Search results for "Dyes"

showing 10 items of 324 documents

Distribution of origin of nitric oxide synthase-immunoreactive nerve fibers in the rat epididymis.

1996

Abstract Distribution of neuronal nitric oxide synthase-immunoreactive (nNOS-IR) nerve fibers and somata in the rat epididymis and major pelvic ganglia was studied by immunohistochemical methods. In the epididymis, the supply of nNOS-IR fibers was highest in the cauda and became progressively fewer toward the caput. In the cauda and corpus, nNOS-IR fibers were distributed throughout the subepithelial tissues and around the epithelium. The pattern of distribution of vasoactive intestinal polypeptide (VIP)- and tyrosine hydroxylase (TH)-immunoreactive fibers in the epididymis was similar but the latter was generally more numerous in a given region as compared to that of nNOS-IR fibers. A popu…

MaleStilbamidinesTyrosine 3-MonooxygenaseVasoactive intestinal peptidePopulationBiologyRats Sprague-DawleyNerve FibersDorsal root ganglionGanglia SpinalmedicineAnimalseducationMolecular Biologyreproductive and urinary physiologyFluorescent DyesEpididymisNeuronseducation.field_of_studyNeurotransmitter AgentsHypogastric PlexusGeneral NeuroscienceVas deferensSmooth muscle contractionAnatomyEpididymisCholine acetyltransferaseImmunohistochemistryEpitheliumRatsbody regionsmedicine.anatomical_structurePhenotypenervous systemNeurology (clinical)Nitric Oxide SynthaseDevelopmental BiologyVasoactive Intestinal PeptideBrain research
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Calcitonin gene-related peptide-like immunoreactivity in spinal cord and superior cervical ganglion of the djungarian hamster (Phodopus sungorus)

1993

The indirect immunofluorescent method was employed to investigate the distribution of calcitonin gene-related peptide-like immunoreactivity (CGRP-LI) in the spinal cord and superior cervical ganglion of the Djungarian hamster Phodopus sungorus. In cross-sections of the spinal cord, immunoreactive fibres and terminals were found in laminae 1 and 2 in high density, in the dorsolateral (Lissauer's) tract, in ventral and lateral horns, and in the area surrounding the central canal. A few CGRP-LI perikarya were seen in the ventral but not the dorsal horn. CGRP-LI was further observed in preganglionic sympathetic neurons which were labelled by retrograde axonal transport of fluoro-gold (FG) follo…

MaleSuperior cervical ganglionPhodopusStilbamidinesAutonomic Fibers PreganglionicCalcitonin Gene-Related PeptideHamsterSuperior Cervical GanglionCalcitonin gene-related peptideBiologyCellular and Molecular NeuroscienceSympathetic Fibers PostganglionicCricetinaemedicineAnimalsFluorescent DyesIntermediolateral nucleusAnatomySpinal cordImmunohistochemistryCircadian RhythmGanglionmedicine.anatomical_structureSpinal Cordnervous systemCervical gangliaLateral funiculusJournal of Chemical Neuroanatomy
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Plasma membrane Ca2+ ATPase 4 is required for sperm motility and male fertility.

2004

Calcium and Ca(2+)-dependent signals play a crucial role in sperm motility and mammalian fertilization, but the molecules and mechanisms underlying these Ca(2+)-dependent pathways are incompletely understood. Here we show that homozygous male mice with a targeted gene deletion of isoform 4 of the plasma membrane calcium/calmodulin-dependent calcium ATPase (PMCA), which is highly enriched in the sperm tail, are infertile due to severely impaired sperm motility. Furthermore, the PMCA inhibitor 5-(and-6)-carboxyeosin diacetate succinimidyl ester reduced sperm motility in wild-type animals, thus mimicking the effects of PMCA4 deficiency on sperm motility and supporting the hypothesis of a pivot…

MaleTime FactorsBiochemistryMiceTestisProtein IsoformsCloning MolecularCation Transport Proteinsreproductive and urinary physiologySperm motilityMice KnockoutRecombination GeneticReverse Transcriptase Polymerase Chain ReactionPlasma Membrane Calcium-Transporting ATPasesFluoresceinsTransport proteinCell biologyBlotting SouthernBiochemistrySperm Motilityendocrine systemDNA ComplementaryGenotypeBlotting WesternMolecular Sequence Datachemistry.chemical_elementSuccinimidesCalcium-Transporting ATPasesFertilization in VitroCalciumBiologyPlasma Membrane Calcium-Transporting ATPasesAnimalsHumansMolecular BiologyFluorescent DyesCalcium metabolismModels Geneticurogenital systemCell BiologyBlotting NorthernSpermProtein Structure TertiaryRatsCalcium ATPaseAlternative SplicingFertilitychemistryMicroscopy FluorescencePlasma membrane Ca2+ ATPaseCalciumThe Journal of biological chemistry
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A comparative study of the sperm nuclear morphometry in cattle, goat, sheep, and pigs using a new computer-assisted method (CASMA-F)

2012

This study was designed to compare the sperm nuclear morphometry of four species of domestic artiodactyls (cattle, sheep, goats, and pigs), using the newly developed automatic computer-assisted sperm morphometry analysis-F. The study was divided into two experiments. In the first experiment, samples from 20 males from each species were collected, diluted, and divided into four sample aliquots. The first was labeled directly with Hoechst 33342, and the others were processed as smears. Between smears, one group was directly labeled with Hoechst after air drying, and the other was fixed either with glutaraldehyde (GLUT), or with methanol, and afterward labeled with Hoechst. Digital images of t…

Maleendocrine systemBOARSwineSperm HeadSemenBiologyAndrologySpecies SpecificityFood AnimalsImage Processing Computer-AssistedAnimalsAir dryingSmall AnimalsFluorescent DyesCell NucleusSheepurogenital systemEquineGoatsAnatomySpermatozoaSpermOpen softwareMicroscopy FluorescenceBenzimidazolesCattleAnimal Science and ZoologyTheriogenology
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Study of nuclear and acrosomal sperm morphometry in ram using a computer-assisted sperm morphometry analysis fluorescence (CASMA-F) method.

2014

The aim of this study was to develop a new method that allows morphometric assessment of the sperm nucleus and acrosome in the ram using fluorescence microscopy and free software. The study was divided into three experiments. In the first experiment, semen smears from 20 ejaculates were fixed and labeled with a propidium iodide-pisum sativum agglutinin (PI/PSA) combination. Digital images of the sperm nucleus, acrosome, and whole sperm head were captured and analyzed using the ImageJ program. The computer-assisted sperm morphometry analysis fluorescence (CASMA-F) method used allowed the differentiation, capture, and morphometric analysis of most sperm nuclei, acrosomes, and whole heads with…

Maleendocrine systemSperm HeadSemenBiologyAndrologyFood AnimalsFluorescence microscopeImage Processing Computer-AssistedAnimalsSmall AnimalsAcrosomeFluorescent DyesSheepStaining and Labelingurogenital systemEquineOptical ImagingPeasSpermFluorescenceSpermatozoaStainingMorphometric analysisAnimal Science and ZoologyPlant LectinsPropidiumTheriogenology
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Toward an integrative and predictive sperm quality analysis in Bos taurus

2017

There is a need to develop more integrative sperm quality analysis methods, enabling researchers to evaluate different parameters simultaneously cell by cell. In this work, we present a new multi-parametric fluorescent test able to discriminate different sperm subpopulations based on their labeling pattern and motility characteristics. Cryopreserved semen samples from 20 Holstein bulls were used in the study. Analyses of sperm motility using computer-assisted sperm analysis (CASA-mot), membrane integrity by acridine orange-propidium iodide combination and multi-parametric by the ISAS®3Fun kit, were performed. The new method allows a clear discrimination of sperm subpopulations based on memb…

Maleendocrine systemmedia_common.quotation_subjectMotilityFertilitySemenBiologyCryopreservationAndrology03 medical and health sciences0302 clinical medicineEndocrinologyFood AnimalsCapacitationAnimalsAcrosomeSperm motilityreproductive and urinary physiologyFluorescent Dyesmedia_common030219 obstetrics & reproductive medicineStaining and Labelingurogenital system0402 animal and dairy science04 agricultural and veterinary sciencesGeneral MedicineSpermatozoa040201 dairy & animal scienceSpermSemen AnalysisCattleAnimal Science and Zoology
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A nitrergic projection from the superior olivary complex to the inferior colliculus of the rat

2003

The present study was conducted to test whether the ascending auditory projection from the superior olivary complex (SOC) of the brainstem to the inferior colliculus (IC) may use nitric oxide (NO) as a neuroactive compound. We identified olivo-collicular projection neurons in subnuclei of the SOC by retrograde neuronal tracing with Fluoro-Gold (FG) injected into the central nucleus of the IC. Sections containing retrograde labelled neurons were subjected to immunohistochemical incubation in an antiserum directed against the enzyme responsible for NO production in nerve cells, neuronal NO synthase (nNOS). The analysis showed that FG-containing neurons as well as nNOS-immunoreactive neurons w…

Maleinorganic chemicalsInferior colliculusStilbamidinesNitric Oxide Synthase Type IOlivary NucleusNitric OxideRats Sprague-Dawleyotorhinolaryngologic diseasesmedicineAnimalsTrapezoid bodyFluorescent DyesNeuronsAfferent PathwaysStaining and LabelingChemistryAnatomyImmunohistochemistryRetrograde tracingInferior ColliculiSensory SystemsRatsNeuronal tracingmedicine.anatomical_structurenervous systemSuperior olivary complexBrainstemNitric Oxide SynthaseNitrergic NeuronNeuroscienceNucleusHearing Research
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An approach to predictive testing of contact sensitizers in vitro by monitoring their influence on endocytotic mechanisms.

1996

Endocytotic activation of epidermal Langerhans cells (LC) by immunogenic haptens is an early event during development of allergic contact dermatitis. In this work a fast and objective flow-cytometric assay for predictive in vitro testing of contact sensitizers by monitoring their influence on endocytotic mechanisms in murine LC was developed. Epidermal cell suspensions were labelled with a monoclonal antibody directed to MHC class II molecules and pH-sensitive fluorochrome-coupled second-step reagents. For untreated LC a significant quenching of fluorescence intensity by internalization of the MHC-antibody complexes into acidic compartments was noticed. Similar results were obtained in the …

Malemedia_common.quotation_subjectImmunologyImmunologic TestsEndocytosischemistry.chemical_compoundMicemedicineConcanavalin AImmunology and AllergyAnimalsInternalizationAllergic contact dermatitisPhorbol 1213-Dibutyratemedia_commonFluorescent DyesMice Inbred BALB CbiologyHistocompatibility Antigens Class IILectinGeneral Medicinemedicine.diseaseFlow CytometryIn vitroEndocytosischemistryConcanavalin ALangerhans CellsImmunologyDermatitis Allergic ContactPhorbolbiology.proteinIrritantsFemaleHaptenInternational archives of allergy and immunology
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Diagnosing Helicobacter pylori in vivo by confocal laser endoscopy.

2005

Background & Aims: Confocal laser endomicroscopy enables subsurface microscopic imaging of living tissue during ongoing endoscopy. This case report describes the in vivo detection of Helicobacter pylori by endomicroscopy.Methods: Endomicroscopy (Pentax, Tokyo, EC-3870CIFK) was performed by using two different contrast stains: Topical Acriflavine in addition to intravenously applied fluorescein netted the surface and allowed identification of focal accumulation of Helicobacter pylori at the surface and in deeper layer of the gastric epithelium. Biopsies were performed at the antrum and corpus for urease testing and histology. In addition, biopsies were cultured for Helicobacter pylori. Cultu…

Malemedicine.medical_specialtyPathologyConfocalAdministration TopicalContrast MediaGastroenterologySensitivity and SpecificityEndoscopy Gastrointestinallaw.inventionHelicobacter InfectionsDiagnosis Differentialchemistry.chemical_compoundIn vivoConfocal microscopylawInternal medicinemedicineEndomicroscopyHumansAcriflavineAgedFluorescent DyesMicroscopy ConfocalHepatologybiologyHelicobacter pyloriGastroenterologyHistologyHelicobacter pyloribiology.organism_classificationchemistryAcriflavineFluoresceinEx vivoGastroenterology
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Principal neurons projecting to the pineal gland in close association with small intensely fluorescent cells in the superior cervical ganglion of rats

1988

The localization in the superior cervical ganglia (SCG) of small, intensely fluorescent (SIF) cells and of principal nerve (PN) cells innervating the pineal gland was examined in adult male Sprague-Dawley rats. PN cells were demonstrated by means of the retrograde neuron-tracing method using the fluorescent tracer Fluoro-Gold (FG) injected into the pineal gland. SIF cells were visualized by the formaldehyde-induced fluorescence method. Twenty-nine percent of the FG-labeled PN cells were found closely associated with SIF cells. In the rostral half of the ganglion, 43% of the SIF cells were situated in juxtaposition to one or several labeled neurons. The possible influence of SIF cells on the…

Malemedicine.medical_specialtySuperior cervical ganglionHistologyStilbamidinesCentral nervous systemEnteroendocrine cellBiologyPineal GlandPathology and Forensic MedicinePineal glandFormaldehydeInternal medicineNeural PathwaysmedicineAnimalsFluorescent DyesNeuronsGanglia SympatheticRats Inbred StrainsCell BiologyRetrograde tracingMolecular biologyRatsGanglionmedicine.anatomical_structureEndocrinologyMicroscopy Fluorescencenervous systemCervical gangliaNeuronCell and Tissue Research
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