Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: EC:1.11.1.7 (peroxidase)
65,474 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The distribution of gamma-aminobutyric acid-immunoreactive (GABA-I) elements was examined in the septal region of the rat brain. The indirect peroxidase-antiperoxidase technique was used with anti-GABA antibodies in normal and colchicine-pretreated rats, with or without use of detergent in the incubation medium. Intraventricular injection of colchicine did not result in any change in the staining of neuronal perikarya. Intraseptal injections increased the intensity of labelling of GABA-I cell bodies in the lateral septal nucleus and increased the number of labelled cells in the medial septal nucleus and diagonal band of Broca (dbB). Triton X-100 added to the incubation media decreased the intensity of staining and number of GABA-I somata in all septal nuclei with a concentration-dependent effect. No change was observed concerning GABA-I varicosities. The septal area, including the lateral, medial, and triangular septal nuclei; the anterior rudiment of the hippocampus; the island of Calleja magna; the septofimbrial nucleus; the bed nucleus of the stria terminalis; and the dbB showed a strong reaction to anti-GABA antibodies with regard to GABA-containing surrounding structures. GABA-I axonal varicosities were observed in all the regions with an uneven distribution. The highest density was found in the dorsal and ventral parts of the lateral septal nucleus and in a band situated between the dbB and the nucleus accumbens. Labelled varicosities were frequently observed surrounding GABA-I and nonimmunoreactive cell bodies. GABA-I somata ranged from 10 to 30 micron in diameter. Small neurons were present in great number at the ventricular border and in the zona limitans. Medium-size and large neurons were mostly observed in the medial part of the dorsal lateral nucleus and in the intermediate lateral nucleus.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Distribution of gamma-aminobutyric acid-immunoreactive neurons in the septal region of the rat brain. 352 64

Antisera specific for gamma-aminobutyric acid (GABA) or its biosynthetic enzyme, glutamate decarboxylase, were used in pre- and postembedding immunocytochemical techniques at the light and electron microscopic levels, to visualize the GABAergic innervation of the hypothalamic supraoptic nucleus. Immunostaining for glutamate decarboxylase or gamma-aminobutyric acid were also combined with oxytocin and vasopressin immunolocalization, thereby permitting evaluation of the contribution of the innervation onto each type of neuron in this nucleus. Light microscopy of semithin plastic sections or vibratome slices stained for glutamate decarboxylase or gamma-aminobutyric acid, with peroxidase-antiperoxidase as immunolabel, revealed an extensive punctate labeling in the supraoptic nucleus and its immediate surroundings. Quantitative analysis of glutamate decarboxylase immunostaining in semithin sections indicated a comparable density of immunopositive punctae at the anterior and posterior levels of the nucleus (14-27 X 10(6) per mm3 tissue). Glutamate decarboxylase- or gamma-aminobutyric acid-immunoreactive cell bodies were never observed within the nucleus although they were detected in the hypothalamus immediately dorsolateral to the nucleus. Electron microscopy of vibratome slices treated with antiglutamate decarboxylase or antigamma-aminobutyric acid and peroxidase-antiperoxidase, or of ultrathin sections stained directly with antigamma-aminobutyric acid and immunoglobulin-coupled colloidal gold, showed that the immuno-reactive punctae represented, in the main, axonal terminals. They invariably contained small, rounded clear vesicles and, at times, one or two larger, dense cored vesicles; they all formed symmetrical synapses onto magnocellular cell bodies and dendrites. Oxytocin and vasopressin neurons were contacted in a similar fashion by glutamate decarboxylase- or gamma-aminobutyric acid-positive boutons in semithin sections of the nucleus stained simultaneously for glutamate decarboxylase and oxytocin and in ultrathin sections stained for glutamate decarboxylase or gamma-aminobutyric acid and oxytocin or vasopressin. Glutamate decarboxylase- or gamma-aminobutyric acid-positive terminals often formed synapses onto two postsynaptic elements in the same plane of section ("double" synapses), a synaptic configuration usually encountered in supraoptic nuclei of lactating animals. In such cases, the postsynaptic somata were oxytocinergic.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Immunocytochemical analysis of the GABAergic innervation of oxytocin- and vasopressin-secreting neurons in the rat supraoptic nucleus. 353 41

Postembedding immunocytochemistry with a gamma-aminobutyric acid (GABA) antiserum was done on semithin sections of cat lateral geniculate nucleus (LGN) previously processed with the rapid-Golgi and gold-toning procedures, to determine which of the three main morphological types (1, 2,3) of neurons in the A-laminae show immunoreactivity and are, therefore, presumably GABAergic. Only type 3 cells were found to be GABA positive. These cells were characterized by small somata and few, scarcely branched dendrites bearing almost exclusively appendages with long slender stalks. Some of these cells have extensive filiform "axonlike" processes originating from different regions of dendrites and having appendages similar to those originating directly from dendrites. Many of these Golgi gold-toned impregnated dendritic appendages of type 3 cells were analyzed in the electron microscope and were identified as typical F2 terminals by their content of pleomorphic synaptic vesicles; by being postsynaptic to retinal (RLP), cortical (RSD), and perigeniculate (F1) terminals; and by being presynaptic to dendrites. In addition, since it was previously demonstrated that glutamic acid decarboxylase (GAD) and GABA-positive cells are not retrogradely labeled with horseradish peroxidase (HRP) from the visual cortex, the present results, by showing that GABA-positive cells have type 3 morphology, provide supporting evidence for the interneuronal nature of type 3 cells in cat LGN.
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PMID:Localization of gamma-aminobutyric acid (GABA) in type 3 cells and demonstration of their source to F2 terminals in the cat lateral geniculate nucleus: a Golgi-electron-microscopic GABA-immunocytochemical study. 354 41

The thalamic reticular nucleus (TRN) of the rat has been studied immunocytochemically using an antiserum against the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). Combined light and electron microscopic investigations by means of peroxidase-antiperoxidase and immunogold labeling show that this nucleus contains a homogeneous population of GABA-immunoreactive neurons receiving extensive GABAergic connections suggestive of self-inhibitory inputs.
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PMID:GABA immunoreactivity in the thalamic reticular nucleus of the rat. A light and electron microscopical study. 354 27

The value of gamma-aminobutyric acid (GABA) immunogold labeling in the quantification of nerve endings was studied in dissociated rat neocortex cultures. Adjacent sections were processed in 3 series according to the same staining protocol. Of all nerve ending profiles examined, 20% appeared to be GABA-positive, while 7% could not be classified. In cultures pretreated with gabaculine, GABA-positive endings were labeled more heavily. Cell bodies could always be discriminated as GABA-positive or GABA-negative. Of all neuronal cell profiles, 14% appeared to be GABA-positive. These neurons could also be identified by light microscopy using the peroxidase-anti-peroxidase method.
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PMID:Postembedding immunocytochemical GABA labeling in rat neocortex cultures: applicability in quantitative studies. 357 66

The laminar distribution and structure of the supragranular cells projecting from primary auditory cortex (AI) to the second auditory cortex (AII) in the cat were studied with horseradish peroxidase. Injections in AII retrogradely labeled somata in ipsilateral cortical layers I-VI of AI. A bimodal laminar disposition was found, with approximately 40% of the labeled cells in layer III, 25% in layer V, and 10-15% each in layers II, IV, and VI; only a few cells were found in layer I. The labeled cells were scattered in small aggregates between which unlabeled neurons were interspersed. There was some, though not a strict, topographical distribution of the labeled cells according to the locus of the injection in AII. Injections in the caudal part of AII labeled cells in more rostral AI, while rostral AII injections labeled cells in more caudal AI. Ventral AII injections labeled more ventrally located AI cells, while more dorsal AII injections labeled more dorsally situated AI cells. AII injections also labeled cells in other auditory cortex subdivisions, including the posterior ectosylvian, ventroposterior, temporal, and dorsal auditory zone/suprasylvian fringe cortical areas, and in some non-auditory cortical areas. In layers II and III, both pyramidal and non-pyramidal cells were labeled. More pyramidal cells were labeled in layer III than layer II (80% vs. 62%), and the proportion of non-pyramidal cells in layer II was more than twice that in layer IV (27% vs. 12%). The types of labeled cells were distinguished from one another on the basis of size, somatic and dendritic shape, and laminar distribution. The profiles of labeled cells in these experiments were compared to, and correlated with, those in Golgi-impregnated material. In layer II, the classes of corticocortical projecting cells consisted of small and medium-sized pyramidal, bipolar, and multipolar cells. Those in layer III included small, medium-sized, and large pyramidal neurons, and bipolar and multipolar cells. The average somatic area of the labeled cells did not differ significantly from that of the unlabeled cells, and both were about equal in somatic size to neurons accumulating tritiated gamma-aminobutyric acid in layers II and III. These findings suggest that there is convergent, ipsilateral input onto AII from every layer in AI, and from other cortical auditory and non-auditory areas. A morphologically heterogeneous population of cells in AI contributes to these projections. Diversity in the cytological origins of corticocortical projections implies functional differences between layers II and III since the latter also projects commissural, while layer II in the cat, does not.
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PMID:Corticocortical connections of cat primary auditory cortex (AI): laminar organization and identification of supragranular neurons projecting to area AII. 372 52

Recent evidence suggests that gamma-aminobutyrate has a profound influence on the activity of premotor neurons in the intermediate grey layer of the superior colliculus. In the present study an antibody to glutamate decarboxylase, the synthesizing enzyme for gamma-aminobutyrate, was used to identify and characterize the structures in the intermediate grey layer of the cat that use gamma-aminobutyrate as a transmitter. The material was examined with both the light and electron microscope. Glutamate decarboxylase immunoreactivity was confined, for the most part, to axon terminals. Glutamate decarboxylase positive terminals almost completely cover the soma and proximal dendrites of the large neurons that are characteristic of this layer. Other glutamate decarboxylase positive terminals contact smaller, presumably more distal dendrites. By combining the glutamate decarboxylase immunocytochemistry with the retrograde transport of horseradish peroxidase in single animals, it was demonstrated that the cells of origin of the major descending efferent pathway from the intermediate grey layer, the predorsal bundle, are heavily contacted by glutamate decarboxylase immunoreactive terminals.
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PMID:Glutamate decarboxylase immunoreactivity in the intermediate grey layer of the superior colliculus in the cat. 383 98

The peroxidase-antiperoxidase immunohistochemical technique was used together with an antiserum to gamma-aminobutyric acid (GABA) to identify GABA-containing structures in the rat basolateral amygdala (ABL). Morphological characteristics of GABA-positive neurons in ABL indicate that they correspond to class II, and perhaps class III, local circuit neurons observed in previous Golgi studies. GABA-positive punctate structures resembling axon terminals were observed both in the neuropil and forming peri-cellular baskets around large unlabeled perikarya in ABL. These results suggest that the strong intrinsic inhibition noted in electrophysiological studies of ABL is due primarily to synapses of GABAergic class II neurons with class I projection neurons.
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PMID:Immunohistochemical identification of gamma-aminobutyric acid-containing neurons in the rat basolateral amygdala. 388 76

To study the morphological substrate for interaction between two chemically distinct neuronal types, two double ultrastructural immunolabeling strategies were employed. In the first, two different electron-dense markers were used to examine simultaneously two different neurotransmitter-related antigens in the hypothalamic supraoptic nucleus in the same thin section. Results obtained with the first method were confirmed with a second approach based on postembedding immunostaining of alternate serial thin sections with different antisera. Antiserum against glutamate decarboxylase, the enzyme responsible for the synthesis of the inhibitory amino acid transmitter gamma-aminobutyric acid (GABA), or antisera against GABA, was used to localize immunoreactive axons in the hypothalamic supraoptic nucleus. With light microscopy, glutamate decarboxylase- and GABA-immunoreactive axon terminals immunostained with peroxidase were found arborizing throughout all areas of the nucleus; terminal boutons were found adjacent to unlabeled somata within the nucleus. Cells containing immunoreactive oxytocin, vasopressin, and neurophysin were localized with peroxidase. Glutamate decarboxylase-immunoreactive axons stained with peroxidase prior to embedding in plastic were demonstrated to contact neurons which contained vesicles immunostained with neurophysin antiserum by a post-embedding immunocytochemical procedure which used immunoglobulins or protein A adsorbed to colloidal gold as a second ultrastructural marker. Quantitative evaluation of post-embedding staining with colloidal gold using a neurophysin primary antiserum indicated a specific antigen localization in neurosecretory vesicles. A critical factor in this double-labeling paradigm was that immunological reagents used in the second series did not cross-react with those used in the first series, regardless of the species of origin of antisera. To provide further verification of GABAergic synapses on neurophysin-containing neurons, alternate serial ultrathin sections were stained with colloidal gold using antisera against either neurophysin or GABA; boutons immunoreactive for GABA made synaptic contact with supraoptic neurons containing neurophysin immunoreactivity. Converging results obtained with these two procedures indicate that GABAergic axons synapse directly on neurons containing oxytocin or vasopressin in the rat hypothalamic supraoptic nucleus.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Dual ultrastructural localization of two neurotransmitter-related antigens: colloidal gold-labeled neurophysin-immunoreactive supraoptic neurons receive peroxidase-labeled glutamate decarboxylase- or gold-labeled GABA-immunoreactive synapses. 390 66

Glutamate decarboxylase (L-glutamate l-carboxylase; EC 4.1.1.15), the enzyme in brain that forms gamma-aminobutyric acid, was made visible on sections of rat cerebellum by use of rabbit antiserum to purified mouse-brain glutamate decarboxylase. Cerebellar sections obtained from rats that were perfused with 4% paraformaldehyde were treated with antiserum against the enzyme or with serum from unimmunized rabbits, washed, and then incubated with peroxidase-labeled goat antibody against rabbit immunoglobulin. The glutamate decarboxylase was made visible on sections by means of the product formed by the action of peroxidase on 3,3'-diaminobenzidine and H(2)O(2). A weak and diffuse reaction was observed in Purkinje cell bodies, suggesting the occurrence of the enzyme within these cells. In addition, an intense, punctate deposition of reaction product was located around the Purkinje cells and around the neurons of the deep cerebellar nuclei, suggesting the impingement of many nerve terminals containing the enzyme upon these neuronal surfaces. No specific reaction product was observed in sections treated with serum from unimmunized rabbits. The distribution of glutamate decarboxylase observed in our preparations is consistent with a large body of indirect biochemical, physiological, and morphological data dealing with the synaptic role of gamma-aminobutyric acid neurons in the cerebellum.
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PMID:Immunohistochemical localization of glutamate decarboxylase in rat cerebellum. 413 Dec 74


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