Search results for "ratón"

showing 10 items of 64 documents

Comparative tumorigenicity of picene and dibenz[a,h]anthracene in the mouse

1990

The carcinogenic activity of the two polycyclic aromatic hydrocarbons (PAHs), picene (benzo[a]chrysene) and dibenz[a,h]anthracene (DBA), was determined in NMRI mice by five different experimental protocols in order to find out if picene is a carcinogen as predicted by recent quantum mechanical calculations in contrast to earlier observations which could not confirm any carcinogenic activity of picene. Single s.c. treatment of adult mice with picene or DBA (308 nmol/animal, each) led to the formation of fibrosarcomas in 63.3% of treated animals regardless of the PAH used. Chronic epicutaneous application of both PAHs (total dose 1.36 mumol) to the back of mice resulted in the development of …

MaleChryseneCancer ResearchLung NeoplasmsSkin NeoplasmsTime FactorsRatónMice Inbred Strainsmedicine.disease_causeChrysenesMicechemistry.chemical_compoundReference ValuesBiological propertyBenz(a)AnthracenesmedicineAnimalsDibenz(ah)anthraceneCarcinogenAnthraceneGeneral MedicineMolecular biologychemistryPiceneCarcinogensFemaleCarcinogenesisCarcinogenesis
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Distinct influence of atypical 1,4-dihydropyridine compounds in azidothymidine-induced neuro- and cardiotoxicity in mice ex vivo.

2008

This study demonstrates the effective protection by compounds of atypical 1,4-dihydropyridine (DHP) series cerebrocrast, glutapyrone and tauropyrone against neuro- and cardiotoxicity caused by the model compound azidothymidine, a well-known mitochondria-compromising anti-HIV drug. In previous in vitro experiments, we have demonstrated distinct effects of these DHP compounds to influence mitochondrial functioning. In the present in vivo experiments, DHP compounds were administered intraperitoneally in mice daily for 2 weeks, per se and in combinations with azidothymidine at doses: azidothymidine 50 mg/kg; cerebrocrast 0.1 mg/kg; glutapyrone 1 mg/kg; and tauropyrone 1 mg/kg. At the end of the…

MaleDihydropyridinesHeart DiseasesRatónAnti-HIV AgentsTaurineApoptosisBiologyPharmacologyToxicologyMiceGlutamatesIn vivomedicineAnimalsPharmacologyCerebral CortexInflammationCardiotoxicityMice Inbred ICRCaspase 3DihydropyridineTranscription Factor RelAGeneral MedicineBiochemistryGene Expression RegulationEnzyme inhibitorApoptosisToxicitybiology.proteinNeurotoxicity SyndromesZidovudineEx vivomedicine.drugBasicclinical pharmacologytoxicology
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Genetic control of C3 production by the S region of the mouse MHC.

1988

SUMMARY The present paper reports evidence indicating that the level of the third complement component (C3) is regulated by the S region of the murine H-2 complex. In fact, using congenic strains of mice we demonstrate that mice with the k haplotype at the S region show high C3 levels, whereas mice with the d haplotype at the S region show low C3 levels.

MaleGeneticsRatónImmunologyHaplotypeH-2 AntigensCongenicMice Inbred StrainsComplement C3ImmunogeneticsBiologyMajor histocompatibility complexHemolysisMajor Histocompatibility ComplexMiceGene Expression RegulationHaplotypesGeneticsbiology.proteinAnimalsAlleles
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Attenuation of sucrose consumption in mice by chronic mild stress and its restoration by imipramine

1995

Chronic exposure to mild unpredictable stressors (CMS) has previously been found to reduce the consumption of palatable, sweet solutions in rats. In the present study, the utility of this procedure was assessed in mice. Male AP mice subjected to CMS showed reduced consumption of a 2% or 4% sucrose solution. This effect was reversed by chronic (3 weeks) treatment with the tricyclic antidepressant imipramine (20 mg/kg per day). These results extend previous reports of a generalized decrease in sensitivity to reward (anhedonia) in rats caused by CMS and the efficacy of antidepressant treatment in this paradigm. Chronic unpredictable mild stress in mice appears to provide a realistic animal mod…

MaleImipramineSucrosemedicine.medical_specialtySucroseRatónmedicine.drug_classmedicine.medical_treatmentTricyclic antidepressantImipramineEatingMicechemistry.chemical_compoundInternal medicineAnimalsMedicinePsychiatryDepression (differential diagnoses)PharmacologyAnalysis of VarianceDepressive DisorderChemotherapyBehavior Animalbusiness.industryAnhedoniaDisease Models AnimalEndocrinologychemistryAntidepressantmedicine.symptombusinessStress Psychologicalmedicine.drugPsychopharmacology
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Development and pathology of echinostoma caproni in experimentally infected mice

2007

In the present article, several parasitological features of mice, each experimentally infected with 75 metacercariae of Echinostoma caproni (Trematoda: Echinostomatidae), were studied during the first 12 wk postinfection. Moreover, the early pathological responses also were analyzed and compared with data previously published on other host species of E. caproni to gain further insight into the factors determining worm rejection or establishment of chronic infections. The results obtained show that the pattern of E. caproni infection in mice is consistent with a highly compatible host–parasite system. This combination is characterized by a high worm establishment, high egg output, and long s…

MaleNeutrophilsRatónEchinostoma caproni:CIENCIAS DE LA VIDA [UNESCO]Host-Parasite InteractionsEchinostomatidaeMiceRandom AllocationUNESCO::CIENCIAS DE LA VIDAAnimalsParasite hostinginfected miceMesenteryIntestinal MucosaechinostomaEcology Evolution Behavior and SystematicsAnalysis of VarianceEchinostomiasisMice Inbred ICRcaproniBiomphalariabiologyHost (biology):CIENCIAS DE LA VIDA::Biología animal (Zoología) ::Parasitología animal [UNESCO]biology.organism_classificationIntestinesUNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología) ::Parasitología animalImmunologyLeukocytes MononuclearParasitologyGoblet CellsTrematodaEchinostoma
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Effects of acute and chronic maprotiline administration on inhibitory avoidance in male mice

2000

The effects of acute and chronic administration of maprotiline (5, 10 or 20 mg/kg, intraperitoneally) were assessed on inhibitory avoidance in male mice. Acute administration of maprotiline before training did not effect training phase latencies, but impaired performance (i.e. produced shorter latencies) in the test at doses of 5 and 20 mg/kg. When given after training, the drug did not modify test latencies at any of the doses used. Chronic administration for 21 days (interrupted 24 h before training) also shortened latencies in the test but not in training. An experiment on the acute effects of maprotiline on analgesia (determination of flinch and jump thresholds for increasing electric f…

MalePain ThresholdAnterograde amnesiaRatónInhibitory postsynaptic potentialDrug Administration ScheduleDevelopmental psychologyNorepinephrine (medication)MiceBehavioral NeuroscienceDrug toleranceThreshold of painAvoidance LearningReaction TimemedicineAnimalsMaprotilineDose-Response Relationship DrugBrainNeural InhibitionDrug ToleranceMaprotilineAnesthesiaMental RecallAntidepressive Agents Second-Generationmedicine.symptomPsychologyReuptake inhibitorInjections Intraperitonealmedicine.drugBehavioural Brain Research
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Differential uptake of systemic fluorochrome Hoechst 33342 in lung and liver metastasis of B16 melanoma.

1992

The growth and vascularization patterns of B16 melanoma colonies in the liver and lungs were measured and compared by histological techniques and dye diffusion patterns after injection of the fluorochrome Hoechst 33342. In the liver, the fluorescent pattern of dye diffusion revealed that uninodular tumours measuring up to 146 microns in diameter were not functionally vascularized. However, when the nodules fused to give rise to multinodular tumours measuring between 256 and 366 microns in diameter, a reticular dye diffusion pattern revealed functional tumour vascularization. In the lungs, subpleural, parenchymal and peritubular (i.e. surrounding blood vessels and airways) tumours were obser…

MalePathologymedicine.medical_specialtyLung NeoplasmsRatónmedicine.medical_treatmentMelanoma ExperimentalBiologyPathology and Forensic MedicineMetastasisMiceParenchymamedicineAnimalsNeoplasm MetastasisMolecular BiologyChemotherapyLungNeovascularization PathologicRespiratory diseaseLiver NeoplasmsCell BiologyGeneral Medicinemedicine.diseaseRadiation therapyMice Inbred C57BLmedicine.anatomical_structureReticular connective tissueBenzimidazolesVirchows Archiv. A, Pathological anatomy and histopathology
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Cryoablation of Human Colorectal Cancerin Vivoin a Nude Mouse Xenograft Model

1998

Abstract Objective: To establish the minimum required temperature in cryoablation of human colorectal cancer cell lines grown as subcutaneous tumors in mice. Methods: Male nu/nu nude mice were inoculated by a sc injection of 1 × 10 6 LoVo ( n = 30) or C170 ( n = 32) cells. After 2 weeks the tumors were frozen using a 3-mm cryotherapy probe (LCS 3000, Cryotech, UK) to temperatures ranging from −8 to −84°C. Results: (LoVo) Of 21 mice evaluable for analysis no tumors recurred in 3 mice which had their tumors frozen to less than −60°C as measured at the presumed tumor/host boundary, whereas all but one tumor recurred in 18 mice which had their tumors frozen to >−60°C. (C170) Of 18 mice evaluabl…

MalePathologymedicine.medical_specialtyRatónColorectal cancermedicine.medical_treatmentTransplantation HeterologousMice NudeRectumCryotherapyGeneral Biochemistry Genetics and Molecular BiologyCryosurgeryMiceNude mousemedicineAnimalsHumansbiologybusiness.industryCryoablationNeoplasms ExperimentalGeneral Medicinebiology.organism_classificationmedicine.diseaseCold Temperaturemedicine.anatomical_structureCryotherapyCell cultureColorectal NeoplasmsGeneral Agricultural and Biological SciencesbusinessNeoplasm TransplantationCryobiology
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Dietary administration of high doses of pterostilbene and quercetin to mice is not toxic.

2009

The aim of this study is to evaluate possible harmful effects of high doses of t-pterostilbene (t-PTER) and quercetin (QUER) in Swiss mice. Mice were fed during 28 days at doses of 0, 30, 300, and 3000 mg/kg body weight/day of t-PTER, QUER, or a mixture of both, t-PTER + QUER, which are equivalent to 5, 50, and 500 times, respectively, the estimated mean human intake of these polyphenols (25 mg/day). Daily oral administration of QUER, t-PTER, or a mixture of both of them did not cause mortality during the experimental period. There were no differences in food and water consumption on sex. No significant body weight gain in the male or female groups was observed. Red blood cell number and th…

MalePterostilbeneRatónFlavonoidPhysiologyBiologyHematocritWeight GainToxicologychemistry.chemical_compoundMiceOral administrationStilbenesmedicineAnimalschemistry.chemical_classificationSex Characteristicsmedicine.diagnostic_testGeneral ChemistryDietRed blood cellmedicine.anatomical_structurechemistryHematocritToxicityErythrocyte CountFemaleQuercetinGeneral Agricultural and Biological SciencesQuercetinJournal of agricultural and food chemistry
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Colonization of adrenal glands and ovaries of mice by HSV-2 variants

1990

HSV-2 strain ER was shown to consist of variants with different pathogenic phenotype: Variant ER+ replicates to high titers in the adrenal glands and the ovaries but much less in the spleen; the testes were not colonized. ER+ migrates to the spinal ganglia and is highly neuroinvasive after i.p. inoculation. Variant ER- replicates 100-1,000 fold less in the adrenal glands and the ovaries, but proceeds to the spinal ganglia without invading the CNS. However, both variants are highly neuropathogenic after direct i.c. injection. We conclude that neuropathogenicity, neuroinvasiveness and the ability to replicate in the adrenal glands as well as ovaries are each determined by different sets of ge…

MaleRatónmedicine.medical_treatmentSpleenOvaryBiologyVirus ReplicationLethal Dose 50MiceSpecies SpecificityVirologyAdrenal GlandsmedicineAnimalsHumansSimplexvirusPropionibacterium acnesVero CellsCells CulturedMice Inbred BALB CAdrenalectomyOvaryAdrenalectomyHerpes SimplexEmbryoGeneral MedicineSilicon DioxideVirologyPhenotypemedicine.anatomical_structureViral replicationVero cellFemaleSpleenArchives of Virology
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