Search results for "contractility"

showing 10 items of 87 documents

Physiological adaptations to resistance training in rats selectively bred for low and high response to aerobic exercise training

2018

New Findings: What is the central question of this study? Can phenotypic traits associated with low response to one mode of training be extrapolated to other exercise-inducible phenotypes? The present study investigated whether rats that are low responders to endurance training are also low responders to resistance training. What is the main finding and its importance? After resistance training, rats that are high responders to aerobic exercise training improved more in maximal strength compared with low-responder rats. However, the greater gain in strength in high-responder rats was not accompanied by muscle hypertrophy, suggesting that the responses observed could be mainly neural in orig…

Malemedicine.medical_specialtyprotein synthesisPhysiologyStimulationHindlimbPhysical strengthArticleMuscle hypertrophy03 medical and health sciences0302 clinical medicineEndurance trainingInternal medicinePhysical Conditioning AnimalMedicineAerobic exerciseAnimalsMuscle Strengthmuscle hypertrophyta315Muscle Skeletallihassolutfibre contractilitybusiness.industryResistance trainingResistance Training030229 sport sciencesGeneral Medicinemuscle stimulationAdaptation PhysiologicalRatsPhysiological AdaptationsEndocrinologyBody Compositionbusiness030217 neurology & neurosurgerylihasvoima
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Active contractility of the lymphangion and coordination of lymphangion chains

1976

PharmacologyChemistryGuinea PigsBiological TransportCell BiologyComputational biologyIntestinesLymphatic SystemContractilityCellular and Molecular NeurosciencePressureAnimalsMolecular MedicineExtracellular SpaceMolecular BiologyLymphangionMathematicsMuscle ContractionExperientia
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Vergleichende Untersuchungen �ber die Wirkung verschiedener Digitoxigeninderivate auf die Kontraktionskraft und den Ca-Austausch isolierter Meerschwe…

1963

An isolierten, elektrisch gereizten Meerschweinchenvorhofen wurde das Verhalten der Kontraktionskraft und des cellularen Ca-Haushaltesunter dem Einflus von Digitoxigenin, Dihydrodigitoxigenin und 3α-Digitoxigenin uber einen weiten Dosierungsbereich vergleichend untersucht. Diese Substanzen zeigten betrachtliche Unterschiede in der Intensitat ihrer positiv inotropen und kontrakturerzeugenden Wirkung. Im positiv inotropen Dosierungsbereich verhielten sich die aquieffektiven Konzentrationen von Digitoxigenin, Dihydrodigitoxigenin und 3α-Digitoxigenin etwa wie 1:20:70. Bei der Messung des transmembranen Ca-Austausches mit 47Ca ergab sich unter Kontrollbedingungen eine nur partielle Markierbarke…

PharmacologyGuinea pigContractilityDigitoxigeninchemistry.chemical_compoundChemistryPharmacology toxicologyGeneral MedicineDIGITALIS GLYCOSIDESMolecular biologyElectric stimulationNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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Functional characterization of α1 -adrenoceptor subtypes in vascular tissues using different experimental approaches:a comparative study

2003

The α1-adrenergic responses of rat aorta and tail artery have been analysed measuring the contractility and the inositol phosphate (IP) formation induced by noradrenaline. Three antagonists, prazosin, 5-methylurapidil (α1A selective) and BMY 7378 (α1D selective) have been used in different experimental procedures. Noradrenaline possesses a greater potency inducing contraction and IP accumulation in aorta (pEC50-contraction=7.32±0.04; pEC50-IPs=6.03±0.08) than in the tail artery (pEC50-contraction=5.71±0.07; pEC50-IPs=5.51±0.10). Although the maximum contraction was similar in both tissues (Emax-tail=619.1±55.6 mg; Emax-aorta-698.2±40.8 mg), there were marked differences in the ability of th…

Pharmacologychemistry.chemical_classificationmedicine.medical_specialtyAortaContraction (grammar)AntagonistBiologyContractilityEndocrinologychemistryInternal medicinemedicine.arterySecond messenger systemmedicinePrazosinAdrenergic antagonistInositol phosphatemedicine.drugBritish Journal of Pharmacology
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Effects of nitric oxide donors on cardiac contractility in wild-type and myoglobin-deficient mice

2002

1. The effects of the nitric oxide (NO) donors S-nitroso-N-acetylpenicillamine (SNAP), sodium(Z)-1-(N,N-diethylamino)diazen-1-ium-1,2-diolate (DEA-NONOate), and (Z)-1-[N-(2-Aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate (DETA-NONOate) on force of contraction (F(c)) were studied in atrial and ventricular muscle strips obtained from wild-type (WT) and myoglobin-deficient (myo(-/-)) mice. 2. SNAP slightly reduced F(c) in preparations from WT mice at concentrations above 100 microM; this effect was more pronounced in myo(-/-) mice. 3. DEA-NONOate reduced F(c) in preparations from myo(-/-) mice to a larger extent than those from WT mice. 4. DETA-NONOate reduced F(c) in preparations…

Pharmacologymedicine.medical_specialtyWild typeSnapNitric oxideContractilitychemistry.chemical_compoundEndocrinologychemistryMyoglobinInternal medicinemedicineSoluble guanylyl cyclaseReceptorIntracellularBritish Journal of Pharmacology
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Hypoxia-induced dysfunction of rat diaphragm

2004

Contains fulltext : 47331.pdf (Publisher’s version ) (Closed access) Oxidants may play a role in hypoxia-induced respiratory muscle dysfunction. In the present study we hypothesized that hypoxia-induced impairment in diaphragm contractility is associated with elevated peroxynitrite generation. In addition, we hypothesized that strenuous contractility of the diaphragm increases peroxynitrite formation. In vitro force-frequency relationship, isotonic fatigability, and nitrotyrosine levels were assessed under hypoxic (Po(2) approximately 6.5 kPa) and hyperoxic (Po(2) approximately 88.2 kPa) control conditions and also in the presence of authentic peroxynitrite (60 min), ebselen (60 min), and t…

Pulmonary and Respiratory MedicineAzolesMalemedicine.medical_specialtyPhysiologyDiaphragmAetiology screening and detection [ONCOL 5]In Vitro TechniquesIsoindolesNitric oxideContractilitychemistry.chemical_compoundTranslational research [ONCOL 3]Physiology (medical)Internal medicineOrganoselenium CompoundsPeroxynitrous AcidmedicineRespiratory muscleAnimalsRespiratory systemEnzyme InhibitorsRats WistarHypoxiaHeart lung and circulation [UMCN 2.1]Renal disorder [IGMD 9]omega-N-MethylarginineNitrotyrosineCell BiologyHypoxia (medical)Tissue engineering and pathology [NCMLS 3]musculoskeletal systemRatsPathogenesis and modulation of inflammation [N4i 1]EndocrinologychemistryBiochemistryMuscle FatigueTyrosineRat DiaphragmLipid Peroxidationmedicine.symptomPeroxynitriteMuscle ContractionAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
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Immunohistochemical and Biomolecular Identification of Orphanin FQ, eNOS, Atrial natriuretic Factor and Oxytocin in Rat Seminal Vesicles

2009

In previous studies performed on rodents, we detected the presence of adreno-cholinergic and peptidergic innervation in seminal vesicles and other organs of the male genital system, such as prostate and ductus deferens, in which we also investigated the expression of NOS and NADPH-diaphorase. During the present project we focused our attention on the expression of some peptides involved in local control of smooth muscle relaxation, contractility, vasodilatation and control of blood flow in rat seminal vesicles. We investigated, through immunohistochemistry and RT-PCR, the presence of four peptides: orphanin, eNOS, ANF and oxytocin. Immunohistochemistry was used to detect the presence of the…

Settore BIO/17 - IstologiaMalemedicine.medical_specialtyNitric Oxide Synthase Type IIIVasodilator AgentsVasodilationOxytocinContractilityParacrine signallingSeminal vesicleEnosInternal medicinemedicineAnimalsOpioid peptideGeneral Veterinarybiologyrat seminal vesicles orphanin eNOS ANF oxytocinSeminal VesiclesGeneral Medicinebiology.organism_classificationImmunohistochemistryRatsEndocrinologymedicine.anatomical_structureOpioid PeptidesOxytocinAtrial Natriuretic FactorHomeostasismedicine.drugAnatomia, Histologia, Embryologia
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Effects of a vitamin D3 analogue in a rat model of bladder outlet obstruction

2006

OBJECTIVES To explore the effect of the vitamin D3 analogue, BXL-628, on some of the consequences of bladder outlet obstruction (BOO), e.g. hypertrophy and loss of contractile function, as vitamin D3 and BXL-628 inhibit prostate and bladder cell growth in vitro, and there are receptors for vitamin D in rat and human bladder. MATERIAL AND METHODS In female rats, BOO was produced by a standardized method; one group received daily BXL-628 (150 µg/kg per day) and the remaining rats received vehicle. Sham-operated rats received BXL-628 or vehicle. After 2 weeks, the conscious rats were assessed by cystometry. Plasma calcium levels were determined and in vitro contractility assessed at the end of…

Vitaminmedicine.medical_specialtyUrologymedia_common.quotation_subjectUrinary BladderUrinationStimulationurologic and male genital diseasesUrinationPotassium ChlorideMuscle hypertrophyRats Sprague-DawleyContractilityBladder outlet obstructionchemistry.chemical_compoundCalcitriolInternal medicinePressuremedicineVitamin D and neurologyAnimalsmedia_commonmedicine.diagnostic_testbusiness.industryCystometryHypertrophyOrgan SizeElectric StimulationRatsUrinary Bladder Neck ObstructionEndocrinologychemistryFemalebusinessMuscle ContractionBJU International
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Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction

2015

Up to 80% of individuals with myotonic dystrophy type 1 (DM1) will develop cardiac abnormalities at some point during the progression of their disease, the most common of which is heart blockage of varying degrees. Such blockage is characterized by conduction defects and supraventricular and ventricular tachycardia, and carries a high risk of sudden cardiac death. Despite its importance, very few animal model studies have focused on the heart dysfunction in DM1. Here, we describe the characterization of the heart phenotype in a Drosophila model expressing pure expanded CUG repeats under the control of the cardiomyocyte-specific driver GMH5-Gal4. Morphologically, expression of 250 CUG repeat…

[SDV]Life Sciences [q-bio]Myotonic dystrophyMedicine (miscellaneous)lcsh:MedicineVentricular tachycardiaImmunology and Microbiology (miscellaneous)DiastoleHeart RateDrosophila ProteinsMyocytes CardiacGeneticsbiologyRNuclear ProteinsHeartPhenotype3. Good healthCell biology[SDV] Life Sciences [q-bio]Drosophila melanogasterPhenotypeDrosophilaDrosophila melanogasterDrosophila ProteinResearch Articlelcsh:RB1-214congenital hereditary and neonatal diseases and abnormalitiesSystoleLongevityNeuroscience (miscellaneous)In situ hybridizationMyotonic dystrophyGeneral Biochemistry Genetics and Molecular BiologyMuscleblindContractilitymedicinelcsh:PathologyAnimalsPentamidineHeart dysfunctionfungilcsh:RArrhythmias Cardiacbiology.organism_classificationmedicine.diseaseMyocardial ContractionSurvival AnalysisDisease Models AnimalTrinucleotide repeat expansionTrinucleotide Repeat Expansion
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Effects of sulphonylureas on spontaneous motility and induced contractions in rat isolated uterus

1986

Abstract To clarify the action of sulphonylureas on calcium, the effect of tolbutamide and ghbenclamide has been investigated on a Ca-dependent process, the contractile activity of uterine smooth muscle. Both sulphonylureas antagonized the contractions evoked by CaCl2 in a non-competitive manner when the uterus was maintained in depolarizing solution and did not affect the spontaneous contractions of rat uterus. The capacity of tolbutamide and ghbenclamide to relax vanadate-induced contraction of rat uterus in Ca-free medium suggests that sulphonylureas may have an intracellular site of action related to cytosolic free Ca levels, or effect a reduction in Ca action.

endocrine systemmedicine.medical_specialtyContraction (grammar)TolbutamideUterusPharmaceutical ScienceMotilitychemistry.chemical_elementIn Vitro TechniquesBiologyCalciumGlibenclamideContractilityUterine ContractionTolbutamideInternal medicineGlyburidemedicineAnimalsHypoglycemic AgentsPharmacologyRats Inbred StrainsVanadiumRatsSulfonylurea CompoundsEndocrinologymedicine.anatomical_structureMechanism of actionchemistryCalciumFemaleVanadatesmedicine.symptommedicine.drugJournal of Pharmacy and Pharmacology
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