Search results for "Andrology"

showing 10 items of 410 documents

Uterine Receptivity and the Ramifications of Ovarian Stimulation on Endometrial Function

2007

Controlled ovarian stimulation (COS) is widely used in assisted reproduction techniques (ART). However, hormonal treatment induces endometrial alterations that may alter implantation rates compared with natural cycles. Endometrial alterations have been observed by histological and biochemical techniques. The recent developments in functional genomics have provided objective tools to analyze the endometrium in natural cycles and evaluate the impact of COS protocols in endometrial development. This article describes the fundamental aspects of endometrial receptivity in natural cycles and reports how COS affects the morphology, biochemistry, and the genomic pattern of the endometrium.

medicine.medical_specialtyEndocrinology Diabetes and Metabolismmedia_common.quotation_subjectUterusOvaryStimulationBiologyEndometriumAndrologyEndometriumEndocrinologyOvulation InductionPregnancyPhysiology (medical)Internal medicinemedicineHumansEmbryo ImplantationMenstrual CycleMenstrual cycleOligonucleotide Array Sequence Analysismedia_commonPrincipal Component AnalysisGene Expression ProfilingGene Expression Regulation DevelopmentalObstetrics and GynecologyGenomicsEndocrinologymedicine.anatomical_structureReproductive MedicineIn uteroFemaleFunction (biology)HormoneSeminars in Reproductive Medicine
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529. PROPROTEIN CONVERTASE 6 PLAYS A CRITICAL ROLE IN MODULATING THE HUMAN ENDOMETRIAL EPITHELIUM FOR RECEPTIVITY AND IMPLANTATION

2009

Successful embryo implantation is an important step in establishing pregnancy, requiring a healthy embryo and a receptive endometrium. Establishment of endometrial receptivity involves morphological and physiological changes initially in the endometrial epithelium, but the underlying molecular mechanisms are not fully understood. We have previously demonstrated that proprotein convertase 5/6 (PC6), a member of the proprotein convertase (PC) family, is up-regulated in the endometrium specifically at implantation in association with epithelial differentiation, in the human and monkey. PCs convert a range of precursor proteins of important functions into their bioactive forms; they are thus r…

medicine.medical_specialtyGene knockdownReproductive immunologyEmbryo cultureEmbryoReproductive technologyTransfectionBiologyEndometriumProprotein convertaseAndrologyEndocrinologymedicine.anatomical_structureEndocrinologyReproductive MedicineInternal medicineGeneticsmedicineAnimal Science and ZoologyMolecular BiologyDevelopmental BiologyBiotechnologyReproduction, Fertility and Development
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Sex-specific reaction of liver ultrastructure in zebra fish (Brachydanio rerio) after prolonged sublethal exposure to 4-nitrophenol

1989

Abstract Morphological alterations of the liver of zebra fish ( Brachydanio rerio ) following prolonged exposure to 0.1, 1 and 5 mg · l −1 4-nitrophenol (4-NP) were investigated by means of light and electron microscopy. Based on marked sexual dimorphism in control animals, liver recactions were both sex- and dose-dependent. Whereas at 0.1 mg·1 −1 only minor changes could be revealed, there were numerous structural modifications at 1 mg·1 −1 : Whereas male fish primarily react with a proliferation of smooth endoplasmic reticulum, female fish display a high degree of fenetrastion within cisternate of the rough endoplasmic reticulum. Both sexes exhibit infiltration of macrophages and lymphocy…

medicine.medical_specialtyHealth Toxicology and MutagenesisEndoplasmic reticulumAnatomyAquatic ScienceMitochondrionBiologymedicine.diseaseSexual dimorphismAndrologymedicine.anatomical_structureToxicitymedicineUltrastructureHistopathologyNuclear membraneInfiltration (medical)Aquatic Toxicology
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Contracting striated muscle fibres differentiated from primary rat pituitary cultures.

1982

Whole pituitaries or adenohypophyses alone of adult female Wistar/ Furth rats were dissociated into single cells by means of two different enzymic disintegration methods. The single-cell suspension was then seeded out and cultured for up to 8 months in tissue culture dishes with untreated and polylysine coated surfaces. The cells were cultured in different sera (horse serum, newborn-calf serum, fetal-calf serum, mixtures of horse and newborn-calf serum, and isogenic rat serum) and also in a serum-free, hormone-supplemented medium. When the cells were cultured in medium containing horse serum (15 %) plus fetal-calf serum (3%) on polylysine-treated surfaces, cell fusion and the development of…

medicine.medical_specialtyHistologyRats Inbred WFBiologyPathology and Forensic MedicineAndrologyCell FusionTissue culturechemistry.chemical_compoundPituitary Gland AnteriorInternal medicinemedicineMyocyteAnimalsPolylysineCells CulturedCell fusionMyogenesisMusclesHorseCell DifferentiationCell BiologyMolecular medicineCulture MediaRatsRat PituitaryEndocrinologyBloodchemistryPolylysinePituitary GlandFemaleMuscle ContractionCell and tissue research
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Vitrification of zona-free rabbit expanded or hatching blastocysts: a possible model for human blastocysts.

2003

BACKGROUND: The purpose of this study was to test the effectiveness of one two-step (A) and two one-step (B1 and B2) vitrification procedures on denuded expanded or hatching rabbit blastocysts held in standard sealed plastic straws as a possible model for human blastocysts. The effect of blastocyst size was also studied on the basis of three size categories (I: diameter <200 μm; II: diameter 200-299 μm; III: diameter ≥300 μm). METHODS: Rabbit expanded or hatching blastocysts were vitrified at day 4 or 5. Before vitrification, the zona pellucida was removed using acidic phosphate buffered saline. For the two-step procedure, prior to vitrification, blastocysts were pre-equilibrated in a solut…

medicine.medical_specialtyHot TemperatureZona freeBiologyAndrologychemistry.chemical_compoundEmbryonic and Fetal DevelopmentmedicineAnimalsHumansVitrificationBlastocystZona pellucidaZona PellucidaCryopreservationTissue SurvivalDimethyl sulfoxideHatchingRehabilitationHistological TechniquesObstetrics and GynecologyEmbryoSurgerymedicine.anatomical_structureBlastocystReproductive MedicinechemistryModels AnimalFemaleRabbitsEthylene glycolHuman reproduction (Oxford, England)
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Human Endometrial Mucin MUC1 Is Up-Regulated by Progesterone and Down-Regulated In Vitro by the Human Blastocyst1

2001

Expression of MUC1 in endometrial epithelium has been suggested to create a barrier to embryo attachment that must be lifted at the time of implantation. In this study, we investigated the hormonal regulation of human endometrial MUC1 in hormone replacement therapy cycles and in the human blastocyst. We also analyzed the embryonic regulation of MUC1 in human endometrial epithelial cells (EECs) during the apposition and adhesion phases of human implantation using two different in vitro models. Our results indicate that endometrial MUC1 mRNA and immunoreactive protein increase in receptive endometrium compared to nonreceptive endometrium. Human blastocysts express MUC1, as demonstrated by rev…

medicine.medical_specialtyImmunocytochemistryEmbryoCell BiologyGeneral MedicineBiologyEndometriumdigestive systemEmbryonic stem celldigestive system diseasesAndrologystomatognathic diseasesAppositionParacrine signallingmedicine.anatomical_structureEndocrinologyReproductive MedicineInternal medicinemedicineBlastocystskin and connective tissue diseasesneoplasmsMUC1Biology of Reproduction
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Embryonic and foetal Islet-1 positive cells in human hearts are also positive to c-Kit.

2011

During embryogenesis, the mammalian heart develops from a primitive heart tube originating from two bilateral primary heart fields located in the lateral plate mesoderm. Cells belongings to the pre-cardiac mesoderm will differentiate into early cardiac progenitors, which express early transcription factors which are also common to the Isl-1 positive cardiac progenitor cells isolated from the developing pharyngeal mesoderm and the foetal and post-natal mice hearts. A second population of cardiac progenitor cells positive to c-Kit has been abundantly isolated from adult hearts. Until now, these two populations have been considered two different sets of progenitor cells present in the heart in…

medicine.medical_specialtyMesodermHistologyTime FactorsPopulationLIM-Homeodomain ProteinsBiophysicsembryoReceptors Cell SurfaceBiologyIsl-1; c-Kit; human heart; embryo; foetusAndrologyFetusfoetus.Antigens CDPregnancyInternal medicinec-Kitmental disordersmedicineHumansMyocytes CardiacProgenitor celleducationlcsh:QH301-705.5Fetuseducation.field_of_studyOriginal PaperLateral plate mesodermMyocardiumEmbryogenesisEndoglinInfant NewbornEmbryoHeartCell BiologyEmbryonic stem cellImmunohistochemistryfoetusProto-Oncogene Proteins c-kitEndocrinologymedicine.anatomical_structureIsl-1 c-Kit human heart embryo foetuslcsh:Biology (General)Isl-1Femalehuman heartpsychological phenomena and processesTranscription FactorsEuropean journal of histochemistry : EJH
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Viability and function of the cryopreserved whole rat ovary: comparison between slow-freezing and vitrification

2011

Objective To investigate four different protocols for cryopreservation of the whole rat ovary with intact vasculature to evaluate whether differences exist in post-thawing viability of the ovary after either vitrification or slow freezing. Design Experimental study. Setting Obstetrics and gynecology department. Animal(s) Immature Sprague-Dawley female rats. Intervention(s) Ovaries were isolated with the vascular tree intact up to the bifurcation of the abdominal aorta and were subsequently cannulated. The ovaries were flushed with increasing concentrations of the cryoprotectant dimethyl sulfoxide (DMSO) to either 1.5 or 7 M. The ovaries underwent cryopreservation by vitrification or passive…

medicine.medical_specialtyNeutral redTime FactorsCryoprotectantApoptosisOvaryBiologyCryopreservationRats Sprague-DawleyTissue Culture TechniquesAndrologychemistry.chemical_compoundCryoprotective AgentsOvarian FollicleFreezingFollicular phasemedicineAnimalsDimethyl SulfoxideVitrificationIncubationCryopreservationTissue SurvivalGynecologyDose-Response Relationship DrugEstradiolCaspase 3Dimethyl sulfoxideOvaryFertility PreservationObstetrics and GynecologyOrgan PreservationImmunohistochemistryVitrificationRatsPerfusionmedicine.anatomical_structureReproductive MedicinechemistryFemaleFertility and Sterility
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Protandric hermaphrodite peculiarities in Amphiprion frenatus Brevoort (Teleostei, Pomacentridae)

1990

Electron microscopy of the male phase of the ovotestis of Amphiprion frenatus, a protandric hermaphrodite, showed no connective tissue between male and female areas and, as the basal lamina was lacking both along the seminiferous tubules and round the previtellogenic oocytes, the male and female germ cells were only separated by their respective surrounding somatic cells (Sertoli and follicle cells). Besides previtellogenic oocytes, oocytes in meiotic prophase and very small (young) previtellogenic oocytes, were detected in the ovarian part, as spermatogenesis proceeded, revealing oogenetic activity. Degeneration of some previtellogenic oocytes and their follicle cells was discernible.

medicine.medical_specialtyOvotestisSomatic cellAquatic ScienceBiologyAndrologyFollicleProphasemedicine.anatomical_structureEndocrinologyHermaphroditeMeiosisInternal medicinemedicineBasal laminaSpermatogenesisEcology Evolution Behavior and SystematicsJournal of Fish Biology
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Effect of the methacrylate-based endodontic sealer Epiphany on rat peritoneal macrophages viability

2011

Objective: To evaluate the effect of the endodontic sealer Epiphany on rat peritoneal macrophages viability. Materials and methods: Peritoneal macrophages were obtained from Wistar rats and resuspended in RPMI- 1640 medium. Undiluted (crude extract) and diluted extracts to 10%, 1%, 0.1%, 0.01%, 0.001% and 0.0001% of Epiphany, AH 26 and AH Plus sealers on RPMI-1640 medium were tested for cytotoxicity to rat peritoneal macrophages using the trypan blue dye exclusion assay. Data were analyzed statistically by the Kruskal-Wallis and Mann-Whitney tests at 5% significance level. Results: Crude extract of Epiphany killed 51% of cells, but was less cytotoxic that crude extracts of AH Plus and AH 26…

medicine.medical_specialtySerial dilutionChemistrymedia_common.quotation_subjectDye exclusionOdontologíaMethacrylate:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludSurgeryAndrologychemistry.chemical_compoundEpiphanyUNESCO::CIENCIAS MÉDICASmedicineCytotoxic T cellTrypan blueCytotoxicityGeneral Dentistrymedia_common
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