Search results for "guinea"

showing 10 items of 412 documents

The role of choline in the release of acetylcholine in isolated hearts.

1978

1. The concentrations of acetylcholine, choline and noradrenaline were estimated in the perfusate (overflow) of isolated hearts of chickens, cats, rabbits and guinea pigs. Neurotransmitter release was evoked by stimulation of both vagus nerves and by direct stimulation of the heart (field stimulation). 2. In the absence of exogenous choline and physostigmine, field stimulation at 20 Hz for 20 min caused an overflow of acetylcholine from the hearts of the 4 species investigated. During vagal stimulation, however, acetylcholine was detected only in the perfusate of the chicken heart. 3. Field stimulation for 2 min caused an overflow of 193 pmol g−1 min−1 acetylcholine and of 666 pmol g−1 min−…

Malemedicine.medical_specialtyPhysostigmineanimal structuresReserpinePhysostigmineGuinea PigsStimulationIn Vitro TechniquesCholinechemistry.chemical_compoundNorepinephrineInternal medicinemedicineCholineAnimalsNeurotransmitterGanglia AutonomicCholinesterasePharmacologybiologyMyocardiumVagus NerveGeneral MedicineReserpineAcetylcholineElectric StimulationEndocrinologychemistrybiology.proteinCatsCholinergicFemaleRabbitsChickensAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Some pharmacological properties of the false cholinergic transmitter acetylpyrrolidinecholine and its precursor pyrrolidinecholine

1976

The acetylchline analogue acetylpyrrolidinecholine as well as the choline analogue pyrrolidinecholine were synthesized and the cholinergic properties of both substances were investigated on the guinea-pig ileum, rat blood pressure and frog rectus abdominis muscle. Acetylpyrrolidinecholine was 3-5 times less potent than acetylcholine on the three preparations tested. The dose-response curves to acetylpyrrolidinecholine were shifted to the right in a parallel manner by atropine and (+)-tubocurarine. The dissociation constants for atropine and (+)-tubocurarine obtained with acetylpyrrolidinecholine as agonist were not different from those obtained with acetylcholine. This indicates that acetyl…

Malemedicine.medical_specialtyPyrrolidinesGuinea PigsRana temporariaNeuromuscular JunctionNeuromuscular transmissionBlood PressureReceptors NicotinicSynaptic TransmissionCholinechemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptormedicineAnimalsAcetylcholine receptorPharmacologyMuscarineMuscarinic acetylcholine receptor M3Muscle SmoothGeneral MedicineReceptors MuscarinicAcetylcholineRatsNicotinic agonistEndocrinologyParasympathomimeticschemistryCholinergicAcetylcholineMuscle Contractionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Formation and release of acetylpyrrolidinecholine (N-methyl, N-acetoxyethylpyrrolidinium) as a false cholinergic transmitter in the myenteric plexus …

1977

1. Longitudinal muscle strips of the guineapig small intestine were incubated with Tyrode solution containing the choline analogue pyrrolidinecholine. At the end of the incubation the concentrations of acetylcholine and its analogue acetylpyrrolidinecholine were determined in the strips by gas chromatography. 2. After 120 min of incubation with 1 mM pyrrolidinecholine, acetylpyrrolidinecholine comprised about 15% of the total amount of acetylcholine plus acetylpyrrolidinecholine. Electrical stimulation (1 Hz) of the strips during the incubation slightly increased the proportion of acetylpyrrolidinecholine to 21%. 3. The acetylcholine content of control strips increased significantly during …

Malemedicine.medical_specialtyPyrrolidinesTime FactorsGuinea PigsMyenteric PlexusStimulationIn Vitro TechniquesGuinea pigchemistry.chemical_compoundInternal medicineIntestine SmallmedicineCholineAnimalsIncubationMyenteric plexusPharmacologyChemistryParasympatholyticsGeneral MedicineSmall intestineAcetylcholineElectric StimulationMuscle DenervationEndocrinologymedicine.anatomical_structureCholinergicFemaleAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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The inhibition by dopamine of cholinergic transmission in the isolated guinea-pig ileum. Mediation through alpha-adrenoceptors.

1982

1. Segments of the guinea-pig ileum were incubated in Tyrode's solution containing 3 μM propranolol. Dopamine, like noradrenaline and clonidine, inhibited the twitch response to field stimulation. The inhibitory action of dopamine remained unchanged in the presence of the dopamine uptake inhibitor nomifensine (1 μM). Tissue from reserpine-pretreated amimals was insensitive to tyramine but the response to dopamine was not affected. It is, therefore, assumed that the effect of dopamine is due to a direct receptor stimulation and not to the release of noradrenaline. 2. The inhibitory action of dopamine was not antagonized by the dopamine receptor antagonists cis-flupenthixol, pimozide or dompe…

Malemedicine.medical_specialtyReserpineApomorphineDopamineGuinea PigsStimulationPharmacologyIn Vitro TechniquesSynaptic TransmissionClonidineNorepinephrineDopamineIleumParasympathetic Nervous SystemInternal medicinemedicineAnimalsTolazolinePharmacologyDose-Response Relationship DrugChemistryGeneral MedicineReceptors Adrenergic alphaDomperidoneReceptors AdrenergicApomorphineNomifensineEndocrinologyDopamine receptorDopamine AntagonistsFemaleSulpiridemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Pharmacological analysis of the responsiveness of guinea-pig lung parenchymal strip to dopamine

1984

Abstract Responses to dopamine were examined in the guinea-pig isolated lung parenchymal strip. Complete cumulative concentration-response curves to dopamine exhibited a biphasic pattern with a small initial contraction at concentrations below 10(-5) M followed by a dose-dependent relaxation at higher concentrations. Phentolamine (10(-5) M) completely abolished the contractile component and enhanced sensitivity and maximal relaxation to dopamine. In the presence of phentolamine, propranolol antagonized the dopamine-induced relaxation (pA2 = 8.54 +/- 0.07). In the presence of propranolol (10(-6) M), dopamine produced a dose-related contraction displaced to the right by phentolamine. Incubati…

Malemedicine.medical_specialtyReserpineContraction (grammar)DopamineGuinea PigsPropranololIn Vitro TechniquesPharmacologyNorepinephrinePhentolamineCocaineDopamineInternal medicinemedicineHaloperidolAnimalsPhentolamineLungPharmacologyChemistryAirway ResistanceIsoproterenolReserpinePropranololAcetylcholineEndocrinologyCatecholamineAcetylcholineResearch Articlemedicine.drugBritish Journal of Pharmacology
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ACTIONS OF PROSTAGLANDIN E2 ON MYOCARDIAL MECHANICS, CORONARY VASCULAR RESISTANCE AND OXYGEN CONSUMPTION IN THE GUINEA-PIG ISOLATED HEART PREPARATION

1975

Abstract 1 In isolated, electrically driven (3 Hz) hearts of guinea-pigs the action of prostaglandin E2 on left ventricular pressure (LVP), oxygen consumption (Qo2) and coronary vascular resistance (CVR) was studied by establishing cumulative concentration-response curves. The hearts were perfused at a constant flow (10 ml/min) with Tyrode solution (Ca++ 1.8 mM) at 32 degrees C. 2 Under control conditions prostaglandin E2 (2.86 X10(-11) -1.43 X 10(-7) M) decreased LVP, QO2 and CVR in a concentration-dependent manner by maximally 27, 18 and 38%, respectively (P less than 0.05). 3 After reserpine pretreatment there were lower initial values for all parameters measured. The effect of prostagla…

Malemedicine.medical_specialtyReserpineTime Factorsmedicine.medical_treatmentGuinea PigsBlood PressureIn Vitro TechniquesCoronary circulationOxygen ConsumptionHeart RateCoronary CirculationInternal medicineHeart ratemedicineAnimalsProstaglandin E2Pharmacologybusiness.industryProstaglandins EHeartReserpineMyocardial Contractionmedicine.anatomical_structureEndocrinologyBlood pressureVascular resistanceVentricular pressureFemaleVascular ResistancebusinessResearch Articlemedicine.drugProstaglandin EBritish Journal of Pharmacology
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INTERACTIONS OF ISOPRENALINE AND PROSTAGLANDIN E2 WITH RESPECT TO MYOCARDIAL CONTRACTILE FORCE, CORONARY VASCULAR RESISTANCE AND MYOCARDIAL OXYGEN CO…

1976

Left ventricular pressure (LVP), left ventricular pressure derivative (LV dp/dtmax), coronary vascular resistance (CVR) and myocardial oxygen consumption (Qo2) were measured simultaneously in isolated, electrically driven hearts of guinea-pigs at constant perfusion rate. 2 LVP, LV dp/dtmax, CVR and Qo2 were greatly decreased by either the addition of prostaglandin E2 (50 ng/ml) to the perfusion fluid or pretreatment of the animals with reserpine. 3 Isoprenaline (0.5 nM to 100 nM) induced increases in LVP, LV dp/dtmax and Qo2. In the presence of prostaglandin E2, there was a parallel shift of the isoprenaline concentration-response curve for LVP and LV dp/dtmax. This effect was not seen, aft…

Malemedicine.medical_specialtyReserpinemedicine.medical_treatmentGuinea PigsIndomethacinProstaglandinBlood PressureNorepinephrinechemistry.chemical_compoundOxygen ConsumptionInternal medicineIsoprenalinemedicineAnimalsDrug InteractionsProstaglandin E2PharmacologyDose-Response Relationship Drugbusiness.industryMyocardiumProstaglandins EIsoproterenolReserpineCoronary VesselsMyocardial ContractionBlood pressuremedicine.anatomical_structurechemistryCardiologyVentricular pressureVascular resistanceFemaleVascular ResistancebusinessResearch Articlemedicine.drugProstaglandin EBritish Journal of Pharmacology
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EFFECTS OF VANADATE ON RESPONSES OF GUINEA-PIG ISOLATED TRACHEA TO SPASMOGENS

1993

Abstract The effects of vanadate on the contractility of the guinea-pig isolated trachea was examined. Vanadate (0·1 Mm) produced a sustained contraction that was abolished in Ca2+-free EGTA (0·1 Mm)-containing physiological salt solution but was resistant to verapamil (1 μm). Vanadate (0·1 Mm) depressed tracheal responses to CaCl2 (in Ca2+-free depolarizing solution), KCl, acetylcholine, histamine and 5-hydroxytryptamine. For vanadate (10 μm), the inhibition of spasmogenic responses only reached statistical significance for histamine and 5-hydroxytryptamine. Caffeine (1 Mm)-induced spasm (trachea at 20°C in the presence of indomethacin (2·8 μm)) was not affected by vanadate (10 μm-0·1 Mm).…

Malemedicine.medical_specialtySerotoninContraction (grammar)Guinea PigsPharmaceutical ScienceIn Vitro TechniquesPotassium ChlorideContractilitychemistry.chemical_compoundInternal medicineCaffeinemedicineAnimalsVanadatePharmacologyChemistryCell MembraneMuscle SmoothAcetylcholineTracheaEGTAEndocrinologyParasympathomimeticsVerapamilVerapamilCalciumFemalemedicine.symptomVanadatesAcetylcholineHistaminemedicine.drugMuscle contractionHistamineMuscle Contraction
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EFFECTS OF PHORBOL 12,13-DIACETATE AND ITS INFLUENCE ON SPASMOGENIC RESPONSES IN NORMAL AND SENSITIZED GUINEA-PIG TRACHEA

1995

Abstract We have studied the effects of phorbol 12,13-diacetate (PDA) and its influence on a variety of spasmogenic responses in trachea isolated in from normal and sensitized guinea-pigs. Tracheal preparations were denuded of epithelium, treated with indomethacin (2·8 μm), and cooled to 20°C. In these experimental conditions, tracheal strips contracted to PDA (0·1 nm-1 μm). Contractions to PDA (1 μm) were greater in sensitized tissues. In normal trachea, contractions to PDA (0·1 μm) were depressed by H-7, 1-(5-isoquinolinyl-sulphonyl)-2-methylpiperazine, (50 μm), amiloride (10 μm), verapamil (10 μm) and Ca2+-free exposure. Similar effects were obtained in sensitized trachea except that PDA…

Malemedicine.medical_specialtySerotoninContraction (grammar)Vasodilator AgentseducationGuinea PigsIndomethacinPharmaceutical ScienceIn Vitro TechniquesPiperazinesPotassium ChlorideGuinea pigAmiloridechemistry.chemical_compoundInternal medicine1-(5-Isoquinolinesulfonyl)-2-MethylpiperazinePhorbol EstersmedicineAnimalsDiureticsProtein Kinase CPharmacologyMuscle Smoothrespiratory systemIsoquinolinesAmilorideTracheaEndocrinologychemistryVerapamilPhorbolVerapamilCalciummedicine.symptomHistamineAcetylcholinemedicine.drugMuscle contractionHistamineMuscle Contraction
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Cholinergic modulation of the release of 5-hydroxytryptamine from the guinea pig ileum.

1987

Isolated segments of the guinea pig ileum were vascularly perfused and the release of 5-HT and its metabolite 5-HIAA into the portal venous effluent determined by HPLC with electrochemical detection. Test substances were applied via the arterial perfusion medium. Oxotremorine inhibited concentration-dependently the release of 5-HT and 5-HIAA (by 47% at 1 mumol/l). Scopolamine (0.1 mumol/l) did not affect the release of 5-HT and 5-HIAA, but antagonized the effect of oxotremorine. In the presence of TTX (1 mumol/l), oxotremorine (1 mumol/l) increased the release of 5-HT by 150% and that of 5-HIAA by 220%. This increase was completely blocked by scopolamine. Hexamethonium (100 mumol/l) and TTX…

Malemedicine.medical_specialtySerotoninMetaboliteGuinea PigsScopolamineHexamethonium CompoundsBiologyIn Vitro TechniquesReceptors NicotinicHexamethoniumGuinea pigchemistry.chemical_compoundIleumInternal medicineMuscarinic acetylcholine receptorOxotremorinemedicineEnterochromaffin CellsAnimalsReceptors CholinergicIntestinal MucosaPharmacologyMuscarineOxotremorineGeneral MedicineEndocrinologynervous systemchemistryEnterochromaffin cellHexamethoniumSerotoninmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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