Search results for "Pharmacology toxicology"

showing 10 items of 253 documents

The positive inotropic effect of phenylephrine in the presence of propranolol. Increase in time to peak force and in relaxation time without increase…

1978

The effects of phenylephrine on the shape of the contraction curve and on the cyclic adenosine 3',5'-monophosphate (c-AMP) content were studied in electrically driven (frequency 0.2 Hz) cat papillary muscles. All experiments were done in the presence of 1 micron propranolol in order to minimize interference from beta-adrenoceptors. 1. Phenylephrine increased the force of contraction in a concentration-dependent manner. Maximal effects (about 200% of control) occurred at 30 micron phenylephrine. 2. The positive inotropic effect (PIE) of phenylephrine was antagonized by phentolamine. Phentolamine, 5 micron, produced a parallel shift of the concentration-response curve for the PIE of phenyleph…

Inotropemedicine.medical_specialtyContraction (grammar)Time FactorsPharmacology toxicologyAdrenergic beta-AntagonistsPropranololIn Vitro TechniquesPhenylephrineHeart RateInternal medicinemedicineCyclic AMPAnimalsDrug InteractionsPhentolaminePhenylephrinePharmacologyChemistryMyocardiumGeneral MedicineAdenosineMyocardial ContractionPropranololC++ AMPStimulation ChemicalEndocrinologyCatsTime to peakmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Effect of DB-c-AMP on mechanical characteristics of ventricular and atrial preparations of several mammalian species

1974

Conflicting results exist about the influence of cyclic N6-2′-O-dibutyryl-AMP (DB-c-AMP) on myocardial contractile force. The present study was designed to examine whether the positive inotropic action of DB-c-AMP is restricted to certain model preparations or whether it can be assumed to represent a more general effect of the drug. Therefore, the effects of DB-c-AMP on myocardial force and on various parameters of the isometric contraction curve were examined in isolated electrically driven (0.5–2Hz) ventricular and atrial preparations of several mammalian species (cat, rabbit, calf, sheep, rat and guinea-pig). The following results were obtained:

Inotropemedicine.medical_specialtyTime FactorsHeart VentriclesGuinea PigsPharmacology toxicologyIsometric exerciseSpecies SpecificityInternal medicinemedicineAnimalsHeart AtriaElectric stimulationPharmacologySheepBucladesineCATSbusiness.industryOrgan SizeGeneral MedicinePapillary MusclesElectric StimulationStimulation ChemicalC++ AMPRatsEndocrinologyBucladesineCatsCattleRabbitsbusinessHeart atriummedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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The effects of morphine on the temporal structure of Wistar rat behavioral response to pain in hot-plate

2016

Rationale: The largest amount of researches on the hot-plate test was carried out using quantitative assessments. However, the evaluation of the relationships among the different elements that compose the behavioral response to pain requires different approaches. Although previous studies have provided clear information on the behavioral structure of the response, no data are available on its temporal structure. Objectives: The objective of this study was to investigate the temporal structure of the behavioral response to pain in Wistar rat tested in hot-plate and how this structure was influenced by morphine-induced analgesia. Methods: The behavior of four groups of subjects tested in hot-…

Male0301 basic medicineHot TemperatureTime FactorsHot-platemedicine.medical_treatmentPharmacology toxicologyPainPhysiologyWistar ratSettore BIO/09 - Fisiologia03 medical and health sciences0302 clinical medicinemedicineNoxious stimulusAnimalsAnimal behaviorHot plateRats WistarSalinePharmacologyBehavior AnimalMorphineMultivariate analysiT-pattern analysiRatsAnalgesics Opioid030104 developmental biologyBehavioral responseMultivariate AnalysisExploratory BehaviorMorphineOpioid analgesicsPsychologyNeuroscience030217 neurology & neurosurgerymedicine.drugPsychopharmacology
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Models with clinically-relevant and life-threatening histamine-related cardiovascular disturbances: Evaluation of the clinical effectiveness of H1/H2…

1996

MaleAllergymedicine.medical_specialtyNeurologySwineClinical effectivenessImmunologyPharmacology toxicologyBlood PressureHistamine Receptor AntagonistsPharmacologyHistamine Releasechemistry.chemical_compoundDogsAnimalsp-Methoxy-N-methylphenethylamineMedicinePharmacologyChi-Square Distributionbusiness.industryPerioperativemedicine.diseaseDisease Models AnimalHistamine H2 AntagonistschemistryHistamine H1 AntagonistsSwine MiniatureFemaleHypotensionbusinessHistamineHistamineInflammation Research
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Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF) - more common than assumed? Report of four cases with transient NIHF and a rev…

2012

Abstract Background Lysosomal storage disorders (LSD) are a rare cause of non immunological hydrops fetalis (NIHF) and congenital ascites. The reported incidence is about 1%. The incidence of idiopathic NIHF is estimated to be about 18%. Patients and methods We report four cases with transient hydrops fetalis resulting from LSD and performed a literature review on LSD with NIHF and congenital ascites in combination. Results At present, 12 different LSDs are described to be associated with NIHF or congenital ascites. Most patients had a family history of NIHF, where the preceding sibling had not been examined. A diagnostic approach to the fetus with NIHF due to suspected LSD either in utero …

MalePathologymedicine.medical_specialtyHydrops FetalisNon-immunological hydrops fetalisPharmacology toxicologylcsh:MedicineLysosomal storage diseaseLysosomal storage disordersClinical approachPregnancyHydrops fetalisAscitesLysosomal storage diseaseHumansMedicineGenetics(clinical)Pharmacology (medical)Genetics (clinical)Medicine(all)business.industryResearchIncidence (epidemiology)lcsh:RTransient hydropsGeneral Medicinemedicine.diseaseCongenital ascitesLysosomal Storage DiseasesImmunologyFemalemedicine.symptombusinessOrphanet Journal of Rare Diseases
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T-pattern analysis of diazepam-induced modifications on the temporal organization of rat behavioral response to anxiety in hole board.

2010

Rationale: By means of t-pattern analysis, it has been observed that the different events, characterizing rat behavior in hole board (HB), present close interrelationships which occur sequentially and with significant constraints on the interval lengths separating them. Objectives: The aim of present research was to study, by means of descriptive and multivariate t-pattern analyses, the effects of the reference anxiolytic drug diazepam (DZP) on temporal structure of a rat’s anxiety-related behavior in HB. Methods: Fifty-six male Wistar rats were tested for 10 min in HB. Video files, collected for each animal, were coded by means of a software coder, and event log files, generated for each s…

MaleTime FactorsPharmacology toxicologyPattern analysisAnxietySettore BIO/09 - FisiologiaDevelopmental psychologymedicineAnimalsRats WistarPharmacologyDiazepamBehavior AnimalDose-Response Relationship DrugMultivariate analysiT-pattern analysiRatsDisease Models AnimalBehavioral responseAnti-Anxiety AgentsMultivariate AnalysisHole boardRatAnxietymedicine.symptomTemporal organizationPsychologyNeuroscienceDiazepammedicine.drugBehavioral ResearchPsychopharmacology
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Comparative effects of the novel vasotocin analogue F-180 vs. vasopressin and terlipressin on systemic and splanchnic isolated vessels from portal hy…

2001

F-180 has been proposed as a new vasopressin analogue for the treatment of portal hypertension. This study investigates the contractile profile of F-180 compared to vasopressin and its analogue terlipressin on isolated systemic and splanchnic vessels from sham-operated and partial portal vein ligated (PPVL) rats. F-180 (10(-9)-10(-6) M), vasopressin (10(-11)-10(-8) M) and terlipressin (10(-9)-10(-4) M) induced contraction of the mesenteric vein, aorta, iliac, tail and mesenteric arteries. The order of potency in these vessels was vasopressin (pD2 approximately 9)F-180 (pD2 approximately 8)terlipressin (pD2 approximately 6). Significant (P0.01) differences between sham-operated and PPVL rats…

MaleVasopressinmedicine.medical_specialtymedicine.drug_classVasopressinsPharmacology toxicologyPortal veinLypressinVasotocinMuscle Smooth VascularRats Sprague-Dawleychemistry.chemical_compoundMesenteric VeinsInternal medicineHypertension PortalmedicineAnimalsVasoconstrictor AgentsPharmacologybusiness.industryGeneral Medicinemedicine.diseaseMesenteric ArteriesRatsEndocrinologychemistryVasoconstrictioncardiovascular systemPortal hypertensionVasopressin AnalogueSplanchnicbusinessTerlipressinTerlipressinmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Effect of theophylline on calcium exchangeability in ventricular myocardium.

1976

The effects of theophylline on contractile force and myocardial calcium exchangeability were studied in isolated, electrically driven Langendorff perfused guinea-pig hearts. Following a 30-min exposure to 45Ca, total cellular calcium and 45Ca activity were measured in right ventricular samples. "Nontoxic" theophylline concentrations (5 x 10(-5) -10(-3) g/ml) which augmented contractile force without producing arrhythmias or contractures had no effect on total tissue calcium and did not alter the size of the fraction of cellular calcium exchangeable under steady-state conditions. A "toxic" concentration of theophylline (2 x 10(-3) g/ml) induced contractures and increased the amount of exchan…

Malemedicine.medical_specialtyHeart VentriclesPharmacology toxicologyGuinea Pigschemistry.chemical_elementCalciumIn Vitro TechniquesVentricular myocardiumTheophyllineInternal medicineCoronary CirculationmedicineAnimalsTheophyllineMyocardial calciumTotal TissuePharmacologyMyocardiumBiological TransportGeneral MedicineMyocardial ContractionElectric StimulationStimulation ChemicalCell calciumEndocrinologychemistryCalciumFemaleTotal calciumExtracellular Spacemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Clinic modelling randomised trials (CMRT's) in animals as a new intermediate between biological experiments and randomised clinical trials: applicati…

1998

Malemedicine.medical_specialtySwinemedicine.medical_treatmentPremedicationImmunologyPharmacology toxicologyRanitidineHistamine ReleaseDouble-Blind MethodMedicineAnimalsDimethindenep-Methoxy-N-methylphenethylamineAnesthesiaCluster randomised controlled trialIntensive care medicineIntraoperative ComplicationsRandomized Controlled Trials as TopicPharmacologybusiness.industryClinical trialDisease Models AnimalHistamine H2 AntagonistsSurgical Procedures OperativeHistamine H1 AntagonistsSwine MiniatureAntihistamineFemalebusinessCimetidineInflammation research : official journal of the European Histamine Research Society ... [et al.]
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Differential inhibition of biphenyl hydroxylation in perfused rat liver

1978

A differential inhibition of biphenyl hydroxylation by alpha-naphthoflavone and metyrapone was observed in isolated perfused rat liver. alpha-Naphthoflavone inhibited 2- and 4-hydroxylation in livers from beta-naphthoflavone-pretreated animals but had no effect on both reactions in livers from phenobarbital-pretreated animals. Metyrapone inhibited 2- and 4-hydroxylation in phenobarbital-stimulated livers, but only insignificant inhibition of 2-hydroxylation and a slight enhancement of 4-hydroxylation by metyrapone was observed in beta-naphthoflavone-stimulated livers. Conjugation of 2-hydroxybiphenyl and 4-hydroxybiphenyl by isolated perfused livers was also studied. 4-Hydroxybiphenyl prefe…

Malemedicine.medical_specialtyTime FactorsPharmacology toxicologyHydroxylationDifferential inhibitionHydroxylationchemistry.chemical_compoundCytochrome P-450 Enzyme SystemBiphenyl metabolismInternal medicinemedicineAnimalsFlavonoidsPharmacologyBiphenylMetyraponeBiphenyl CompoundsGeneral MedicineMetyraponeRatsEndocrinologyLiverchemistryDepression ChemicalPhenobarbitalRat livermedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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