Search results for "Urine"

showing 10 items of 924 documents

Alpha-adrenergic drugs in retrograde ejaculation.

1974

6 men with complete or partial loss of ejaculation as a result of retroperitoneal lymphadenectomy (performed because of testicular tumor) were treated with an intravenous injection of 60 mg synephrine. Synephrine stimulates adrenergic alpha-receptors. Only 1 man with sustained retrograde ejaculation improved following treatment showing antegrade ejaculation. This temporary restoration of fertility was thought to be due to an increase in bladder neck tone and prevention of backflow of semen into the bladder as a result of stimulation of adrenergic alpha-receptors.

Retrograde ejaculationInfertilityAdultMalemedicine.medical_specialtyEjaculationPopulationUrologyAdrenergicSemenStimulationCell CountUrineurologic and male genital diseasesMedicineHumansEjaculationeducationeducation.field_of_studybusiness.industrySynephrineObstetrics and Gynecologymedicine.diseaseSpermatozoaSurgeryMasturbationNeck of urinary bladderReproductive MedicineSurgical Procedures OperativeInjections IntravenousLymph Node ExcisionGenital Diseases MalebusinessFertility and sterility
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Evaluating diagnostic indicators of urogenital Schistosoma haematobium infection in young women: A cross sectional study in rural South Africa

2018

BackgroundUrine microscopy is the standard diagnostic method for urogenital S. haematobium infection. However, this may lead to under-diagnosis of urogenital schistosomiasis, as the disease may present itself with genital symptoms in the absence of ova in the urine. Currently there is no single reliable and affordable diagnostic method to diagnose the full spectrum of urogenital S. haematobium infection. In this study we explore the classic indicators in the diagnosis of urogenital S. haematobium infection, with focus on young women.MethodsIn a cross-sectional study of 1237 sexually active young women in rural South Africa, we assessed four diagnostic indicators of urogenital S. haematobium…

Rural PopulationPhysiologyCross-sectional studylcsh:MedicineArtificial Gene Amplification and ExtensionUrineUrinePolymerase Chain ReactionGastroenterologySchistosomiasis haematobiaSouth Africa0302 clinical medicineMedicine and Health SciencesSchistosomiasis030212 general & internal medicinelcsh:Scienceqy_185Schistosoma haematobiumMultidisciplinarybiologyEukaryotawc_810Latent class modelBody Fluids3. Good healthHelminth Infectionsqx_355SchistosomaFemaleAnatomyResearch ArticleNeglected Tropical DiseasesAdultmedicine.medical_specialtyAdolescentUrogenital SchistosomiasisImaging TechniquesUrology030231 tropical medicineImage AnalysisResearch and Analysis MethodsSensitivity and SpecificityYoung Adult03 medical and health sciencesDiagnostic MedicineHelminthsInternal medicineparasitic diseasesParasitic DiseasesmedicineHumansAnimalsSex organMolecular Biology TechniquesMolecular BiologySchistosomaIncontinencebusiness.industryGenitourinary systemlcsh:ROrganismsBiology and Life SciencesGold standard (test)Tropical Diseasesbiology.organism_classificationwj_20InvertebratesSchistosoma HaematobiumCross-Sectional Studieslcsh:QbusinessPLOS ONE
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Guanosine modulates K+ membrane currents in SH-SY5Y cells: involvement of adenosine receptors

2022

AbstractGuanosine (GUO), widely considered a key signaling mediator, is implicated in the regulation of several cellular processes. While its interaction with neural membranes has been described, GUO still is an orphan neuromodulator. It has been postulated that GUO may eventually interact with potassium channels and adenosine (ADO) receptors (ARs), both particularly important for the control of cellular excitability. Accordingly, here, we investigated the effects of GUO on the bioelectric activity of human neuroblastoma SH-SY5Y cells by whole-cell patch-clamp recordings. We first explored the contribution of voltage-dependent K+ channels and, besides this, the role of ARs in the regulation…

SH-SY5Y cellElectrophysiologyPhysiologyPhysiology (medical)Clinical BiochemistryCellular excitabilityPotassium channelPurinePatch-clampSettore BIO/09 - Fisiologia
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On-line in-tube solid phase microextraction coupled to capillary liquid chromatography-diode array detection for the analysis of caffeine and its met…

2019

Abstract In-tube solid phase microextraction (IT-SPME) coupled on-line to capillary liquid chromatography with diode array detection provides a simple and fast analytical methodology for the simultaneous quantitation of caffeine and its three primary metabolites (theobromine, paraxanthine and theophylline) in micro samples of serum, saliva and urine matrices. The sample amount required for one analysis was only 2.5 μL of saliva, 6.25 μL of serum or 40 μL of urine, a requirement for its implementation in a hospital laboratory for preterm newborns, where sample availability is a major problem. In standard conditions, 25 μL of diluted saliva or serum (or 100 μL of urine) were processed by IT-S…

SalivaAnalyteClinical BiochemistryPharmaceutical ScienceUrineUrineSolid-phase microextraction01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundTheophyllineCaffeineDrug DiscoverymedicineHumansSalivaTheobromineSolid Phase MicroextractionSpectroscopyParaxanthineDetection limitChromatography010405 organic chemistryElution010401 analytical chemistry0104 chemical scienceschemistryCalibrationTheobromineBiological samples Capillary liquid chromatography In-tube solid-phase microextraction TrimethylxanthinesChromatography Liquidmedicine.drug
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A single method for recovery and concentration of enteric viruses and bacteria from fresh-cut vegetables

2011

Fresh-cut vegetables are prone to be contaminated with foodborne pathogens during growth, harvest, transport and further processing and handling. As most of these products are generally eaten raw or mildly treated, there is an increase in the number of outbreaks caused by viruses and bacteria associated with fresh vegetables. Foodborne pathogens are usually present at very low levels and have to be concentrated (i.e. viruses) or enriched (i.e. bacteria) to enhance their detection. With this aim, a rapid concentration method has been developed for the simultaneous recovery of hepatitis A virus (HAV), norovirus (NV), murine norovirus (MNV) as a surrogate for NV, Escherichia coli O157:H7, List…

Salmonellaved/biology.organism_classification_rank.speciesReal-Time Polymerase Chain Reactionmedicine.disease_causeMicrobiologyMicrobiologyMiceEnterobacteriaceaeListeria monocytogenesVegetablesmedicineAnimalsHumansFood microbiologyEnterovirusbiologyved/biologyPathogenic bacteriaGeneral Medicinebiology.organism_classificationListeria monocytogenesEnterobacteriaceaeFood MicrobiologyNorovirusBacteriaFood ScienceMurine norovirusInternational Journal of Food Microbiology
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Evaluation of mycotoxins and their metabolites in human breast milk using liquid chromatography coupled to high resolution mass spectrometry

2014

Humans can be exposed to mycotoxins through the food chain. Mycotoxins are mainly found as contaminants in food and could be subsequently excreted via biological fluids such as urine or human breast milk in native or metabolised form. Since breast milk is usually supposed as the only food for new-borns, the occurrence of mycotoxins in thirty-five human milk samples was evaluated by a newly developed method based on QuEChERS extraction and UHPLC-HRMS detection. The method described here allows the detection of target mycotoxins in order to determine the quality of this initial feeding. The method has been fully validated, with recoveries ranging from 64% to 93% and relative standard deviatio…

Sample preparationFood ContaminationUrineBreast milkQuechersOrbitrapBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundLiquid chromatography-high resolution mass spectrometrylawPregnancyEnvironmental ChemistryHumansSample preparationMycotoxinHuman breast milkSpectroscopyChromatography High Pressure LiquidChromatographyMilk HumanChemistryHuman milkInfant Newbornfood and beveragesReproducibility of ResultsContaminationMycotoxinsOrbitrapFemaleBiomarkersAnalytica Chimica Acta
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Towards sarcosine determination in urine for prostatic carcinoma detection

2019

Abstract Sarcosine, a potential biomarker for prostate cancer, can be detected in a solid state enzyme based biosensor using sarcosine oxidase, with particle immobilised reagents. A novel fusion protein of the fluorescent protein, mCherry, sarcosine oxidase (SOx), and the polypeptide R5 (R52-mCherry-SOx-R5-6 H), was explored, which allowed self-immobilization on silica microparticles and long-term (90 days +) retention of activity, even at room temperature. In contrast, commercial wildtype SOx lost activity in a few days. A silica-R52-mCherry-SOx-R5-6H microparticle sensor for determination of sarcosine in urine, linked the SOx coproduct, H2O2, to a measurement catalysed by horseradish pero…

Sarcosine02 engineering and technologyUrine010402 general chemistry01 natural sciencesHorseradish peroxidasechemistry.chemical_compoundMaterials ChemistryElectrical and Electronic EngineeringMicroparticleInstrumentationSarcosine oxidasechemistry.chemical_classificationChromatographybiologyMetals and Alloys021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnzymechemistrybiology.proteinUric acid0210 nano-technologyBiosensorSensors and Actuators B: Chemical
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Fast one-step liquid chromatography determination of purine compounds in blood with photodiode array detector

2012

Settore BIO/10 - BiochimicaSettore MED/26 - Neurologiapurine compoundHPLC
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Comprehensive proteomic overview of EPS-urine for the identification of novel prostate cancer biomarkers.

2010

Settore BIO/13 - Biologia ApplicataEPS-Urine Proteome biomarkers discovery
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In-depth proteomic analyses of expressed prostatic secretions in urine for identification of prostate-enriched proteins

2012

Settore BIO/13 - Biologia ApplicataProteomicprostate cancerEPS-urine
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