Search results for "Fixative"

showing 10 items of 15 documents

Could formaldehyde induce mutagenic and cytotoxic effects in buccal epithelial cells during anatomy classes?

2017

Background Due to increased formaldehyde exposure, carcinogenic to humans, several researches have been studying the potential toxicity and the safe levels for human beings. The aim of this study was to investigate mutagenicity and cytotoxicity in buccal epithelial exfoliated cells (BEC) of students subjected to formaldehyde (FA) during anatomy classes. Material and Methods BEC were collected periodically from 17 volunteers of undergraduate programs, who had participated in practical anatomy classes, before and after FA exposure. Cells were stained according to Feulgen method and then micronucleus test was applied. A total of 1,500 cells were assessed per individual in this study for the mi…

0301 basic medicineMaleProgrammed cell death03 medical and health sciencesFixativesYoung Adult0302 clinical medicineFormaldehydeMedicineCytotoxic T cellHumansFeulgen stainALDEÍDOSCytotoxicityGeneral DentistryCarcinogenOral Medicine and Pathologybusiness.industryCytotoxinsResearchMouth MucosaEpithelial Cells030206 dentistryBuccal administrationAnatomy:CIENCIAS MÉDICAS [UNESCO]030104 developmental biologyOtorhinolaryngologyMutagenesisMicronucleus testUNESCO::CIENCIAS MÉDICASSurgeryFemaleAnatomybusinessMicronucleusMedicina Oral, Patología Oral y Cirugía Bucal
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A survey of clearing techniques for 3D imaging of tissues with special reference to connective tissue

2016

AbstractFor 3-dimensional (3D) imaging of a tissue, 3 methodological steps are essential and their successful application depends on specific characteristics of the type of tissue. The steps are 1° clearing of the opaque tissue to render it transparent for microscopy, 2° fluorescence labeling of the tissues and 3° 3D imaging. In the past decades, new methodologies were introduced for the clearing steps with their specific advantages and disadvantages. Most clearing techniques have been applied to the central nervous system and other organs that contain relatively low amounts of connective tissue including extracellular matrix. However, tissues that contain large amounts of extracellular mat…

0301 basic medicinePathologymedicine.medical_specialtyTissue FixationHistologyClinical BiochemistryGingiva3D histochemistryConnective tissueBenzoatesSpecimen HandlingExtracellular matrixFixatives03 medical and health sciencesImaging Three-DimensionalDermis3D imagingmedicineClearingAnimalsHumansSkinFluorescent DyesMicroscopy ConfocalStaining and LabelingLight-sheet microscopyHistocytochemistryChemistryPhenyl EthersPhenyl EthersExtracellular matrixCell Biology030104 developmental biologymedicine.anatomical_structureConnective TissueLight sheet fluorescence microscopyClearingBenzyl AlcoholProgress in Histochemistry and Cytochemistry
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Activity of O 6 -methylguanine DNA methyltransferase in mononuclear blood cells of formaldehyde-exposed medical students

1999

A recent study reported that exposure of student embalmers in Cincinnati to high concentrations of formaldehyde (2 mg/m3) reduced the activity of the DNA repair protein O6-methylguanine DNA methyltransferase (MGMT). Reduction in a DNA repair enzyme may strongly increase the cancer risk not only with respect to the repair-enzyme causing agent but with respect to all carcinogens causing lesions subject to repair by the enzyme in question. Thus, we examined whether formaldehyde exposure of 57 medical students during their anatomy course at two different Universities in Germany influenced MGMT activity in mononuclear blood cells. Mean formaldehyde exposure of 41 students was 0.2 +/- 0.05 mg/m3 …

AdultMalemedicine.medical_specialtyPathologyStudents MedicalTime FactorsMethyltransferaseAlcohol DrinkingDNA repairHealth Toxicology and MutagenesisFormaldehydeToxicologyPeripheral blood mononuclear cellDNA methyltransferaseFixativesO(6)-Methylguanine-DNA Methyltransferasechemistry.chemical_compoundFormaldehydeInternal medicineHypersensitivitymedicineHumansneoplasmsCarcinogenchemistry.chemical_classificationbusiness.industrySmokingEnvironmental ExposureGeneral MedicineEndocrinologyEnzymechemistryData Interpretation StatisticalToxicityLeukocytes MononuclearFemalebusinessArchives of Toxicology
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Involvement of protein kinase Cdelta in contact-dependent inhibition of growth in human and murine fibroblasts.

2001

There is evidence that protein kinase C delta (PKCdelta) is a tumor suppressor, although its physiological role has not been elucidated so far. Since important anti-proliferative signals are mediated by cell-cell contacts we studied whether PKCdelta is involved in contact-dependent inhibition of growth in human (FH109) and murine (NIH3T3) fibroblasts. Cell-cell contacts were imitated by the addition of glutardialdehyde-fixed cells to sparsely seeded fibroblasts. Downregulation of the PKC isoforms alpha, delta, epsilon, and mu after prolonged treatment with 12-O-tetradecanoylphorbol-13-acetate (TPA, 0.1 microM) resulted in a significant release from contact-inhibition in FH109 cells. Bryosta…

Cancer ResearchTime FactorsBryostatin 1ImmunoprecipitationActive Transport Cell NucleusDown-RegulationBiologychemistry.chemical_compoundFixativesLactonesMiceDownregulation and upregulationGeneticsmedicineAnimalsHumansProtein IsoformsBenzopyransEnzyme InhibitorsFibroblastProtein kinase AMolecular BiologyProtein kinase CProtein Kinase CChemotaxisCell CycleAcetophenones3T3 CellsFibroblastsBryostatinsMolecular biologyBlotIsoenzymesProtein Kinase C-deltamedicine.anatomical_structurechemistryGlutaralTetradecanoylphorbol AcetateMacrolidesMitogensRottlerinCell DivisionProtein BindingOncogene
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Regionalization of epididymal duct and epithelium in rats and mice by automatic computer-aided morphometric analysis.

2005

Aim: To establish a rat and mouse epididymal map based on the use of the Epiquatre automatic software for histologic image analysis. Methods: Epididymides from five adult rats and five adult mice were fixed in alcoholic Bouin’s fixative and embedded in paraffin. Serial longitudinal sections through the medial aspect of the organ were cut at 10 µm and stained with hematoxylin and eosin. As determined from major connective tissue septa, nine subdivisions of the rat epididymis and seven for the mouse were determined, consisting of five sub-regions in the caput (rat and mouse), one (mouse) or three (rat) in the corpus and one in the cauda (rat and mouse). Using the Epiquatre software, several t…

EpididymisMalePathologymedicine.medical_specialtyRat EpididymisComputersUrologyH&E stainConnective tissueGeneral MedicineAnatomyBiologyEpididymisEpitheliumEpitheliumRatsAutomationMicemedicine.anatomical_structureMorphometric analysismedicineAnimalsDuct (anatomy)FixativeAsian journal of andrology
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Localization of Ca(2+)-stores and tissue compartments with a Ca(2+)-binding capacity in the organ of Corti of the guinea-pig by electron energy-loss …

1992

SUMMARY The addition of 10 mM CaCl2 to glutaraldehyde fixative leads to the formation of small electron-dense deposits in the organ of Corti of the guinea-pig. These precipitates are mainly attached to cell membranes in contact with different extracellular lymphatic fluids. A higher number of precipitates is localized in the acellular parts of tectorial and basilar membrane. Electron energy-loss spectroscopy (EELS) was used to determine the elemental composition of the deposits formed. The spectra showed a prominent signal at the Ca2+ L2,3 ionization edge. Oxygen could also be detected in all the precipitates analysed. EELS analysis of mitochondria of the inner and outer hair cells after co…

HistologyGuinea PigsAnalytical chemistrychemistry.chemical_elementCalciumPathology and Forensic Medicinechemistry.chemical_compoundCalcium ChlorideHair Cells AuditorymedicineExtracellularAnimalsInner earOrgan of CortiFixativeOrganellesElectron energy loss spectroscopyMitochondriaOxygenMicroscopy ElectronMembranemedicine.anatomical_structurechemistryOrgan of CortiBiophysicsCalciumGlutaraldehydeElectron Probe MicroanalysisJournal of microscopy
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Fixation conditions affect the intensity but not the pattern of NADPH-diaphorase staining as a marker for neuronal nitric oxide synthase in rat olfac…

1994

NADPH-diaphorase (NADPH-d) is commonly used as a histochemical marker for the neuronal form of the enzyme nitric oxide synthase (NOS). A recent biochemical study showed that in broken-cell preparations NADPH-d activity did not fully represent NOS and that NOS-unrelated NADPH-d activity was suppressed during fixation. Because it is unknown whether fixation also affects NOS-associated NADPH-d activity, we investigated the effects of various widely used fixatives on NADPH-d staining in relation to NOS immunoreactivity, obtained with polyclonal antibodies, in rat olfactory bulb. We found that the intensity of NADPH-d staining associated with NOS, as well as that unrelated to NOS, depends on fi…

MalePathologymedicine.medical_specialtyTissue FixationHistologyLysineSensitivity and SpecificityStainImmunoenzyme TechniquesRats Sprague-DawleymedicineAnimalsFixativeNeuronschemistry.chemical_classificationStaining and LabelingbiologyChemistryNADPH DehydrogenaseOlfactory BulbMolecular biologyRatsOlfactory bulbStainingNitric oxide synthaseEnzymePolyclonal antibodiesbiology.proteinAmino Acid OxidoreductasesNitric Oxide SynthaseAnatomyBiomarkersJournal of Histochemistry & Cytochemistry
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Computer assisted morphometric analysis of ram sperm heads: Evaluation of different fixative techniques

1998

The recent development of automated systems for morphometric sperm head analysis has provided a series of objective parameters which have facilitated the standardization of morphological semen evaluation. This current work attempts to establish the optimum fixing conditions for the morphometric characterization of ram spermatozoa. Ejaculates were obtained from 5 Merino rams used for periodic collection of semen and were diluted at 1:50 with TEST medium. Air-dried smears were fixed either in ethanol-ether (1:1), 50% methanol, 2% glutaraldehyde or SUZA fixative, in which case the smear was pretreated with chloramine. The samples were then stained with commercial kit Hemacolor. Once the prepar…

MaleTissue FixationHigh variabilitySemenBiologyTeratozoospermiaAndrologyFixativeschemistry.chemical_compoundFood AnimalsImage Processing Computer-AssistedAnimalsSmall AnimalsFixativeFixation (histology)SheepSperm CountEquineMethanolAnatomySpermatozoaSpermchemistryGlutaralComputer-assisted morphometric analysisAnimal Science and ZoologyGlutaraldehydeTheriogenology
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Femoropopliteal prosthetic bypass with glutaraldehyde stabilized human umbilical vein (HUV).

2007

Objective Femoropopliteal bypass still is the standard surgical therapy for disabling claudication and critical ischemia. When autologous vein is not suitable synthetic or biological prostheses may be considered. Second generation glutaraldehyde tanned human umbilical vein (HUV) graft was chosen for above and below knee femoropopliteal bypass when autologous vein was not available. A single center experience regarding long-term graft function, secondary reinterventions, and potential biodegeneration of the HUV is presented. Methods Between January 1994 and January 2005, 211 consecutive femoropopliteal bypass operations with HUV (65 above knee and 146 below knee) were performed in 197 patien…

Malemedicine.medical_specialtyUmbilical VeinsTime FactorsTissue FixationAnastomosisProsthesis DesignSeverity of Illness IndexBlood Vessel Prosthesis ImplantationFixativesAneurysmIschemiamedicineHumansPopliteal ArteryDerivationVeinVascular PatencyAgedRetrospective StudiesUltrasonographyAged 80 and overBioprosthesismedicine.diagnostic_testbusiness.industryGreat saphenous veinGraft Occlusion VascularThrombosisIntermittent ClaudicationMiddle Agedmedicine.diseaseLimb SalvageThrombosisSurgeryBlood Vessel ProsthesisFemoral Arterymedicine.anatomical_structureTreatment OutcomeLower ExtremityGlutaralAngiographySurgeryFemaleRadiologymedicine.symptombusinessClaudicationCardiology and Cardiovascular MedicineFollow-Up StudiesJournal of vascular surgery
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Improvement of the butyl methacrylate-paraffin embedment.

1983

The excellent butyl methacrylate-paraffin method as an embedment for light microscopy has been technically improved. More uniform and reproducible polymerization has been obtained by using a vacuum oven to degas the polymerizing mixture and to replace the air with nitrogen at 650 Torr. The amount of benzoyl peroxide required must be determined for each batch of butyl methacrylate. A teflon lined, reusable metal mold and a method of one-step blocking of tissues in preparation for sectioning are also described.

Materials scienceStaining and LabelingEmbedmentHistological Techniquestechnology industry and agriculturechemistry.chemical_elementBenzoyl peroxideNitrogenButyl methacrylateVacuum furnaceFixativeschemistryChemical engineeringPolymerizationPolymethacrylic AcidsParaffinTorrPolymer chemistryMicroscopymedicineMethacrylatesAnatomymedicine.drugStain technology
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