Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P20366 (substance P)
 21,176 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The distribution of substance P-like (SP) and vasoactive intestinal polypeptide-like (VIP) structures was studied using an indirect immunoperoxidase technique in the mediterranean barbel Barbus meridionalis and in the rainbow trout Salmo gairdneri. SP-like positive fibers were observed in the inner strata of the mediterranean barbel olfactory bulb, mainly the granule cell and the plexiform layers. Ganglion cells and fibers of the terminal nerve were also labeled. No SP-positive structure was found in the olfactory bulb of the rainbow trout. On the contrary, the VIP antiserum used displayed very strong immunostaining in the olfactory nerve fiber layer of Salmo gairdneri, whereas those fibers in Barbus meridionalis showed no immunoreactivity. After a complete transection of the olfactory tract and a survival time of 20 days, SP-immunostained fibers were not observed. Thus, they can presumably be identified as centrifugal fibers, coursing from the telencephalic hemispheres through the olfactory tracts, into the olfactory bulb. The VIP immunoreactivity was confined to the olfactory fibers, both in the olfactory nerve and the olfactory bulb. The positive immunostaining disappeared after chemical lesion of the olfactory mucosa. These observations demonstrate that the olfactory bulb of freshwater teleosts exhibits a high degree of heterogeneity in its immunocytochemical distribution pattern, this pattern also differing from previous reports on higher vertebrates.
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PMID:Interspecies differences in the substance P- and vasoactive intestinal polypeptide-like immunoreactivities in the olfactory bulb of Salmo gairdneri and Barbus meridionalis. 169 Aug 15

1. The effects of 5-hydroxytryptamine3 (5-HT3) receptor antagonists on the behavioural hyperactivity response which results from injection of the neurokinin receptor agonist [pGlu5, MePhe8, Sar9]-substance P (5-11) (DiMe-C7) into the ventral tegmental area (VTA) of the rat midbrain have been determined. 2. Subcutaneous administration of ondansetron (GR38032) (0.001-0.3 mg kg-1), GR65630 (0.01 mg kg-1), ICS 205-930 (0.1 mg kg-1) and MDL 72222 (0.1 mg kg-1), inhibited the DiMe-C7-induced hyperactivity response. 3. The effects of ondansetron on DiMe-C7-induced changes in dopamine and 5-HT metabolism in discrete areas of rat forebrain were studied in order to investigate further the possible mechanism of action of 5-HT3 antagonists in modifying mesolimbic dopaminergic systems. 4. Intra-VTA administration of DiMe-C7 increased levels of dihydroxyphenylacetic acid (DOPAC) in the nucleus accumbens, olfactory tubercules and right amygdala, indicating increased mesolimbic dopamine metabolism. DOPAC levels were not significantly increased in the frontal cortex, left amygdala or striatum. Dopamine levels were not altered in any of these brain areas. DiMe-C7 also increased 5-hydroxyindoleacetic acid (5-HIAA) levels in the amygdala but this was only statistically significant in the right amygdala. 5-HT levels were not changed significantly by DiMe-C7 treatment. 5. In control rats, pretreatment with ondansetron (0.1 mg kg-1) had no effect on the levels of dopamine, 5-HT or their metabolites, but in rats given DiMe-C7, ondansetron significantly inhibited the increase in DOPAC levels in the nucleus accumbens. 6. These results are in agreement with the proposed facilitatory role of 5-HT3 receptor activation on mesolimbic dopaminergic transmission, and suggest that 5-HT3 antagonists may have important therapeutic indications for the treatment of CNS disorders in which mesolimbic dopamine systems are perturbed.
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PMID:Effect of 5-HT3 receptor antagonists on responses to selective activation of mesolimbic dopaminergic pathways in the rat. 169 72

The respiratory and olfactory mucosae of rats and mice were examined at ultrastructural levels for the presence of intraepithelial nerve endings. Immunocytochemical studies utilizing antisera directed against substance P and calcitonin gene-related peptide (CGRP) revealed numerous intraepithelial peptide-immunoreactive fibers near the basal region of the epithelium. Occasional transepithelial fibers were observed to extend outward to nearly reach the epithelial surface. In no cases, however, did the transepithelial fibers reach the surface, but instead, stopped at the line of tight junctions approximately 1 micron from the surface. No specialized contacts between the nerve fibers and the epithelial cells were observed. The transepithelial fibers provide a possible anatomical substrate for the sensitivity of the trigeminal nerve to many air-borne chemical stimuli. That potential chemical stimuli must traverse the tight-junctional barrier may explain why lipid solubility is related to effectiveness for trigeminal stimuli.
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PMID:Ultrastructure of substance P- and CGRP-immunoreactive nerve fibers in the nasal epithelium of rodents. 169 45

In the search for particular neurons that stain selectively and can be identified, the cerebral ganglia (brains) of the crayfish Cherax destructor and the crab Leptograpsus variegatus were immunocytochemically treated with a monoclonal antibody raised against substance P. Four large neurons in the cerebral ganglion of the crayfish and crab label selectively with a monoclonal antibody raised against substance P. Two of the large neurons have their cell bodies in the protocerebrum and two in the deutocerebrum in both animals. Each protocerebral cell in both animals projects through the ipsilateral and contralateral olfactory lobes to end among the lateral cell somata of the olfactory lobe and not in the neuropile. Electron micrographs show the presence of synapses within the cell somata area and on the cell somata themselves. Each deutocerebral cell in both animals projects only ipsilaterally and ends within the neuropile of the olfactory lobes. The immunoreactivity to substance P antibody and the shapes and the unique projections of the four cells suggest that they are homologous in the two species. Synaptic connections between axons and cell somata are rare in the arthropods but have been found on the Kenyon cells of the mushroom bodies of Limulus. This raises questions about homologies between the crustacean olfactory lobe and the mushroom bodies of Limulus and insects.
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PMID:Substance P antibody reveals homologous neurons with axon terminals among somata in the crayfish and crab brain. 169 54

The distribution and incidence of substance P (SP)- and Met-enkephalin-Arg6-Gly7-Leu8 (ENK-8)-like immunoreactive granule cells in the main and accessory olfactory bulbs of male rats was studied immunohistochemically. In the granule cell layer of the main olfactory bulb, numerous ENK-8-like immunoreactive granule cells were observed but SP-like immunoreactive ones were rare (less than 1%). On the other hand, in the granule cell layer of the accessory olfactory bulb, both SP-like immunoreactive and ENK-8-like immunoreactive granule cells were numerous. 15-20% of these neurons contained both the peptides.
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PMID:Peptidergic granule cell populations in the rat main and accessory olfactory bulb. 169 71

The family of mammalian tachykinin receptors consists of substance P receptor (SPR), neuromedin K receptor (NKR) and substance K receptor (SKR). In this investigation, tissue and regional distributions of the mRNAs for the three rat tachykinin receptors were investigated by blot-hybridization and RNase-protection analyses using the previously cloned receptor cDNAs. SPR mRNA is widely distributed in both the nervous system and peripheral tissues and is expressed abundantly in the hypothalamus and olfactory bulb, as well as in the urinary bladder, salivary glands and small and large intestines. In contrast, NKR mRNA is predominantly expressed in the nervous system, particularly in the cortex, hypothalamus and cerebellum, whereas SKR mRNA expression is restricted to the peripheral tissues, being abundant in the urinary bladder, large intestine, stomach and adrenal gland. Thus, the mRNAs for the three tachykinin receptors show distinct patterns of expression between the nervous system and peripheral tissues. Blot-hybridization analysis in combination with S1 nuclease protection and primer-extension analyses revealed that there are two large forms of SKR mRNA expressed commonly in the peripheral tissues, and two additional small forms of the mRNA expressed specifically in the adrenal gland and eye. These analyses also showed that the multiple forms of SKR mRNA differ in the lengths of the 5' mRNA portions, and that the two small forms of the mRNA, if translated, encode a truncated SKR polypeptide lacking the first two transmembrane domains. This investigation thus provides the comprehensive analysis of the distribution and mode of expression of the mRNAs for the multiple peptide receptors and offers a new basis on which to interpret the diverse functions of multiple tachykinin peptides in the CNS and peripheral tissues.
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PMID:Tissue distribution and quantitation of the mRNAs for three rat tachykinin receptors. 170 Nov 45

Density and pattern of nerve fibers with neuropeptide Y-like immunoreactivity (NPY-LI) and substance P-like immunoreactivity (SP-LI) in the rat dura mater encephali were investigated by light and electron microscopy using whole-mount preparations. NPY-LI fibers are observed throughout the encephalic dura mater. A remarkable net of NPY-LI nerve fibers is located in the walls of the sagittal and transverse sinuses. Beyond that NPY-LI network, distinct NPY-LI nerve fibers or plexus occur in the rostral falx, parietal dura mater of the olfactory bulb, supratentorial dura mater, parietal dura mater of the cerebellum, tentorium cerebelli and the ventral dura mater. Electron microscopic studies reveal that NPY-LI is exclusively located in unmyelinated axons of small and large nerve fiber bundles, with or without a perineural sheath. Immunopositive C-fibers are predominantly associated with the vascular bed. SP-LI nerve fibers have a moderate and more uniform distribution in the encephalic dura mater. A distinct plexus of SP-LI fibers follows the branches of the middle meningeal artery and the adjacent dura mater. SP-LI fibers are most prominent in the parietal dura mater of the cerebellum. Fine beaded SP-LI fibers, arising from larger SP-LI fiber bundles, are observed in close association to the capillary bed. SP-LI axons are all unmyelinated. They are found in larger nerve fiber bundles with a perineural sheath or in Schwann cells lacking any perineural sheath. The function of NPY-LI and SP-LI nerve fibers in the rat dura mater is discussed in relation to their topography, density and termination.
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PMID:Neuropeptide Y- and substance P-like immunoreactive nerve fibers in the rat dura mater encephali. 170 Dec 89

The autoradiographic distribution of neurokinin (NK)-1 receptors was visualized in the rat brain using the highly selective ligand, [3H]-[Sar9,Met(O2)11]-substance P. This ligand apparently binds to a single class of high affinity (Kd = 1.4 +/- 0.5 nM), low capacity (Bmax = 160 +/- 3.0 fmol/mg protein) sites in rat brain membrane preparations. The ligand selectivity profile reveals that substance P (SP) and unlabeled [Sar9,Met(O2)11]-SP are potent competitors of [3H]-[Sar9,Met(O2)11]-SP binding while NK-2 and NK-3 analogues are virtually inactive demonstrating the selectivity of this radioligand for the NK-1 receptor class. Autoradiographic data show that [3H]-[Sar9,Met(O2)11]-SP binding sites are broadly but discretely distributed in rat brain, the highest densities of sites being located in the external plexiform layer of the olfactory bulb, striatum, olfactory tubercule, amygdala-hippocampal area, endopiriform and entorhinal cortices, superior colliculus, locus coeruleus and substantia gelatinosa of the spinal cord. This distribution is similar, but not identical, to that previously reported for NK-1 sites using less selective ligands such as [125I]Bolton-Hunter SP. For example, some difference in labelling patterns are observed in the hippocampal formation. This could be explained by the existence of NK-1 receptor subtypes, only one of them being recognized by [3H]-[Sar9,Met(O2)11]-SP or by the greater selectivity of this radioligand for NK-1 over NK-2 and NK-3 receptor classes.
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PMID:Autoradiographic distribution of brain neurokinin-1/substance P receptors using a highly selective ligand [3H]-[Sar9,Met(O2)11]-substance P. 170 54

Substance P (SP)-ir and opioid-ir structures were studied in the cat main olfactory bulb (MOB), accessory olfactory bulb (AOB), and olfactory peduncle. In the MOB, the opioid-ir and the majority of the SP-ir neurons belong to the granule cell type. SP-ir granule cells reside in the deeper granule cell layer, whereas opioid-ir granule cells reside in the superficial granule cell layer, internal plexiform, and mitral cell layer. Many granule cells are observed in the external plexiform and glomerular layer. Other granule cells were found in the bulbar/peduncular white matter, the taenia tecta, and the genu of the corpus callosum. A new substance P-ir cell type was identified in the glomerular layer. This cell type was also identified by using the technique of intracellular injection of Lucifer Yellow. The cell type corresponds neither to the external tufted type nor to the short axon cell types described so far. The AOB resembles the MOB with respect to large numbers of SP-ir and opioid-ir granule cells. In addition, a few opioid-ir neurons, probably superficial mitral cells, were found in the glomerular layer. The AOB is surrounded by islands of immunoreactive granule cells, which connect to the granule cell layer by extremely long processes. Opioid-ir and SP-ir beaded axons pass through the olfactory peduncle terminating on granule cells, and ascend as far as the glomerular layer. All subdivisions of the anterior olfactory nucleus (AON) contain immunoreactive terminal fields. Afferent fibers and terminal plexuses derive from a population of immunoreactive neurons located predominantly in the region of the septo-olfactory junction. They have large somata. Their axons form recurrent collaterals, some of which run rostrally in the peduncular white matter. Others ascend caudally towards the septal region. The fibers seem to remain ipsilaterally, since the olfactory limb of the anterior commissure and the commissure proper are devoid of SP-ir and opioid-ir fibers. During development SP and opioid immunoreactivity were found only in differentiated granule cells. The peptides were not detectable in migrating or immature granule cells, as identified in Golgi-impregnated material. The granule cell population largely develops during postnatal life. The number of opioid-ir granule cells increases slowly and continuously, reaching the adult level not before the sixth postnatal month. Strikingly, SP-ir granule cell number increases fast and reaches a transient peak during the second month. Thereafter it declines (40% decrease) to the adult density, which is similar to that of opioid-ir granule cells.
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PMID:Substance P- and opioid-immunoreactive structures in olfactory centers of the cat: adult pattern and postnatal development. 170 69

The gene for the rat substance P receptor has been cloned, its genomic structure determined, and the patterns of mRNA expression extensively analyzed. Unlike many genes encoding G protein-coupled receptors, the protein-coding region of this gene is divided into five exons consisting of 965, 195, 151, 197, and 2,010 base pairs. The substance P receptor gene extends more than 45 kilobases in length, and the splice sites for the exons occur at the borders of the sequences encoding putative membrane-spanning domains. The transcription initiation site has been defined by solution hybridization-nuclease protection and nucleotide sequence analyses, and lies downstream of a conventional TATA sequence. Substance P receptor mRNA levels in various tissues have been quantitated using solution hybridization-nuclease protection assays and were found to comprise from 0.00008 to 0.0016% of total RNA levels. Relatively high levels of substance P receptor mRNA are seen in the urinary bladder and the sublingual salivary gland, whereas moderate levels are observed for the submandibular salivary gland, striatum, hippocampus, midbrain, and olfactory bulb with lower levels in the remainder of the central nervous system and alimentary canal. These results are discussed in relation to the evolutionary role of multiple exons for a G protein-coupled receptor and with regard to the locations and mechanisms of substance P receptor gene expression.
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PMID:Organization, structure, and expression of the gene encoding the rat substance P receptor. 170 52


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