrix component; (b) release of an inhibitor by the matrix in culture; or (c) inhibitory properties of the matrix macromolecules themselves. Our results suggest that mechanism (c) is most likely. The reasons are, first, that culture of EC or RPE cells on several different extracellular matrix substrates in the presence of logarithmically increasing concentrations of acidic or basic fibroblast growth factors (aFGF or bFGF) leads to a vertical shift of the plots of cell number after 4 days in culture vs. log growth factor concentration for both types of cells. The same result obtains when cells are cultured with logarithmically increasing concentrations of all-trans retinoic acid, which inhibits EC but not RPE cell proliferation in a dose-dependent fashion. This is consistent with mechanism (b) or (c), but not (a), for which one would expect a horizontal shift. Second, washing the matrices prior to the plating of cells with 1M NaCl, which elutes aFGF and partially elutes bFGF molecules from basement membranes, does not alter the growth of cells plated after the wash. This suggests also that growth factor binding to the matrix is not a likely mechanism for the observed inhibition. Incubation of matrices with culture medium prior to plating cells does not usually alter the ability of the medium thus "conditioned" to support cell growth, arguing against the possibility that the matrices release a soluble activator or inhibitor of such growth. However, in some experiments performed with lots of Matrigel (a commercially available basement membrane extract from a murine tumor) obtained prior to mid-1991, media "conditioned" by incubation with this matrix did show enhanced ability to facilitate EC and RPE cell proliferation. Finally, if RPE cells or EC are plated on various substrates, allowed to attach for 24 hr., and then the same or other substrates are poured over the cells, the effect on proliferation of the matrices plated on the apical surfaces of the cells is often less than that of matrices plated adjacent to their basal surfaces. Although in most cases these differences are not statistically significant, there is an apparent trend.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Subcellular localization of neuronal nitric oxide synthase in turtle retina: electron immunocytochemistry.

Recent studies imaging nitric oxide (NO) production in the retina have indicated a much wider distribution of NO production than would be suggested by previous light-microscopic localizations of neuronal nitric oxide synthase (nNOS). To help resolve this discrepancy, the present study analyzed the ultrastructural localization of nNOS-like immunoreactivity (-LI) in all layers of the retina. In the ellipsoids of rod photoreceptors and the accessory elements of double cones, nNOS-LI was associated with some atypical mitochondria. In the outer plexiform layer, nNOS-LI was in some postsynaptic horizontal and bipolar cell processes at photoreceptor ribbon synapses. In some amacrine and ganglion cell somata, nNOS-LI was diffusely localized in the cytoplasm and associated with the endoplasmic reticulum. In the inner plexiform layer, nNOS-LI diffusely filled some amacrine cell processes, while in other amacrine cells nNOS-LI was selectively localized at the presynaptic specializations of conventional synapses. Neuronal NOS-LI was also found at membrane specializations in bipolar cell terminals that were distinct from their normal ribbon synapses. Finally, some nNOS-LI was found in mitochondria in Muller cells. The diverse subcellular localizations of nNOS-LI indicates that NO may play distinct functional roles in many retinal cells, which correlates well with the widespread NO production found in previous NO imaging studies.

Amacrine Cells↗

Topography of cones and rods in the tree shrew retina.

The topographical distribution of cones and rods in the tree shrew retina was analysed quantitatively in whole-mounted retinae and horizontal semithin sections stained with cresyl violet or toluidine blue. The outer nuclear layer consists of a single layer of photoreceptor nuclei with the rod nuclei slightly displaced towards the outer plexiform layer. This facilitated quantification of the photoreceptor populations. The density of cones ranges from 12,000/mm2 in the peripheral retina to a maximum of 36,000/mm2 in the inferior retina. Unlike ganglion cell density, the density of cones does not peak in the temporal retina. Rod density, between 500/mm2 and 3,500/mm2, also peaks in the inferior retina, but not in the same region as cone density. Rods constitute from 1 to 14% of the photoreceptor population, depending on retinal location, and have a local minimum at the central area. Amongst the cones a regularly arrayed subpopulation of presumed blue-sensitive cones is distinguished by its special staining properties. These cones constitute between 4 and 10% of the cone population depending on retinal location. A second, irregularly spaced, subpopulation of possibly pathological cones is also described.

Animals↗

The d-wave of the rod electroretinogram of rat originates in the cone pathway.

We studied the off-response of the rat ERG evoked with long duration, mesopic stimuli during light and dark adaptation, and after intravitreal injection of aspartate and (+/-)-cis-piperidine-2,3-dicarboxylic acid (PDA). At stimulus offset, the dark-adapted ERG always showed a rapid negative deflection followed by a positive deflection after which the potential returned to baseline. When the stimulus was turned off in the presence of a background of scotopic intensity, the positive deflection consisted of two components. One component was relatively small, fast, and insensitive to rod light adaptation. It resembled the d-wave of the rod ERG. The other component was slow and its amplitude grew with rod light adaptation. In the presence of aspartate, the fast-positive component was absent from the ERG while the remaining positive-going decay of the receptor potential had a time course similar to that of the slow-positive component in the untreated eye. Scotopically matched red and blue stimuli of mesopic intensity elicited equal ERG responses from the dark-adapted eye, including the two positive components in the off-response. These stimuli were also used to assess changes in the ERG off-response during recovery from a strong bleach. Even though the cone contribution to the rat ERG is very small, the presence of a small positive-going component in the off-response following an intense bleach suggested that this response originated from the cone pathway. PDA which suppresses the light response of hyperpolarizing bipolar cells and horizontal cells selectively eliminated the fast-positive component from the ERG. The findings of this study are inconsistent with the idea that the d-wave reflects the decay of the rod receptor potential. They support the possibility that signals from rods cross rod-cone gap junctions at mesopic light intensities, and drive second-order neurons in the cone pathway.

Animals↗

Association amacrine cells of Ramón y Cajal: rediscovery and reinterpretation.

In 1895, by means of the Golgi method, Santiago Ramón y Cajal discovered a cell having a unique morphology in the avian retina. This cell had its cell body in the amacrine cell level of the inner nuclear layer, only a few rudimentary dendrites at the outermost level of the inner plexiform layer (IPL), and a long axon coursing horizontally and terminating in the IPL. Despite having defined amacrine cells as cells without axons, Cajal named this cell type "association amacrine cell" (AAC). This discovery was not confirmed by other investigators for nearly a century. Very recently, however, isthmo-optic target cells (IOTCs), which receive the terminals of centrifugal fibers emanating from the isthmo-optic nucleus, have been identified as one type of AAC. As summarized and discussed in this review, the morphology of the AACs as described by Cajal has been completely confirmed. However, since these cells appear to be classical polarized, monoaxonal neurons and lack the dendritic interactions that are typical of amacrine cells, they should be regarded as a distinct type of retinal interneuron and not as amacrine cells.

Animals↗

Structural basis of the functional development of the retina in the cichlid Tilapia leucosticta (teleostei).

The differentiation of retinal cells has been studied with special reference to the formation of functionally important structures. Three phases could be revealed: from day 3 to day 6 retinal cells in the mostly advanced central part show signs of general cell differentiation (formation of ribosomes, endoplasmic reticulum, mitochondria). In the second phase from day 6 to day 9 characteristic nerve cell structures appear (neurites, dendrites, synapses, receptor outer and inner segments). In the last phase from day 9 to day 12 these special structures attain their final, mature appearance, synapses seem ready for function, dendritic invaginations and synaptic ribbons are formed, twin cones become arranged in mosaic patterns. This developmental order conforms to a gradient running from the ganglion cells to the receptors. Neurites and dendrites appear in the ganglion cells on day 3, in the intermediate neuron layer not before day 4. The horizontal cells are the last ones to differentiate out of the intermediate neurons. The inner plexiform layer synapses are structurally mature before those from the outer plexiform layer. The receptor inner and outer segments differentiate from the 5th day up to the time the young fish is able to see (day 13). The last structures to appear are dendritic invaginations and synaptic ribbons in the receptor terminals, and the twin cone mosaic. It is assumed that the ability to see is achieved only when these structures have been formed.

Animals↗

Evidence that different cation chloride cotransporters in retinal neurons allow opposite responses to GABA.

GABA gating an anion channel primarily permeable to chloride can hyperpolarize or depolarize, depending on whether the chloride equilibrium potential (E(Cl)) is negative or positive, respectively, to the resting membrane potential (E(rest)). If the transmembrane Cl(-) gradient is set by active transport, those neurons or neuronal regions that exhibit opposite responses to GABA should express different chloride transporters. To test this, we immunostained retina for the K-Cl cotransporter (KCC2) that normally extrudes chloride and for the Na-K-Cl cotransporter (NKCC) that normally accumulates chloride. KCC2 was expressed wherever E(Cl) is either known or predicted to be negative to E(rest) (ganglion cells, bipolar axons, and OFF bipolar dendrites), whereas NKCC was expressed wherever E(Cl) is either known or predicted to be positive to E(rest) (horizontal cells and ON bipolar dendrites). Thus, in the retina, the opposite effects of GABA on different cell types and on different cellular regions are probably primarily determined by the differential targeting of these two chloride transporters.

Animals↗

GABA-like immunoreactivity in the vertebrate retina: a species comparison.

Rabbit antisera directed against gamma-amino butyric acid (GABA) conjugated to bovine serum albumin was used to localize neurons containing GABA-like immunoreactivity in the retinas of nine species of animals: human, cat, rabbit, rat, chicken, turtle, frog, mudpuppy and goldfish. The retinas of all species contained GABA-like labeling in several populations of amacrine cells in the inner nuclear layer, cells in the ganglion-cell layer that may include displaced amacrine cells and in fibers in the inner plexiform layer and in the optic nerve fiber layer. Labeled horizontal cells were found in cat and in all non-mammalian retinas. Labeled interplexiform cells were found in rat, rabbit, cat and human retinas. Labeled bipolar cells were restricted to frog and mudpuppy retinas. The distribution of anti-GABA is usually similar to that of anti-glutamic acid decarboxylase and neuronal [3H]GABA uptake, indicating good correspondence between these 'GABAergic' markers. However, several significant differences among these markers are discussed.

Animals↗

Studies of retinal representations within the cat's optic tract.

The manner in which each retina can be mapped onto a single cross section of the optic tract of the cat has been defined by neuroanatomical methods. It has been found that the contralateral nasal hemi-retina and both temporal hemi-retinae are represented in each tract by multiple, rough maps which partially overlap one another. All maps show the same general orientation, with area centralis represented dorsomedially, lower retina represented dorsolaterally, and upper retina represented ventromedially. The peripheral part of the horizontal meridian is represented ventrolaterally. Labeling all of the fibers from one eye by axonal degeneration or autoradiographic methods shows that the crossed map is displaced dorsally and medially relative to the uncrossed map, leaving a dorsomedial crescent of pure crossed fibers. Localized retinal lesions or injections of 3H-amino acid show the general orientation of the maps. Lesions within the dorsomedial pure crossed crescent show that fibers in this crescent arise from retinal areas close to the optic disc, near the site of the early fetal fissure. Localized injections of horseradish peroxidase into the optic tract show the relationships of the several maps in terms of the retinal distribution of retrogradely labeled retinal ganglion cells. They show that axons of large and small cells map ventrolaterally in the tract while intermediate sizes map dorsomedially. They confirm that the crossed map is displaced relative to the uncrossed maps. It is suggested that the optic tract develops by fibers taking a position in the tract in accordance with their time of arrival at the chiasm. The several maps are displaced because they develop sequentially and the optic tract can be read as a developmental record, the most dorsomedial axons being the oldest.

Animals↗

A model of anuran retina relating interneurons to ganglion cell responses.

A model is presented which accounts for many characteristic response properties used to classify anuran ganglion cell types while being consistent with data concerning interneurons. In the model color is ignored and input stimuli are assumed to be only black and white at high contrast. We show that accurate ganglion cell responses are obtained even with simplified receptors and horizontal cells: Receptors are modeled as responding with a step change, while horizontal cells respond only to global changes in intensity brought about by full field illumination changes. A hyperpolarizing and depolarizing bipolar cell are generated by subtracting local receptor and horizontal potentials. Two transient amacrine cells (On and Off) are generated using a high-pass filter like mechanism with a thresholded output which responds to positive going changes in the corresponding bipolar cell potentials. The model shows how a selective combination of bipolar and amacrine channels can account for many of the response properties used to classify the anuran ganglion cell types (class-0 through 4) and makes several experimental predictions.

Animals↗

Connexions between retinal neurons with identified neurotransmitters.

Dopaminergic and indoleamine accumulating neurons can be demonstrated both in the light and the electron microscopes. Considerable differences have been found between different animal species. There are two types of dopaminergic neurons, the interamacrine cells and the interplexiform cells. The interamacrine cells contact only other amacrine cells. They receive synapses from other amacrine cells which are likely to operate with, e.g. GABA or glycine as neurotransmitter. The dopamine turnover in the dopaminergic interamacrine cells is very rapidly activated by light. Dopaminergic interplexiform neurons are known only in teleost fish and New World monkeys. They have approximately the same contacts in the inner plexiform layer as the interamacrine cells, but, in addition, send processes to the outer plexiform layer and there contact both horizontal cells and bipolar cells. The function of the dopaminergic neurons has not been determined. The indoleamine accumulating amacrine neurons are in Cebus monkeys, cats and rabbits contacted by bipolar cells in dyads and form reciprocal synapses with them. They are also contacted by amacrine cells and make synapses on other with them. They are also contacted by amacrine cells and make synapses on other amacrine cells and on ganglion cells. The contacts are different in teleost fish, where the indoleamine accumulating cells mainly contact other amacrine cells only. The transmitter of the indoleamine accumulating neurons is debated in mammals but is most likely 5-hydroxytryptamine in other vertebrates.

Animals↗

The intrinsic organization of the nucleus lentiformis mesencephali magnocellularis: a light- and electron-microscopic examination.

The nucleus lentiformis mesencephali magnocellularis (nLMmc) is an essential part of the accessory optic nuclei and is responsible for stabilization of the horizontal eye movement. The morphology of this nucleus and its intrinsic structural connectivity were studied with Golgi, biotinylated dextran amine anterograde immunotracer and GABA immunostaining methods by light and electron microscopy. In the Golgi preparations neurons of large, medium-large, medium and small sizes were distinguished. The small neurons are GABA-immunopositive local circuit neurons, the others are proposed to be partly projection, partly local circuit neurons. The large and medium-large projection neurons are located in a tight topographical relationship observed in the Golgi preparations. The dendrites of the large and medium-large cells are also observed to be in close proximity with each other, and also with retinal fibre terminals. The morphological arrangement suggests that the retinal fibres make synaptic contacts with dendrites from both types of cell, and this is confirmed by the examination of retinal fibre terminals using electron microscopy. The optic fibre terminals establish synaptic contacts with small dendritic branches, dendritic processes and dendritic spines of large and medium-large neurons in the nLMmc. This arrangement allows the two types of nLMmc neuron access to very similar, if not identical, inputs, which may facilitate some of the different aspects of visual processing. Optic transmission by these cells may be modulated by the GABA-immunopositive terminals from various local circuit neurons, and very probably from GABAergic myelinated fibres as well, which may originate from the contralateral nLMmc and/or the visual Wulst.

Animals↗

The distribution and kinetics of visual pigments in the owl monkey retina.

An imaging fundus reflectometer has been used to study the distribution and regeneration of visual pigments in the retina of the owl monkey, Aotes trivirgatus. Measurements were made over an area of retina from 10 degrees nasal to 30 degrees temporal on the horizontal meridian, and from 5 degrees inferior to 30 degrees superior on the vertical meridian. The measured density differences vary with retinal location, with values in the central retina higher than those in more peripheral regions. The area of high density differences is roughly circular, with the highest values (approximately 0.3 log units) centred on or near the area centralis. Spectral measurements are consistent with a rod visual pigment absorbing maximally at about 518 nm, and indicate that the contribution of cone pigments to the imaging fundus reflectometer (IFR) data is negligible everywhere within the retinal area studied. The distribution of density differences is shown to correlate well with anatomical data for receptor and ganglion cell populations. Bleaching the visual pigment with brief intense lights leads to the extensive formation of the long-lived photoproduct metarhodopsin 3. Complete regeneration of rhodopsin following a full bleaching exposure (whether of brief or extended duration) takes more than 60 min and the time course of its recovery cannot be described accurately by first order kinetics.

Animals↗

Experimental induction of an abnormal ipsilateral visual field representation in the geniculocortical pathway of normally pigmented cats.

In the normally pigmented neonatal cat, many ganglion cells in temporal retina project to the contralateral dorsal lateral geniculate nucleus (LGNd) and medial interlaminar nucleus (MIN). Most of these cells are eliminated during postnatal development. If one optic tract is sectioned at birth, much of this exuberant projection from the contralateral temporal retina is stabilized (Leventhal et al., 1988b). To determine how the abnormal projection from the contralateral temporal retina is accommodated in the central visual pathways, neuronal activity was recorded in the visual thalamus and cortex of adult cats whose optic tracts were sectioned as neonates. The recordings showed that up to 20 degrees of the ipsilateral hemifield is represented in the LGNd and MIN. Recordings from areas 17 and 18 of the intact visual cortex showed that up to 20 degrees of the ipsilateral visual field is also represented and that the ipsilateral representation is organized as in a Boston Siamese cat (Hubel and Wiesel, 1971; Shatz, 1977; Cooper and Blasdel, 1980) or a heterozygous albino cat (Leventhal et al., 1985b). The extent of the ipsilateral visual field representation was greater in area 18 than in area 17; the extent of the ipsilateral hemifield representation in areas 17 and 18 varied with elevation, increasing with distance from the horizontal meridian. The receptive fields of cells in the LGNd and visual cortex subserving contralateral temporal retina were abnormally large. Otherwise, their receptive field properties seemed normal. In the same animals studied physiologically, HRP was injected into the ipsilateral hemifield representation in the LGNd and MIN of the intact hemisphere. The topographic distribution of the alpha and beta cells, respectively, labeled by these injections correlated with the elevation-related changes in the ipsilateral visual field representation in areas 18 and 17. Our results indicate that the retinotopic organization of the mature geniculocortical pathway reflects the abnormal pattern of central projections of ganglion cells in neonatally optic tract sectioned cats. Thus, if they do not die, retinal ganglion cells normally eliminated during development are capable of making seemingly normal, functional connections. The finding that an albino-like representation of the ipsilateral hemifield can be induced in the visual cortex of normally pigmented cats suggests that the well-documented defects in the geniculocortical pathways of albinos are secondary to the initial misrouting of ganglion cells at the optic chiasm (Kliot and Shatz, 1985) and not a result of albinism per se.

Albinism↗

The decussation of the retinothalamic pathway in the cat, with a note on the major meridians of the cat's eye.

We have studied the naso-temporal division of the retinothalamic pathway of the cat by making large unilateral injections of horseradish peroxidase into the lateral geniculate nucleus. In confirmation of previous work, our retinal whole-mounts show a distinct vertical decussation line separating the contralaterally projecting nasal retina from the ipsilaterally projecting temporal retina. The ipsilateral decussation line is quite sharp, while the contralateral decussation is somewhat more diffuse, with numbers of large cells extending a few degrees into the temporal retina. However, in contrast to the results of optic tract section, our material (demonstrating the thalamic component only) does not reveal any significant population of contralaterally projecting small cells across most of the temporal retina. The previous observation of approximately 200 micrometer of naso-temporal overlap in the area centralis is confirmed here, and evidence is presented that this overlap may increase at eccentricities above the horizontal meridian. Taken together with previously published data, this demonstration of the vertical decussation line has allowed us to estimate the relative inclinations of the major meridians of the cat's eye.

Animals↗

Putative neurotransmitters in the retinae of three urodele species (Triturus alpestris, Salamandra salamandra, Pleurodeles waltli).

The immunocytochemical localization of several substances with putative neurotransmitter or modulator properties was investigated in the retinae of three urodele species. Gamma-aminobutyric acid-like immunoreactive labelling appeared in different types of amacrine and horizontal cells. In addition, labelled fibres in the optic nerve were detected. It was not possible to determine whether these fibres were ganglion-cell axons or part of an efferent projection. Endogenous serotonin was found in several populations of amacrine cells including stratified and diffuse types. Glucagon-like immunoreactivity appeared in one bistratified amacrine cell type, and neurotensin-like immunoreactivity was detected in a single monostratified amacrine cell type. Metenkephalin-like-immunoreactive labelling was type. Metenkephalin-like-immunoreactive labelling was rare but found in several sublaminae of the inner plexiform layer. Thus each peptide-like-immunoreactive cell type makes up a distinct and unique population of cells and probably has a special functional role in retinal processing. There are striking similarities in the peptide-like immunoreactive patterns of Triturus alpestris and Necturus maculosus whereas in Ambystomatidae the peptide-like-immunoreactive systems appear to be differently organized. This supports the hypothesis that Salamandridae and Proteidae are more closely related to each other than to the Ambystomatidae.

Animals↗