Search results for "Toxicity"

showing 10 items of 2261 documents

Organometallic complexes with biological molecules: V.In vivo cytotoxicity of diorganotin(IV)-amoxicillin derivatives in mitotic chromosomes ofrutilu…

1995

In order to test in vivo cytotoxicity of diorganotin(IV)-amoxicillin (amox) derivatives, mitotic chromosomes of Rutilus rubilio (Pisces, Cyprinidae) have been analyzed using two different chromosome-staining techniques. Results gathered after exposure of fish to the free amox.3H 2 O, R 2 SnClamox.2H 2 O, and R 2 Snamox 2 .2H 2 O (R = methyl, butyl and phenyl ; amox - = 6-[D(-)-β-amino-p-hydroxyphenylacetamido]penicillinate) suggest that methyl derivatives seem to exert a lower cytotoxicity than butyl and phenyl ones and that R 2 Snamox 2 .2H 2 O derivatives are more toxic than R 2 Snclamox.2H 2 O at both 10 -5 and 10 -7 mol dm -3 concentrations. The following structural lesions have been id…

biologyChemistryStereochemistryChromosomeGeneral Chemistrybiology.organism_classificationmedicine.disease_causeChromosome aberrationInorganic ChemistryMoleCyprinidaemedicineRutilusCytotoxicityMitosisGenotoxicityApplied Organometallic Chemistry
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Three New Medicagenic Acid Saponins from Polygala micranthaGuill. & Perr.

2011

Three new medicagenic acid saponins, micranthosides A–C (1–3), were isolated from the roots of Polygala micranthaGuill. & Perr., along with six known presenegenin saponins. Their structures were elucidated on the basis of extensive 1D- and 2D-NMR experiments (1H, 13C, DEPT, COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3-O-β-D-glucopyranosylmedicagenic acid 28-[O-β-D-galactopyranosyl-(14)-O-β-D-xylopyranosyl-(14)-O-α-L-rhamnopyranosyl-(12)-β-D-fucopyranosyl] ester (1), 3-O-β-D-glucopyranosylmedicagenic acid 28-[O-6-O-acetyl-β-D-galactopyranosyl-(14)-O-β-D-xylopyranosyl-(14)-O-α-L-rhamnopyranosyl-(12)-β-D-fucopyranosyl] ester (2), and 3-O-{O-β-D-glucopyranosyl-(13)-O-[β-D-gluc…

biologyChemistryStereochemistryOrganic ChemistryDEPTMass spectrometrybiology.organism_classificationBiochemistryCatalysisPolygalaMedicagenic acidInorganic ChemistryHuman colon cancerDrug DiscoveryPhysical and Theoretical ChemistryCytotoxicityTwo-dimensional nuclear magnetic resonance spectroscopyHeteronuclear single quantum coherence spectroscopyHelvetica Chimica Acta
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Acute toxicity of some chlorinated phenols, catechols and cresols to trout.

1981

biologyChemistryTroutHealth Toxicology and MutagenesisCatecholsGeneral MedicineToxicologybiology.organism_classificationPollutionAcute toxicityLethal Dose 50TroutCresolsChlorinated phenolsPhenolsEnvironmental chemistryEcotoxicologyAnimalsBiotransformationSalmonidaeChlorophenolsBulletin of environmental contamination and toxicology
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Drivers of topoisomerase II poisoning mimic and complement cytotoxicity in AML cells

2019

Recently approved cancer drugs remain out-of-reach to most patients due to prohibitive costs and only few produce clinically meaningful benefits. An untapped alternative is to enhance the efficacy and safety of existing cancer drugs. We hypothesized that the response to topoisomerase II poisons, a very successful group of cancer drugs, can be improved by considering treatment-associated transcript levels. To this end, we analyzed transcriptomes from Acute Myeloid Leukemia (AML) cell lines treated with the topoisomerase II poison etoposide. Using complementary criteria of co-regulation within networks and of essentiality for cell survival, we identified and functionally confirmed 11 druggabl…

biologyCombination therapybusiness.industryTopoisomeraseMyeloid leukemiatopoisomerase II poisonscombination therapyCell killingOncologygene expressioncancer essentialitybiology.proteinmedicineCancer researchDNA damageCytotoxic T cellCytotoxicitybusinessEtoposidePI3K/AKT/mTOR pathwayResearch Papermedicine.drugOncotarget
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BER, MGMT, and MMR in defense against alkylation-induced genotoxicity and apoptosis

2001

Methylating carcinogens and cytostatic drugs induce different methylation products in DNA. In cells not expressing the repair protein MGMT or expressing it at a low level, O6-methylguanine is the major genotoxic, recombinogenic, and apoptotic lesion. Genotoxicity and apoptosis triggered by O6-methylguanine require mismatch repair (MMR). In cells expressing O6-methylguanine-DNA methyl transferase (MGMT) at a high level or for agents producing low amounts of O6-methylguanine, N-alkylations become the major genotoxic lesions. N-Alkylations are repaired by base excision repair (BER). In mammalian cells, naturally occurring mutants of BER have not been detected, which points to the importance of…

biologyDNA polymeraseTransfectionBase excision repairmedicine.disease_causeMolecular biologyDNA glycosylaseCancer researchbiology.proteinmedicineTranscriptional regulationAP siteDNA mismatch repairGenotoxicity
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Effects of Pulp and Paper Mill Effluent (BKME) on Physiology and Biochemistry of the Roach (Rutilus rutilus L.)

1996

The effects of bleached kraft pulp and paper mill effluent (BKME) on the roach (Rutilus rutilus L.) were studied under experimental and natural field conditions. In the acute experiment (72 h exposure to the concentrated BKME), the roach suffered from a general stress syndrome, characterized by a significant increase of cortisol and blood glucose, as well as a significant decrease of leucocrit and total plasma protein. In three weeks' exposure in a polluted and an unpolluted lake and in fish caught from the same lakes, the more specific effects of BKME treatments appeared. During the three weeks' exposure, slight hyperglycaemia as well as a decrease in a transaminase activity (GPT) and incr…

biologyEcologybusiness.industryHealth Toxicology and MutagenesisPulp (paper)Paper millGeneral Medicineengineering.materialToxicologybiology.organism_classificationPollutionTransaminaseAnimal scienceKraft processToxicityengineeringEcotoxicologyRutilusbusinessEffluentArchives of environmental contamination and toxicology
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Tumoricidal Activity of Endothelial Cells

2001

The mechanism of NO- and H(2)O(2)-induced tumor cytotoxicity was examined during B16 melanoma (B16M) adhesion to the hepatic sinusoidal endothelium (HSE) in vitro. We used endothelial nitric-oxide synthetase gene disruption and N(G)-nitro-l-arginine methyl ester-induced inhibition of nitric-oxide synthetase activity to study the effect of HSE-derived NO on B16M cell viability. Extracellular H(2)O(2) was removed by exogenous catalase. H(2)O(2) was not cytotoxic in the absence of NO. However, NO-induced tumor cytotoxicity was increased by H(2)O(2) due to the formation of potent oxidants, likely ( small middle dot)OH and (-)OONO radicals, via a trace metal-dependent process. B16M cells culture…

biologyEndotheliumChemistryEbselenCell BiologyGlutathioneBiochemistryMolecular biologychemistry.chemical_compoundmedicine.anatomical_structureBiochemistryCatalasebiology.proteinmedicineCytotoxic T cellButhionine sulfoximineViability assayCytotoxicityMolecular BiologyJournal of Biological Chemistry
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Accumulation of Pb and Zn in Bidens triplinervia and Senecio sp. spontaneous species from mine spoils in Peru and their potential use in phytoremedia…

2012

Abstract Heavy metal toxicity has become a global concern due to the ever-increasing contamination of soil, water and crops. Until recent decades little has been known about the remediation of mining sites using spontaneous plants in Latin America. Soil and plant samples were taken in Peru, at a polymetallic mine (mainly silver, lead and copper) in Cajamarca Province, Hualgayoc district. Top soils (0–20 cm) were analyzed for physical and chemical properties by standard methods. Total Pb and Zn concentrations in top soils were determined by ICP-OES. Similar metals in plants were analyzed separately (aerial and root system). Ti content was used as an indicator for contamination of plant sampl…

biologyEnvironmental remediationBidens triplinerviaMetal toxicitySeneciobiology.organism_classificationPhytoremediationGeochemistry and PetrologyLoamEnvironmental chemistryBotanySoil waterEnvironmental scienceEconomic GeologyHyperaccumulatorJournal of Geochemical Exploration
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P4‐256: POSITIVE FEEDBACK LOOP OF APC/C‐CDH1‐MEDIATED EXCITOTOXICITY IN ALZHEIMER'S DISEASE

2014

biologyEpidemiologybusiness.industryHealth PolicyExcitotoxicityDiseasemedicine.disease_causeCDH1Psychiatry and Mental healthCellular and Molecular NeuroscienceDevelopmental Neurosciencebiology.proteinmedicineNeurology (clinical)Geriatrics and GerontologybusinessNeurosciencePositive feedbackAlzheimer's & Dementia
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Oxidative Stress And Ubiquitin Ligases: Their Involvement In Alzheimer’s Disease Pathophysiology

2015

Oxidative stress is a major hallmark in Alzheimer’s Disease. We showed that amyloid beta (Aβ 1-42 ), induces mitochondrial oxidative stress. We focused on dysregulations of ubiquitin ligases in Alzheimer’s and their relation to oxidative stress. The anaphase-promoting complex/cyclosome (APC/C)-Cdh1 ubiquitin ligase has a role as cell cycle regulator in proliferating cells and, recently another role in the regulation the degradation of key glycolytic enzyme 6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase-3 has been found (Almeida et al., 2012). Herrero-Mendez et al. observed in 2009 that inhibition of Cdh1 leads to an upregulation of Pfkfb3 in neurons and that this results in the activ…

biologyGlutaminaseAmyloid betaGlutamate receptorExcitotoxicityPentose phosphate pathwaymedicine.disease_causeBiochemistryUbiquitin ligaseCell biologyBiochemistryUbiquitinPhysiology (medical)biology.proteinmedicineOxidative stressFree Radical Biology and Medicine
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