يعرض 1 - 20 نتائج من 2,185 نتيجة بحث عن '"oxygen radical absorbance capacity"', وقت الاستعلام: 0.64s تنقيح النتائج
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    المساهمون: D. Mercatante, D. Ansorena, A. Taticchi, I. Astiasarán, M. Servili, M. T. Rodriguez-Estrada

    وصف الملف: ELETTRONICO

    Relation: info:eu-repo/semantics/altIdentifier/pmid/36670884; info:eu-repo/semantics/altIdentifier/wos/WOS:000919536000001; volume:12; issue:1; firstpage:1; lastpage:13; numberofpages:13; journal:ANTIOXIDANTS; https://hdl.handle.net/11585/920001; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85146797333; https://www.mdpi.com/2076-3921/12/1/22

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    المصدر: Revista Investigación en Salud Universidad de Boyacá; Vol. 9 No. 2 (2022): Revista Investigación en Salud Universidad de Boyacá; 194-213 ; Revista Investigación en Salud Universidad de Boyacá; Vol. 9 Núm. 2 (2022): Revista Investigación en Salud Universidad de Boyacá; 194-213 ; Revista Investigación en Salud Universidad de Boyacá; Vol. 9 N.º 2 (2022): Revista Investigación en Salud Universidad de Boyacá; 194-213 ; 2539-2018 ; 2389-7325 ; 10.24267/23897325.v9n2

    وصف الملف: application/pdf

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Database. 2010;2010:bap024. https://doi.org/10.1093/database/bap024; Rothwell JA, Urpi-Sarda M, Boto-Ordoñez M, Knox C, Llorach R, Eisner R, et al. Phenol-Explorer 2.0: a major update of the Phenol-Explorer database integrating data on polyphenol metabolism and pharmacokinetics in humans and experimental animals. Database. 2012;2012:bas031. https://doi.org/10.1093/database/bas031; Rothwell JA, Perez-Jimenez J, Neveu V, Medina-Remón A, M’Hiri N, García-Lobato P, et al. Phenol-Explorer 3.0: a major update of the Phenol-Explorer database to incorporate data on the effects of food processing on polyphenol content. Database. 2013;2013:bat070. https://doi.org/10.1093/database/bat070; Stepanenko AA, Dmitrenko V V. Pitfalls of the MTT assay: Direct and off-target effects of inhibitors can result in over/underestimation of cell viability. Gene. diciembre de 2015;574(2):193-203. https://doi.org/10.1016/j.gene.2015.08.009; Angius F, Floris A. Liposomes and MTT cell viability assay: an incompatible affair. Toxicol Vitro Int J Publ Assoc BIBRA. marzo de 2015;29(2):314-9. https://doi.org/10.1016/j.tiv.2014.11.009; Gomez Perez M, Fourcade L, Mateescu MA, Paquin J. Neutral Red versus MTT assay of cell viability in the presence of copper compounds. Anal Biochem. octubre de 2017;535:43-6. https://doi.org/10.1016/j.ab.2017.07.027; Karakaş D, Ari F, Ulukaya E. The MTT viability assay yields strikingly false-positive viabilities although the cells are killed by some plant extracts. Turk J Biol Turk Biyol Derg. 2017;41(6):919-25. https://doi.org/10.3906/biy-1703-104; Cassiem W, de Kock M. The anti-proliferative effect of apricot and peach kernel extracts on human colon cancer cells in vitro. BMC Complement Altern Med. 2019;19(1):32. https://doi.org/10.1186/s12906-019-2437-4; Patra S, Pradhan B, Nayak R, Behera C, Das S, Patra SK, et al. 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BioMed Res Int. 2020;2020:8857428. https://doi.org/10.1155/2020/8857428; Hosseini FS, Noroozi Karimabad M, Hajizadeh MR, Khoshdel A, Khanamani Falahati-Pour S, Mirzaei MR, et al. Evaluating of Induction of Apoptosis by Cornus mass L. Extract in the Gastric Carcinoma Cell Line (AGS). Asian Pac J Cancer Prev APJCP. 2019;20(1):123-30. https://doi.org/10.31557/APJCP.2019.20.1.123; Desta KT, Kim GS, Abd El-Aty AM, Raha S, Kim M-B, Jeong JH, et al. Flavone polyphenols dominate in Thymus schimperi Ronniger: LC-ESI-MS/MS characterization and study of anti-proliferative effects of plant extract on AGS and HepG2 cancer cells. J Chromatogr B Analyt Technol Biomed Life Sci. 2017;1053:1-8. https://doi.org/10.1016/j.jchromb.2017.03.035; Pagliara V, Nasso R, Di Donato P, Finore I, Poli A, Masullo M, et al. Lemon Peel Polyphenol Extract Reduces Interleukin-6-Induced Cell Migration, Invasiveness, and Matrix Metalloproteinase-9/2 Expression in Human Gastric Adenocarcinoma MKN-28 and AGS Cell Lines. Biomolecules. 2019;9(12):833. https://doi.org/10.3390/biom9120833; Hallmann E, Kazimierczak R, Marszalek K, Drela N, Kiernozek E, Toomik P, et al. The Nutritive Value of Organic and Conventional White Cabbage (Brassica Oleracea L. Var. Capitata) and Anti-Apoptotic Activity in Gastric Adenocarcinoma Cells of Sauerkraut Juice Produced Therof. J Agric Food Chem. septiembre de 2017;65(37):8171-83. https://doi.org/10.1021/acs.jafc.7b01078; Chen D-L, Sheng H, Zhang D-S, Jin Y, Zhao B-T, Chen N, et al. The circular RNA circDLG1 promotes gastric cancer progression and anti-PD-1 resistance through the regulation of CXCL12 by sponging miR-141-3p. Mol Cancer. 15 de diciembre de 2021;20(1):166. https://doi.org/10.1186/s12943-021-01475-8; Liu ML, Zhang SJ. Effects of resveratrol on the protein expression of survivin and cell apoptosis in human gastric cancer cells. J BUON Off J Balk Union Oncol. 2014;19(3):713-7.; Yang Y, Huang X, Chen S, Ma G, Zhu M, Yan F, et al. Resveratrol induced apoptosis in human gastric carcinoma SGC-7901 cells via activation of mitochondrial pathway. Asia Pac J Clin Oncol. 2018;14(5):e317-24. https://doi.org/10.1111/ajco.12841; Yang T, Zhang J, Zhou J, Zhu M, Wang L, Yan L. Resveratrol inhibits Interleukin-6 induced invasion of human gastric cancer cells. Biomed Pharmacother Biomedecine Pharmacother. 2018;99:766-73. https://doi.org/10.1016/j.biopha.2018.01.153; Nowdijeh AA, Moosavi MA, Hosseinzadeh S, Soleimani M, Sabouni F, Hosseini-Mazinani M. Anti-oxidant and Selective Anti-proliferative Effects of the Total Cornicabra Olive Polyphenols on Human Gastric MKN45 Cells. Iran J Biotechnol. 2019;17(1):e1967. https://doi.org/10.21859/ijb.1967; Liu B, Li Z. Black Currant (Ribes nigrum L.) Extract Induces Apoptosis of MKN-45 and TE-1 Cells Through MAPK- and PI3K/Akt-Mediated Mitochondrial Pathways. J Med Food. 2016;19(4):365-73. https://doi.org/10.1089/jmf.2015.3521; Arcone R, Palma M, Pagliara V, Graziani G, Masullo M, Nardone G. Green tea polyphenols affect invasiveness of human gastric MKN-28 cells by inhibition of LPS or TNF-alpha induced Matrix Metalloproteinase-9/2. Biochim Open. 2016;3:56-63. https://doi.org/10.1016/j.biopen.2016.10.002; Jing X, Cheng W, Wang S, Li P, He L. Resveratrol induces cell cycle arrest in human gastric cancer MGC803 cells via the PTEN-regulated PI3K/Akt signaling pathway. Oncol Rep. 2016;35(1):472-8. https://doi.org/10.3892/or.2015.4384; Zhang Q, Wang X, Cao S, Sun Y, He X, Jiang B, et al. Berberine represses human gastric cancer cell growth in vitro and in vivo by inducing cytostatic autophagy via inhibition of MAPK/mTOR/p70S6K and Akt signaling pathways. Biomed Pharmacother Biomedecine Pharmacother. agosto de 2020;128:110245. https://doi.org/10.1016/j.biopha.2020.110245; Mieszala K, Rudewicz M, Gomulkiewicz A, Ratajczak-Wielgomas K, Grzegrzolka J, Dziegiel P, et al. Expression of genes and proteins of multidrug resistance in gastric cancer cells treated with resveratrol. Oncol Lett. 2018/02/12 ed. 2018;15(4):5825-32. https://doi.org/10.3892/ol.2018.8022; Venancio VP, Cipriano PA, Kim H, Antunes LMG, Talcott ST, Mertens-Talcott SU. Cocoplum (Chrysobalanus icaco L.) anthocyanins exert anti-inflammatory activity in human colon cancer and non-malignant colon cells. Food Funct. enero de 2017;8(1):307-14. https://doi.org/10.1039/c6fo01498d; Emanuele S, Notaro A, Palumbo Piccionello A, Maggio A, Lauricella M, D’Anneo A, et al. Sicilian Litchi Fruit Extracts Induce Autophagy versus Apoptosis Switch in Human Colon Cancer Cells. Nutrients. 12 de octubre de 2018;10(10):1490. https://doi.org/10.3390/nu10101490; Kim D-H, Park K-W, Chae IG, Kundu J, Kim E-H, Kundu JK, et al. Carnosic acid inhibits STAT3 signaling and induces apoptosis through generation of ROS in human colon cancer HCT116 cells. Mol Carcinog. junio de 2016;55(6):1096-110. https://doi.org/10.1002/mc.22353; Signorelli P, Fabiani C, Brizzolari A, Paroni R, Casas J, Fabrias G, et al. Natural grape extracts regulate colon cancer cells malignancy. Nutr Cancer. 2015;67(3):494-503. https://doi.org/10.1080/01635581.2015.1004591; Chalons P, Courtaut F, Limagne E, Chalmin F, Cantos-Villar E, Richard T, et al. Red Wine Extract Disrupts Th17 Lymphocyte Differentiation in a Colorectal Cancer Context. Mol Nutr Food Res. abril de 2020;e1901286. https://doi.org/10.1002/mnfr.201901286; Jiang T, Wang H, Liu L, Song H, Zhang Y, Wang J, et al. CircIL4R activates the PI3K/AKT signaling pathway via the miR-761/TRIM29/PHLPP1 axis and promotes proliferation and metastasis in colorectal cancer. Mol Cancer. 18 de diciembre de 2021;20(1):167. https://doi.org/10.1186/s12943-021-01474-9; Sharma N, Sharma A, Bhatia G, Landi M, Brestic M, Singh B, et al. Isolation of Phytochemicals from Bauhinia variegata L. Bark and Their In Vitro Antioxidant and Cytotoxic Potential. Antioxid Basel Switz. octubre de 2019;8(10). https://doi.org/10.3390/antiox8100492; Gao Y, Li W, Jia L, Li B, Chen YC, Tu Y. Enhancement of (-)-epigallocatechin-3-gallate and theaflavin-3-3’-digallate induced apoptosis by ascorbic acid in human lung adenocarcinoma SPC-A-1 cells and esophageal carcinoma Eca-109 cells via MAPK pathways. Biochem Biophys Res Commun. agosto de 2013;438(2):370-4. https://doi.org/10.1016/j.bbrc.2013.07.078; Stavrou IJ, Christou A, Kapnissi-Christodoulou CP. Polyphenols in carobs: A review on their composition, antioxidant capacity and cytotoxic effects, and health impact. Food Chem. 15 de diciembre de 2018;269:355-74. https://doi.org/10.1016/j.foodchem.2018.06.152; Ruskovska T, Maksimova V, Milenkovic D. Polyphenols in human nutrition: from the in vitro antioxidant capacity to the beneficial effects on cardiometabolic health and related inter-individual variability - an overview and perspective. Br J Nutr. 14 de febrero de 2020;123(3):241-54. https://doi.org/10.1017/S0007114519002733; Mutungi MM, Muema FW, Kimutai F, Xu Y-B, Zhang H, Chen G-L, et al. Antioxidant and Antiproliferative Potentials of Ficus glumosa and Its Bioactive Polyphenol Metabolites. Pharm Basel Switz. 15 de marzo de 2021;14(3). https://doi.org/10.3390/ph14030266; Merighi S, Travagli A, Tedeschi P, Marchetti N, Gessi S. Antioxidant and Antiinflammatory Effects of Epilobium parviflorum, Melilotus officinalis and Cardiospermum halicacabum Plant Extracts in Macrophage and Microglial Cells. Cells. 8 de octubre de 2021;10(10). https://doi.org/10.3390/cells10102691; Mangmool S, Kunpukpong I, Kitphati W, Anantachoke N. Antioxidant and Anticholinesterase Activities of Extracts and Phytochemicals of Syzygium antisepticum Leaves. Mol Basel Switz. 30 de mayo de 2021;26(11). https://doi.org/10.3390/molecules26113295; Fonseca-Hernández D, Lugo-Cervantes EDC, Escobedo-Reyes A, Mojica L. Black Bean (Phaseolus vulgaris L.) Polyphenolic Extract Exerts Antioxidant and Antiaging Potential. Mol Basel Switz. 6 de noviembre de 2021;26(21). https://doi.org/10.3390/molecules26216716; Song S, Lee Y-M, Lee YY, Yeum K-J. Oat (Avena sativa) Extract against Oxidative Stress-Induced Apoptosis in Human Keratinocytes. Mol Basel Switz. 13 de septiembre de 2021;26(18). https://doi.org/10.3390/molecules26185564; Zhu K-X, Lian C-X, Guo X-N, Peng W, Zhou H-M. Antioxidant activities and total phenolic contents of various extracts from defatted wheat germ. Food Chem. 2011;126(3):1122-6. https://doi.org/10.1016/j.foodchem.2010.11.144; Ramos A, Visozo A, Piloto J, García A, Rodríguez CA, Rivero R. Screening of antimutagenicity via antioxidant activity in Cuban medicinal plants. J Ethnopharmacol. agosto de 2003;87(2-3):241-6. https://doi.org/10.1016/s0378-8741(03)00156-9; Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. diciembre de 1983;65(1-2):55-63. https://doi.org/10.1016/0022-1759(83)90303-4; Wang Y, Chu F, Lin J, Li Y, Johnson N, Zhang J, et al. Erianin, the main active ingredient of Dendrobium chrysotoxum Lindl, inhibits precancerous lesions of gastric cancer (PLGC) through suppression of the HRAS-PI3K-AKT signaling pathway as revealed by network pharmacology and in vitro experimental verification. J Ethnopharmacol. 28 de octubre de 2021;279:114399. https://doi.org/10.1016/j.jep.2021.114399; Deng P, Li K, Gu F, Zhang T, Zhao W, Sun M, et al. LINC00242/miR-1-3p/G6PD axis regulates Warburg effect and affects gastric cancer proliferation and apoptosis. Mol Med Camb Mass. 29 de enero de 2021;27(1):9. https://doi.org/10.1186/s10020-020-00259-y; Quintana-Castillo JC, Ávila-Gómez IC, Ceballos-Ruiz JF, Vargas-Muñoz LJ, Estrada-Gómez S. Efecto citotóxico de fosfolipasas A2 del veneno de Crotalus durissus cumanensis de Colombia. Rev Investig En Salud Univ Boyacá. 24 de julio de 2017;4(1):16-37. https://doi.org/10.24267/23897325.194; Denizot F, Lang R. Rapid colorimetric assay for cell growth and survival: Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. J Immunol Methods. 1986;89(2):271-7. https://doi.org/10.1016/0022-1759(86)90368-6; Banfalvi G. Methods to detect apoptotic cell death. Apoptosis. 2017;22(2):306-23. https://doi.org/10.1007/s10495-016-1333-3; Kumar P, Nagarajan A, Uchil PD. Analysis of Cell Viability by the MTT Assay. Cold Spring Harb Protoc. junio de 2018;2018(6). https://doi.org/10.1101/pdb.prot095505; van Tonder A, Joubert AM, Cromarty AD. Limitations of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay when compared to three commonly used cell enumeration assays. BMC Res Notes. febrero de 2015;8:47. https://doi.org/10.1186/s13104-015-1000-8; Abel SDA, Baird SK. Honey is cytotoxic towards prostate cancer cells but interacts with the MTT reagent: Considerations for the choice of cell viability assay. Food Chem. febrero de 2018;241:70-8. https://doi.org/10.1016/j.foodchem.2017.08.083; Kari S, Subramanian K, Altomonte IA, Murugesan A, Yli-Harja O, Kandhavelu M. Programmed cell death detection methods: a systematic review and a categorical comparison. Apoptosis Int J Program Cell Death. agosto de 2022;27(7-8):482-508. https://doi.org/10.1007/s10495-022-01735-y; Feldman AT, Wolfe D. Tissue processing and hematoxylin and eosin staining. Methods Mol Biol Clifton NJ. 2014;1180:31-43. https://doi.org/10.1007/978-1-4939-1050-2_3; Errami Y, Naura AS, Kim H, Ju J, Suzuki Y, El-Bahrawy AH, et al. Apoptotic DNA fragmentation may be a cooperative activity between caspase-activated deoxyribonuclease and the poly(ADP-ribose) polymerase-regulated DNAS1L3, an endoplasmic reticulum-localized endonuclease that translocates to the nucleus during apoptosis. J Biol Chem. 1 de febrero de 2013;288(5):3460-8. https://doi.org/10.1074/jbc.M112.423061; Jamali T, Kavoosi G, Safavi M, Ardestani SK. In-vitro evaluation of apoptotic effect of OEO and thymol in 2D and 3D cell cultures and the study of their interaction mode with DNA. Sci Rep. 25 de octubre de 2018;8(1):15787. https://doi.org/10.1038/s41598-018-34055-w; Julien O, Wells JA. Caspases and their substrates. Cell Death Differ. agosto de 2017;24(8):1380-9. https://doi.org/10.1038/cdd.2017.44; Kesavardhana S, Malireddi RKS, Kanneganti T-D. Caspases in Cell Death, Inflammation, and Pyroptosis. Annu Rev Immunol. 26 de abril de 2020;38:567-95. https://doi.org/10.1146/annurev-immunol-073119-095439; Cheng K-C, Wang C-J, Chang Y-C, Hung T-W, Lai C-J, Kuo C-W, et al. Mulberry fruits extracts induce apoptosis and autophagy of liver cancer cell and prevent hepatocarcinogenesis in vivo. J Food Drug Anal. 2020;28(1):84-93. https://doi.org/10.1016/j.jfda.2019.06.002; Qin Y, Ma Z, Dang X, Li W, Ma Q. Effect of resveratrol on proliferation and apoptosis of human pancreatic cancer MIA PaCa-2 cells may involve inhibition of the Hedgehog signaling pathway. Mol Med Rep. noviembre de 2014;10(5):2563-7. https://doi.org/10.3892/mmr.2014.2511; Xu S, Yao J, Ainiwaer M, Hong Y, Zhang Y. Analysis of Bacterial Community Structure of Activated Sludge from Wastewater Treatment Plants in Winter. BioMed Res Int. 2018;2018:1-8. https://doi.org/10.1155/2018/8278970; Xu J, Liu D, Niu H, Zhu G, Xu Y, Ye D, et al. Resveratrol reverses Doxorubicin resistance by inhibiting epithelial-mesenchymal transition (EMT) through modulating PTEN/Akt signaling pathway in gastric cancer. J Exp Clin Cancer Res CR. enero de 2017;36(1):19. https://doi.org/10.1186/s13046-016-0487-8; https://revistasdigitales.uniboyaca.edu.co/index.php/rs/article/view/916

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    المصدر: Potato Research, 65 (3)

    وصف الملف: application/application/pdf

    Relation: info:eu-repo/semantics/altIdentifier/wos/000774593900001; info:eu-repo/grantAgreement/EC/FP7/608422; http://hdl.handle.net/20.500.11850/542308

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    المساهمون: Département Sciences Analytiques et Interactions Ioniques et Biomoléculaires (DSA-IPHC), Institut Pluridisciplinaire Hubert Curien (IPHC), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Centre de Recherches sur la Cognition Animale - UMR5169 (CRCA), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)-Centre de Biologie Intégrative (CBI), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Toulouse Mind & Brain Institut (TMBI), Université Toulouse - Jean Jaurès (UT2J), Université de Toulouse (UT)-Université de Toulouse (UT)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université Toulouse - Jean Jaurès (UT2J), Université de Toulouse (UT)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT), Physiologie de la reproduction et des comportements Nouzilly (PRC), Institut Français du Cheval et de l'Equitation Saumur (IFCE)-Université de Tours (UT)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

    المصدر: ISSN: 0377-8401.

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