Search results for "Luteolin"

showing 10 items of 31 documents

Effects of Lycopene, Indole-3-Carbinol, and Luteolin on Nitric Oxide Production and iNOS Expression are Organ-Specific in Rats

2010

Effects of Lycopene, Indole-3-Carbinol, and Luteolin on Nitric Oxide Production and iNOS Expression are Organ-Specific in RatsNatural compounds are known to modify NO content in tissues; however, the biological activity of polyphenol-rich food often does not correspond to the effects of individual polyphenols on NO synthase activity. The aim of this study was to see how natural compounds luteolin, indole-3-carbinol, and lycopene modify NO production in rat tissues and change the expression of the iNOS gene and protein. Indole-3-carbinol produced multiple effects on the NO level; it significantly decreased NO concentration in blood, lungs, and skeletal muscles and increased it in the liver. …

Malemedicine.medical_specialtyIndolesNitric Oxide Synthase Type IIInflammationNitric OxideToxicologyNitric oxidechemistry.chemical_compoundLycopeneInternal medicineGene expressionmedicineIndole-3-carbinolAnimalsRats WistarLuteolinMuscle SkeletalLungPublic Health Environmental and Occupational HealthBrainSkeletal muscleBiological activityCarotenoidsLycopeneRatsmedicine.anatomical_structureEndocrinologyLiverchemistrymedicine.symptomLuteolinArchives of Industrial Hygiene and Toxicology
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Influence of anti-inflammatory flavonoids on degranulation and arachidonic acid release in rat neutrophils.

1994

We assessed the effects of 24 flavonoid derivatives, reported as anti-inflammatory, on lysosomal enzyme secretion and arachidonic acid release in rat neutrophils. Amentoflavone, quercetagetin- 7-O -glucoside, apigenin, fisetin, kaem pferol, luteolin and quercetin were the most potent inhibitors of β-glucuronidase and lysozyme release. The first com pound was also able to inhibit basal release. These flavonoids besides chrysin and to a reduced extent, naringenin, significantly inhibited arachidonic acid release from membranes. A correlation between degranulation and arachidonic acid release was found for this series of compounds. Structureactivity relationships and implications for the anti-…

NaringeninNeutrophilsAmentoflavoneBiologyGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundStructure-Activity RelationshipAnimalsheterocyclic compoundsChrysinGlucuronidaseFlavonoidsArachidonic AcidMolecular StructureAnti-Inflammatory Agents Non-Steroidalfood and beveragesRatsN-Formylmethionine Leucyl-PhenylalaninechemistryBiochemistryApigeninRegression AnalysisArachidonic acidMuramidaseKaempferolLysosomesLuteolinFisetinZeitschrift fur Naturforschung. C, Journal of biosciences
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A Nutraceutical Containing Chlorogenic Acid and Luteolin Improves Cardiometabolic Parameters in Subjects with Pre-Obesity: A 6-Month Randomized, Doub…

2023

Pre-obesity is a condition that predisposes to the risk of developing obesity, cardiovascular diseases (CVD), and diabetes. Our previous study demonstrated that a Cynara cardunculus (L.) based nutraceutical named Altilix® (Bionap, Italy), containing chlorogenic acid and luteolin extracts, was able to improve several hepatic and cardio-metabolic parameters. Given this background, we conducted a post-hoc analysis of the Altilix® study in order to analyze the supplement’s effects in the subgroup of pre-obesity subjects on anthropometry (weight and waist circumference), glucose metabolism (HbA1C, HOMA-IR, and HOMA-β), lipid profile (total cholesterol, triglycerides, LDL-chole…

Nutrition and Dieteticschlorogenic acidpre-obesity; chlorogenic acid; luteolin; cardiometabolic parametersluteolinpre-obesitycardiometabolic parametersFood ScienceNutrients; Volume 15; Issue 2; Pages: 462
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Cytotoxic phytochemicals from the crude extract of Tetrapleura tetraptera fruits towards multi-factorial drug resistant cancer cells.

2020

Abstract Ethnopharmacological relevance Tetrapleura tetraptera is an African medicinal spice used in traditional medicine to treat several ailments including cancer. Aim of the study The present study was designed to evaluate the cytotoxicity of the dichloromethane-methanol (1:1) extract of the fruits of Tetrapleura tetraptera (TTF) and its constituents: (3R, 4S)-3,4-dimethyloxetan-2-one (1), luteolin (2), stigmasterol (4), 3-O-[6′-O-undecanoyl-β-D-glucopyranosyl]stigmasterol (6), olean-12-en-3-β-O-D-glucopyranoside (7), 3-O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosylurs-12-en-28-oic acid (8), 3-O-β-D-glucopyranosyl-(1 → 3)-β-D-glucopyranosyl-27-hydroxyolean-12-ene-28-oic acid (9), methyl…

Tetrapleura tetrapteraPhytochemicalsApoptosis03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500302 clinical medicineBetulinic acidNeoplasmsDrug DiscoveryCytotoxic T cellHumansTetrapleuraCytotoxicity030304 developmental biologyPharmacologychemistry.chemical_classificationMembrane Potential Mitochondrial0303 health sciencesReactive oxygen speciesbiologyDose-Response Relationship DrugPlant ExtractsHep G2 Cellsbiology.organism_classificationHCT116 CellsMolecular biologyAntineoplastic Agents PhytogenicDrug Resistance MultipleMatrix MetalloproteinasesOxidative StresschemistryApoptosisDrug Resistance Neoplasm030220 oncology & carcinogenesisCaspasesFruitCancer cellReactive Oxygen SpeciesLuteolinSignal TransductionJournal of ethnopharmacology
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Prunella vulgaris L. Upregulates eNOS Expression in Human Endothelial Cells

2010

The purported effects of "circulation-improving" herbs used in traditional Chinese medicine (TCM) show striking similarities with the vascular actions of nitric oxide (NO) produced by the endothelial NO synthase (eNOS). We have previously reported that Salviae miltiorrhizae radix and Zizyphi spinosae semen upregulate eNOS expression. In the present study, we studied the effect on eNOS gene expression of 15 Chinese herbs with potential effects on the vasculature, and identified Prunella vulgaris L. (PVL) (flowering spike) as a potent eNOS-upregulating agent. In EA.hy 926 cells, a cell line derived from human umbilical vein endothelial cells (HUVEC), an aqueous extract of PVL increased eNOS …

Time FactorsNitric Oxide Synthase Type IIIEndotheliumCell SurvivalBlotting WesternPrunella vulgarisCynarosidePharmacologyNitric OxideGene Expression Regulation EnzymologicCell LineNitric oxidechemistry.chemical_compoundUrsolic acidEnosmedicineHumansPrunellaRNA MessengerDose-Response Relationship DrugbiologyEndothelial CellsGeneral Medicinebiology.organism_classificationUp-RegulationNitric oxide synthasemedicine.anatomical_structureComplementary and alternative medicinechemistryChild Preschoolbiology.proteinLuteolinDrugs Chinese HerbalThe American Journal of Chinese Medicine
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Phytochemical Investigation of the Labiate Dorystoechas hastata

1988

Abstract Carnosol (11,12-dihydroxyabieta-8,11,13-trien-20-oic acid 20,7-lactone), and rosmanol (7α, 11, 12-trihydroxy-abieta-8, 11, 13-trien-20 oic acid-20, 6-lactone), two abietane diterpenes previously isolated from Rosmarinus officinalis, have been isolated from leaves of Dorystoechas hastata. Luteolin, luteolin-7-glucoside, 6-methoxyluteolin-7-glucoside, caffeic acid and chlorogenic acid have also obtained from the same source. The co-occurrence of carnosol, rosmanol and 6-methoxyluteolin-7-glucoside support the close relationship of these two genera.

biologyPlant Sciencebiology.organism_classificationCarnosolRosmarinuschemistry.chemical_compoundchemistryChlorogenic acidPhytochemicalBotanyOfficinalisCaffeic acidLuteolinEcology Evolution Behavior and SystematicsAbietaneGiornale botanico italiano
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Über die Verbreitung von Flavonoiden bei akrokarpen Laubmoosen

1978

Summary The methanolic extract from the sporophytes of the moss Ceratodon purpureus (L.) Brid . (Ditrichaceae) contains one flavonoid. It was isolated and purified by means of paper chromatography and identified by cochromatography with authentic material and by UV-spectral data as luteolin. No glycosides of either luteolin or another flavonoid could be detected.

chemistry.chemical_classificationCeratodon purpureusbiologyFlavonoidGlycosideSporophyteGeneral MedicineDitrichaceaebiology.organism_classificationMossPaper chromatographychemistry.chemical_compoundchemistryBotanyLuteolinZeitschrift für Pflanzenphysiologie
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Chemical Constituents of Urospermum picroides

1992

Seven phenolic compounds were isolated from the aerial parts of U. picroides. They were identified by UV spectra, TLC and HPLC-DAD as luteolin, luteolin-7-glucoside, quercetin, quercetin-3-galactoside, kaempferol-3-galactoside, chlorogenic and isochlorogenic acids. Other phenolics were characterized by HPLC-DAD analysis: gallic, protocatechuic, caffeic, ferulic and isoferulic acids, quercetin-3-glucoside and luteolin-4′-glucoside.

chemistry.chemical_classificationChromatographybiologyStereochemistryFlavonoidbiology.organism_classificationGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundUv spectrachemistryChemotaxonomyChemical constituentsPhenolsUrospermum picroidesQuercetinLuteolinZeitschrift für Naturforschung C
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A chemotaxonomic survey of Sonchus subgenus Sonchus

1993

Abstract Five species of Sonchus subgenus Sonchus were surveyed for their phenolic constituents. Seven flavonoids were identified: luteolin, luteolin-7-glucoside, apigenin, apigenin-3-glucoside, quercetin, quercetin-3-glucoside and quercetin-3-galactoside; three were phenolic acids; caffeic, chlorogenic and isochlorogenic; and two were coumarins: aesculetin and cichoriin. Their systematic significance for this genus is discussed.

chemistry.chemical_classificationbiologyFlavonoidAsteraceaebiology.organism_classificationBiochemistrychemistry.chemical_compoundchemistrySonchusChemotaxonomyBotanyApigeninSubgenusAesculetinLuteolinEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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Die Flavonoide von Riccia fluitans L.

1978

Summary Five flavonoids of Riccia fluitans were analysed by means of paper chromatography and uv-spectral data. One substance was identified as luteolin, the others are glycosides of apigenin and luteolin: apigenin-7-O-glucuronide, luteolin-7-O-glucuronide, luteolin-7-O-glucuronide-3’-O-rhamnoside and luteolin-6,8-di-C-glycoside (lucenin).

chemistry.chemical_classificationchemistry.chemical_compoundPaper chromatographybiologychemistryApigeninBotanyGlycosideGeneral MedicineRiccia fluitansbiology.organism_classificationLuteolinZeitschrift für Pflanzenphysiologie
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