Search results for "Bridged Bicyclo Compounds"

showing 10 items of 47 documents

Group II metabotropic glutamate receptor activation by agonist LY379268 treatment increases the expression of brain derived neurotrophic factor in th…

2009

A number of in vitro and in vivo studies using selective agonists have indicated a neuroprotective role for group-II metabotropic glutamate (mGlu2/3) receptors in various models of neuronal injury. Although an interplay among neurotrophic factors and mGlu2/3 receptors signalling system has been suggested as possible mechanism involved on neuroprotection, at present poor information are available concerning the in vivo regulation by mGlu2/3 receptors activation of specific neurotrophic factors. By using in situ hybridization and western blotting methods the aim of present study was to analyse the potential regulatory role of selective mGluR2/3 agonist LY379268 treatment on brain derived neur…

Malemedicine.medical_specialtyTime Factorsmedicine.drug_classTropomyosin receptor kinase BBiologyReceptors Metabotropic GlutamateHippocampusSettore BIO/09 - FisiologiaMiceNeurotrophic factorsInternal medicineExcitatory Amino Acid AgonistsmedicineAnimalsRNA MessengerAmino Acidsneurotrophic factorNeuronsBrain-derived neurotrophic factorDose-Response Relationship DrughippocampuBrain-Derived Neurotrophic FactorGeneral NeuroscienceGlutamate receptorBrainLY379268Bridged Bicyclo Compounds HeterocyclicReceptor antagonistUp-RegulationMice Inbred C57BLMetabotropic receptorEndocrinologyBDNFXanthenesMetabotropic glutamate receptorcerebral cortexMetabotropic glutamate receptor 2Excitatory Amino Acid AntagonistsmGlu2/3 receptor
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Wavelength-Selective Softening of Hydrogel Networks.

2021

Photoresponsive hydrogels hold key potential in advanced biomedical applications including tissue engineering, regenerative medicine, and drug delivery, as well as intricately engineered functions such as biosensing, soft robotics, and bioelectronics. Herein, the wavelength-dependent degradation of bio-orthogonal poly(ethylene glycol) hydrogels is reported, using three selective activation levels. Specifically, three chromophores are exploited, that is, ortho-nitrobenzene, dimethyl aminobenzene, and bimane, each absorbing light at different wavelengths. By examining their photochemical action plots, the wavelength-dependent reactivity of the photocleavable moieties is determined. The wavele…

Materials scienceLightCell SurvivalNanotechnologyBiocompatible MaterialsCell LinePolyethylene Glycolschemistry.chemical_compoundMiceBimaneTissue engineeringCell AdhesionAnimalsGeneral Materials ScienceNitrobenzenesBioelectronicsDrug CarriersMechanical Engineeringtechnology industry and agricultureHydrogelsChromophoreBridged Bicyclo Compounds HeterocyclicchemistryMechanics of MaterialsDrug deliverySelf-healing hydrogelsBiosensorEthylene glycolAdvanced materials (Deerfield Beach, Fla.)
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Dual modulation of striatal acetylcholine release by hyperforin, a constituent of St. John's wort.

2002

Extracts of the medicinal plant St. John's wort (Hypericum perforatum) are widely used for the treatment of mild to moderate depression. Hyperforin, a constituent of St. John's wort, is known to inhibit the sodium-dependent uptake of catecholamines and amino acids into synaptic nerve endings, probably by interference with mechanisms controlling the synaptic sodium concentration. Because de novo synthesis of acetylcholine (ACh) is dependent on sodium-dependent high-affinity choline uptake, we studied the effect of hyperforin on choline (Ch) uptake in vitro and on striatal ACh release in vivo using microdialysis. In rat brain synaptosomes, hyperforin inhibited high-affinity choline uptake wit…

MicrodialysisPharmacologyMotor ActivityPhloroglucinolCholineRats Sprague-Dawleychemistry.chemical_compoundBridged Bicyclo CompoundsIn vivomedicineCholineAnimalsReceptors CholinergicIC50PharmacologyChemistryTerpenesHypericum perforatumBiological TransportAcetylcholineCorpus StriatumAnti-Bacterial AgentsRatsHyperforinSystemic administrationMolecular MedicineAcetylcholineHypericummedicine.drugThe Journal of pharmacology and experimental therapeutics
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Stimulation of hippocampal acetylcholine release by hyperforin, a constituent of St. John’s Wort

2004

Abstract Extracts of the medicinal plant St. John’s Wort ( Hypericum perforatum ) are widely used in the therapy of affective disorders and have been reported to exert antidepressant, anxiolytic, and cognitive effects in experimental and clinical studies. We here report that hyperforin, the major active constituent of the extract, increases the release of acetylcholine from rat hippocampus in vivo as determined by microdialysis. Hippocampal acetylcholine levels were increased by 50–100% following the systemic administration of pure hyperforin at doses of 1 and 10 mg/kg. The effect was almost completely suppressed by local perfusion with calcium-free buffer or with tetrodotoxin (1 μM). We co…

Microdialysismedicine.drug_classMicrodialysisTetrodotoxinPhloroglucinolPharmacologyHippocampusAnxiolyticRats Sprague-DawleyBridged Bicyclo Compoundschemistry.chemical_compoundmedicineAnimalsAnesthetics LocalNeurotransmitterPlant ExtractsTerpenesGeneral NeuroscienceHypericum perforatumAcetylcholineAnti-Bacterial AgentsRatsHyperforinchemistryAntidepressantCholinergicHypericumAcetylcholinemedicine.drugNeuroscience Letters
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Pharmacological activity of C10-substituted analogs of the high-affinity kainate receptor agonist dysiherbaine

2009

Kainate receptor antagonists have potential as therapeutic agents in a number of neuropathologies. Synthetic modification of the convulsant marine toxin neodysiherbaine A (NDH) previously yielded molecules with a diverse set of pharmacological actions on kainate receptors. Here we characterize three new synthetic analogs of NDH that contain substituents at the C10 position in the pyran ring of the marine toxin. The analogs exhibited high-affinity binding to the GluK1 (GluR5) subunit and lower affinity binding to GluK2 (GluR6) and GluK3 (GluR7) subunits in radioligand displacement assays with recombinant kainate and AMPA receptors. As well, the natural toxin NDH exhibited approximately 100-f…

Models MolecularAgonistKainic acidPatch-Clamp TechniquesTime FactorsStereochemistrymedicine.drug_classProtein subunitGreen Fluorescent ProteinsGlutamic AcidKainate receptorAMPA receptorMolecular Dynamics SimulationLigandsTransfectionTritiumBinding CompetitiveArticleMembrane PotentialsRadioligand AssayStructure-Activity RelationshipCellular and Molecular Neurosciencechemistry.chemical_compoundReceptors Kainic AcidExcitatory Amino Acid AgonistsmedicineRadioligandHumansReceptoralpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidCell Line TransformedPharmacologyAlanineKainic AcidDose-Response Relationship DrugMolecular StructureChemistryBridged Bicyclo Compounds HeterocyclicProtein SubunitsBiochemistryMutagenesis Site-DirectedMarine toxinNeuropharmacology
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Full Domain Closure of the Ligand-binding Core of the Ionotropic Glutamate Receptor iGluR5 Induced by the High Affinity Agonist Dysiherbaine and the …

2009

The prevailing structural model for ligand activation of ionotropic glutamate receptors posits that agonist efficacy arises from the stability and magnitude of induced domain closure in the ligand-binding core structure. Here we describe an exception to the correlation between ligand efficacy and domain closure. A weakly efficacious partial agonist of very low potency for homomeric iGluR5 kainate receptors, 8,9-dideoxyneodysiherbaine (MSVIII-19), induced a fully closed iGluR5 ligand-binding core. The degree of relative domain closure, approximately 30 degrees , was similar to that we resolved with the structurally related high affinity agonist dysiherbaine and to that of l-glutamate. The ph…

Models MolecularAgonistStereochemistrymedicine.drug_classGlutamic AcidKainate receptorCrystallography X-RayLigandsBiochemistryPartial agonistCell LineReceptors Kainic AcidmedicineHumansComputer SimulationAmino AcidsReceptorMolecular BiologyAlanineBinding SitesChemistryMechanisms of Signal TransductionGlutamate receptorHydrogen BondingCell BiologyBridged Bicyclo Compounds HeterocyclicLigand (biochemistry)Protein Structure TertiaryProtein SubunitsIonotropic glutamate receptorProtein BindingIonotropic effectJournal of Biological Chemistry
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Abyssomicin E, a highly functionalized polycyclic metabolite from Streptomyces species.

2007

Abyssomicin E (1), a new polycyclic metabolite with a C19 skeleton, was isolated from Streptomyces sp. (HKI0381). Its chemical structure was determined by comprehensive NMR and MS spectroscopic analyses. For the first time in this recently discovered class of compounds, the absolute stereochemistry was directly established by subsequent single-crystal X-ray diffraction study using anomalous dispersion with copper radiation.

Models MolecularbiologyMolecular StructureChemistryStereochemistryChemical structureMetaboliteOrganic ChemistryGeneral MedicineAbyssomicin Ebiology.organism_classificationBridged Bicyclo Compounds HeterocyclicBiochemistryStreptomycesStreptomyces speciesStreptomyceschemistry.chemical_compoundOrganic chemistryPhysical and Theoretical ChemistryOrganic letters
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The essential oil of turpentine and its major volatile fraction (alpha- and beta-pinenes): a review.

2010

This paper provides a summary review of the major biological features concerning the essential oil of turpentine, its origin and use in traditional and modern medicine. More precisely, the safety of this volatile fraction to human health, and the medical, biological and environmental effects of the two major compounds of this fraction (alpha- and beta-pinenes) have been discussed.

Modern medicineTraditional medicineTurpentinePharmacology toxicologyPublic Health Environmental and Occupational HealthMEDLINETurpentineFraction (chemistry)General Medicinelaw.inventionHuman healthBridged Bicyclo CompoundslawMonoterpenesOils VolatileAnimalsHumansPlant OilsEssential oilBicyclic MonoterpenesInternational journal of occupational medicine and environmental health
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Antibacterial Activity and Anticancer Activity of Rosmarinus officinalis L. Essential Oil Compared to That of Its Main Components

2012

In this study, Rosmarinus officinalis L. essential oil and three of its main components 1,8-cineole (27.23%), α-pinene (19.43%) and β-pinene (6.71%) were evaluated for their in vitro antibacterial activities and toxicology properties. R. officinalis L. essential oil possessed similar antibacterial activities to α-pinene, and a little bit better than β-pinene, while 1,8-cineole possessed the lowest antibacterial activities. R. officinalis L. essential oil exhibited the strongest cytotoxicity towards three human cancer cells. Its inhibition concentration 50% (IC50) values on SK-OV-3, HO-8910 and Bel-7402 were 0.025‰, 0.076‰ and 0.13‰ (v/v), respectively. The cytotoxicity of all the test sampl…

Pharmaceutical ScienceRosmarinusAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawDrug DiscoveryFood scienceCytotoxicityBicyclic Monoterpenesbiologyantibacterial activities18-cineoleAnti-Bacterial AgentsChemistry (miscellaneous)α-pineneOfficinaliscytotoxicityMolecular MedicineAntibacterial activityCell SurvivalMicrobial Sensitivity TestsRosmarinus officinalis L.Articlelcsh:QD241-441Bridged Bicyclo CompoundsInhibitory Concentration 50lcsh:Organic chemistryCell Line TumorBotanyOils Volatile<em>Rosmarinus officinalis </em>L.; 18-cineole; α-pinene; β-pinene; antibacterial activities; cytotoxicityHumansPhysical and Theoretical ChemistryIC50Essential oilEucalyptolBacteriaPlant ExtractsOrganic ChemistryCyclohexanolsbiology.organism_classificationAntineoplastic Agents PhytogenicRosmarinusβ-pineneEucalyptolchemistryMonoterpenesDrug Screening Assays AntitumorHuman cancerMolecules; Volume 17; Issue 3; Pages: 2704-2713
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Novel Analogs and Stereoisomers of the Marine Toxin Neodysiherbaine with Specificity for Kainate Receptors

2007

Antagonists for kainate receptors (KARs), a family of glutamategated ion channels, are efficacious in a number of animal models of neuropathologies, including epilepsy, migraine pain, and anxiety. To produce molecules with novel selectivities for kainate receptors, we generated three sets of analogs related to the natural marine convulsant neodysiherbaine (neoDH), and we characterized their pharmacological profiles. Radioligand displacement assays with recombinant alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and KARs demonstrated that functional groups at two positions on the neoDH molecule are critical pharmacological determinants; only binding to the glutamate receptor …

PharmacologyAgonistAlaninemedicine.drug_classChemistryProtein subunitStereoisomerismKainate receptorAMPA receptorBridged Bicyclo Compounds HeterocyclicLigand (biochemistry)ArticleCell LineReceptors Kainic AcidBiochemistryConvulsantmedicineHumansMolecular MedicineMarine ToxinsReceptorMarine toxinJournal of Pharmacology and Experimental Therapeutics
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