PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 7789446-0 1995 The colocalization of parvalbumin and calbindin-D28k with GABA in the subnucleus caudalis of the rat spinal trigeminal nucleus. gamma-Aminobutyric Acid 58-62 parvalbumin Rattus norvegicus 22-33 7789446-1 1995 The colocalization of two calcium-binding proteins, parvalbumin (PV) and calbindin-D28k (CaB), which have been reported to be markers of specific subpopulations of neurons in the central nervous system, with the inhibitory amino acid neurotransmitter gamma-amino-butyric acid (GABA) was investigated in neurons of laminae I-IV of the subnucleus caudalis of the rat spinal trigeminal nucleus by using post-embedding immunocytochemical methods. gamma-Aminobutyric Acid 251-275 parvalbumin Rattus norvegicus 52-63 7789446-1 1995 The colocalization of two calcium-binding proteins, parvalbumin (PV) and calbindin-D28k (CaB), which have been reported to be markers of specific subpopulations of neurons in the central nervous system, with the inhibitory amino acid neurotransmitter gamma-amino-butyric acid (GABA) was investigated in neurons of laminae I-IV of the subnucleus caudalis of the rat spinal trigeminal nucleus by using post-embedding immunocytochemical methods. gamma-Aminobutyric Acid 277-281 parvalbumin Rattus norvegicus 52-63 7723933-8 1995 Because GABA and parvalbumin are colocalized in the MS-DBB neurons, the results suggest that the level of parvalbumin is decreased, but that the cells are not lost. gamma-Aminobutyric Acid 8-12 parvalbumin Rattus norvegicus 106-117 7526265-3 1994 Parvalbumin-immunoreactivity was restricted to those GABA-immunoreactive neurons that also showed glycine-immunoreactivity and was not co-localized with neuropeptide Y-immunoreactivity or NADPH diaphorase activity. gamma-Aminobutyric Acid 53-57 parvalbumin Rattus norvegicus 0-11 7870301-13 1994 Postembedding immunocytochemistry for GABA revealed that parvalbumin-immunoreactive boutons in synaptic contact with medium spiny neurons were GABA-positive. gamma-Aminobutyric Acid 38-42 parvalbumin Rattus norvegicus 57-68 7870301-13 1994 Postembedding immunocytochemistry for GABA revealed that parvalbumin-immunoreactive boutons in synaptic contact with medium spiny neurons were GABA-positive. gamma-Aminobutyric Acid 143-147 parvalbumin Rattus norvegicus 57-68 1688284-6 1991 However, parvalbumin immunoreactivity, present normally in a subpopulation of GABA-immunoreactive dentate basket cells, was absent on the stimulated side. gamma-Aminobutyric Acid 78-82 parvalbumin Rattus norvegicus 9-20 1346522-7 1992 The majority of surviving GABA-ergic neurons expressed immunoreactivity to parvalbumin, a marker for striatal GABA-ergic interneurons. gamma-Aminobutyric Acid 26-30 parvalbumin Rattus norvegicus 75-86 1346522-7 1992 The majority of surviving GABA-ergic neurons expressed immunoreactivity to parvalbumin, a marker for striatal GABA-ergic interneurons. gamma-Aminobutyric Acid 110-114 parvalbumin Rattus norvegicus 75-86 1284972-8 1992 These results (1) identify a population of presumed inhibitory neurons that apparently form commissural projections; (2) document that all of these cells contain the calcium-binding protein parvalbumin; and (3) indicate that the vast majority of commissurally projecting hilar neurons are neither parvalbumin- nor GABA-immunoreactive. gamma-Aminobutyric Acid 314-318 parvalbumin Rattus norvegicus 190-201 7507722-3 1993 Calretinin cells and parvalbumin cells were also immunoreactive for GABA. gamma-Aminobutyric Acid 68-72 parvalbumin Rattus norvegicus 21-32 1797867-0 1991 Different populations of parvalbumin- and calbindin-D28k-immunoreactive neurons contain GABA and accumulate 3H-D-aspartate in the dorsal horn of the rat spinal cord. gamma-Aminobutyric Acid 88-92 parvalbumin Rattus norvegicus 25-36 1797867-7 1991 A high proportion of PV-immunoreactive perikarya were also stained for GABA in laminae II and III (70.0% and 61.2% respectively). gamma-Aminobutyric Acid 71-75 parvalbumin Rattus norvegicus 21-23 1797867-11 1991 These results show that out of the two calcium-binding proteins, CaBP is a characteristic protein of a small subpopulation of neurons using excitatory amino acids and PV is a characteristic protein of a subpopulation of neurons utilizing GABA as a transmitter. gamma-Aminobutyric Acid 238-242 parvalbumin Rattus norvegicus 167-169 1952098-1 1991 In the adult rat brain, the calcium-binding protein parvalbumin is preferentially associated with spontaneously fast-firing, metabolically active neurons and coexists with gamma-amino-butyric acid (GABA) in cortical inhibitory interneurons. gamma-Aminobutyric Acid 172-196 parvalbumin Rattus norvegicus 52-63 1952098-1 1991 In the adult rat brain, the calcium-binding protein parvalbumin is preferentially associated with spontaneously fast-firing, metabolically active neurons and coexists with gamma-amino-butyric acid (GABA) in cortical inhibitory interneurons. gamma-Aminobutyric Acid 198-202 parvalbumin Rattus norvegicus 52-63 1952098-6 1991 In the gamma-aminobutyric acid (GABA)-containing interneurons of the cerebral cortex and the hippocampus, as well as in the Purkinje cells of the cerebellum, parvalbumin only appears postnatally. gamma-Aminobutyric Acid 7-30 parvalbumin Rattus norvegicus 158-169 1952098-6 1991 In the gamma-aminobutyric acid (GABA)-containing interneurons of the cerebral cortex and the hippocampus, as well as in the Purkinje cells of the cerebellum, parvalbumin only appears postnatally. gamma-Aminobutyric Acid 32-36 parvalbumin Rattus norvegicus 158-169 3945815-0 1986 Parvalbumin in most gamma-aminobutyric acid-containing neurons of the rat cerebral cortex. gamma-Aminobutyric Acid 20-43 parvalbumin Rattus norvegicus 0-11 2289971-4 1990 Double labeling of single neurons with both the GABA and parvalbumin antisera showed that all parvalbumin neurons were positive for GABA, but some GABA labelled neurons were not immunoreactive for parvalbumin. gamma-Aminobutyric Acid 132-136 parvalbumin Rattus norvegicus 94-105 2289971-4 1990 Double labeling of single neurons with both the GABA and parvalbumin antisera showed that all parvalbumin neurons were positive for GABA, but some GABA labelled neurons were not immunoreactive for parvalbumin. gamma-Aminobutyric Acid 132-136 parvalbumin Rattus norvegicus 94-105 2289971-4 1990 Double labeling of single neurons with both the GABA and parvalbumin antisera showed that all parvalbumin neurons were positive for GABA, but some GABA labelled neurons were not immunoreactive for parvalbumin. gamma-Aminobutyric Acid 132-136 parvalbumin Rattus norvegicus 94-105 2289971-4 1990 Double labeling of single neurons with both the GABA and parvalbumin antisera showed that all parvalbumin neurons were positive for GABA, but some GABA labelled neurons were not immunoreactive for parvalbumin. gamma-Aminobutyric Acid 132-136 parvalbumin Rattus norvegicus 94-105 2289971-6 1990 The relationship of the GABA-containing parvalbumin neurons to the striatal mosaic organization was determined by using immunocytochemistry for another calcium binding protein, calbindin D28K, to label the matrix compartment of the striatum. gamma-Aminobutyric Acid 24-28 parvalbumin Rattus norvegicus 40-51 2924151-0 1989 Kindling induced changes in parvalbumin immunoreactivity in rat hippocampus and its relation to long-term decrease in GABA-immunoreactivity. gamma-Aminobutyric Acid 118-122 parvalbumin Rattus norvegicus 28-39 2924151-6 1989 Co-localization study in controls showed that 32% of PV-immunoreactive somata were also immunopositive for GABA. gamma-Aminobutyric Acid 107-111 parvalbumin Rattus norvegicus 53-55 2924151-10 1989 Here we demonstrate that the presence of the calcium-binding protein parvalbumin seems to exert a protective effect against the process that leads to a decrease in GABA content. gamma-Aminobutyric Acid 164-168 parvalbumin Rattus norvegicus 69-80 3945815-3 1986 With semithin frozen sections, it is possible to demonstrate that most GABA neurons in the rat somatosensory cortex contain the calcium-binding protein parvalbumin and that parvalbumin is found virtually only in GABA neurons. gamma-Aminobutyric Acid 212-216 parvalbumin Rattus norvegicus 173-184 3945815-5 1986 The specific role of parvalbumin in GABA-containing cortical cells may be related to controlling the effectiveness of their inhibitory action. gamma-Aminobutyric Acid 36-40 parvalbumin Rattus norvegicus 21-32 28944879-1 2017 Calbindin-D28k (CB), calretinin (CR) and parvalbumin (PV), which regulate cytosolic free Ca2+ concentrations in neurons, are chemically expressed in gamma-aminobutyric acid (GABA)ergic neurons that regulate the degree of glutamatergic excitation and output of projection neurons. gamma-Aminobutyric Acid 149-172 parvalbumin Rattus norvegicus 41-52 31016783-2 2019 In the OB, gamma-aminobutyric acid (GABA), as an inhibitory neurotransmitter, is secreted from GABAergic neurons which contain parvalbumin (a calcium-binding protein). gamma-Aminobutyric Acid 11-34 parvalbumin Rattus norvegicus 127-138 31016783-2 2019 In the OB, gamma-aminobutyric acid (GABA), as an inhibitory neurotransmitter, is secreted from GABAergic neurons which contain parvalbumin (a calcium-binding protein). gamma-Aminobutyric Acid 36-40 parvalbumin Rattus norvegicus 127-138 28834708-2 2017 The activity of these neurons is tightly controlled by g-aminobutyric acid (GABA)ergic interneurons, especially by those expressing parvalbumin (PV) and calretinin (CR). gamma-Aminobutyric Acid 55-74 parvalbumin Rattus norvegicus 132-143 28834708-2 2017 The activity of these neurons is tightly controlled by g-aminobutyric acid (GABA)ergic interneurons, especially by those expressing parvalbumin (PV) and calretinin (CR). gamma-Aminobutyric Acid 55-74 parvalbumin Rattus norvegicus 145-147 28834708-2 2017 The activity of these neurons is tightly controlled by g-aminobutyric acid (GABA)ergic interneurons, especially by those expressing parvalbumin (PV) and calretinin (CR). gamma-Aminobutyric Acid 76-80 parvalbumin Rattus norvegicus 132-143 28834708-2 2017 The activity of these neurons is tightly controlled by g-aminobutyric acid (GABA)ergic interneurons, especially by those expressing parvalbumin (PV) and calretinin (CR). gamma-Aminobutyric Acid 76-80 parvalbumin Rattus norvegicus 145-147 28834708-4 2017 Thus, the present study investigates whether neurons expressing PV or CR co-express specific GABA, acetylcholine and/or dopamine receptors in the basolateral amygdala of the rat. gamma-Aminobutyric Acid 93-97 parvalbumin Rattus norvegicus 64-66 28944879-1 2017 Calbindin-D28k (CB), calretinin (CR) and parvalbumin (PV), which regulate cytosolic free Ca2+ concentrations in neurons, are chemically expressed in gamma-aminobutyric acid (GABA)ergic neurons that regulate the degree of glutamatergic excitation and output of projection neurons. gamma-Aminobutyric Acid 174-178 parvalbumin Rattus norvegicus 41-52 28214898-2 2016 Substantial evidence suggests that abnormalities in inhibitory gamma-aminobutyric acid (GABA) interneuron function, especially in the parvalbumin subtype of GABA interneuron, both developmentally and in adulthood, may contribute mechanistically to cognitive deficits and psychotic symptoms in schizophrenia. gamma-Aminobutyric Acid 63-86 parvalbumin Rattus norvegicus 134-145 29021744-11 2017 This effect is prevented by the local application of omega-agatoxin, suggesting that it may in part depend on GABA release by fast-spiking parvalbumin (PV)-expressing cortical interneurons. gamma-Aminobutyric Acid 110-114 parvalbumin Rattus norvegicus 139-150 28214898-2 2016 Substantial evidence suggests that abnormalities in inhibitory gamma-aminobutyric acid (GABA) interneuron function, especially in the parvalbumin subtype of GABA interneuron, both developmentally and in adulthood, may contribute mechanistically to cognitive deficits and psychotic symptoms in schizophrenia. gamma-Aminobutyric Acid 88-92 parvalbumin Rattus norvegicus 134-145 28214898-2 2016 Substantial evidence suggests that abnormalities in inhibitory gamma-aminobutyric acid (GABA) interneuron function, especially in the parvalbumin subtype of GABA interneuron, both developmentally and in adulthood, may contribute mechanistically to cognitive deficits and psychotic symptoms in schizophrenia. gamma-Aminobutyric Acid 157-161 parvalbumin Rattus norvegicus 134-145 24946277-6 2014 Additionally, we found layer-specific increases in GABA release sites originating from calbindin, calretinin, and parvalbumin interneurons, implying that there is a re-wiring of the interneuronal network. gamma-Aminobutyric Acid 51-55 parvalbumin Rattus norvegicus 114-125 26044967-2 2015 In schizophrenia for example, changes in GABA neurons [reduced expression of glutamic acid decarboxylase (GAD), parvalbumin (PV) and the GABA reuptake transporter (GAT1)] suggest reduced cortical GABA synthesis and release; these changes are hypothesized to cause the cognitive deficits observed in this disorder. gamma-Aminobutyric Acid 41-45 parvalbumin Rattus norvegicus 112-123 26044967-2 2015 In schizophrenia for example, changes in GABA neurons [reduced expression of glutamic acid decarboxylase (GAD), parvalbumin (PV) and the GABA reuptake transporter (GAT1)] suggest reduced cortical GABA synthesis and release; these changes are hypothesized to cause the cognitive deficits observed in this disorder. gamma-Aminobutyric Acid 41-45 parvalbumin Rattus norvegicus 125-127 25528062-5 2015 Additionally, a decrease in PV-labeled axon terminals of GABA-ergic cells, likely reflecting the perisomatic inhibitory innervation of pyramidal neurons, was observed in the medial prefrontal cortices in both sexes. gamma-Aminobutyric Acid 57-61 parvalbumin Rattus norvegicus 28-30 25620912-7 2014 Animals exposed to GWIR-chemicals and stress for 4 weeks displayed reduced numbers of PV-expressing GABA-ergic interneurons in the dentate gyrus and NPY-expressing interneurons in the CA1 and CA3 subfields. gamma-Aminobutyric Acid 100-104 parvalbumin Rattus norvegicus 86-88 23146738-8 2012 CONCLUSIONS: The expression changes of PV and GAD67 in SZ can be simulated using the SZ development model induced by MK-801, which might affect the development of the GABA system in the PFC and hippocampus by downregulating KCC2 expression. gamma-Aminobutyric Acid 167-171 parvalbumin Rattus norvegicus 39-41 24815212-0 2014 Sex differences in diazepam effects and parvalbumin-positive GABA neurons in trait anxiety Long Evans rats. gamma-Aminobutyric Acid 61-65 parvalbumin Rattus norvegicus 40-51 21220766-2 2011 Most GABA cells of rat frontal cortex have at least 1 of 6 chemical markers (parvalbumin, calretinin, alpha-actinin-2, somatostatin, vasoactive intestinal polypeptide, and cholecystokinin), with each chemical class comprising several distinct neuronal subtypes having specific physiological and morphological characteristics. gamma-Aminobutyric Acid 5-9 parvalbumin Rattus norvegicus 77-88 22591370-11 2012 Parvalbumin-expressing GABA-ergic interneurons regulate the primary neuronal output from hippocampus that is important for memory and behavior. gamma-Aminobutyric Acid 23-27 parvalbumin Rattus norvegicus 0-11 22342346-3 2012 We sought to determine whether T-817MA would ameliorate sensorimotor gating deficits and loss of parvalbumin (PV)-positive gamma-aminobutyric acid (GABA) neurons in the brain of rats transiently exposed to MK-801, an N-methyl-d-aspartate receptor blocker, in the neonatal stage, as an animal model of schizophrenia. gamma-Aminobutyric Acid 123-146 parvalbumin Rattus norvegicus 97-108 21238466-10 2012 These findings suggest that abnormal cortical glutamate transmission, possibly driven by pathological changes in GABA function in parvalbumin-positive fast-spiking interneurons, may underlie some of the cognitive deficits in schizophrenia. gamma-Aminobutyric Acid 113-117 parvalbumin Rattus norvegicus 130-141 21376086-4 2011 After extinction, neuronal activation was visualized by c-Fos for overall activity and parvalbumin immunoreactivity for gamma-aminobutyric acid (GABA) neuron in brain areas linked to anxiety (medial prefrontal cortex and amygdala). gamma-Aminobutyric Acid 120-143 parvalbumin Rattus norvegicus 87-98 21376086-4 2011 After extinction, neuronal activation was visualized by c-Fos for overall activity and parvalbumin immunoreactivity for gamma-aminobutyric acid (GABA) neuron in brain areas linked to anxiety (medial prefrontal cortex and amygdala). gamma-Aminobutyric Acid 145-149 parvalbumin Rattus norvegicus 87-98 23738215-0 2012 T-817MA, but Not Haloperidol and Risperidone, Restores Parvalbumin-Positive gamma -Aminobutyric Acid Neurons in the Prefrontal Cortex and Hippocampus of Rats Transiently Exposed to MK-801 at the Neonatal Period. gamma-Aminobutyric Acid 76-100 parvalbumin Rattus norvegicus 55-66 23738215-1 2012 The number of parvalbumin (PV)-positive gamma -aminobutyric acid (GABA) neurons is decreased in the brain of rats transiently exposed to MK-801, an N-methyl-D-aspartate (NMDA) receptor blocker, in the neonatal stage (Uehara et al. gamma-Aminobutyric Acid 40-64 parvalbumin Rattus norvegicus 14-25 23738215-1 2012 The number of parvalbumin (PV)-positive gamma -aminobutyric acid (GABA) neurons is decreased in the brain of rats transiently exposed to MK-801, an N-methyl-D-aspartate (NMDA) receptor blocker, in the neonatal stage (Uehara et al. gamma-Aminobutyric Acid 40-64 parvalbumin Rattus norvegicus 27-29 23738215-1 2012 The number of parvalbumin (PV)-positive gamma -aminobutyric acid (GABA) neurons is decreased in the brain of rats transiently exposed to MK-801, an N-methyl-D-aspartate (NMDA) receptor blocker, in the neonatal stage (Uehara et al. gamma-Aminobutyric Acid 66-70 parvalbumin Rattus norvegicus 14-25 23738215-1 2012 The number of parvalbumin (PV)-positive gamma -aminobutyric acid (GABA) neurons is decreased in the brain of rats transiently exposed to MK-801, an N-methyl-D-aspartate (NMDA) receptor blocker, in the neonatal stage (Uehara et al. gamma-Aminobutyric Acid 66-70 parvalbumin Rattus norvegicus 27-29 23738215-4 2012 We herein sought to determine whether T-817MA, haloperidol (HPD), or risperidone (RPD) would ameliorate the decrease in the number of PV-positive GABA neurons in the medial prefrontal cortex (mPFC) and hippocampus of the model animals. gamma-Aminobutyric Acid 146-150 parvalbumin Rattus norvegicus 134-136 20113193-4 2010 In contrast, numbers of neurons that expressed the calcium-binding protein parvalbumin, which is a marker interneurons that express the inhibitory neurotransmitter gamma-aminobutyric acid (GABAergic neurons) were decreased for wild-type (Wt) rats on the VA-deficient diet and for Wt rats treated with morphine. gamma-Aminobutyric Acid 164-187 parvalbumin Rattus norvegicus 75-86 17340116-1 2007 RATIONALE: Neurodevelopmental deficits of parvalbumin-immunoreactive gamma-aminobutyric acid (GABA)ergic interneurons in prefrontal cortex have been reported in schizophrenia. gamma-Aminobutyric Acid 69-92 parvalbumin Rattus norvegicus 42-53 17467185-5 2007 Of the subtypes of GABA interneurons identified by expression of several calcium-binding proteins, a significantly higher percentage of neurons expressing IR for parvalbumin also expressed 5-HT(2C)R-IR than did the percentage of neurons expressing calbindin-IR or calretinin-IR that also expressed 5-HT(2C)R-IR. gamma-Aminobutyric Acid 19-23 parvalbumin Rattus norvegicus 162-173 17467185-6 2007 Since parvalbumin is located in basket and chandelier GABA interneurons which project to cell body and initial axon segments of pyramidal cells, respectively, these results raise the possibility that the 5-HT(2C)R in the mPFC acts via the parvalbumin-positive GABAergic interneurons to regulate the output of pyramidal cells in the rat mPFC. gamma-Aminobutyric Acid 54-58 parvalbumin Rattus norvegicus 6-17 17340116-1 2007 RATIONALE: Neurodevelopmental deficits of parvalbumin-immunoreactive gamma-aminobutyric acid (GABA)ergic interneurons in prefrontal cortex have been reported in schizophrenia. gamma-Aminobutyric Acid 94-98 parvalbumin Rattus norvegicus 42-53 17177263-1 2007 Evidence for the existence of different populations of gamma-aminobutyric acid (GABA)-ergic neurons in the substantia nigra comes partially from anatomical studies, which have shown there to be little if any overlap between the calcium-binding proteins parvalbumin and calretinin in individual neurons, suggesting that these may represent neuronal subtypes with distinct electrophysiological and/or anatomical properties. gamma-Aminobutyric Acid 80-84 parvalbumin Rattus norvegicus 253-264 12064777-4 2002 Double immunohistochemical staining revealed that the parvalbumin immunoreactive presynaptic perikarya and dendrites contained GABA. gamma-Aminobutyric Acid 127-131 parvalbumin Rattus norvegicus 54-65 16413119-3 2006 GABA neurons of the rat neocortex co-localize with calcium-binding proteins [parvalbumin, carletinin, calbindin D28k] and neuropeptides (vasoactive intestinal polypeptide, somatostatin). gamma-Aminobutyric Acid 0-4 parvalbumin Rattus norvegicus 77-88 15913953-6 2005 Light and electron microscopic immunocytochemical investigations prove that the parvalbumin-immunoreactive calyciform complexes contain also GABA, that are likely to be inhibitory. gamma-Aminobutyric Acid 141-145 parvalbumin Rattus norvegicus 80-91 17008398-2 2007 gamma-Amino-butyric acid (GABA)ergic interneurons comprise the bulk of local inhibitory circuitry in brain, many of which contain the calcium binding protein, parvalbumin (PV). gamma-Aminobutyric Acid 0-24 parvalbumin Rattus norvegicus 159-170 17008398-2 2007 gamma-Amino-butyric acid (GABA)ergic interneurons comprise the bulk of local inhibitory circuitry in brain, many of which contain the calcium binding protein, parvalbumin (PV). gamma-Aminobutyric Acid 26-30 parvalbumin Rattus norvegicus 159-170 16420437-3 2006 In schizophrenia, decreases in inhibitory gamma-aminobutyric acid (GABA)-containing interneurons that express the calcium-binding protein parvalbumin have been reported in the prefrontal cortex and hippocampus. gamma-Aminobutyric Acid 42-65 parvalbumin Rattus norvegicus 138-149 16420437-3 2006 In schizophrenia, decreases in inhibitory gamma-aminobutyric acid (GABA)-containing interneurons that express the calcium-binding protein parvalbumin have been reported in the prefrontal cortex and hippocampus. gamma-Aminobutyric Acid 67-71 parvalbumin Rattus norvegicus 138-149 15238432-4 2005 Increased density of PV-ir GABA interneurons in the ACC at 1 day withdrawal was reproduced in rats repeatedly injected with apomorphine or with SKF-38393. gamma-Aminobutyric Acid 27-31 parvalbumin Rattus norvegicus 21-23 11169468-7 2001 Using newly developed methods designed to copreserve and colocalize GABA and polypeptide immunoreactivities with increased sensitivity, the authors report that virtually all hippocampal interneuron somata that are immunoreactive for parvalbumin (PV), calbindin, calretinin, somatostatin (SS), neuropeptide Y, cholecystokinin, and vasoactive intestinal peptide exhibited clearly detectable, somal, GABA-like immunoreactivity (LI). gamma-Aminobutyric Acid 397-401 parvalbumin Rattus norvegicus 233-244 9268067-5 1997 Dual-label fluorescence confocal microscopic studies with a 5-HT2A antibody and a mouse monoclonal antibody to parvalbumin, a marker of a subset of gamma aminobutyric acid (GABA)ergic interneurons in the cortex, demonstrated that although some cells expressing 5-HT2A-li were interneurons, most were not. gamma-Aminobutyric Acid 148-171 parvalbumin Rattus norvegicus 111-122 11311534-2 2001 In order to investigate the role of GABA in early development of forebrain interneurons, we determined the survival of parvalbumin-immunoreactive GABAergic interneurons in the adult rat striatum following prenatal exposure to either GABA(A) receptor agonist or antagonist. gamma-Aminobutyric Acid 146-150 parvalbumin Rattus norvegicus 119-130 11516833-7 2001 Parvalbumin-positive neurons constituted 19-43% of GABA-immunoreactive neurons in the basolateral amygdala, depending on the nucleus. gamma-Aminobutyric Acid 51-55 parvalbumin Rattus norvegicus 0-11 10509647-1 1999 PURPOSE: To evaluate the hypothesis that the expression of the calcium-binding protein parvalbumin (PV) in a subpopulation of gamma-aminobutyric acid (GABA)ergic neurons is an appropriate molecular marker for the effect on ocular dominance plasticity of monocular deprivation during the postnatal sensitive period. gamma-Aminobutyric Acid 126-149 parvalbumin Rattus norvegicus 87-98 10509647-1 1999 PURPOSE: To evaluate the hypothesis that the expression of the calcium-binding protein parvalbumin (PV) in a subpopulation of gamma-aminobutyric acid (GABA)ergic neurons is an appropriate molecular marker for the effect on ocular dominance plasticity of monocular deprivation during the postnatal sensitive period. gamma-Aminobutyric Acid 126-149 parvalbumin Rattus norvegicus 100-102 10509647-1 1999 PURPOSE: To evaluate the hypothesis that the expression of the calcium-binding protein parvalbumin (PV) in a subpopulation of gamma-aminobutyric acid (GABA)ergic neurons is an appropriate molecular marker for the effect on ocular dominance plasticity of monocular deprivation during the postnatal sensitive period. gamma-Aminobutyric Acid 151-155 parvalbumin Rattus norvegicus 87-98 10509647-1 1999 PURPOSE: To evaluate the hypothesis that the expression of the calcium-binding protein parvalbumin (PV) in a subpopulation of gamma-aminobutyric acid (GABA)ergic neurons is an appropriate molecular marker for the effect on ocular dominance plasticity of monocular deprivation during the postnatal sensitive period. gamma-Aminobutyric Acid 151-155 parvalbumin Rattus norvegicus 100-102 9788283-1 1998 The presence of interconnections between cholinergic and parvalbumin (PARV)-containing gamma aminobutyric acid (GABA)ergic septohippocampal projection neurons is still a matter of debate. gamma-Aminobutyric Acid 87-110 parvalbumin Rattus norvegicus 57-68 9788283-1 1998 The presence of interconnections between cholinergic and parvalbumin (PARV)-containing gamma aminobutyric acid (GABA)ergic septohippocampal projection neurons is still a matter of debate. gamma-Aminobutyric Acid 112-116 parvalbumin Rattus norvegicus 57-68 10462693-4 1999 In rat basal forebrain, cholinergic and parvalbumin-containing gamma-aminobutyric acid-ergic cells demonstrated GLUT4 immunoreactivity, whereas calretinin-, calbindin-D-, and neuronal nitric oxide synthase-containing neurons did not express GLUT4 protein. gamma-Aminobutyric Acid 63-86 parvalbumin Rattus norvegicus 40-51 9511925-3 1998 In this study, we analyzed, at the light and electron microscopic level, the distribution and morphology of PV-ir neurons and their relationship with GABA in adult and developing rats. gamma-Aminobutyric Acid 150-154 parvalbumin Rattus norvegicus 108-110 9416916-1 1997 We study the neurogenesis of a distinct subclass of rat striatum gamma-aminobutyric acid (GABA)ergic interneurons marked by the calcium-binding protein parvalbumin (PV). gamma-Aminobutyric Acid 65-88 parvalbumin Rattus norvegicus 152-163 9416916-1 1997 We study the neurogenesis of a distinct subclass of rat striatum gamma-aminobutyric acid (GABA)ergic interneurons marked by the calcium-binding protein parvalbumin (PV). gamma-Aminobutyric Acid 90-94 parvalbumin Rattus norvegicus 152-163 9268067-5 1997 Dual-label fluorescence confocal microscopic studies with a 5-HT2A antibody and a mouse monoclonal antibody to parvalbumin, a marker of a subset of gamma aminobutyric acid (GABA)ergic interneurons in the cortex, demonstrated that although some cells expressing 5-HT2A-li were interneurons, most were not. gamma-Aminobutyric Acid 173-177 parvalbumin Rattus norvegicus 111-122 8720498-1 1996 The possible coexistence of the calcium-binding protein, parvalbumin, with the major inhibitory neurotransmitter, gamma-aminobutyric acid (GABA), and its synthesizing enzyme, glutamate decarboxylase (GAD), was studied in nonpyramidal cells of the rat medial and lateral entorhinal cortex. gamma-Aminobutyric Acid 114-137 parvalbumin Rattus norvegicus 57-68 8720498-1 1996 The possible coexistence of the calcium-binding protein, parvalbumin, with the major inhibitory neurotransmitter, gamma-aminobutyric acid (GABA), and its synthesizing enzyme, glutamate decarboxylase (GAD), was studied in nonpyramidal cells of the rat medial and lateral entorhinal cortex. gamma-Aminobutyric Acid 139-143 parvalbumin Rattus norvegicus 57-68 8720498-4 1996 The colocalization analysis revealed that all parvalbumin-immunoreactive neurons (mirror technique n = 688 and confocal microscopy n = 644) in all layers of the medial and lateral entorhinal cortex were also immunopositive for GABA or GAD. gamma-Aminobutyric Acid 227-231 parvalbumin Rattus norvegicus 46-57 8720498-5 1996 Parvalbumin-cells made up 52% of the GABA cells in most of the layers in the medial and lateral entorhinal cortex. gamma-Aminobutyric Acid 37-41 parvalbumin Rattus norvegicus 0-11 9177765-5 1997 The results show that the majority of PV (100%), SOM (89.8%) and CR (93.9%) staining neurons are GABA positive. gamma-Aminobutyric Acid 97-101 parvalbumin Rattus norvegicus 38-40 9184110-1 1997 Physiological/anatomical studies of rat frontal cortex in vitro have distinguished subpopulations of gamma-aminobutyric acid (GABA)-expressing inhibitory interneurons defined by expression of the calcium-binding proteins, parvalbumin (PV) and calbindin (CA). gamma-Aminobutyric Acid 126-130 parvalbumin Rattus norvegicus 235-237 9028774-1 1997 In the septal complex, both parvalbumin and calbindin neurons cocontain GABA. gamma-Aminobutyric Acid 72-76 parvalbumin Rattus norvegicus 28-39