Search results for "contraction"

showing 10 items of 1092 documents

P1 and P2 receptors in the rat duodenal smooth muscle

1989

Pharmacologymedicine.medical_specialtyAdenosineDose-Response Relationship DrugDuodenumPurinergic receptorReceptors PurinergicMuscle SmoothIsometric exerciseIn Vitro TechniquesBiologyIn vitroRatsAdenosine Triphosphatemedicine.anatomical_structureEndocrinologySmooth muscleIsometric ContractionInternal medicinemedicineDuodenumAnimalsReceptorMuscle ContractionPharmacological Research
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Activation of soluble guanylyl cyclase by YC-1 in aortic smooth muscle but not in ventricular myocardium from rat

1997

1 The effects of YC-1 (3-(5′-hydroxymethyl-2′-furyl)-1-benzyl indazole), an activator of soluble guanylyl cyclase, on tension, levels of cyclic GMP and cyclic AMP, and cardiac L-type Ca2+-current (ICa(L)) were investigated in aortic smooth muscle and ventricular heart muscle from rat. 2 YC-1 (0.1–30 μM) induced a concentration-dependent relaxation in aortic rings precontracted with phenylephrine (3 μM). The relaxant effects of YC-1 were reversed by 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (30 μM; ODQ), potentiated by zaprinast (10 μM) and antagonized by Rp-8-Br-cGMPS (100 μM). 3 In ventricular heart muscle strips, YC-1 (30 μM) exhibited no effects on force of contraction (Fc) in the abse…

Pharmacologymedicine.medical_specialtyAortaContraction (grammar)Chemistrychemistry.chemical_compoundEndocrinologyIsoprenalineInternal medicinemedicine.arterycardiovascular systemmedicinePlatelet aggregation inhibitormedicine.symptomSoluble guanylyl cyclaseZaprinastPhenylephrineVasoconstrictionmedicine.drugBritish Journal of Pharmacology
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Zur Wirkung von Oxytocin auf einen autorhythmischen glatten Gefässmuskel

1972

The influence of oxytocine on the spontaneously contractile portal vein of the rat has been investigated. This octapeptide decreases the active tension and abolished it completely at a concentration of 5×10−7g/ml. The effect is not caused by an adrenergic mechanism but by a direct action on the smooth muscle cell.

Pharmacologymedicine.medical_specialtyChemistryPortal veinAdrenergicCell BiologyCellular and Molecular NeuroscienceEndocrinologySmooth muscleOxytocinInternal medicinemedicineMolecular MedicineActive tensionmedicine.symptomMolecular BiologyMuscle contractionmedicine.drugExperientia
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Kinetische Analyse der Calcium-Kompartimente im Meerschweinchenherzen unter Kontrollbedingungen und Strophanthineinwirkung

1974

A quantitative analysis of myocardial Ca-metabolism was carried out on isolated, isovolumetric (10 ml/min) perfused guinea pig hearts by combined determinations of the total Ca-content and kinetics of 45Ca-efflux (collecting period 60 min) (Fig. 1). The kinetics of 45Ca-uptake was estimated by extrapolating 45Ca-efflux curves of heart muscles isotopically loaded for different times (2, 5, 10, 30 60 min) to the end of the loading-period (Fig. 2).

Pharmacologymedicine.medical_specialtyChromatographyChemistryPharmacology toxicologyGeneral MedicineHeart musclesOuabainGuinea pigEndocrinologyInternal medicinemedicineQuantitative analysis (chemistry)Isovolumetric contractionmedicine.drugNaunyn-Schmiedeberg's Archives of 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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Über die Beeinflussung der Ca-Aufnahme in Lipidextrakte aus Mikrosomen und Mitochondrien des Herzens durch Digitoxin

1970

Lipids were isolated by chloroform-methanol extraction from mitochondrial and microsomal fractions of guinea-pig hearts. In the presence of digitoxin (10−9-10−6 g/ml) 15–30% more radioactive Ca was taken up by the lipid extracts than under control conditions, but the total amount of Ca in this phase remained unchanged. Thus, digitoxin produced an increase in the specific activity of the lipid-bound Ca which may be explained by an increased exchangeability of this Ca fraction. This effect of digitoxin might result in an improved availability of the lipid-bound Ca for Ca-dependent functions (e.g. contraction) of the heart muscle cell.

Pharmacologymedicine.medical_specialtyContraction (grammar)DigitoxinChemistryCell Biologycarbohydrates (lipids)Cellular and Molecular NeuroscienceEndocrinologyInternal medicinepolycyclic compoundsmedicineMicrosomeMolecular Medicinelipids (amino acids peptides and proteins)Heart Muscle CellSpecific activityMolecular Biologymedicine.drugExperientia
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Effects ofThymus species extracts on rat duodenum isolated smooth muscle contraction

1989

The diethylether, ethylacetate and butanolic extracts from Thymus webbianus and Thymus leptophyllus were tested for spasmolytic activity. Pre-incubation of the isolated rat duodenum with these extracts for 10 min produced a concentration-dependent inhibition of acetylcholine-induced contractions. This effect was at least ten times greater with the apolar extracts than with the polar extracts.

Pharmacologymedicine.medical_specialtyEndocrinologySmooth muscleInternal medicinemedicineRat Duodenumlipids (amino acids peptides and proteins)Smooth muscle contractionBiologyPhytotherapy Research
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Histamine inhibits spontaneous activity of the uterus of the progesterone-treated rat

1993

Pharmacologymedicine.medical_specialtyGeneral NeuroscienceUterusHistamine H1 receptorBiologychemistry.chemical_compoundmedicine.anatomical_structureEndocrinologychemistryHistamine H2 receptorIn uteroInternal medicinemedicineCatecholamineLiberationmedicine.symptomHistamineMuscle contractionmedicine.drugJournal of Autonomic 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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Evidence that ATP or a related purine is an excitatory neurotransmitter in the longitudinal muscle of mouse distal colon

2007

Background and purpose: This study analysed the contribution of the purinergic system to enteric neurotransmission in the longitudinal muscle of mouse distal colon. Experimental approach: Motor responses to exogenous ATP and to nerve stimulation in vitro were assessed as changes in isometric tension. Key results: ATP induced a concentration-dependent contraction, reduced by 4-[[4-formyl-5-hydroxy-6-methyl-3-[(phosphonooxy)methyl]-2-pyridinyl]azo]-1,3-benzene disulphonic acid (PPADS), suramin, P2Y purinoreceptor desensitisation with adenosine 5’-O-2-thiodiphosphate (ADPβS), and atropine, but unaffected by P2X purinoceptor desensitisation with α,β-methylene ATP (α,β-meATP) and by 2,2-dimethyl…

Pharmacologymedicine.medical_specialtyP2Y receptorPurinergic receptorNeurotransmissionBiologyAdenosinechemistry.chemical_compoundAdenosine diphosphatePurinergic AntagonistsEndocrinologychemistryInternal medicinemedicinePPADSmedicine.symptomMuscle contractionmedicine.drugBritish Journal of Pharmacology
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