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Biomedical subjects

R Weiler

Publications and source records attributed to R Weiler.

At least 73 records · Page 4Linked to original sources
PubMed1989

Reduced light responsiveness of the cone pathway during prolonged darkness does not result from an increase of dopaminergic activity in the fish retina.

Dopaminergic activity in the fish retina during prolonged darkness was analyzed by monitoring total dopamine (DA) content, dihydroxyphenylacetic acid (DOPAC) and endogenous release of DA. Whereas DOPAC values drop to a third within the first 90 min of darkness, the releasable pool of DA increases by a third during this period. Endogenous release of DA drops to about 25% within the first 30 min and remains at this low level during continuous darkness. These data demonstrate that the electrophysiologically observed sensitivity reduction of horizontal cells during prolonged darkness is not due to an increase of dopaminergic activity during this period.

3,4-Dihydroxyphenylacetic Acid↗
PubMed1989

An immunological study on chromogranin A and B in human endocrine and nervous tissues.

Antisera were raised against synthetic peptides derived from the primary amino acid sequence of human chromogranin B. These antisera recognized in one- and two-dimensional immunoblotting a component previously designated as chromogranin B. In human chromaffin granules, the major endogenous processing product of chromogranin B is formed by proteolytic cleavage of the protein near the C-terminus. Immunohistochemical localizations were obtained with antisera against human chromogranins A and B and against a synthetic peptide corresponding to the B sequence. In human tissues, chromogranin B is co-stored with chromogranin A in the adrenal medulla, the anterior pituitary, parafollicular cells of the thyroid, in some cells of the endocrine pancreas and in some enterochromaffin cells, whereas only chromogranin A is found in the parathyroid gland and enterochromaffin cells of the gastric corpus mucosa. In the nervous system, no immunostaining was observed for chromogranin A and only a weak one for chromogranin B in some cells of the spinal cord. However, the Purkinje cells of the cerebellum were strongly positive for chromogranin B.

Chromogranin A↗
PubMed1989

Enkephalinergic modulation of the dopamine system in the turtle retina.

One subpopulation of amacrine interneurons in the turtle retina was shown to contain met-enkephalin by means of immunocytochemistry, and another was demonstrated to have a high-affinity uptake system for [3H]-dopamine by means of autoradiography. Although the amacrine soma size, density, and distribution of their neurites in IPL substrata was similar in retinas in which met-enkephalin and dopamine were localized, combined light microscope immunocytochemistry-autoradiography demonstrated that these two neurotransmitter systems did not coexist in the same cells. Because the two amacrine cell subtypes ramify in the same IPL substrata, neuronal interaction between them is possible. Release experiments showed that the potassium-induced release of [3H]-dopamine from the superfused turtle retina was reduced by 40% when enkephalin was added to the superfusate. The inhibition of [3H]-dopamine release could be blocked by the addition of naloxone. The addition of enkephalin had no effect of the potassium-induced release of [3H]-GABA from the superfused retina. These findings suggest that an enkephalinergic modulation of the dopaminergic amacrine cell system exists in the turtle retina.

Animals↗
PubMed1988

Mesencephalic innervation of the turtle retina by a single serotonin-containing neuron.

Co-localization of retrograde transported Nuclear yellow and serotonin immunoreactivity revealed the existence of a central serotonergic projection to the retina in the turtle Pseudemys scripta elegans. This serotonergic retinopetal system consists of only one fiber originating in the contralateral caudal mesencephalon. In the retina, the fiber arborizes exclusively in the temporal hemisphere, covering about one third of the total retinal surface. Interestingly this projecting area lies in the part of the retina, to which binocular perception can be attributed.

5,7-Dihydroxytryptamine↗
PubMed1988

Physiological and morphological characterization of OFF-center amacrine cells in the turtle retina.

OFF-center amacrine cells were intracellularly recorded and stained with Lucifer yellow to investigate the cell correlations between photoresponses and morphological features. All OFF-amacrine cells were monostratified and branched within the outer half of the inner plexiform layer. In the flat-mounted retina, however, three distinct morphological classes were distinguishable, which correlated with observed physiological differences. Class 1 consisted of wide-field, stellate amacrine cells with long, thin processes, which branched only close to the soma. The diameter of the circular dendritic field ranged from 0.8 mm to 2.0 mm. Their photoresponse to spot stimulation was a hyperpolarization during light-ON and a small depolarization after light-OFF. They showed strong antagonistic center-surround organization of the receptive field. Its size was approximately equal to the dendritic field size. Class 2 consisted of wide-field, giant amacrine cells with a "central" dendritic field formed by thick dendrites, and a "peripheral" dendritic field formed by a few long and thin, "axonlike" processes. The shape of the dendritic field was elongated, with the long axis parallel to the visual streak. Their receptive field size was considerably smaller than their dendritic field size, which was several millimeters of diameter along the long axis. Their photoresponse to spot stimulation was a fast depolarization after light-OFF, and about 50% of these cells showed strong antagonistic center-surround receptive field organization. Class 3 consisted of small- or medium-field, "starburstlike" amacrine cells with circular dendritic fields of 0.1 mm to 0.6 mm diameter. Their fine, beaded dendrites branched predominantly in the distal parts of the dendritic field. their photoresponses to light were similar to those of the giant amacrine cells; however, their receptive field size exceeded the dendritic field size. Radial sections of the retinas with labeled cells were incubated in antisera to reveal the putative transmitters GABA, serotonin, neurotensin, met-enkephalin and glucagon. No immunoreactivity with these antisera was detected within the stained OFF-center amacrine cells.

Animals↗
PubMed1988

Glutamate and dopamine modulate synaptic plasticity in horizontal cell dendrites of fish retina.

Horizontal cell dendrites protruding into the cone pedicles in fish retina exhibit a light-dependent plasticity. In a light-adapted retina they form numerous spinules having membrane densities at their tips. These spinules disappear during dark adaptation. Experiments with light- or dark-adapted retinas which were incubated in glutamate or its agonists and antagonists, respectively, revealed that this putative cone transmitter is able to reduce the expression of spinules in a light-adapted retina. Dopamine, on the other hand, induces the formation of spinules in a dark-adapted retina and haloperidol reduces the expression in a light-adapted retina. These data suggest a control of spinules plasticity through two retinal neurotransmitter systems.

Animals↗
PubMed1988

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↗
PubMed1988

Immunological studies on the occurrence and properties of chromogranin A and B and secretogranin II in endocrine tumors.

We investigated a variety of endocrine tumors for the presence of chromogranins A and B and secretogranin II. These antigens were identified by one- and two-dimensional immunoblotting and in some cases by immunohistochemistry. An antigen corresponding in electrophoretic behavior to adrenal chromogranin A was present in all types of tumors, including insulinomas, oat cell carcinomas, and Merkel cell tumors of the skin. Chromogranin B had a much more limited distribution. This antigen could not be detected in parathyroid adenomas, oat cell carcinomas, or Merkel cell tumors, either by immunoblotting and immunohistochemistry. The occurrence of secretogranin II was similar to that of chromogranin B, with the exception of a positive reaction in Merkel cell tumors. In benign pheochromocytomas, all three antigens were found consistently; whereas in two of three malignant pheochromocytomas, chromogranin B was absent. Our study establishes that in most cases chromogranins and secretogranin in tumors are identical to the adrenal antigens, but that these antigens are not always stored together. Chromogranin A is the most widely distributed marker for endocrine tumors.

Adrenal Gland Neoplasms↗
PubMed1987

Morphometric analysis of serotoninergic bipolar cells in the retina and its implications for retinal image processing.

The entire population of retinal serotoninergic bipolar cells in the turtle Pseudemys scripta elegans was labeled by immunocytochemical methods. This allowed a systematic analysis to be made of the morphological variabilities among a functionally homogeneous neuronal population. The analyzed morphological characteristics included: size of the Landolt club, size of the soma, lateral extension of the ramification within the outer plexiform layer, course of the axon across the inner nuclear layer, pattern of the axonal ramification within the inner plexiform layer, lateral extension of these ramifications, and density of the cells. Whereas characteristics 1-4 and 7 show a morphological variability strictly related to the location of the bipolar cell with respect to the visual streak, a fovealike structure, characteristics 5 and 6 show no such correlation. The size of the soma increases by a factor of 4 from the visual streak toward the periphery. The area covered by the ramification in the OPL increases from 330 micron 2 at the visual streak to 50,000 microns 2 at the dorsal and ventral edges of the retina. The coverage factor remains the same throughout the retina, as well as the area covered by the ramifications in the IPL, which is about 2,000 microns 2. At the visual streak and at 110 degrees ventral and 68 degrees dorsal of the visual streak, the bipolar axons cross the INL perpendicularly. In between the axons take an oblique course leading to an axon-induced shift between input and output of up to 250 microns.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

Chromogranin A and B and secretogranin II in bronchial and intestinal carcinoids.

Carcinoid tumours (bronchial and intestinal) were analyzed by immunoblotting for the presence of chromogranin A, B and secretogranin II. In all tumours an antigen corresponding in electrophoretic behaviour to adrenal chromogranin A was present. Lung carcinoids (3 out of 5) contained a relatively high concentration of a proteoglycan form of this antigen in addition. Chromogranin B was found in all tumours. In one and two dimensional immunoblotting it appeared identical to the corresponding adrenal antigen. Secretogranin II was also present, however concentrations (especially in intestinal carcinoids) were low and variable. Furthermore, in intestinal tumours it differed from the adrenal antigen by having a slightly higher molecular size and a more alkaline pI. Immunohistochemistry revealed that the tumour tissues stained positively for all three antigens. For secretogranin II the staining in intestinal tumours was relatively weak and quite variable. These results should provide a defined basis for immunohistochemical screening of carcinoids for the chromogranin/secretogranin antigens.

Bronchial Neoplasms↗
PubMed1986

Immunocytochemical localization of serotonin in intracellularly analyzed and dye-injected ganglion cells of the turtle retina.

Combining intracellular recording techniques with immunocytochemistry revealed the existence of serotonin within a few ganglion cells of the turtle retina. Lucifer yellow was intracellularly injected into physiologically classified ganglion cells. Sections containing labeled somata were subsequently incubated with an antibody directed against serotonin and immunoreactivity was revealed using horseradish peroxidase as a marker. In 3 ganglion cells the two markers were co-localized. These cells ramified in layers 2 and 3 of the inner plexiform layer and produced color opponent ON-OFF photoresponses.

Animals↗
PubMed1985

Kainic acid-induced release of serotonin from OFF-bipolar cells in the turtle retina.

The immunofluorescence of antibody-labelled serotonin was used as an indicator for the amount of intracellular serotonin. Incubation in Ringer solution containing serotonin and pargyline increased the immunofluorescence which was subsequently decreased in a calcium-dependent manner by incubation in high-potassium Ringer. If preloaded retinas were exposed to 10 microM kainic acid, the immunofluorescence decreased in a time-dependent way. This kainic acid-induced release was blocked by piperidine dicarboxylic acid. These results support the idea that serotonin is a transmitter in OFF-bipolar cells.

Animals↗
PubMed1985

Mesencephalic pathway to the retina exhibits enkephalin-like immunoreactivity.

Using immunocytochemical methods it was possible to demonstrate a small number of fibers within the optic nerve of the turtle Pseudemys scripta elegans exhibiting Met-enkephalin-like immunoreactivity. The fibers project to the retina where they ramify within the inner plexiform layer in the region of the visual streak. Retrograde labelling with Nuclear Yellow in combination with immunocytochemical staining revealed the origin of these fibers within visceral nuclei of the caudal mesencephalon. The existence of a mesencephalic, enkephalinergic pathway to the retina will facilitate further studies of opiate action in the retina by offering the possibility of selectively stimulating the endogenous release.

Animals↗
PubMed1985

Morphological and pharmacological analysis of putative serotonergic bipolar and amacrine cells in the retina of a turtle, Pseudemys scripta elegans.

Using immunocytochemical methods, we have been able to demonstrate serotonin-like immunoreactivity (SLI) in amacrine and bipolar cells of the turtle retina. Inhibition of monoamine oxidase with pargyline drastically increases the amount of 5-hydroxytryptamine within both cell types. The indoleamine 6-hydroxytryptamine is taken up by both cell types and both types are destroyed within 10 days following intraocular injection of 5,7-dihydroxytryptamine. Increasing the external potassium concentration induces release of serotonin in both cell types. Our data support the idea that these neurons use serotonin during neuronal processing. Morphologically, amacrine and bipolar cells with SLI can be subdivided into two and three subclasses, respectively, based on their ramification pattern within the inner plexiform layer. A comparison of the morphological data with those of intracellularly stained amacrine and bipolar cells suggests that all bipolar cells with SLI are center-hyperpolarizing cells and all amacrine cells center-depolarizing cells.

Animals↗
PubMed1985

S-neurons and not L-neurons are the source of GABAergic action in the ocellar retina.

Electrophysiological evidence obtained with current- and voltage clamp experiments from single L-neurons of the ocellar nerve of locust (Locusta migratoria) questions a direct synaptic feedback from these neurons onto the photoreceptors. The synaptic currents recorded under voltage clamp reflected the photoresponse of the L-neuron, despite the fact it developed no synaptic activity under these conditions. This result is contrary to GABAergic feedback models proposed in the literature. Electrophysiological recordings, as well as immunocytochemistry revealing GABA and glutamate decarboxylase, indicated a possible contribution of S-neurons in such a feedback system. A population of probable S-neurons whose somas were in the pars intercerebralis adjacent to the ocellar nerve tracts was heavely labelled. About 10 fibres entered each tract and formed a dense network of fine arborizations within the ocellar plexiform layer. L-neurons showed no GABA-immunoreactivity. Based on these data a new model for GABAergic feedback is proposed and discussed.

Animals↗
PubMed1984

Light-dependent change of cone-horizontal cell interactions in carp retina.

Carp H2 horizontal cells were investigated at various stages of dark and light adaptation. Their state of adaptation was verified by evaluating in computer reconstructed serial sections the number of small, fingerlike protrusions originating from H1 processes. These so-called spinules are absent in the dark-adapted state and are reformed during light adaptation. Intracellular recordings showed that long-wave-induced depolarization thought to be mediated by sign-inverted feedback from H1 horizontal cells onto green-sensitive cones could not be demonstrated in completely dark-adapted specimens. This type of response only developed with increasing light adaptation. Following electrophysiological characterization, the cells were injected with horseradish peroxidase and identified light and electronmicroscopically. Our results show a good correlation between the number of spinules and the degree of electrophysiological feedback suggesting that the spinules may be the sites of the feedback synapses in teleost retinas. Several models of synaptic transmission from H1 terminals to cone pedicles are discussed.

Animals↗