Search results for "Andrology"

showing 10 items of 410 documents

Aneuploidy as a consequence of senescence and ovariectomy in the golden hamster (Mesocricetus auratus).

1978

The hypothesis of the preferred X-chromosome loss in elder human females was reevaluated in the golden hamster: early castration of females proved that the increase of aneuploid cells is correlated with the loss of the ovaries. But here, and in old females, aneuploidy consisted of random loss of excess of chromosomes, in no case an X-chromosome.

Senescencemedicine.medical_specialtyAgingX ChromosomeAneuploidyBone Marrow CellsBiologyAndrologyCellular and Molecular Neurosciencechemistry.chemical_compoundInternal medicineCricetinaemedicineAnimalsCastrationMolecular BiologyX chromosomePharmacologyCell Biologymedicine.diseasebiology.organism_classificationAneuploidyEndocrinologyCastrationchemistryMolecular MedicineAneuploid CellsFemaleHuman FemalesMesocricetusGolden hamsterExperientia
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Age-associated telomere shortening in mouse oocytes

2013

Abstract Background Oocytes may undergo two types of aging. The first is induced by exposure to an aged ovarian microenvironment before being ovulated, known as ‘reproductive or maternal aging’, and the second by either a prolonged stay in the oviduct before fertilization or in vitro aging prior to insemination, known as ‘postovulatory aging’. However, the molecular mechanisms underlying these aging processes remain to be elucidated. As telomere shortening in cultured somatic cells triggers replicative senescence, telomere shortening in oocytes during reproductive and postovulatory aging may predict developmental competence. This study aimed to ascertain the mechanisms underlying altered te…

Senescencemedicine.medical_specialtyTime FactorsSomatic cellMouse oocyteReproductive medicineIn situ hybridizationBiologyReal-Time Polymerase Chain Reactionmedicine.disease_causeAndrologyMiceEndocrinologyHuman fertilizationPostovulatory agingInternal medicineReproductive agingmedicineAnimalsTelomeraseIn Situ Hybridization FluorescenceTelomere ShorteningResearchTertAge FactorsObstetrics and GynecologyTelomereTelomereEndocrinologyCellular MicroenvironmentReproductive MedicineOxidative stressOocytesOviductFemaleReactive Oxygen SpeciesOxidative stressMaternal AgeDevelopmental BiologyReproductive Biology and Endocrinology
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Expression of vascular endothelial growth factor receptors in the endometrium of septate uterus.

2008

Objective To compare the messenger RNA (mRNA) expression of vascular endothelial growth factor (VEGF) receptors (KDR, Flt-1, and sflt) in the different endometrial locations of septate uterus and normal uterus. Design Prospective, observational study. Setting University teaching hospital. Patient(s) Twelve women with complete septate uterus undergoing hysteroscopic metroplasty and 12 women with normal uterus. Intervention(s) Endometrial tissue samples were obtained from the endometrium covering the septum and the endometrium lining the lateral wall of the uterus. Moreover, endometrial samples were obtained from patients with normal uterus. Main Outcome Measure(s) Differences in the mRNA exp…

SeptateAdultmedicine.medical_specialtyUterusBiologyEndometriumAndrologychemistry.chemical_compoundEndometriumInternal medicinemedicineHumansProspective StudiesRNA MessengerReceptorRegulation of gene expressionMessenger RNAVascular Endothelial Growth Factor Receptor-1urogenital systemUterusObstetrics and GynecologyVascular Endothelial Growth Factor Receptor-2Vascular endothelial growth factormedicine.anatomical_structureEndocrinologyReceptors Vascular Endothelial Growth FactorReproductive MedicinechemistryGene Expression RegulationCase-Control StudiesFemaleSeptate uterusFertility and sterility
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Effect of different cryopreservation protocols on the metaphase II spindle in human oocytes.

2008

The aim of this study was to evaluate the impact of different cryopreservation protocols on the repolymerization of metaphase (M)II spindles in human oocytes. Fresh aspirated donor oocytes were cryopreserved 3–4 h after retrieval using four different protocols: slow freezing using 1.5 mol/l 1,2-propanediol (PROH) + 0.2 mol/l sucrose (n = 36); 1.5 mol/l PROH + 0.3 mol/l sucrose (n = 34); 1.5 mol/l PROH + 0.3 mol/l sucrose with Na + depleted–choline replaced media (n = 27), and vitrification by the Cryotip method (n = 23). The control group comprised 34 fresh oocytes. Three hours after thawing, surviving and control oocytes were fixed for meiotic spindle/chromatin assessment. Survival rates w…

Slow freezingCryopreservationSucroseObstetrics and GynecologySpindle ApparatusBiologyCryopreservationAndrologychemistry.chemical_compoundMeiosisReproductive MedicinechemistryMeiosisMoleBotanyFreezingOocytesHumansVitrificationFemaleIncubationMetaphaseMetaphaseDevelopmental BiologyReproductive biomedicine online
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Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure

2002

The fertilized mouse egg actively demethylates the paternal genome within a few hours after fertilization, whereas the maternal genome is only passively demethylated by a replication-dependent mechanism after the two-cell stage. This evolutionarily conserved assymetry in the early diploid mammalian embryo may have a role in methylation reprogramming of the two very different sets of sperm and egg chromatin for somatic development and formation of totipotent cells. Immunofluorescence staining with an antibody against 5-methylcytosine (MeC) showed that the incidence of abnormal methylation patterns differs between mouse two-cell embryos from superovulated females, nonsuperovulated matings, an…

Somatic cellCleavage Stage OvumFluorescent Antibody TechniqueSuperovulationAcetaldehydeFertilization in VitroBiologyAndrologyMiceGeneticsmedicineAnimalsBlastocystEnzyme InhibitorsGeneticsEmbryo cultureEmbryoCell BiologyMethylationDNA MethylationSpermmedicine.anatomical_structureembryonic structuresDNA methylationReprogrammingDevelopmental BiologyMolecular Reproduction and Development
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The influence of bone allograft processing on osteoblast attachment and function

2004

In order to assess the influence of eight different sterilisation and disinfection methods for bone allografts on adhesion, proliferation, and differentiation of human bone marrow stromal cells (BMSC), cells were grown in culture and then plated onto pieces of human bone allografts. Following processing methods were tested: autoclavation (AUT), low-temperature-plasma sterilisation of demineralised allografts (D-LTP), ethylene oxide sterilisation (EtO), fresh frozen bone (FFB), 80 degrees C-thermodisinfection (80 degrees C), gamma-irradiation (Gamma), chemical solvent disinfection (CSD), and Barrycidal-disinfection (BAR). The seeding efficiency was determined after one hour to detect the num…

Stromal cellCell Survivalmedicine.medical_treatmentOsteocalcinPopulationGene ExpressionBone Marrow CellsIn Vitro TechniquesBone graftingAndrologyCell AdhesionmedicineHumansTransplantation HomologousOrthopedics and Sports MedicineViability assayCell adhesioneducationCells CulturedBone Marrow Transplantationeducation.field_of_studyOsteoblastsbiologyChemistrySterilizationCell DifferentiationOsteoblastAlkaline PhosphataseTransplantationmedicine.anatomical_structureImmunologyOsteocalcinbiology.proteinStromal CellsCell DivisionJournal of Orthopaedic Research
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Preeclampsia: a defect in decidualization is associated with deficiency of Annexin A2.

2020

Background Decidualization defects in the endometrium have been demonstrated at the time of delivery in women with severe preeclampsia and to linger for years, which suggests a maternal contribution to the pathogenesis of this condition. Global transcriptional profiling reveals alterations in gene expression, which includes down-regulation of Annexin A2 in severe preeclampsia patients with decidualization resistance. Objective We investigated the functional role of Annexin A2 deficiency during endometrial decidualization and its potential contribution to shallow trophoblast invasion during implantation and subsequent placentation using in vitro and in vivo modeling. Study Design Annexin A2 …

Stromal cellGene ExpressionEndometriumAndrology03 medical and health sciencesMice0302 clinical medicinePre-EclampsiaAnnexinCell MovementPregnancymedicineDeciduaAnimalsHumans030212 general & internal medicineEmbryo ImplantationRNA Small InterferingAnnexin A2Cells Cultured030219 obstetrics & reproductive medicinemedicine.diagnostic_testbusiness.industryObstetrics and GynecologyDecidualizationPlacentationTrophoblastActinsPlacentationProlactinTrophoblastsInsulin-Like Growth Factor Binding Protein 1Disease Models Animalmedicine.anatomical_structureFemaleStromal CellsbusinessAnnexin A2Endometrial biopsyAmerican journal of obstetrics and gynecology
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Freezing without surrounding cryomedium preserves the endothelium and its function in human internal mammary arteries

2005

Abstract Purpose Cryopreserved human blood vessels may become important tools in bypass surgery. Optimal cryopreservation of an arterial graft should, therefore, preserve both histological and physiological characteristics of smooth muscle and endothelium comparable to the unfrozen artery. Methods Rings from human internal mammary arteries (IMA) were investigated in vitro either unfrozen or after immersion into a cryomedium (RPMI 1640 containing 1.8 M Me2SO and 0.1 M sucrose) and cryostorage with and without surrounding medium. Results In unfrozen IMA, neither contractile responses to noradrenaline (NA) nor endothelium-dependent relaxant responses to acetylcholine (ACH) was modified after e…

SucrosePathologymedicine.medical_specialtyEndotheliumBiologyGeneral Biochemistry Genetics and Molecular BiologyCryopreservationAndrologyNorepinephrinechemistry.chemical_compoundCryoprotective AgentsFreezingmedicineHumansDimethyl SulfoxideEndotheliumMammary ArteriesPhorbol 1213-DibutyrateProtein Kinase CProtein kinase CCryopreservationDose-Response Relationship DrugDimethyl sulfoxideTemperatureMuscle SmoothGeneral MedicineAcetylcholineCulture MediaCold TemperatureEnzyme ActivationMicroscopy ElectronDose–response relationshipmedicine.anatomical_structurechemistryCarcinogensMicroscopy Electron ScanningMammary arteryEndothelium VascularTissue PreservationGeneral Agricultural and Biological SciencesAcetylcholinemedicine.drugArteryCryobiology
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Isolated in-vitro perfusion of pig hearts obtained from the abattoir: an alternative to animal experiments?

1994

Isolated pig hearts (German farm pigs) were characterized after global in-vivo ischaemia as a potential alternative to in-vivo animal studies. Hearts were harvested from adult farm swine at the abattoir 10.3 +/- 2.1 min after incision of the carotid artery. They were immediately perfused and thereafter stored in ice-cold cardioplegic (St Thomas's) solution. After 38 +/- 3 min, retrograde perfusion was started with oxygenated pig blood (37 degrees C; 5000 U Heparin.l-1; pH 7.38 +/- 0.1; 11 mmol glucose.l-1) at a flow rate of 85 ml.min-1 100 g-1 wet weight (gww-1) for 30 min (n = 10). Additionally, shortly after obtaining the hearts, ATP and CP content were measured by enzymatic tests in 10 p…

SwineSodiumCarotid arterieschemistry.chemical_elementMyocardial Reperfusion InjuryCalciumIn Vitro TechniquesSodium ChlorideAnimal Testing AlternativesPotassium ChlorideAndrologyCalcium ChlorideReperfusion therapyHeart rateRetrograde perfusionMedicineAnimalsMagnesiumCardioplegic SolutionsMyocardial Stunningbusiness.industryMagnesiumMyocardiumHeartAnatomyPerfusionBicarbonateschemistryCardiology and Cardiovascular MedicinebusinessPerfusionAbattoirsEuropean heart journal
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The Influence of Hyaluronic Acid Biofunctionalization of a Bovine Bone Substitute on Osteoblast Activity In Vitro

2021

Bovine bone substitute materials (BSMs) are used for oral bone regeneration. The objective was to analyze the influence of BSM biofunctionalization via hyaluronic acid (HA) on human osteoblasts (HOBs). BSMs with ± HA were incubated with HOBs including HOBs alone as a negative control. On days 3, 7 and 10, cell viability, migration and proliferation were analyzed by fluorescence staining, scratch wound assay and MTT assay. On days 3, 7 and 10, an increased cell viability was demonstrated for BSM+ compared with BSM− and the control (each p ≤ 0.05). The cell migration was enhanced for BSM+ compared with BSM− and the control after day 3 and day 7 (each p ≤ 0.05). At day 10, an accelerated wound…

Technology02 engineering and technologyArticleAndrology03 medical and health scienceschemistry.chemical_compound0302 clinical medicineHyaluronic acidhyaluronic acidmedicineGeneral Materials ScienceMTT assayViability assayxenograftoral regenerationBone regenerationMicroscopyQC120-168.85TbovineQH201-278.5biofunctionalizationosteoblastsOsteoblastCell migration030206 dentistrybone substituteEngineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyIn vitroTK1-9971Bovine bonemedicine.anatomical_structureDescriptive and experimental mechanicschemistryElectrical engineering. Electronics. Nuclear engineeringTA1-20400210 nano-technologyMaterials
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