Search results for "caffeine"

showing 10 items of 118 documents

Perceived tiredness among adolescents and its association with sleep habits and use of psychoactive substances

1997

This study investigated the variation in perceived tiredness among 11, 13 and 15-year-old Finnish adolescents (n = 4187). Additionally interrelationships between sleep habits, use of psychoactive substances (alcohol, tobacco and coffee) and perceived tiredness among 15-year-olds were examined. This study is part of an international, WHO-coordinated survey of school children's health and lifestyle (the HBSC Study). In Finland, research data represented the whole country. The data were collected in March-May 1994. Pupils responded anonymously to a standardized questionnaire during a class period. Subjective tiredness was very common and increased with age among adolescents. Perceived tirednes…

MaleSleep Wake Disordersmedicine.medical_specialtyAdolescentSubstance-Related DisordersCognitive NeuroscienceStructural equation modelingBehavioral NeuroscienceSex FactorsCaffeineAge relatedTobaccomedicineHumansChildPsychiatryAssociation (psychology)FatigueResearch dataEthanolAge FactorsGeneral MedicineSleep in non-human animalsPlants ToxicHealth promotionAdolescent BehaviorFemaleFeeling tiredPsychologyClinical psychologyJournal of Sleep Research
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Sleep and sleepiness in shift-working tram drivers

2020

Driver sleepiness contributes to traffic accidents. However, sleepiness in urban public transport remains an understudied subject. To fill this gap, we examined the sleepiness, sleep, and on-duty sleepiness countermeasures (SCMs) in 23 tram drivers working morning, day, and evening shifts for three weeks. Sleepiness was measured using Karolinska Sleepiness Scale (KSS). Nocturnal total sleep time (TST) was measured with wrist actigraphy. SCMs and naps were self-reported with a smartphone application. Caffeine and napping were considered effective SCMs. Severe sleepiness (KSS >= 7) was observed in 22% of shifts with no differences between shift types. Rest breaks were associated with slight r…

MaleSleepinessTime FactorsväsymysTransportationAudiologySmartphone applicationFATIGUEunettomuusROAD0302 clinical medicineWork Schedule Tolerance11. SustainabilityMedicineSafety Risk Reliability and Quality050107 human factorsSleep lossMorningRISKkuljettajatraitiovaununkuljettajatREST05 social sciencesAccidents TrafficHAULMiddle Aged030210 environmental & occupational health3142 Public health care science environmental and occupational healthvuorotyöFemaleSleep (system call)Sleep lossAdultAutomobile DrivingCAFFEINEmedicine.medical_specialtyEvening515 Psychologyurban transportationPhysical Therapy Sports Therapy and RehabilitationHuman Factors and ErgonomicsINDIVIDUAL-DIFFERENCESsleep lossuni (lepotila)03 medical and health sciencesSleep Disorders Circadian RhythmCOUNTERMEASURESHumans0501 psychology and cognitive sciencesdriver fatigueEngineering (miscellaneous)unihäiriötbusiness.industryUrban transportationActigraphySleep timeDriver fatigueUrban transportationkaupunkiliikenneliikenneonnettomuudetSleepbusiness
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An inhibitory sex pheromone tastes bitter for Drosophila males

2007

1932-6203 (Electronic) Journal Article; Sexual behavior requires animals to distinguish between the sexes and to respond appropriately to each of them. In Drosophila melanogaster, as in many insects, cuticular hydrocarbons are thought to be involved in sex recognition and in mating behavior, but there is no direct neuronal evidence of their pheromonal effect. Using behavioral and electrophysiological measures of responses to natural and synthetic compounds, we show that Z-7-tricosene, a Drosophila male cuticular hydrocarbon, acts as a sex pheromone and inhibits male-male courtship. These data provide the first direct demonstration that an insect cuticular hydrocarbon is detected as a sex ph…

Malelcsh:MedicineEvolutionary Biology/Sexual BehaviorInsectCourtshipToxicologySexual Behavior Animal0302 clinical medicineMatingSex Attractantslcsh:Science[SDV.BDD]Life Sciences [q-bio]/Development Biologymedia_commonAnimal biologyNeurons0303 health sciencesPhysiology/Sensory SystemsSex CharacteristicsMultidisciplinaryNeuroscience/Behavioral Neurosciencebiology[SDV.BA]Life Sciences [q-bio]/Animal biologyBiologie du développementDevelopment Biology3. Good healthCell biologyDrosophila melanogasterSex pheromoneTastePheromoneDrosophila melanogasterSex characteristicsResearch Articleanimal structuresGenotypemedia_common.quotation_subject03 medical and health sciencesCaffeineBiologie animaleEcology/Behavioral EcologyAnimalsHomosexuality MaleLighting030304 developmental biologyEvolutionary Biology/Animal Behaviorlcsh:Rfungibiology.organism_classificationSex Attractantslcsh:Q030217 neurology & neurosurgery
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Endogenous adenosine inhibits hippocampal CA1 neurones: further evidence from extra- and intracellular recording.

1988

Extracellular and intracellular recordings from CA1 pyramidal neurones of rats in vitro were used to study the effects of endogenous and exogenously applied adenosine. The adenosine receptor antagonist, caffeine, enhanced the intracellular recorded e.p.s.p.-i.p.s.p. sequence evoked by stimulation of the stratum radiatum which is antagonized by exogenous adenosine. The late, potassium dependent i.p.s.p. was not antagonized. The adenosine uptake inhibitor, nitrobenzylthioinosine (NBTI), mimicked the effects of exogenously applied adenosine. The effects of NBTI and of exogenously applied adenosine were antagonized by caffeine in the same manner. Exposure to adenosine deaminase enhanced the evo…

Malemedicine.medical_specialtyAdenosineAdenosine DeaminasePharmacologyIn Vitro TechniquesAdenosine receptor antagonistHippocampusAdenosine A1 receptorchemistry.chemical_compoundAdenosine deaminaseThioinosineInternal medicineCaffeinemedicineAnimalsEvoked PotentialsPharmacologyNeuronsbiologyChemistryRats Inbred StrainsGeneral MedicinePurinergic signallingAdenosineAdenosine receptorRatsElectrophysiologyEndocrinologybiology.proteinCaffeineIntracellularmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Effects of alkylxanthines on contractility of diaphragm fibres isolated from normal and sensitized guinea-pigs.

1993

Abstract This study investigates the effects of alkylxanthines on twitch tension generated by electrical stimulation (supramaximal pulses, 0·2 ms duration, 1 Hz) of diaphragm muscle fibres isolated from normal and actively-sensitized guinea-pigs. Caffeine, theophylline and theobromine increased, in a concentration-dependent manner (50–500 μm), twitch tension in normal and sensitized diaphragm. Caffeine (500 μm) enhanced contractility to a greater extent than theophylline or theobromine. Twitch potentiation by caffeine (500 μm) was significantly greater in sensitized diaphragm. Verapamil (0·1–100 μm) did not alter twitch contractions in the absence or presence of alkylxanthines in normal or …

Malemedicine.medical_specialtyAdenosineDiaphragmGuinea PigsPharmaceutical ScienceIn Vitro TechniquesDantroleneDantroleneContractilitychemistry.chemical_compoundTheophyllineInternal medicineCaffeinemedicineAnimalsTheophyllineRespiratory systemRats WistarPharmacologyMuscle SmoothSerum Albumin Bovinemusculoskeletal systemElectric StimulationDiaphragm (structural system)Bronchodilator AgentsCulture MediaRatsEndocrinologychemistryVerapamilXanthinesEnprofyllineTheobromineCalciumFemaleImmunizationmedicine.symptomCaffeineExtracellular Spacemedicine.drugMuscle contractionMuscle ContractionThe Journal of pharmacy and pharmacology
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An electrophysiological study of the ontogenesis of adenosine receptors in the CA1 area of rat hippocampus

1990

Abstract The depressant effect of adenosine (Ad) was studied electrophysiologically in hippocampal slices from 5-, 10-, 15-, 20-, 30- and 120-day-old rats. Ad (10μM) depressed the field EPSP in CA1 to the same extent in all age groups. Caffeine (Caf), an Ad receptor antagonist, enhanced and nitrobenzylthioinosine (NBI), an Ad uptake blocker, depressed the field EPSP. Both these effects were, however, less prominent in slices from younger animals, a finding consistent with lower extracellular levels of endogenous Ad in neonatal rats.

Malemedicine.medical_specialtyAdenosinemedicine.drug_classAction PotentialsHippocampusBiologyHippocampal formationHippocampuschemistry.chemical_compoundAdenosine A1 receptorDevelopmental NeuroscienceThioinosineCaffeineInternal medicinemedicineAnimalsmusculoskeletal neural and ocular physiologyReceptors PurinergicRats Inbred StrainsReceptor antagonistAdenosineAdenosine receptorRatsEndocrinologynervous systemchemistryExcitatory postsynaptic potentialFemaleCaffeineDevelopmental Biologymedicine.drugDevelopmental Brain Research
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The effect of S-(+)-boldine on the α1-adrenoceptor of the guinea-pig aorta

1996

1. The cardiovascular activity of S-(+)-boldine, an aporphine alkaloid structurally related to papaverine, was determined. The work includes functional studies on guinea-pig isolated aorta contracted with noradrenaline, caffeine, KCl or Ca2+, and on guinea-pig trachea contracted with acetylcholine or histamine. 2. S-(+)-boldine inhibited in a concentration-dependent manner the contractile response evoked by noradrenaline (10 microM) in guinea-pig aorta (IC50 = 1.4 +/- 0.2 microM) while the KCl depolarizing solution (60 mM)- or the Ca2+ (1 mM)-induced contractions were only partially affected by boldine up to 300 microM. In contrast, papaverine relaxed noradrenaline (NA), KCl or Ca2+ induced…

Malemedicine.medical_specialtyAporphinesContraction (grammar)Phosphodiesterase InhibitorsMuscle RelaxationGuinea PigsAorta ThoracicIn Vitro TechniquesPhosphatidylinositolsMuscle Smooth Vascularchemistry.chemical_compoundCaffeinePapaverineReceptors Adrenergic alpha-1Internal medicinemedicine.arterymedicinePrazosinAnimalsBoldineThoracic aortaAdrenergic alpha-AntagonistsPharmacologyPapaverineParasympatholyticsCalcium Channel BlockersTracheaEndocrinologychemistryCompetitive antagonistAdrenergic alpha-1 Receptor AntagonistsHistamineAcetylcholineResearch Articlemedicine.drugBritish Journal of Pharmacology
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Characterization of two different Ca2+ entry pathways dependent on depletion of internal Ca2+ pools in rat aorta

1998

Ryanodine (10 microM), thapsigargin (1 microM) and cyclopiazonic acid (10 microM) produced a slow, sustained contractile response in rat aorta that only can be observed in Ca2+-containing solution. In Ca2+-free medium, no response to the drugs was obtained, which suggests that the contraction elicited in presence of Ca2+ is mainly due to the contribution of extracellular influx. This Ca2+ entry does not depend on the opening of dihydropyridine-dependent Ca2+-channels for nimodipine does not affect this. Noradrenaline (1 microM) induced a biphasic response in Ca2+-free medium that was mediated by two different Ca2+ compartments, one of which is common to caffeine (10 mM), and is also deplete…

Malemedicine.medical_specialtyIndolesThapsigarginContraction (grammar)Phosphodiesterase InhibitorsVasodilator AgentsAorta ThoracicIn Vitro TechniquesMuscle Smooth VascularNorepinephrinechemistry.chemical_compoundCaffeineInternal medicinemedicine.arterymedicineExtracellularAnimalsVasoconstrictor AgentsRats WistarCa2 entryNimodipinePharmacologyAortaRyanodineRyanodine receptorGeneral MedicineRatsEndocrinologychemistryBiophysicsThapsigarginCalciumCalcium ChannelsCyclopiazonic acidMuscle Contractionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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The effects of phorbol 12,13-diacetate on responses of guinea-pig isolated trachea to methylxanthines, isoprenaline and ryanodine

1994

1. Using guinea-pig isolated trachea, we have studied how phorbol 12,13-diacetate (PDA) modulates mechanical responses of the tissue to methylxanthines, isoprenaline and ryanodine. 2. Caffeine (10 microM-5 mM), theophylline (10 microM-5 mM) and isoprenaline (1 nM-1 microM), each inhibited the spontaneous tone of the trachea. Pretreatment with PDA (0.1-10 microM) converted relaxant responses to high concentrations of the methylxanthines into contractions. PDA produced no equivalent effect against isoprenaline. Pretreatment with verapamil (1 or 10 microM), nifedipine (0.1 microM) or incubation with Ca(2+)-free, EGTA (0.1 mM)-containing physiological salt solution (PSS) suppressed the contract…

Malemedicine.medical_specialtyMuscle RelaxationGuinea PigsMepyramineIn Vitro TechniquesCalcium Chloridechemistry.chemical_compoundTheophyllineCaffeineIsoprenalineInternal medicinePhorbol EstersmedicineAnimalsDrug InteractionsTheophyllinePharmacologyRyanodineRyanodine receptorIsoproterenolMuscle SmoothCold TemperatureTracheaEndocrinologyMuscle relaxationVerapamilchemistryMuscle SpasticityXanthinesPotassiumTrachealis muscleVerapamilFemaleCaffeineResearch ArticleHistamineMuscle Contractionmedicine.drugBritish 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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