Search results for "Tissue distribution"

showing 10 items of 240 documents

Cell-specific accumulation patterns of gentamicin in the guinea pig cochlea.

2015

Intratympanic gentamicin therapy has become a popular treatment modality for Meniere's disease (MD) through controlled elimination of vertigo spells caused by the balance organ. However, the known ototoxic properties of aminoglycosides lead to cochlear damage. In order to gain more information about cellular preferences for aminoglycoside accumulation within the cochlea, gentamicin was immuno histochemically localized by light microscopy in male guinea pigs 1 and 7 days after intratympanic application (n = 8 ears/incubation time). Differences in the gentamicin-specific cellular storage capacities were quantified by determination of the local immuno staining intensities. Gentamicin was detec…

MalePathologymedicine.medical_specialtyCell typeGuinea PigsBiological Transport ActiveBiologyotorhinolaryngologic diseasesmedicineAnimalsHumansTissue DistributionSpiral ganglionCochleaMeniere DiseaseInjection IntratympanicAminoglycosideGap JunctionsAnatomyImmunohistochemistrySensory SystemsStainingCochleamedicine.anatomical_structureOrgan of CortiSpiral ligamentModels AnimalGentamicinsense organsGentamicinsmedicine.drugHearing research
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Kinetics of Photofrin II in perifocal brain edema.

1993

Photodynamic therapy is under intense investigation as a possible adjuvant for the treatment of malignant tumors of the central nervous system. It relies on the fact that photosensitizers are selectively taken up or retained by malignant tissue. However, most brain tumors are accompanied by substantial vasogenic edema as a consequence of blood-brain barrier disruption within the tumor, leading to extravasation and propagation of plasma constituents into the surrounding brain tissue. Systemically administered photosensitizers may enter healthy tissue together with the edema fluid, possibly leading to sensitization of tissues outside the tumor. To test this hypothesis, vasogenic edema was ind…

MalePathologymedicine.medical_specialtymedicine.medical_treatmentCentral nervous systemPhotodynamic therapyBrain EdemaCerebral edemaLesionchemistry.chemical_compoundEdemamedicineAnimalsPhotosensitizerTissue DistributionRats WistarFluorescein isothiocyanatebusiness.industryBrain Neoplasmsmedicine.diseaseExtravasationRatsCold TemperatureDisease Models Animalmedicine.anatomical_structurechemistryMicroscopy FluorescencePhotochemotherapySurgeryDihematoporphyrin EtherNeurology (clinical)medicine.symptombusinessFluorescein-5-isothiocyanateExtravasation of Diagnostic and Therapeutic MaterialsNeurosurgery
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Photoperiod effects on bombesin- and cholecystokinin-like immunoreactivity in the suprachiasmatic nuclei of the Djungarian hamster (Phodopus sungorus)

1991

The immunocytochemical distribution of the putative satiety peptides bombesin (BBS) and cholecystokinin (CCK) were studied in the hypothalamic suprachiasmatic nuclei (SCN) of male and female Djungarian hamsters (Phodopus sungorus) held under either long (light/dark, LD 16:8 h) or short (LD 8:16) photoperiod. The animals were killed by perfusion with a fixative at the middle of the light period and the tissue was processed by routine immunohistochemical methods. Perikarya exhibiting BBS- or CCK-like immunoreactivity (LI) were found in the SCN of animals of all groups. Sex-related differences were not observed. In contrast, long-term exposure to short days decreased the number of neurons exhi…

MalePeriodicityendocrine systemmedicine.medical_specialtyTime FactorsLightNeuropeptideHamsterBiologychemistry.chemical_compoundCricetinaeInternal medicinemedicineAnimalsTissue DistributionCholecystokininSuprachiasmatic nucleusGeneral Neurosciencedigestive oral and skin physiologyBombesinbiology.organism_classificationImmunohistochemistryPhodopusEndocrinologymedicine.anatomical_structurechemistryHypothalamusBombesinFemaleSuprachiasmatic NucleusCholecystokininPeriventricular nucleushormones hormone substitutes and hormone antagonistsNeuroscience Letters
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Induction of the fatty acid transport protein 1 and acyl-CoA synthase genes by dimer-selective rexinoids suggests that the peroxisome proliferator-ac…

2000

The intracellular fatty acid content of insulin-sensitive target tissues determines in part their insulin sensitivity. Uptake of fatty acids into cells is a controlled process determined in part by a regulated import/export system that is controlled at least by two key groups of proteins, i.e. the fatty acid transport protein (FATP) and acyl-CoA synthetase (ACS), which facilitate, respectively, the transport of fatty acids across the cell membrane and catalyze their esterification to prevent their efflux. Previously it was shown that the expression of the FATP-1 and ACS genes was controlled by insulin and by peroxisome proliferator-activated receptor (PPAR) agonists in liver or in adipose t…

MalePeroxisome proliferator-activated receptor gammaTime FactorsReceptors Retinoic AcidRetinoic acidReceptors Cytoplasmic and NuclearPeroxisome proliferator-activated receptorTretinoinRetinoid X receptorBiologyFatty Acid-Binding ProteinsBiochemistryMicechemistry.chemical_compoundCoenzyme A LigasesTumor Cells CulturedAnimalsHumansTissue DistributionMolecular BiologyNucleic Acid Synthesis InhibitorsCell Nucleuschemistry.chemical_classificationDose-Response Relationship DrugFatty AcidsMembrane ProteinsFatty acidMembrane Transport ProteinsSerum Albumin Bovine3T3 CellsCell BiologyFatty Acid Transport ProteinsRatsRats ZuckerRetinoic acid receptorRetinoid X ReceptorschemistryBiochemistryDactinomycinFree fatty acid receptorRNAPeroxisome proliferator-activated receptor alphaCaco-2 CellsCarrier ProteinsTranscription Factors
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Physiologically based metformin pharmacokinetics model of mice and scale-up to humans for the estimation of concentrations in various tissues

2020

Metformin is the primary drug for type 2 diabetes treatment and a promising candidate for other disease treatment. It has significant deviations between individuals in therapy efficiency and pharmacokinetics, leading to the administration of an unnecessary overdose or an insufficient dose. There is a lack of data regarding the concentration-time profiles in various human tissues that limits the understanding of pharmacokinetics and hinders the development of precision therapies for individual patients. The physiologically based pharmacokinetic (PBPK) model developed in this study is based on humans’ known physiological parameters (blood flow, tissue volume, and others). The missing tissue-s…

MalePhysiologyAdipose tissueType 2 diabetesPharmacology030226 pharmacology & pharmacyMice0302 clinical medicineAnimal CellsRed Blood CellsMedicine and Health SciencesTissue Distribution0303 health sciencesMultidisciplinarySimulation and ModelingQRMetforminBody Fluids3. Good healthMetforminBloodmedicine.anatomical_structureSmall IntestineMedicineAnatomyCellular TypesResearch Articlemedicine.drugPhysiologically based pharmacokinetic modellingScienceExcretionCmaxResearch and Analysis MethodsModels BiologicalBlood Plasma03 medical and health sciencesPharmacokineticsmedicineAnimalsHumansHypoglycemic AgentsComputer SimulationPharmacokinetics030304 developmental biologyPharmacologyBlood CellsDose-Response Relationship Drugbusiness.industryBiology and Life SciencesKidneysRenal SystemCell BiologyBlood flowmedicine.diseaseSmall intestineGastrointestinal TractDiabetes Mellitus Type 2Physiological ProcessesbusinessDigestive SystemPLOS ONE
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PINK1 displays tissue-specific subcellular location and regulates apoptosis and cell growth in breast cancer cells.

2010

The PINK1 gene is mutated in the germ line of patients with hereditary early-onset Parkinson disease, and PINK1 prosurvival function at neuronal mitochondria has been related with the etiology of this disease. However, the expression and function of PINK1 protein in nonneuronal tissues has not been determined yet. Here, we have analyzed PINK1 protein expression and subcellular distribution in normal and neoplastic human tissues and investigated the function of PINK1 in breast carcinoma cells. PINK1 protein, as stained by a specific anti-PINK1 monoclonal antibody, was widely expressed in human tissues, displaying high expression in epithelial tissues and in the central nervous system and low…

MaleProgrammed cell deathLung NeoplasmsApoptosisBreast NeoplasmsBiologymedicine.disease_causePathology and Forensic MedicineMiceCell Line TumormedicineAnimalsHumansTissue DistributionCell ProliferationCell growthCancermedicine.diseaseSquamous carcinomaCancer researchCarcinoma Squamous CellEctopic expressionFemaleBreast diseaseCarcinogenesisBreast carcinomaProtein KinasesHuman pathology
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Nucleoside phosphotransferase in animal tissues. Tissue distribution and kinetic properties

1985

Amphibian, avian and mammal tissues contain a nucleoside phosphotransferase clearly different from those previously described in vegetables and bacteria. Whatever the animal source, the enzyme showed many similar characteristics as far as substrate specificity, dependence upon Mg2+, instability at 37 degrees C, and the protecting effect of nucleotides were concerned. Moreover, when submitted to gel filtration, the enzyme behaved in all cases as a dissociable high molecular weight protein, whose degree of association was controlled by nucleotides. In amphibian and avian tissues multiple forms of the enzyme seem to be present which differ for the substrate concentration at half-maximal veloci…

MaleRanidaeClinical BiochemistryKineticsSize-exclusion chromatographyChick EmbryoBiologySubstrate SpecificityCricetinaeSettore BIO/10 - BiochimicaNucleoside phosphotransferaseIntestine SmallTestisAnimalsNucleotideMagnesiumHorsesMolecular Biologychemistry.chemical_classificationEffectorPhosphotransferasesTemperatureBrainCell BiologyGeneral Medicinebiology.organism_classificationRatsKineticsEnzymeNucleoside phosphotransferaseTissue distributionchemistryBiochemistryChromatography GelCattleRabbitsChickensPhosphotransferasesBacteriaSpleen
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Pregnane X receptor and yin yang 1 contribute to the differential tissue expression and induction of CYP3A5 and CYP3A4.

2012

The hepato-intestinal induction of the detoxifying enzymes CYP3A4 and CYP3A5 by the xenosensing pregnane X receptor (PXR) constitutes a key adaptive response to oral drugs and dietary xenobiotics. In contrast to CYP3A4, CYP3A5 is additionally expressed in several, mostly steroidogenic organs, which creates potential for induction-driven disturbances of the steroid homeostasis. Using cell lines and mice transgenic for a CYP3A5 promoter we demonstrate that the CYP3A5 expression in these organs is non-inducible and independent from PXR. Instead, it is enabled by the loss of a suppressing yin yang 1 (YY1)-binding site from the CYP3A5 promoter which occurred in haplorrhine primates. This YY1 sit…

MaleReceptors SteroidDrugs and DevicesMolecular Sequence Datalcsh:MedicineSequence HomologyMice TransgenicBiologyModels BiologicalMolecular GeneticsMiceDogsGene expressionMolecular Cell BiologyGeneticsAnimalsCytochrome P-450 CYP3AHumansTissue DistributionEvolutionary SystematicsPharmacokineticsEnzyme inducerBinding sitelcsh:ScienceBiologyCYP3A5 GeneCells CulturedPhylogenyYY1 Transcription FactorPregnane X receptorEvolutionary BiologyMultidisciplinaryCYP3A4Base SequenceYY1lcsh:RPregnane X ReceptorComputational BiologyPromoterMolecular biologyOrganismal EvolutionMice Inbred C57BLNephrologyEnzyme Inductionbiology.proteinMedicinelcsh:QFemaleResearch ArticlePloS one
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Studies of the expression of the cytochrome P450IA, P450IIB, and P450IIC gene family in extrahepatic and hepatic tissues.

1990

We have studied the expression of three P-450 gene subfamilies in hepatic and extrahepatic tissues using the sensitive RNAse A protection assay. Members of the P450IA subfamily, which encodes the major methylcholanthrene-inducible cytochromes P-450, were found to be not expressed in extrahepatic tissues of untreated animals, raising the question whether these P-450 play a role in the metabolism of carcinogens in unexposed individuals. In contrast, members of the P450IIB family, some of which encode the major phenobarbital-inducible cytochromes P-450, were found to be expressed in some extrahepatic tissues of untreated rats and here most notably in the lung and in sebaceous glands. Members o…

MaleSubfamilyCytochromeRNase PHealth Toxicology and MutagenesisCytochrome P-450 Enzyme SystemCytochrome P-450 CYP1A2Gene familyCytochrome c oxidaseAnimalsTissue DistributionGeneRegulation of gene expressionMessenger RNAbiologyPublic Health Environmental and Occupational HealthRNA ProbesMolecular biologyRatsBiochemistryLiverMultigene Familybiology.proteinFemaleOxidoreductasesResearch ArticleEnvironmental Health Perspectives
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Controlled Iontophoretic Delivery in Vitro and in Vivo of ARN14140—A Multitarget Compound for Alzheimer’s Disease

2019

ARN14140 is a galantamine-memantine conjugate that acts upon both cholinergic and glutamatergic pathways for better management of Alzheimer's disease. Poor oral bioavailability and pharmacokinetics meant that earlier preclinical in vivo studies employed intracerebroventricular injection to administer ARN14140 directly to the brain. The aim of the present study was to evaluate the feasibility of using constant current transdermal iontophoresis for the noninvasive systemic delivery of ARN14140 and to quantify the amounts present in the blood and the brain. Preliminary experiments in vitro were performed using porcine skin and validated with human skin. Cumulative ARN14140 permeation across th…

MaleSwineSkin Absorptionbrain deliveryBiological AvailabilityPharmaceutical ScienceHuman skin02 engineering and technologyPharmacologyAdministration Cutaneous030226 pharmacology & pharmacyPermeability03 medical and health sciences0302 clinical medicineDrug StabilityPharmacokineticsIn vivoDrug DiscoveryARN14140AnimalsBrain/metabolismHumansSkin/metabolismMedicineTissue DistributionRats WistarNootropic Agents/administration & dosage/pharmacokineticsTransdermalddc:615galantamine-memantine conjugateAlzheimer Disease/drug therapyIontophoresisbusiness.industryGalantamine/administration & dosage/pharmacokineticsiontophoresiIontophoresisMemantine/administration & dosage/pharmacokinetics021001 nanoscience & nanotechnologyIn vitroRatsBioavailabilityHeterocyclic Compounds 4 or More Rings/administration & dosage/pharmacologytransdermalFeasibility StudiesMolecular MedicineCholinergic0210 nano-technologybusinessMolecular Pharmaceutics
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