Search results for "guinea"

showing 10 items of 412 documents

Tetanus Toxin Inhibits Neuroexocytosis Even When Its Zn2+-dependent Protease Activity Is Removed

1995

Tetanus toxin (TeTX) is a dichain protein that blocks neuroexocytosis, an action attributed previously to Zn(2+)-dependent proteolysis of synaptobrevin (Sbr) by its light chain (LC). Herein, its cleavage of Sbr in rat cerebrocortical synaptosomes was shown to be minimized by captopril, an inhibitor of certain metalloendoproteases, whereas this agent only marginally antagonized the inhibition of noradrenaline release, implicating a second action of the toxin. This hypothesis was proven by preparing three mutants (H233A, E234A, H237A) of the LC lacking the ability to cleave Sbr and reconstituting them with native heavy chain. The resultant dichains were found to block synaptosomal transmitter…

CaptoprilSynaptobrevinProteolysismedicine.medical_treatmentGuinea PigsInhibitory postsynaptic potentialmedicine.disease_causeBiochemistryExocytosisNorepinephrinechemistry.chemical_compoundTetanus ToxinCadaverineAplysiaEndopeptidasesmedicineAnimalsEnzyme InhibitorsNeurotransmitterMolecular BiologyCerebral CortexTransglutaminasesProteasemedicine.diagnostic_testbiologyToxinHydrolysisWild typeCell Biologybiology.organism_classificationRecombinant ProteinsRatsZincBiochemistrychemistryAplysiaBiophysicsSynaptosomesJournal of Biological Chemistry
researchProduct

Pyridinedicarboxylates, the first mechanism-derived inhibitors for prolyl 4-hydroxylase, selectively suppress cellular hydroxyprolyl biosynthesis. De…

1987

Two pyridinedicarboxylates, predicted [Hanauske-Abel (1983) M.D.-Ph.D. Thesis, Philipps Universität Marburg] and later found to be potent reversible inhibitors of purified prolyl 4-hydroxylase [Majaama, Hanauske-Abel, Günzler & Kivirikko (1984) Eur. J. Biochem. 138, 239-245] were investigated with respect to their effect on hydroxyprolyl biosynthesis in the fibroblast/collagen and the macrophage/Clq systems, and the effect was compared with that of the iron chelator 2,2′-dipyridyl, the compound usually employed to inhibit cellular hydroxyprolyl formation. Only the enzyme-mechanism-derived pyridinedicarboxylates were highly selective inhibitors, and only they lacked overt cytotoxicity. M…

Cell typeCell SurvivalComplement Activating EnzymesGuinea PigsProcollagen-Proline DioxygenaseBiologyBiochemistrychemistry.chemical_compoundBiosynthesisComplement C1In vivomedicineAnimalsHumansSecretionPicolinic AcidsFibroblastCytotoxicityMolecular BiologyCells CulturedDose-Response Relationship DrugComplement C1qEndoplasmic reticulumCell BiologyFibroblastsHydroxyprolineMicroscopy Electronmedicine.anatomical_structureBiochemistrychemistryLipophilicityCollagenResearch ArticleBiochemical Journal
researchProduct

Electron microscopic localization of nitric oxide I synthase in the organ of Corti of the guinea pig

1997

Nitric oxide synthase (NOS) activity has been detected previously in the mammalian cochlea at a light microscopic level. Here we present results of electron microscopic analysis for post-embedding immunoreactivity of neural-type NOS I in the cochlea of the guinea pig. Strong enzyme immunoreactivity was identified in the cytoplasm of inner and outer hair cells. Gold-labeled NOS I antibodies were mainly located in electron-dense areas of the cytoplasm, whereas electron-lucent regions of the receptor cells were nearly free from any immunoreactivity. In both types of hair cells anti-NOS I antibodies were also visible in the cuticular plates, hair bundles and nuclei. Further ultrastructural anal…

Cell typeGuinea PigsBiologyPitch DiscriminationReference ValuesHair Cells AuditorymedicineAnimalsInner earOrgan of CortiCochleaLamina reticularisGeneral MedicineImmunohistochemistryCell biologyIsoenzymesMicroscopy Electronmedicine.anatomical_structureOtorhinolaryngologyBiochemistryCytoplasmOrgan of CortiUltrastructuresense organsHair cellNitric Oxide SynthaseSignal TransductionEuropean Archives of Oto-Rhino-Laryngology
researchProduct

Volatile constituents of aerial parts of three endemic Centaurea species from Turkey: Centaurea amanicola Hub.-Mor., Centaurea consanguinea DC. and C…

2008

The volatile constituents of the aerial parts of Centaurea amanicola Hub.-Mor., Centaurea consanguinea DC. and Centaurea ptosimopappa Hayek were extracted by hydrodistillation and analysed by GC and GC-MS. Altogether 94 components were identified. Sesquiterpenoids, fatty acids and carbonylic compounds were the most abundant components in the oils. Hexadecanoic acid and (Z,Z )-9,12-octadecadienoic acid were the main fatty acids in all the examined samples, that showed different patterns of composition. The study on the biological activity of the oils showed an action mainly against the Gram-positive pathogens.

Centaurea amanicola Centaurea consanguinea Centaurea ptosimopappa essential oil GC/MS antimicrobial activityChromatography GasTurkeyOils VolatilePlant OilsCentaureaSettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaMicrobial Sensitivity TestsPlant Components AerialGram-Positive BacteriaGas Chromatography-Mass SpectrometryAnti-Bacterial AgentsNatural product research
researchProduct

Diffusion in slice preparations bathed in unstirred solutions

1987

A diffusion model is described here, which allows for the estimations of drug concentration changes in porous media, such as in slice tissues of the central nervous system (CNS) bathed in unstirred solutions following abrupt changes of drug concentration. This model may be used for the interpretation of data obtained in neuropharmacological studies if (i) the diffusion coefficient of the molecules under investigation is constant within the excised tissue, (ii) drug molecules are diffusing only in the extracellular space (ECS) and are not bound by the tissue, (iii) drug molecules diffuse mainly within one dimension, (iv) the drug concentration in the bath is changed within 5 s, and (v) the b…

Central Nervous SystemGuinea PigsIn Vitro TechniquesHippocampusTortuosityIonDiffusionchemistry.chemical_compoundExtracellularAnimalsWaferDiffusion (business)Molecular BiologyTetramethylammoniumGeneral NeuroscienceOsmolar ConcentrationModels TheoreticalQuaternary Ammonium CompoundsSolutionsMicroelectrodechemistryEvaluation Studies as TopicBiophysicsNeurology (clinical)Porous mediumMicroelectrodesDevelopmental BiologyBrain Research
researchProduct

The Properdin System: Composition and Function

1978

. This article summarizes the physicochemical data on the factors which compose the properdin system in guinea pig and man. The following other topics are discussed: (1) Activation of the properdin system; (2) Formation of the initiating and amplification C3 convertases; (3) Formation of the C5 convertase, and (4) Regulatory control mechanisms of the properdin system.

Chemical PhenomenaProperdinChemistryChemistry PhysicalGuinea PigsComplement C5Complement C3Complement C3-C5 ConvertasesHematologyGeneral MedicineCell biologyC5-convertaseRegulatory controlImmunologyComplement C3bProperdinAnimalsHumansComplement Factor DFunction (biology)Complement Factor BVox Sanguinis
researchProduct

Struktur-Wirkungs-Beziehungen bei Histaminanaloga, 24. Mitt. Absolute Konfiguration und histaminartige Wirkung der Enantiomere von 4-(2-Aminopropyl)-…

1982

Es werden die Racematspaltung von 4-(2-Aminopropyl)-5-methyl-imidazol (1), die Bestimmung der absoluten Konfiguration sowie die histaminartige Wirksamkeit der Enantiomere am Ileum (H1) und Atrium (H2) des Meerschweinchens beschrieben. Structure-Activity Relationships of Histamine Analogues, XXIV: Absolute Configuration and Histamine-Type Activity of the Enantiomers of 4-(2-Aminopropyl)-5-methylimidazole The resolution of 4-(2-aminopropyl)-5-methylimidazole (1), the determination of the absolute configuration and the histamine-type activity of the enantiomers on the guinea pig ileum (H1) and atrium (H2) are reported.

ChemistryStereochemistryDrug DiscoveryAbsolute configurationPharmaceutical ScienceEnantiomerGuinea pig ileumMolecular conformationArchiv der Pharmazie
researchProduct

3,4-trans-4-Aryl-3-(1-pyridinio)-1,2,3,4-tetrahydropyridine-6-thiolates—new group of potential cardiotonic drugs

2005

Abstract 3,4- trans -4-Aryl-3-(1-pyridinio)-1,2,3,4-tetrahydropyridine-6-thiolates 6 – 11 were prepared by a Michael reaction of N -acetonylpyridinium chloride with 3-aryl-2-cyanothioacrylamides or by a one-pot three-carbon condensation of N -acetonylpyridinium chloride, aromatic aldehyde and 2-cyanothioacetamide, and their cardiotonic properties were studied. 3,4- trans -5-cyano-2-hydroxy-2-methyl-4-(3-nitrophenyl)-3-(1-pyridinio)-1,2,3,4-tetrahydropyridine-6-thiolate 8 was considered as a lead compound in this series since it in vitro experiments (spontaneously beating rat atria) showed a cardiotonic activity similar to that of milrinone 2 , however compound 8 induced activity at lover co…

ChronotropicCardiotonic AgentsPyridinesStereochemistryGuinea PigsBlood PressureCardiac activityIn Vitro TechniquesCardiotonic AgentsAldehydeChlorideChemical synthesischemistry.chemical_compoundHeart RateGroup (periodic table)Drug DiscoverymedicineAnimalsSulfhydryl CompoundsRats WistarPharmacologychemistry.chemical_classificationCardiotonic drugsArylOrganic ChemistryGeneral MedicineRatschemistryMilrinoneLead compoundMilrinonemedicine.drugEuropean Journal of Medicinal Chemistry
researchProduct

The lack of the effect of DA-1 and DA-2 dopamine agonists on the isolated guinea-pig atria.

1987

1 The effects of dopamine and both DA-1 and DA-2 dopamine receptor agonists have been studied on the contractile force of electrically driven guinea-pig left atria and frequency of spontaneously beating right atria. 2 Pretreatment of animals with reserpine caused a parallel rightward shift of the concentration-response curve to dopamine of either preparation. 3 Propranolol, but not domperidone, shifted to the right the dose-response curve for the positive inotropic and chronotropic effects of dopamine. 4 Neither apomorphine, fenoldopam, bromocriptine nor piribedil had effects on the frequency and contractile force of the isolated guinea-pig atria. 5 These results suggest that DA-1 and DA-2 …

ChronotropicMalemedicine.medical_specialtyFenoldopamApomorphineVasodilator AgentsGuinea PigsPharmacologyFenoldopamIn Vitro TechniquesReceptors DopaminePiribedilDopamineInternal medicinemedicineAnimalsBromocriptinePharmacologyChemistryGeneral NeurosciencePiribedilHeartReserpineBenzazepinesPropranololBromocriptineDomperidoneElectric StimulationApomorphineEndocrinologyDopamine receptorcardiovascular systemFemalemedicine.drugJournal of autonomic pharmacology
researchProduct

Study on the histamine-like activity of guanfacine

1990

Abstract The effects of guanfacine have been studied on guinea-pig isolated atria and diethylstilboestrol-treated rat isolated uterus to determine whether it possesses histamine-like activity. Guanfacine produced a concentration-dependent negative chronotropic effect which was not modified by ranitidine (0.1 μM). In rat isolated uterus contracted by KCl, clonidine (5–5000 μM) produced concentration-dependent relaxation which was blocked by ranitidine (0.1 μM), but guanfacine only produced relaxation at high concentrations (100–1000 μM), and this was not affected by ranitidine (0.1 μM). It is concluded that guanfacine, unlike clonidine, does not produce effects due to activation of H2-recept…

Chronotropicmedicine.medical_specialtyGuinea PigsUterusPharmaceutical SciencePharmacologyClonidinePotassium ChlorideGuinea pigRanitidineUterine Contractionchemistry.chemical_compoundInternal medicinemedicineAnimalsHeart AtriaDiethylstilbestrolPharmacologyDose-Response Relationship Drugbusiness.industryRats Inbred StrainsMyocardial ContractionGuanfacineRatsGuanfacineClonidineEndocrinologymedicine.anatomical_structureMechanism of actionchemistryFemalemedicine.symptombusinessAdrenergic alpha-AgonistsHistaminemedicine.drugJournal of Pharmacy and Pharmacology
researchProduct