Search results for "STIMULATION"

showing 10 items of 2192 documents

A pharmacological study ofAraujia sericifera B. extracts in rodents

1995

The present study analyses the pharmacological activity in in vitro and in vivo models of different extracts obtained from Araujia sericifera. The hexane extract of fruits lacked toxicity, but exhibited an analgesic effect in models of chemical and thermal stimulation. Such an extract was the only one which exhibited antiinflammatory actions. The intrinsic effect on arterial blood pressure was biphasic: at low doses it significantly increased blood pressure, whereas at high doses it exerted the opposite effect. On isolated organs it produced a marked decrease in the maximum effect of histamine and acetylcholine. The dichloromethanol extract of fruits decreased arterial pressure and the maxi…

PharmacologybiologyChemistryBiological activityStimulationPharmacologyPharmacognosybiology.organism_classificationchemistry.chemical_compoundToxicitymedicineSerotoninAraujia sericiferaAcetylcholineHistaminemedicine.drugPhytotherapy Research
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Evaluation of the acute toxicity, analgesic and CNS activities of different species ofTeucrium genus

1995

Methanol and dichloromethanol extracts of the leaves and stems of four Teucrium species (T. cartaginenses, T. flavum, T. pumillum and T. buxifolium) have been tested for their toxicity, analgesic and central depressor effects. The intraperitoneal administration of the different extracts showed a CNS depressant activity in mice, but they lacked anticonvulsive effects. When tested for analgesic activity none of the extracts increased the threshold of pain thermal stimulus. However, the methanol and dichloromethanol extracts of T. cartaginenses and T. buxifolium species showed a significant analgesic effect in models of pain induced by chemical or mechanical stimulation.

PharmacologybiologyChemistryTEUCRIUM CARTAGINENSES EXTRACTSTEUCRIUM FLAVUM EXTRACTSAnalgesicCentral nervous systemTEUCRIUM BUXIFOLIUM EXTRACTSStimulationBiological activityEFFECTS ON CNSPharmacologybiology.organism_classificationAcute toxicityTeucriumANALGESIAmedicine.anatomical_structureThreshold of painToxicitymedicineTEUCRIUM PUMILLUM EXTRACTSPhytotherapy Research
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Studies on the gastric anti-ulcer activity of hypolaetin-8-glucoside

1988

The gastric anti-ulcer activity of hypolaetin-8-O-β-D-glucoside (H-8-G), a flavonoid isolated from Sideritis leucantha, has been studied in rats. This compound significantly reduced gastric lesions induced by ethanol or acetylsalicylic acid (ASA), with an increase in mucus production. In the pylorus-ligated rat, H-8-G did not affect the volume of gastric secretion but decreased its acidity and peptic activity. The anti-ulcer activity of this flavonoid does not depend on stimulation of cell proliferation in the rat gastric mucosa. Our results suggest that H-8-G activity is related to its cytoprotective effects [mediated by endogenous prostaglandins (PGs) and associated to an increase in gast…

Pharmacologychemistry.chemical_classificationEthanolbiologyCell growthPepticdigestive oral and skin physiologyFlavonoidStimulationEndogenyPharmacologybiology.organism_classificationdigestive system diseaseschemistry.chemical_compoundmedicine.anatomical_structurechemistryBiochemistryGastric mucosamedicineSideritis leucanthaPhytotherapy Research
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Transcriptional and post-transcriptional analysis of peroxisomal protein encoding genes from rat treated with an hypolipemic agent, ciprofibrate

1995

The treatment of rats with ciprofibrate, a potent peroxisome proliferator, led to increased levels of the peroxisomal acyl-CoA oxidase (ACO) mRNA. How ciprofibrate functions to elevate ACO mRNA is not known. To help determine the mechanism of ciprofibrate action, in vitro transcription assays were performed. It was determined that ciprofibrate was responsible for a 3.5-fold stimulation of the rate of ACO transcription within 24 hr of ingestion. It was also observed that the transcription rate stimulation following a 2-week ciprofibrate treatment of Wistar rats was maintained following 4 weeks of ciprofibrate withdrawal. Re-introduction of the drug after the 4-week pause resulted in greater …

Pharmacologychemistry.chemical_classificationmedicine.medical_specialtyOxidase testPeroxisome proliferator-activated receptorStimulationPeroxisomeBiologyBiochemistryEndocrinologychemistryMechanism of actionInternal medicineGene expressionmedicineAcyl-CoA oxidaseCiprofibratemedicine.symptommedicine.drugBiochemical Pharmacology
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The control of amygdaloid and temporal paroxysmal activity by the caudate nucleus

1971

In gatti curarizzati ed in gatti portatori di elettrodi a dimora e liberi di muoversi, la stimolazione ripetitiva ad alta frequenza del nucleo caudato inibisce la comparsa sia dei fenomeni bioelettrici parossistici focalizzati nell'amigdala e nella corteccia temporale sia dei fenomeni comportamentali omologabili all'epilessia psicomotoria.

Pharmacologymedicine.medical_specialtyCaudate nucleusCell BiologyBiologyAmygdalaElectric StimulationTemporal LobeCellular and Molecular NeuroscienceEndocrinologyEpilepsy Temporal LobeSeizuresAnesthesiaInternal medicineCatsmedicineAnimalsMolecular MedicineCaudate NucleusMolecular BiologyExperientia
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Dose-dependent biphasic leptin-induced proliferation is caused by non-specific IL-6/NF-κB pathway activation in human myometrial cells

2015

Background and Purpose Leptin, an adipokine synthesized by the placenta during pregnancy, has been proposed for the management of preterm labour (PTL), as it is able to prevent in vitro uterine contractility and remodelling associated with labour onset. Another common feature of labour onset is the phenotypic switch of myometrial smooth muscle cells from a proliferative to a hypertrophic state. As proliferative effects have been demonstrated for leptin in other tissues, we aimed to investigate its ability to induce myometrial proliferation and thus to maintain uterine quiescence. Experimental Approach We stimulated human primary myometrial smooth muscle cells with leptin in the presence or …

Pharmacologymedicine.medical_specialtyLeptin receptorLeptindigestive oral and skin physiologyMyometriumAdipokineStimulationBiologyEndocrinologyInternal medicinemedicineMyocyteSignal transductionReceptorBritish Journal of Pharmacology
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Adrenoceptor-mediated changes of excitation and contraction in isolated heart muscle preparations.

1989

The inotropic effects of sympathetic stimulation on the heart are mainly ascribed to the activation of beta-adrenoceptors. However, several findings suggest that alpha-adrenoceptors also may help mediate the inotropic response to catecholamines under certain conditions. The onset of the positive inotropic effect mediated by beta-adrenoceptors occurs within seconds and is associated with a faster rate of relaxation. Both beta 1- and beta 2-adrenoceptors are stimulatorily coupled to the enzyme adenylate cyclase, thereby leading to the generation of cyclic AMP. Cyclic AMP increases the slow inward calcium current and enhances the uptake of calcium into the sarcoplasmic reticulum. GTP-binding p…

Pharmacologymedicine.medical_specialtyMuscarineAdrenergic receptorAdenylate kinaseStimulationHeartIn Vitro TechniquesAdenosine receptorCyclaseMyocardial ContractionReceptors AdrenergicBeta-1 adrenergic receptorchemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineAnimalsHumansmedicine.symptomCardiology and Cardiovascular MedicineMuscle contractionJournal of cardiovascular pharmacology
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Calcium dependence of the evoked arginine vasopressin release by electrical stimulation and by L-glutamate.

1989

Pharmacologymedicine.medical_specialtyPituitary glandVasopressinArgininechemistry.chemical_elementStimulationCalciumBiologyIn Vitro TechniquesElectric StimulationRatsArginine Vasopressinmedicine.anatomical_structureEndocrinologychemistryGlutamatesPituitary Gland PosteriorL glutamateInternal medicinemedicineAnimalsCalciumElectric stimulationPharmacological research
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NANC inhibitory neurotransmission in mouse isolated stomach: involvement of nitric oxide, ATP and vasoactive intestinal polypeptide

2003

1. The neurotransmitters involved in NANC relaxation and their possible interactions were investigated in mouse isolated stomach, recording the motor responses as changes of endoluminal pressure from whole organ. 2. Field stimulation produced tetrodotoxin-sensitive, frequency-dependent, biphasic responses: rapid transient relaxation followed by a delayed inhibitory component. 3. The inhibitor of the synthesis of nitric oxide (NO), l-NAME, abolished the rapid relaxation and significantly reduced the slow relaxation. Apamin, blocker of Ca2+-dependent K+ channels, or ADPbetaS, which desensitises P2y purinoceptors, reduced the slow relaxation to 2-8 Hz, without affecting that to 16-32 Hz or the…

Pharmacologymedicine.medical_specialtyRelaxation (psychology)Vasoactive intestinal peptideStimulationNeurotransmissionApaminchemistry.chemical_compoundMuscle relaxationEndocrinologychemistryInternal medicinemedicineBiophysicsSodium nitroprussideNeurotransmittermedicine.drugBritish Journal of Pharmacology
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Tachykinergic neurotransmission is enhanced in duodenum from dystrophic (mdx ) mice

2005

1 Duodenal longitudinal muscle of mdx mice, an animal model for Duchenne muscular dystrophy, showed a decrease in the electrically evoked nonadrenergic, noncholinergic (NANC) inhibitory responses associated with a reduction of the participation of nitric oxide (NO). In this study, we investigated whether the impairment of NO could also lead to alterations in the NANC excitatory transmission. 2 Nerve-evoked responses consisted of an inhibitory phase followed, at the end of stimulation, by an excitatory response characterised by an increase in amplitude of the spontaneous contractions. In mdx mice, the amplitude of the nerve-evoked contractions was significantly higher than in normals. 3 N(om…

Pharmacologymedicine.medical_specialtySubstance PStimulationBiologyNeurotransmissionApaminchemistry.chemical_compoundEndocrinologychemistryInternal medicineExcitatory postsynaptic potentialmedicineSodium nitroprussideNeurokinin ASoluble guanylyl cyclasemedicine.drugBritish Journal of Pharmacology
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