ABSTRACT
The seizure-induced molecular and functional alterations of glutamatergic transmission in the hippocampus have been investigated. Daily repeated epileptic seizures were induced for 12 days by intraperitoneal administration of 4-aminopyridine (4-AP; 4.5 mg/kg) in adult Wistar rats. The seizure symptoms were evaluated on the Racine's scale. One day after the last injection, the brains were removed for in vitro electrophysiological experiments and immunohistochemical analysis. The glutamate receptor subunits NR1, NR2A, NR2B, GluR1, GluR1(flop), GluR2, and KA-2 were studied using the histoblotting method. The semi-quantitative analysis of subunit immunoreactivities in hippocampal layers was performed with densitometry. In the hippocampus, increase of GluR1, GluR1(flop) and NR2B immunostaining was observed in most of the areas and layers. The significant decrease of GluR2 staining intensity was observed in the CA1 and dentate gyrus. Calcium permeability of hippocampal neurons was tested by a cobalt uptake assay in hippocampal slices. The uptake of cobalt increased in the CA1 area and dentate gyrus, but not in the CA3 region following 4-AP treatment. Effects of AMPA and NMDA (N-methyl-d-aspartate) glutamate receptor antagonists (1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine hydrochloride (GYKI 52466) and D-APV respectively) were measured in hippocampal slices using extracellular recording. Analysis of the population spikes revealed the reduced effectiveness of the AMPA receptor antagonist GYKI 52466, while the effect of the NMDA receptor antagonist d-(2R)-amino-5-phosphonovaleric acid was similar to controls. The results demonstrated that repeated convulsions induced structural and functional changes in AMPA receptor-mediated transmission, while NMDA and kainate receptor systems displayed only alterations in receptor subunit composition.
Subject(s)
Gene Expression Regulation/physiology , Hippocampus/metabolism , Hippocampus/physiopathology , Receptors, Glutamate/metabolism , Seizures/pathology , 2-Amino-5-phosphonovalerate/pharmacology , 4-Aminopyridine , Action Potentials/drug effects , Action Potentials/physiology , Animals , Benzodiazepines/pharmacology , Biophysics , Calcium/metabolism , Cobalt/metabolism , Electric Stimulation , Excitatory Amino Acid Antagonists/pharmacology , Gene Expression Regulation/drug effects , Hippocampus/drug effects , Hippocampus/pathology , In Vitro Techniques , Male , Neurons/drug effects , Neurons/metabolism , Protein Subunits/metabolism , Rats , Rats, Wistar , Receptors, Glutamate/classification , Seizures/chemically induced , Seizures/metabolism , Seizures/physiopathology , Synaptic Transmission/drug effects , Synaptic Transmission/physiologyABSTRACT
BACKGROUND: The contribution of brain edema to brain swelling in cases of traumatic brain injury (TBI) remains a critical problem. We believe that inflammatory reactions may play a fundamental role in brain swelling following a head injury. Although possible roles of microglia activation and the release of mediators have been suggested, direct evidence of cellular immune reactivity in diffuse brain injury following closed head trauma is lacking. Accordingly, the objective of this study was to assess the temporal pattern of microglia activation and lymphocyte migration in an experimental model of TBI. METHOD: An impact acceleration TBI model was utilized to induce diffuse brain damage in adult Wistar rats. The animals were separated into three groups: unoperated controls, sham-operated controls and trauma group. At various times after TBI induction (5 min-24 h), rats were perfused transcardially. Sagittal brain sections were analyzed with immunohistochemical markers of CD3 to reveal the presence of T-lymphocytes, and by immunochemistry for the detection of CD11b to reveal microglia activation within the brain parenchyma. FINDINGS: In the control groups, scattered T-cells were found in the brain parenchyma. In the trauma group, TBI induced microglia activation and a transient biphasic T-cell infiltration of the brain parenchyma in all regions was found, beginning as early as 30 min post injury and reaching its maximum values at 45 min and 3 h after trauma induction. CONCLUSION: These results lead us to suggest that the acute response to severe head trauma with early edema formation is likely to be associated with inflammatory events which might be triggered by activated microglia and infiltrating lymphocytes. It is difficult to overestimate the clinical significance of these observations, as the early and targeted treatment of patients with severe head injuries with immunosuppressive medication may result in a far more favorable outcome.
Subject(s)
Brain Injuries/immunology , Head Injuries, Closed/immunology , Immunity, Cellular/immunology , Acceleration , Animals , Brain/immunology , Brain/pathology , Brain Edema/immunology , Brain Edema/pathology , Brain Injuries/pathology , CD11b Antigen/analysis , CD3 Complex/immunology , Disease Models, Animal , Head Injuries, Closed/pathology , Intracranial Pressure/physiology , Lymphocytosis/immunology , Lymphocytosis/pathology , Male , Microglia/immunology , Microglia/pathology , Rats , T-Lymphocytes/immunology , T-Lymphocytes/pathologyABSTRACT
Nerve cells in the substantia nigra pars compacta (SNPC) are known to express tyrosine hydroxylase (TH). By means of light and electron microscopical immunohistochemical techniques, we have shown that the dopaminergic neurons of SNPC express also kynurenine aminotransferase (KAT-I), the enzyme taking part in the formation of kynurenic acid, a neuroprotectant which is one of the endogeneous antagonists of N-methyl-d-aspartate receptors. It was also found that microglial cells and astrocytes express KAT-I. It has been shown that the highly selective dopaminergic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), widely used as a model of Parkinson's disease (PD), affects not only TH of dopaminergic neurons in the SNPC but also their KAT-I immunoreactivity as well: MPTP treatment decreased the number and optical density of KAT-I immunoreactive SNPC neurons. Decrease of KAT-I after MPTP treatment has been proved also by Western blot analysis. MPTP also reduced KAT-I immunoreactivity of microglial cells, except for those involved in reactive gliosis, which were arranged in groups surrounding affected neurons of the SNPC; also the number of KAT-I immunoreactive (IR) astroglial cells was increased in SNPC. We conclude that MPTP treatment may have a dual effect: in addition to being deleterious for neurons expressing TH and KAT-I, it also affects glial cells which could exacerbate the neurodegenerative process characterizing PD.
Subject(s)
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine/pharmacology , Dopamine Agents/pharmacology , Gene Expression Regulation, Enzymologic/drug effects , Substantia Nigra/drug effects , Transaminases/metabolism , Animals , Blotting, Western/methods , CD11b Antigen/metabolism , Cell Count/methods , Female , Glial Fibrillary Acidic Protein/metabolism , Immunohistochemistry/methods , Male , Mice , Mice, Inbred C57BL , Microglia/drug effects , Microglia/metabolism , Microscopy, Immunoelectron/methods , Neurons/drug effects , Neurons/metabolism , Neurons/ultrastructure , Substantia Nigra/metabolism , Substantia Nigra/ultrastructure , Time Factors , Transaminases/genetics , Tyrosine 3-Monooxygenase/metabolismABSTRACT
The immunohistochemical localization of c-fos protein in the CNS neurons was studied in a model of generalized epilepsy induced by the intraperitoneal injection of 4-aminopyridine to adult Wistar rats. This specific blocker of the voltage-dependent potassium channels proved to be suitable for use in the investigation of epileptogenesis. Following the treatment of adult rats with 5 mg kg of 4-aminopyridine, the animals experienced generalized seizures. At the end of the experiment, the rats were briefly anesthetized and perfused with fixative. Frozen coronal plane sections were cut and processed for immunohistochemistry, using polyclonal c-fos antibody. The number and distribution of immunostained cell nuclei in the hippocampus were analyzed in detail with the help of a digital microscope camera and a morphometry program. The highest level of immunostaining was detected in most of the structures at 3 h, but the level had decreased to the control level by 5 h following 4-aminopyridine injection. In the dentate fascia, immunostaining was highest at 1 h and then decreased slowly until 5 h post-injection. The activated neuronal assemblies were analyzed with the aid of parvalbumin c-fos double immunostaining. These countings revealed the highest inhibitory interneuronal activation in every part of the hippocampus (including the dentate fascia) at 3 h post-injection. The results indicate that systemic 4-aminopyridine induces limbic seizures, which are probably initiated in the entorhinal cortex.
Subject(s)
Cell Nucleus/metabolism , Epilepsy, Generalized/metabolism , Hippocampus/metabolism , Neurons/metabolism , Proto-Oncogene Proteins c-fos/metabolism , 4-Aminopyridine , Animals , Epilepsy, Generalized/chemically induced , Male , Rats , Rats, Wistar , Time FactorsABSTRACT
It is widely accepted that Abeta plays a pivotal role in the pathogenesis of Alzheimer's disease (AD) [27]. Attention has been focused mainly on how extracellular Abeta exerts its effects on neuronal cells [7,11,16,32]. However, neuronal degeneration from an accumulation of intracellular Abetax-42 (iAbeta42) occurs in presenilin 1 (PS1) mutant mice without extracellular Abeta deposits [5]. In the present study, intracellular deposits of iAbeta42 are correlated with apoptotic cell death in AD and PS-1 familial AD (PS1 FAD) brains by means of triple staining with antibodies to Abeta, TUNEL, and staining with Hoechst 33342. Neurons simultaneously positive for iAbeta42 and the TUNEL assay were significantly more abundant in AD brains than in controls. The number of apoptotic neurons with intracellular neurofibrillary tangles (iNFTs) was insignificant. Our results indicate that intraneuronal deposition of a neurotoxic form of Abeta seems to be an early event in the neurodegeneration of AD.
ABSTRACT
The central regulation of the preovulatory LH surge requires a complex sequence of interactions between neuronal systems that impinge on LH-releasing hormone (LHRH)-synthesizing neurons. The reported absence of estrogen receptors (ERs) in LHRH neurons indicates that estrogen-receptive neurons that are afferent to LHRH neurons are involved in mediating the effects of this steroid. We now present evidence indicating that central histaminergic neurons, exclusively located in the tuberomammillary complex of the caudal diencephalon, serve as an important relay in this system. Evaluation of this system revealed that 76% of histamine-synthesising neurons display ERalpha-immunoreactivity in their nucleus; furthermore histaminergic axons exhibit axo-dendritic and axo-somatic appositions onto LHRH neurons in both the rodent and the human brain. Our in vivo studies show that the intracerebroventricular administration of the histamine-1 (H1) receptor antagonist, mepyramine, but not the H2 receptor antagonist, ranitidine, can block the LH surge in ovariectomized estrogen-treated rats. These data are consistent with the hypothesis that the positive feedback effect of estrogen in the induction of the LH surge involves estrogen-receptive histamine-containing neurons in the tuberomammillary nucleus that relay the steroid signal to LHRH neurons via H1 receptors.
Subject(s)
Brain/metabolism , Histamine/metabolism , Neurons/metabolism , Receptors, Estrogen/metabolism , Animals , Brain/cytology , Gonadotropin-Releasing Hormone/biosynthesis , Histamine H1 Antagonists/pharmacology , Histamine H2 Antagonists/pharmacology , Humans , Luteinizing Hormone/blood , Mammillary Bodies/metabolism , Neurosecretory Systems/physiology , Rats , Tissue Distribution/physiologyABSTRACT
The neurons of the thalamic reticular nucleus are among the main targets of corticothalamic projections and their vulnerability in pathological conditions is well established. The present experiments aimed at the description and immunocytochemical characterization of the neurons of the thalamic reticular nucleus activated in neocortical seizures. Focal seizures were induced by the topical application of isotonic, isohydric 4-aminopyridine solution to the sensorimotor neocortex of adult, anesthetized Wistar rats. The animals were perfused with fixative after 1 and 2 h of recorded seizure activity. Coronal plane vibratome sections were incubated with cocktails of polyclonal c-fos and monoclonal parvalbumin antisera. Labeled cells in the thalamic reticular nucleus were counted and related to total cell counts. Neurons and neuropil showed strong parvalbumin immunoreactivity. Double-stained sections revealed that 55.32% of the parvalbumin-positive cell population expressed c-fos protein in their cell nuclei at the end of the 1 h seizure period. This ratio decreased to 43.5% following 2 h seizure. Labeled cells, although less in number were also observed in the contralateral thalamic reticular nucleus. Since parvalbumin labels GABAergic cells, it is tempting to speculate that this activation of intrathalamic inhibiton might exert an important anticonvulsant protection on other thalamic nuclei.
Subject(s)
Epilepsy, Absence/metabolism , Geniculate Bodies/metabolism , Motor Cortex/metabolism , Neurons/metabolism , 4-Aminopyridine/pharmacology , Animals , Cell Count , Electroencephalography , Epilepsy, Absence/chemically induced , Epilepsy, Absence/physiopathology , Geniculate Bodies/drug effects , Geniculate Bodies/physiopathology , Male , Motor Cortex/drug effects , Motor Cortex/physiopathology , Neurons/drug effects , Neurons/physiology , Parvalbumins/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Rats , Rats, WistarABSTRACT
The cholinergic neuronal structures and their synaptic connections in the main olfactory bulb of adult rats were analysed by using choline acetyltransferase immunocytochemistry. Within the glomeruli, cholinergic nerve fibers were restricted to strands which subdivided the neuropil into small compartments, the interior of which contained sensory axons but was devoid of cholinergic axons. Small numbers of choline acetyltransferase neurons were detected in all layers. Ultrastructural analysis revealed selective triadic synaptic relationships with different neuron classes in the intraglomerular area and in the external plexiform layer. These triads were made up of (i) a cholinergic axon, (ii) one or several periglomerular or granule cell dendrites, and (iii) usually one relay cell dendrite. In these triads, asymmetric cholinergic synapses were selectively focused on dendrites (gemmules and spines) of periglomerular or granule cells. Within the glomerulus, mitral and tufted cell dendrites were closely apposed to some cholinergic axon varicosities, most abundantly near arborizations of the apical dendrites. However, cholinergic synapses were never seen on any relay cell dendrite. In the external plexiform layer, cholinergic synapses were present on all parts of the superficial short-axon cells. In the internal plexiform layer and the granule cell layer, cholinergic axon varicosities exhibited close apposition or asymmetric synapses with granule cell gemmules. The data suggest that cholinergic projections from the basal forebrain to the main olfactory bulb focus synaptic innervation on interneurons. On relay cells, direct acetylcholine effects may occur, but these must be based on non-synaptic acetylcholine release at the surface of their dendrites.
Subject(s)
Choline O-Acetyltransferase/immunology , Cholinergic Fibers/physiology , Olfactory Bulb/physiology , Presynaptic Terminals/ultrastructure , Animals , Immunohistochemistry , Microscopy, Electron , Neural Pathways/physiology , Prosencephalon/physiology , Rats , Rats, WistarABSTRACT
The distributions of axons immunoreactive for [Leu]- or [Met]enkephalin and GABA were studied in the superior cervical ganglion of adult rats. The antigens were visualized separately and in combination with neuropeptide Y by the immunoperoxidase technique, using reaction end-products of different colors. Similarities and differences were found in the light-microscopic innervation patterns of enkephalin- and GABA-immunoreactive nerve fibers. Both fiber systems were heterogeneously distributed within the superior cervical ganglion, forming denser networks in its rostral part than elsewhere in the ganglion. The appearance of labeled nerve fibers differed in the two systems. Enkephalin-immunoreactive axons exhibited dotted profiles due to a strong immunoreaction in the axonal varicosities as compared with that in the intervaricose segments, whereas GABA-positive fibers were evenly labeled in both parts of the axons. The most marked difference between the innervation patterns from enkephalin- and GABA-immunoreactive axons was the presence of bundles of varicose axons in conjunction with the basket-like aggregation of enkephalin-immunoreactive nerve terminals. The possibility that enkephalins and GABA are co-localized in certain axons was excluded in double-labeling studies, silver intensification being used for the first antigen and the nickel-enhanced diaminobenzidine reaction for the second antigen. Different subsets of principal neurons were richly innervated in a basket-like manner by axons immunoreactive for enkephalins and GABA. Additionally, combined staining with antisera against either enkephalin and neuropeptide Y or GABA and neuropeptide Y revealed that both subsets of principal neurons richly innervated either by enkephalin-immunoreactive or by GABA-immunoreactive axons were devoid of neuropeptide Y immunoreactivity. Thus, the enkephalinergic and GABAergic axons have different subpopulations of neuropeptide Y-negative principal neurons as targets in the superior cervical ganglion. These results provide further evidence that sympathetic ganglion cells can be classified on the basis of their receiving input from different sources.
Subject(s)
Axons/physiology , Enkephalins/metabolism , Ganglia, Sympathetic/physiology , Neurons/physiology , Neuropeptide Y/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Axons/metabolism , Female , Ganglia, Sympathetic/metabolism , Immunohistochemistry , Male , Neurons/metabolism , Rats , Rats, Wistar , Tissue DistributionABSTRACT
Neurochemical and immunohistochemical evidence suggests that the superior cervical ganglion (SCG) contains all components of a gamma-aminobutyric acid (GABA)ergic transmission system, which includes GABAergic axons of unknown origin. The number of nerve fibers with and without GABA-like immunoreactivity was determined in interganglionic connectives at all cervical and thoracic levels of the paravertebral sympathetic trunk. In addition, the distribution of GABA-immunoreactive (IR) neurons was established within the ganglion chain and compared with the relative frequency of principal neurons richly innervated by GABA-IR axon terminals. The following results were obtained: 1) the total number of nerve fibers in cross sections did not significantly vary between the cervical levels, but it increased steadily from upper to lower thoracic segments; 2) in contrast, the number of GABA-IR fibers decreased from the cervical sympathetic trunk below the SCG (approximately 300 fibers) down to the seventh to tenth thoracic ganglion, below which no such fiber was seen; 3) GABA-IR nerve fibers originate from a subclass of GABA-IR cells; these are small, bipolar neurons with predominantly ascending, unmyelinated axon-like processes; 4) the number of principal neurons richly innervated by GABA-IR nerve fibers decreased from the SCG to the upper thoracic ganglia, and was very small below; and 5) apart from basket-like innervation, GABA-IR axons also formed diffuse networks around GABA-negative principal neurons predominantly in cervical and upper thoracic ganglia. These data suggest that the GABAergic innervation of paravertebral sympathetic ganglia is more complex than previously suspected. What appears as preganglionic afferents from several spinal segments (C8-Th7) innervate GABAergic neurons in the sympathetic trunk which have ascending axons and focus their inhibitory effects on the cervical sympathetic ganglia, predominantly the SCG. These data suggest that GABAergic small interganglionic neurons form a feed-forward inhibition system, which may be driven by multisegmental spinal input in the paravertebral sympathetic ganglion chain.
Subject(s)
Ganglia, Sympathetic/chemistry , Neural Inhibition , gamma-Aminobutyric Acid/analysis , Afferent Pathways/chemistry , Afferent Pathways/cytology , Animals , Axons/ultrastructure , Ganglia, Sympathetic/cytology , Myelin Sheath/ultrastructure , Nerve Fibers/chemistry , Nerve Fibers/ultrastructure , RatsABSTRACT
After peripheral transection of the facial nerve, immunostaining of astrocytic gap junction protein changed in the corresponding brainstem nucleus of the rat. Enhanced connexin-43 immunoreactivity was restricted to the ipsilateral facial nucleus and to astrocytes surrounding lesioned motoneurons. This reaction is focally distinct, and marks only a part of the astrocytic network indicating a local plasticity of intercellular coupling. These results suggest that astrocytes work as sensors of signals which either depend on the integrity of neighboring neurons or inform about neuronal disorders.
Subject(s)
Astrocytes/metabolism , Brain Stem/physiology , Facial Nerve/physiology , Membrane Proteins/metabolism , Animals , Astrocytes/immunology , Axons/physiology , Brain Stem/immunology , Brain Stem/metabolism , Connexins , Facial Nerve/immunology , Facial Nerve/metabolism , Immunohistochemistry , Membrane Proteins/immunology , Motor Neurons/immunology , Motor Neurons/physiology , Nerve Degeneration/drug effects , Neuronal Plasticity/drug effects , Neuronal Plasticity/physiology , Rats , Up-Regulation/drug effectsABSTRACT
Morphological features of nerve fibers and synapses containing GABA and [Met]enkephalin were studied at the light and electron microscopic levels in the superior cervical ganglia of rats by pre- and postembedding immunohistochemistry. Both GABA and [Met]enkephalin immunoreactivities were found in varicose nerve fibers, forming diffuse networks which were denser in the rostral than in the caudal part of each ganglion. For both antigens rich and basket-like innervation was observed around some of the principal neurons. The GABA-immunoreactive fibers were evenly stained, while in case of [Met]enkephalin-positive nerve fibers the varicosities showed intensive immunopositivity only. Postembedding immunochemistry revealed that both inhibitory substances were located in axon varicosities which established asymmetric synapses of Gray I type. Fine structural investigation revealed that GABA-like immunoreactivity was confined in the nerve endings to the clear synaptic vesicles of 40 nm diameter, whereas the immunogold particles, indicating the occurrence of [Met]enkephalin, were located over the large dense-cored vesicles of 120 nm diameter. The clear and dense-cored vesicles were, however, mixed in the nerve endings labeled by either neurotransmitter substance. Interestingly, the [Met]enkephalin-immunopositive axon terminals were found, consequently, in synaptic contacts with dendrites containing dense bodies in a row underlying the postsynaptic membrane thickening. Since nerve terminals with GABA-like immunoreactivity established synapses of Gray I type without such subjunctional bodies, one can reasonably assume that, in spite of similarities in termination pattern, there is no co-existence of GABA and enkephalin in the axons in the superior cervical ganglion.
Subject(s)
Enkephalin, Methionine/analysis , Ganglia, Sympathetic/cytology , Nerve Endings/ultrastructure , Nerve Fibers/ultrastructure , Neurons/cytology , Synapses/ultrastructure , gamma-Aminobutyric Acid/analysis , Animals , Axons/ultrastructure , Dendrites/ultrastructure , Ganglia, Sympathetic/ultrastructure , Immunohistochemistry , Microscopy, Immunoelectron , Neurons/ultrastructure , Rats , Rats, WistarABSTRACT
We examined the distribution of gamma-aminobutyric acid-like immunoreactivity (GABA-LI) in the rat kidney by light and electron microscopy. In vibratome sections, GABA-LI was present in both the renal medulla and cortex. The inner stripe of the outer medulla was most heavily and almost homogeneously labeled, whereas GABA-LI in the cortex was mainly confined only to some tubules. GABA-positive structures involved the epithelial cells of the thin and the thick ascending limbs of the loop of Henle, the connecting tubules, and the collecting ducts. In GABA-positive connecting tubules and collecting ducts the immunoreactivity was present in the cytoplasm of about half of the epithelial cells. As revealed by electron microscopy, the labeled cells in the collecting tubules were the light (principal) cells. No GABA-LI occurred in neuronal structures. These findings are consistent with the presence of a non-neuronal GABA system in the rat kidney. Furthermore, the specific distribution of GABA in the tubular epithelium suggests a functional significance of this amino acid in tubular transport processes.
Subject(s)
Kidney/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Immunohistochemistry , Kidney/ultrastructure , Male , Microscopy, Electron , Neurons/metabolism , RatsABSTRACT
The cholinergic innervation of the mouse superior cervical ganglion was investigated by means of immunocytochemistry using a well-characterized monoclonal antibody against choline acetyltransferase (ChAT). Immunopositive nerve fibers entered the superior cervical ganglion from the cervical sympathetic trunk. Light-microscopically, these fibers appeared to be heterogeneously distributed among the principal ganglion cells. The rostral part of the ganglion contained more ChAT-positive fibers then the middle or the caudal one. The axons branched several times before forming numerous varicosities. Most of the ChAT-stained fibers and varicosities aggregated in glomerula-like neuropil structures that were surrounded by principal ganglion cell bodies, whereas others were isolated or formed little bundles among principle neurons. None of the neurons or other cell types in the ganglion exhibited ChAT-positivity. ChAT-immunoreactive fibers disappeared from the ganglion 5 or 13 days after transection of the cervical sympathetic trunk. At the ultrastructural level, most axon terminals and synapses showed ChAT-immunoreactivity. An ultrastructural analysis indicated that immunostained synapses occurred directly on the surface of neuronal soma (1.8%) and dendritic shafts (17.6%). Synapses were often seen on soma spines (18.4%) and on dendritic spines (62.2%). All immunoreactive synapses were of the asymmetric type. The results provide immunocytochemical evidence for a heterogeneous cholinergic innervation of the ganglion and the principal neurons.
Subject(s)
Choline O-Acetyltransferase/metabolism , Ganglia, Sympathetic/enzymology , Animals , Antibodies, Monoclonal/immunology , Axons/enzymology , Axons/ultrastructure , Choline O-Acetyltransferase/immunology , Female , Ganglia, Sympathetic/ultrastructure , Immunohistochemistry , Male , Mice , Microscopy, Electron , Nerve Fibers/enzymology , Nerve Fibers/ultrastructure , Synapses/enzymology , Synapses/ultrastructureABSTRACT
The distribution of gamma-aminobutyric acid (GABA) in the rat kidney was examined by immunocytochemical techniques. GABA-like immunoreactivity (GABA-LI) was predominantly confined to the renal tubules, including the ascending parts of the distal tubules, and the loops of Henle, the collecting tubules and ducts, and the connective parts of the convoluted tubules. In GABA-positive cortical tubules, about half of the epithelial cells were labelled. The labelled cell type showed the ultrastructural features of principal cells. Depolarizing stimulation by ouabain and high K+ concentration evoked the efflux of endogenous GABA from kidney slices. The present findings, along with previous results, suggest that GABA released from renal tubular epithelium, and transported with the urine, might be involved in the modulation of contractility in the urinary tract.
Subject(s)
Kidney Tubules/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Chromatography, High Pressure Liquid , Epithelium/drug effects , Epithelium/metabolism , Immunohistochemistry , Kidney Tubules/drug effects , Male , Microscopy, Electron , Ouabain/pharmacology , Potassium/pharmacology , Rats , Spectrometry, FluorescenceABSTRACT
Choline acetyltransferase immunocytochemistry was used to detect the presence and distribution of cholinergic through-fibers in the superior cervical ganglion of adult mice. The results revealed a great number of choline acetyltransferase-positive axons in the cervical sympathetic trunk and the varicose terminal axons involved in the innervation of the principal ganglionic cells within the ganglion. Immunostained axons were scarce or absent in the external or internal carotid nerves. The immunocytochemical results argue against the physiological importance of cholinergic through-fibers in the postganglionic nerves.
Subject(s)
Choline O-Acetyltransferase/analysis , Ganglia, Sympathetic/chemistry , Animals , Carotid Arteries/innervation , Female , Immunoenzyme Techniques , Male , Mice , Mice, Inbred Strains , Nerve Fibers/chemistryABSTRACT
The distribution of gamma-aminobutyric acid (GABA)-like and glutamate decarboxylase (GAD)-like immunoreactivity was studied in the cervical sympathetic ganglion complex of rats, including the intermediate and inferior cervical ganglia and the uppermost thoracic ganglion. GABA-positive axons may enter the ganglion complex via its caudal end. Others apparently arise from small GABA-positive cell bodies which are scattered among principal neurons, within clusters of SIF cells and in bundles of GABA-negative axons. The majority of these cells is located in the lower half of the ganglion complex. Principal neurons did not react with antibodies against GABA or GAD. An unevenly distributed mesh-work of GABA-immunoreactive axons was seen in each of the ganglia. Immunoreactive axons formed numerous varicosities. Some of them were aggregated in a basket-like form around a subpopulation of GABA-negative principal ganglion cell bodies. Electron-microscopic immunocytochemistry revealed that GABA-positive nerve fibers establish asymmetric synaptic junctions with dendritic and somatic spines of principal neurons, whereas postsynaptic densities are inconspicuous or absent on dendritic shafts and somata. The results suggest that in the cervical sympathetic ganglion complex principal neurons are not GABAergic, but are innervated by axons which react with both antibodies against GAD and/or GABA antibodies and originate from a subpopulation of small neurons.
Subject(s)
Ganglia, Sympathetic/metabolism , Glutamate Decarboxylase/metabolism , gamma-Aminobutyric Acid/metabolism , Animals , Axons/metabolism , Axons/ultrastructure , Cervical Vertebrae , Female , Ganglia, Sympathetic/cytology , Ganglia, Sympathetic/ultrastructure , Immunohistochemistry , Male , Microscopy, Electron , Rats , Rats, Inbred StrainsABSTRACT
The immunomorphological characteristics of interstitial macrophages with PAS-positive granules were studied in experimental Escherichia coli pyelonephritis in rats, using an anti-E. coli antibody. Immunohistochemical, immunoelectron microscopical, as well as light- and electron microscopical findings were compared at twelve time points between 2 days and 13 weeks after infection. Macrophages with PAS-positive granules were present in the inflammatory infiltrates from the 7th day. The granules were phagolysosomes, filled predominantly with myelin figures. The myelin figures originated mainly from the constituents of the bacterial wall and reacted with the anti-E. coli antibody even 13 weeks after infection. The storage of bacterial residues with preserved antigenic structures for several weeks after infection indicates disturbed phagolysosomal elimination of the bacterial substances in the PAS-positive macrophages. In the formation of macrophages with PAS-positive granules, lysosomal overloading with large amounts of bacteria and cell debris is assumed, leading to consumption of the lysosomal enzymes, consequent incomplete breakdown and retention of the bacterial residues.
Subject(s)
Antigens, Bacterial/analysis , Escherichia coli/isolation & purification , Macrophages/microbiology , Pyelonephritis/microbiology , Animals , Cytoplasmic Granules/pathology , Escherichia coli/immunology , Immunoenzyme Techniques , Immunohistochemistry , Kidney Tubules/pathology , Lymphocytes/pathology , Lysosomes/pathology , Macrophages/pathology , Male , Microscopy, Immunoelectron , Necrosis , Neutrophils/pathology , Periodic Acid-Schiff Reaction , Pyelonephritis/pathology , Rats , Rats, Inbred StrainsABSTRACT
The superior cervical ganglion of rats contains a considerable number of nerve fibers with GABA-like immunoreactivity which show a nonuniform distribution within the ganglion. The topography of these fibers has been analyzed by using antibodies raised against GABA-BSA-glutaraldehyde complexes. GABA-positive axons and axon varicosities accumulated around a subpopulation of principal ganglion cells forming basketlike patterns. These neurons richly innervated by GABA-positive axons (RIG-neurons) in turn were aggregated in patches with strong immunoreactivity. The size and packing density of the patches containing RIG-neurons and GABA-positive axons approaching them had rostral-to-caudal and medial-to-lateral gradients. Similar patterns were found in right and left ganglia. In five ganglia, a quantitative analysis revealed on average 1,344 RIG-neurons per ganglion representing about 5% of the total neuron population, with small variations (standard deviation 122) despite the highly variable shape of the ganglia. The distribution of RIG-neurons resembles that of neurons sending their axons into the internal carotid nerve. To check this possible correlation, HRP was injected into the eye and applied to the transected external carotid nerve. Double staining for the retrogradely transported peroxidase and GABA immunohistochemistry revealed that RIG-neurons formed a small subpopulation of retrogradely labelled neurons in both experiments. This suggests that RIG-neurons innervate various target organs. This conclusion is in agreement with the observation that RIG-neurons also exist in other sympathetic ganglia. Data presented suggest that sympathetic ganglion cells can be classified on the basis of non-uniform innervation patterns formed by axons that use different neurotransmitters.
Subject(s)
Ganglia, Sympathetic/cytology , gamma-Aminobutyric Acid/metabolism , Animals , Axons/metabolism , Cell Count , Ganglia, Sympathetic/metabolism , Immunohistochemistry , Male , Rats , Rats, Inbred StrainsABSTRACT
By the immunohistochemical demonstration of SR calcium ATPase and myoglobin a fibre classification method was developed. Fast fibres showed intense, while slow fibres weak SR calcium ATPase reactivity. Immunohistochemical reaction of myoglobin characterized the oxidative metabolic state of fibres similar to the succinate dehydrogenase (SDH) reaction. By means of SR calcium ATPase and myoglobin immunohistochemistry fibres were classified as slow oxidative (SO), fast oxidative glycolytic (FOG) and fast glycolytic (Fg) groups. The SR calcium ATPase activity of the different fibres varied in the FG greater than FOG greater than SO order, while myoglobin immunoreactivity in the FOG greater than SO greater than FG order. Both proteins studied preserved their antigenicities in Bouin's fixative or in formol-acetate and paraffin embedding. The light microscopic immunogold-silver method was found suitable also for electron microscopy. The silver intensification of small particle-size (5 nm) gold conjugate results in a reaction with the joint advantages of high sensitivity and optimal visibility. The described immunohistochemical method proved to be suitable for the retrospective differentiation of human biopsy materials.