Search results for "Histaminergic"

showing 10 items of 10 documents

Brain histamine depletion enhances the behavioural sequences complexity of mice tested in the open-field: Partial reversal effect of the dopamine D2/…

2017

Markers of histaminergic dysregulation were found in several neuropsychiatric disorders characterized by repetitive behaviours, thoughts and stereotypies. We analysed the effect of acute histamine depletion by means of i. c.v. injections of alpha-fluoromethylhistidine, a blocker of histidine decarboxylase, on the temporal organization of motor sequences of CD1 mice behaviour in the open-field test. An ethogram encompassing 9 behavioural components was employed. Durations and frequencies were only slightly affected by treatments. However, as revealed by multivariate t-pattern analysis, histamine depletion was associated with a striking increase in the number of behavioural patterns. We found…

0301 basic medicineMaleDopaminePharmacologyT-pattern analysisSettore BIO/09 - FisiologiaOpen fieldAlpha-fluoromethilhistidine03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compoundMiceRandom Allocation0302 clinical medicineDopamineDopamine receptor D2medicineAnimalsPharmacologyReceptors Dopamine D2Multivariate analysiAntagonistHistaminergicReceptors Dopamine D3BrainHistidine decarboxylaseGrooming030104 developmental biologychemistryExploratory BehaviorDopamine AntagonistsSulpirideSulpiridePsychology030217 neurology & neurosurgeryHistaminemedicine.drugHistamineNeuropharmacology
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The effects of histamine on the isolated mouse uterus

2000

1. A study is made of the contractile and relaxant effects, and mechanism of action, of histamine on isolated uterus from mice treated with diethylstilboestrol, employing acetylcholine and adrenaline as contractile and relaxant standard agents. 2. Concentration-response curves for histamine agonists were obtained in the absence and presence of selective histaminergic blocking drugs (clemizole, ranitidine and thioperamide) and indomethacin. A number of experiments were carried out in uterus from reserpinised mice. Concentration-response curves for acetylcholine and adrenaline were also obtained in the absence and presence of their selective antagonist (atropine and propranolol). 3. In isolat…

Atropinemedicine.medical_specialtyVasodilator AgentsHistamine AntagonistsHistamine agonistHistamine AgonistsRanitidineMiceUterine Contractionchemistry.chemical_compoundInternal medicinemedicineAnimalsDrug InteractionsDiethylstilbestrolPharmacologyThioperamideDose-Response Relationship DrugChemistryGeneral NeuroscienceUterusHistaminergicParasympatholyticsAcetylcholineClemizoleAtropineEndocrinologyFemaleAcetylcholineHistamineHistaminemedicine.drugJournal of Autonomic Pharmacology
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Effects of histamine on dentate granule cells in vitro

1990

Abstract Hippocampal slices from rat brain were exposed to histamine and related substances in a perfusion chamber. Granule cells of the dentate gyrus were studied with conventional extra- and intracellular recording and a single electrode voltage clamp. Histamine caused, through activation of H 2 -receptors, a small depolarization, an increase in the number of synaptic and action potentials, a block of the long lasting (but not the early) component of spike afterhyperpolarizations and a reduction of the accommodation of action potential firing. These effects were mimicked by forskolin (suggests activation of adenylate cyclase). In voltage clamp, histamine blocked a long lasting calcium-dep…

General NeuroscienceDentate gyrusColforsinHistaminergicAction PotentialsRats Inbred StrainsIn Vitro TechniquesPerforant pathInhibitory postsynaptic potentialHippocampusMembrane PotentialsRatschemistry.chemical_compoundmedicine.anatomical_structurechemistryHistamine H2 receptormedicineExcitatory postsynaptic potentialBiophysicsAnimalsHistamine H3 receptorNeuroscienceHistamineAdenylyl CyclasesHistamineNeuroscience
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CLONIDINE, A PARTIAL AGONIST OF THE HISTAMINERGIC H2 RECEPTORS?

1978

Histamine H2 receptorChemistryHistaminergicmedicinePharmacologyPartial agonistClonidinemedicine.drug
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Effects of histamine on spontaneous electrical activity of neurons in rat suprachiasmatic nucleus

1991

Abstract The hypothalamic suprachiasmatic nucleus (SCN) is thought to be a light-entrained pacemaker in mammals, inducing a wide range of endogenous circadian events. In rat brain, histaminergic (HAergic) fibres are particulary rich in the hypothalamus. This prompted an investigation of the influence of bath-applied HAergic compounds on the spontaneous electrical activity of SCN neurons, recorded extracellularly in the hypothalamic slice preparation. Cells activated by bath application of HA ( n = 28) outnumbered those inhibited by HA ( n = 6). 48% of cells tested ( n = 28) were unresponsive to HA application. HA-induced activation of SCN neurons' discharge rate could be suppressed by the H…

Malemedicine.medical_specialtyCentral nervous systemAction PotentialsBiologyNeurotransmissionHistamine receptorInternal medicinemedicineAnimalsCircadian rhythmNeuronsPyrilamineSuprachiasmatic nucleusGeneral NeuroscienceHistaminergicRats Inbred StrainsCircadian RhythmRatsElectrophysiologyEndocrinologymedicine.anatomical_structurenervous systemHypothalamusSuprachiasmatic Nucleussense organsCimetidineHistamineNeuroscience Letters
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Brain histamine and oleoylethanolamide restore behavioral deficits induced by chronic social defeat stress in mice.

2021

The physiological mechanisms underlying the complex interplay between life stressors and metabolic factors is receiving growing interest and is being analyzed as one of the many factors contributing to depressive illness. The brain histaminergic system modulates neuronal activity extensively and we demonstrated that its integrity is necessary for peripheral signals such as the bioactive lipid mediator oleoylethanolamide (OEA) to exert its central actions. Here, we investigated the role of brain histamine and its interaction with OEA in response to chronic social defeat stress (CSDS), a preclinical protocol widely used to study physio-pathological mechanisms underlying symptoms observed in d…

Neurophysiology and neuropsychologyPhysiologyHistidine decarboxylaseNeurosciences. Biological psychiatry. NeuropsychiatryT-pattern analysis OxytocinT-pattern analysisOxytocinSettore BIO/09 - FisiologiaBiochemistrySocial interactionSocial defeatRecognition memory03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compoundOleoylethanolamide0302 clinical medicineEndocrinologyMedicineChronic stressOriginal Research ArticleNeurotransmitterRC346-429Molecular BiologySocial stressEndocrine and Autonomic Systemsbusiness.industryHistidine decarboxylase; Oxytocin; Recognition memory; Social interaction; T-pattern analysisQP351-495HistaminergicHistidine decarboxylase030227 psychiatrychemistryNeurology. Diseases of the nervous systembusinessNeuroscience030217 neurology & neurosurgeryHistamineRC321-571Neurobiology of stress
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Modulatory effects of the serotonergic and histaminergic systems on reaction to light in the crustacean Gammarus pulex

2013

Serotonin modulates reaction to light in many animals. In the freshwater amphipod Gammarus pulex, exogenous administration of serotonin induces a transient reversal of photic behaviour from strong photophobia to photophily. We have elucidated further the neuromodulation of photic behaviour in G. pulex by using in vivo pharmacology and behavioural testing. Using several mammalian 5-HT receptor antagonists and agonists, we provide evidence for a role of serotonin receptors in the 5-HT-dependent regulation of G. pulex photic behaviour, possibly involving 5-HTR2 subtype. Serotonin-induced photophily was blocked by the 5-HT receptor antagonists, mianserin, cyproheptadine, and ritanserin, but not…

Serotoninmedicine.medical_specialtyKetanserinLightMovementHistamine AntagonistsRitanserinPharmacologySerotonergicCellular and Molecular NeuroscienceHistamine receptorSerotonin AgentsNeuromodulationInternal medicinemedicineAnimalsAmphipoda5-HT receptorPharmacologyBehavior AnimalChemistryHistaminergicDrug Synergismmedicine.anatomical_structureEndocrinologysense organsSerotoninHistaminemedicine.drugNeuropharmacology
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Synthesis and Characterization of New Bivalent Agents as Melatonin- and Histamine H3-Ligands

2014

Melatonin is an endogenous molecule involved in many pathophysiological processes. In addition to the control of circadian rhythms, its antioxidant and neuroprotective properties have been widely described. Thus far, different bivalent compounds composed by a melatonin molecule linked to another neuroprotective agent were synthesized and tested for their ability to block neurodegenerative processes in vitro and in vivo. To identify a novel class of potential neuroprotective compounds, we prepared a series of bivalent ligands, in which a prototypic melatonergic ligand is connected to an imidazole-based H3 receptor antagonist through a flexible linker. Four imidazolyl-alkyloxy-anilinoethylami…

StereochemistryHistamine AntagonistsLigandsMelatonin receptorMT<sub>2</sub>ArticleCatalysisInorganic Chemistrylcsh:ChemistryHistamine receptorPiperidinesH<sub>3</sub> antagonistsHumansReceptors Histamine H3Physical and Theoretical ChemistryBinding siteReceptormelatonin receptorMolecular Biologylcsh:QH301-705.5SpectroscopyBinding SitesReceptor Melatonin MT2ChemistryReceptor Melatonin MT1MT1Organic ChemistryMT2ImidazolesHistaminergicMT<sub>1</sub>General Medicinemelatonin receptor; MT1; MT2; H3 antagonists; bivalent ligandsLigand (biochemistry)Protein Structure TertiaryComputer Science ApplicationsMelatonergicMolecular Docking SimulationBiochemistrylcsh:Biology (General)lcsh:QD1-999bivalent ligandsHistamine H3 receptorH3 antagonistsProtein BindingInternational Journal of Molecular Sciences
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Properties of tuberomammillary histamine neurones and their response to galanin.

1991

Histaminergic neurones in the tuberomammillary nucleus possess electrophysiological properties which distinguish them from other neurones in their neighborhood. Their resting potential is -50 mV and they are spontaneously active at about 2 Hz in a slice preparation. They display a transient outward rectification and an anomalous inward rectification. Bath application of galanin (0.1 microM) reduced their firing rate significantly and hyperpolarized them slightly.

medicine.medical_specialtyBath applicationMammillary BodiesImmunologyAction PotentialsGalaninToxicologyMembrane Potentialschemistry.chemical_compoundSlice preparationInternal medicinemedicineAnimalsPharmacology (medical)GalaninNeuronsPharmacologyHistaminergicTuber CinereumResting potentialRatsElectrophysiologyElectrophysiologyEndocrinologymedicine.anatomical_structurenervous systemchemistryBiophysicsPeptidesTuberomammillary nucleusHistamineHistamine
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Pharmacological characterization and autoradiographic localization of histamine H2 receptors in human brain identified with [125I]iodoaminopotentidin…

1992

125I-Aminopotentidine (125I-APT), a reversible probe of high specific radioactivity and high affinity and selectivity for the H2 receptor, was used to characterize and localize this histamine receptor subtype in human brain samples obtained at autopsy. On membranes of human caudate nucleus, specific 125I-APT binding at equilibrium revealed a single component, with a dissociation constant of 0.3 nM and maximal capacity of about 100 fmol/mg of protein. At 0.2 nM, 125I-APT specific binding, as defined with tiotidine, an H2-receptor antagonist chemically unrelated to iodoaminopotentidine, represented 40-50% of the total. Specific 125I-APT binding was inhibited by a series of typical H2-receptor…

medicine.medical_specialtyHistamine H1 receptorHippocampal formationBiologyBiochemistryGuanidinesIodine RadioisotopesCellular and Molecular Neurosciencechemistry.chemical_compoundHistamine receptorHistamine H2 receptorInternal medicinemedicineHumansReceptors Histamine H2Tissue DistributionReceptorHistaminergicBrainHuman brainEndocrinologymedicine.anatomical_structurechemistryHistamine H2 AntagonistsAutoradiographyHistamineJournal of neurochemistry
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