Search results for "Capsaicin"

showing 10 items of 63 documents

Modulation by opioids and by afferent sensory neurones of prostanoid protection of the rat gastric mucosa.

1992

1. Pretreatment with capsaicin, to deplete sensory neuropeptides from primary afferent neurones or the administration of morphine (9 mg kg-1, i.v.), which can inhibit neuropeptide release, augmented gastric mucosal injury induced by a 5 min challenge with intragastric ethanol in the rat, as assessed by macroscopic and histological evaluation. 2. Morphine administration substantially attenuated the protective actions of the prostaglandin analogue 16,16 dimethyl prostaglandin E2 (dm PGE2; 0.5-20 micrograms kg-1, p.o.) against ethanol-induced damage. This reduced degree of protection by dmPGE2 was not however, the consequence of the enhanced level of damage. 3. These actions of morphine in red…

MaleNarcoticsmedicine.medical_specialtymedicine.drug_classProstaglandinNeuropeptideNalorphine(+)-NaloxoneDinoprostonechemistry.chemical_compoundInternal medicinemedicineAnimalsNeurons AfferentProstaglandin E2PharmacologyEthanolMorphinebusiness.industryNaloxoneRats Inbred StrainsRatsEndocrinologychemistryCapsaicinGastric MucosaMorphineProstaglandinsProstaglandin analogueCapsaicinbusinessmedicine.drugResearch ArticleBritish journal of pharmacology
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Explicit episodic memory for sensory-discriminative components of capsaicin-induced pain: Immediate and delayed ratings

2008

Pain memory is thought to affect future pain sensitivity and thus contribute to clinical pain conditions. Systematic investigations of the human capacity to remember sensory features of experimental pain are sparse. In order to address long-term pain memory, nine healthy male volunteers received intrader- mal injections of three doses of capsaicin (0.05, 1 and 20 lg, separated by 15 min breaks), each given three times in a balanced design across three sessions at one week intervals. Pain rating was performed using a computerized visual analogue scale (0-100) digitized at 1/s, either immediately online or one hour or one day after injection. Subjects also recalled their pains one week later.…

MalePain ThresholdRecallVisual analogue scalePainSensory systemAdaptation PhysiologicalPain ratingYoung Adultchemistry.chemical_compoundDiscrimination PsychologicalMemory Short-TermAnesthesiology and Pain MedicineNeurologychemistryCapsaicinDuration (music)AnesthesiaSensory System AgentsHumansNeurology (clinical)CapsaicinPsychologyEpisodic memoryBurning PainPain
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Presynaptic effects of anandamide and WIN55,212-2 on glutamatergic nerve endings isolated from rat hippocampus

2006

We examined the effects of the endocannabinoide-anandamide (AEA), the synthetic cannabinoid, WIN55,212-2, and the active phorbol ester, 4-beta-phorbol 12-myristate 13-acetate (4-beta-PMA), on the release of [(3)H]d-Aspartate ([(3)H]d-ASP) from rat hippocampal synaptosomes. Release was evoked with three different stimuli: (1) KCl-induced membrane depolarization, which activates voltage-dependent Ca(2+) channels and causes limited neurotransmitter exocytosis, presumably from ready-releasable vesicles docked in the active zone; (2) exposure to the Ca(2+) ionophore-A23187, which causes more extensive transmitter release, presumably from intracellular reserve vesicles; and (3) K(+) channel block…

MaleSettore BIO/14 - FARMACOLOGIAPolyunsaturated AlkamideshippocampusMorpholinesmedicine.medical_treatmentPresynaptic TerminalsArachidonic AcidsNaphthalenesExocytosisCellular and Molecular Neurosciencechemistry.chemical_compoundGlutamatesglutamate releasemedicineAnimalsanandamideActive zoneRats WistarNeurotransmitterCannabinoidCalcimycinProtein kinase CSynaptosomeArachidonic AcidChemistrysynaptosomesDepolarizationCell BiologyAnandamideHippocampal synaptosomeCalcium Channel BlockersBenzoxazinesRatsBiochemistryBiophysicsTetradecanoylphorbol AcetateCannabinoidCapsaicinEndocannabinoidsNeurochemistry International
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PE-11, a peptide derived from chromogranin B, in the rat eye.

2010

The aim of the study was to investigate the presence and distribution of PE-11, a peptide derived from chromogranin B, in the rat eye. For this purpose, newborn rats were injected with a single dosage of 50mg/kg capsaicin subcutaneously under the neck fold and after three months, particular eye tissues were dissected and the concentration of PE-11-like immunoreactivity was determined by radioimmunoassay. Furthermore, PE-11-like immunoreactivities were characterized in an extract of the rat eye by reversed phase HPLC. Then, the distribution pattern of PE-11 was investigated in the rat eye and rat trigeminal ganglion by immunofluorescence. As a result, PE-11 was present in each tissue of the …

Malemedicine.medical_specialtyCorneal endotheliumgenetic structuresSensory Receptor CellsPhysiologyRadioimmunoassayFluorescent Antibody TechniqueIrisBiologyEyeBiochemistryRetinaCorneaRats Sprague-DawleyCellular and Molecular NeuroscienceTrigeminal ganglionEndocrinologyCiliary bodyNerve FibersInternal medicineCorneamedicineAnimalsChromatography High Pressure LiquidRetinaCiliary BodyOptic Nerveeye diseasesPeptide FragmentsScleraGanglionRatsEndocrinologymedicine.anatomical_structureAnimals NewbornTrigeminal Ganglionsense organsChoroidCapsaicinNeurogliaScleraChromogranin BPeptides
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NEONATAL CAPSAICIN TREATMENT DOES NOT PREVENT SPLANCHNIC VASODILATATION IN PORTAL-HYPERTENSIVE RATS

1994

It has been suggested that the peripheral sensory neurons are involved in the splanchnic hemodynamic changes of portal hypertension. Therefore the influence of permanent ablation of sensory neurons by neonatal capsaicin pretreatment (50 mg/kg, subcutaneously) on the development of the hyperdynamic splanchnic circulation in portal-hypertensive rats was studied. In adulthood, portal hypertension was induced with partial portal vein ligation. In study 1, systemic and splanchnic hemodynamics were measured by means of a radiolabeled-microsphere technique in portal-hypertensive rats, under ketamine anesthesia, pretreated with capsaicin or vehicle. Mean arterial pressure, heart rate, cardiac index…

Malemedicine.medical_specialtyMean arterial pressureCalcitonin Gene-Related PeptidePortal venous pressureHemodynamicschemistry.chemical_compoundInternal medicineHypertension PortalmedicineAnimalsNeurons AfferentSplanchnic CirculationRats WistarHepatologySplanchnic Circulationbusiness.industryHemodynamicsmedicine.diseaseRatsmedicine.anatomical_structureEndocrinologyAnimals NewbornchemistryGastric MucosaRegional Blood FlowCapsaicinVascular resistancePortal hypertensionCapsaicinSplanchnicbusinessDigestive SystemDilatation Pathologic
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Gastric acid secretory responses induced by peptone are mediated by capsaicin-sensitive sensory afferent neurons

1992

The involvement of capsaicin-sensitive afferent neurons in modulating acid-secretory responses to peptone, a product of protein digestion, has been investigated in the continuously perfused stomach of the urethan-anesthetized rat. Systemic neonatal pretreatment with capsaicin, which destroys primary afferent neurons, does not modify basal levels of acid secretion. Acid responses to intragastric perfusion with isotonic (0.5, 1, and 2.4%) or hypertonic (10 and 20%) solutions of peptone were reduced in capsaicin-treated rats. Intragastric perfusion with hypertonic mannitol (18%) did not stimulate secretion of acid. Systemic capsaicin pretreatment did not modify acid responses to intraperitone…

Malemedicine.medical_specialtyPhysiologyProtein digestionmedicine.medical_treatmentVagotomyGastric Acidchemistry.chemical_compoundPhysiology (medical)Internal medicineAnimalsMedicineNeurons AfferentGanglionectomyGanglia SympatheticHepatologybusiness.industryGastroenterologyRats Inbred StrainsVagotomyGanglionectomyRatsVagus nervePerfusionPentagastrinEndocrinologyHypotonic SolutionschemistryCapsaicinPeptonesReflexGastric acidFemaleCapsaicinbusinessmedicine.drug
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The role of the dentist in the diagnosis and management of patients with oral mucosal diseases

2021

Based on a few case reports of oral mucosal diseases a number of questions is raised about the role of dentists-general practitioners in the diagnostic procedure and management of patients with such diseases. For instance, are dentists prepared to prescribe topical corticosteroids and should dentists be taught how and when to take a biopsy? And how about palpation of the neck? A strong recommendation is made to take clinical pictures for proper documentation and, if needed, for telediagnostic procedures. Another issue relates to the communication between dentists and dental specialists when dealing with patients with oral diseases. In case of a patient suffering from burning mouth syndrome …

Orofacial painmedicine.medical_specialtyDentistsMEDLINEReviewBurning Mouth SyndromePalpationcapsaicinoral epithelial dysplasiaFacial PainBiopsymedicineHumansGeneral DentistryUNESCO:CIENCIAS MÉDICASMaxillofacial surgeonsOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryGeneral surgeryapoptosischiliBurning mouth syndromeoral cancerstomatognathic diseasescell proliferationOtorhinolaryngologySurgerymedicine.symptombusinessMouth DiseasesMedicina oral patologia oral y cirugia bucal
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Capsaicin differentially modulates voltage-activated calcium channel currents in dorsal root ganglion neurones of rats

2005

It is discussed whether capsaicin, an agonist of the pain mediating TRPV1 receptor, decreases or increases voltage-activated calcium channel (VACC) currents (ICa(V)). ICa(V) were isolated in cultured dorsal root ganglion (DRG) neurones of rats using the whole cell patch clamp method and Ba 2+ as charge carrier. In large diameter neurones (>35Am), a concentration of 50AM was needed to reduce ICa(V) (activated by depolarizations to 0 mV) by 80%, while in small diameter neurones (30Am), the IC50 was 0.36 AM. This effect was concentration dependent with a threshold below 0.025 AM and maximal blockade (>80%) at 5AM. The current–voltage relation was shifted to the hyperpolarized direction with an…

Pain ThresholdPatch-Clamp TechniquesTRPV1TRPV Cation ChannelsN-type calcium channelSecond Messenger SystemsMembrane PotentialsGanglia SpinalAnimalsL-type calcium channelPatch clampRats WistarMolecular BiologyCell SizeNeuronsDose-Response Relationship DrugVoltage-dependent calcium channelChemistryGeneral NeuroscienceCalcium channelT-type calcium channelCalciseptineAnatomyRatsRats Inbred LewBiophysicsCalcium ChannelsNeurology (clinical)CapsaicinSignal TransductionDevelopmental BiologyBrain Research
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Topical capsaicin application and axon reflex vasodilatation of the tongue: A videocapillaroscopic study

2006

The aim of this study was to evaluate the effects of topical capsaicin application on human lingual mucosa and to assess if neurogenic inflammation might have a role in the pathogenesis of lingual diseases. Thirty patients (16 males and 14 females; mean age: 41.46 +/- 11.8 years; range: 23-60) were examined in our laboratory. The neurogenic inflammation was experimentally induced in the lingual mucosa close to 1) the left margin of the tongue and 2) the right margin of the tongue after ipsilateral nerve trunk anesthesia. The characteristics of lingual microcirculation were observed using computerized videocapillaroscopic techniques. The vasodilatation was observed close to the left margin o…

PharmacologyNeurogenic inflammationTopical capsaicinbusiness.industryVasodilationAnatomyBurning mouth syndromeMicrocirculationchemistry.chemical_compoundmedicine.anatomical_structurechemistryCapsaicinTongueAnesthesiaReflexMedicinePharmacology (medical)Axon reflexmedicine.symptomAxonbusinessMethods and Findings in Experimental and Clinical Pharmacology
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Involvement of nitric oxide and tachykinins in the effects induced by protease-activated receptors in rat colon longitudinal muscle

2003

The aim of the present study was to verify a possible involvement of nitric oxide (NO) and of tachykinins in the contractile and relaxant effects caused by the activation of protease-activated receptor (PAR)-1 and PAR-2 in the longitudinal muscle of rat colon. Mechanical responses to the PAR-1 activating peptides, SFLLRN-NH2 (10 nM–10 μM) and TFLLR-NH2 (10 nM–10 μM), and to the PAR-2-activating peptide, SLIGRL-NH2 (10 nM–10 μM), were examined in vitro in the absence and in the presence of different antagonists. The relaxation induced by SFLLRN-NH2, TFLLR-NH2 and SLIGRL-NH2 was antagonised by the inhibitor of NO synthase L-Nω-nitroarginine methyl ester (300 μM), or by the inhibitor of the gu…

Pharmacologymedicine.medical_specialtyContraction (grammar)AntagonistMotilityInflammationNitric oxidechemistry.chemical_compoundEndocrinologychemistryCapsaicinInternal medicinemedicineNK1 receptor antagonistmedicine.symptomReceptorBritish Journal of Pharmacology
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