dc.creatorRamos Elizagaray, Sabina Irantxu
dc.creatorQuiroga, Patricia Liliana
dc.creatorPerez, Roberto Daniel
dc.creatorSosa, Carlos Manuel
dc.creatorPérez, Carlos A.
dc.creatorBongiovanni, Guillermina Azucena
dc.creatorSoria, Elio Andres
dc.date.accessioned2021-12-07T22:46:40Z
dc.date.accessioned2022-10-15T02:35:57Z
dc.date.available2021-12-07T22:46:40Z
dc.date.available2022-10-15T02:35:57Z
dc.date.created2021-12-07T22:46:40Z
dc.date.issued2019-06-29
dc.identifierRamos Elizagaray, Sabina Irantxu; Quiroga, Patricia Liliana; Perez, Roberto Daniel; Sosa, Carlos Manuel; Pérez, Carlos A.; et al.; Effect of the aqueous extract of Lantana grisebachii Stuck: against bioaccumulated arsenic-induced oxidative and lipid dysfunction in rat splenocytes; Taylor & Francis; Journal of Dietary Supplements; 16; 4; 29-6-2019; 401-407
dc.identifier1939-0211
dc.identifierhttp://hdl.handle.net/11336/148435
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4335791
dc.description.abstractArsenic (As) is a worldwide immunotoxic agent that is in contaminated waters and consumed by mammals. Phytotherapy may counteract its harmful effects. Lantana grisebachii Stuck (LG, Verbenaceae) and its extract are proposed as protective, given vvits in vitro bioactivity. The aim was to determine the protective capacity of the aqueous LG extract on splenocytes exposed in vivo to arsenic. Splenocytes were obtained from an arsenicosis model (Wistar rats consuming orally 0 [control; C] or 5 mg/Kg/d of As) that received 0-100 mg/Kg/d of LG extract for 30 days. As content (total reflection X-ray fluorescence), fatty acid profile (gas chromatography), γ-glutamyl transpeptidase activity (Szasz method), peroxides (xylenol orange-based assay), and nitrites (Griess reaction) were then assayed in viable splenocytes. Data were analyzed with ANOVA and the Tukey´s test (p < .05). It was observed that the splenocytes contained 2.2 mg/Kg of this elemental arsenic. With γ-glutamyl transpeptidase inhibition and consequent triggering of hydroperoxides (p < .05), it was observed to increase saturated fatty acids and alter lipid profiles. LG treatment avoided damaging effects with values similar to unexposed C (p < .05), and cellular arsenic concentration (p < .0001). In conclusion, the aqueous extract of L. grisebachii counteracted arsenic toxicity in rat splenocytes by preventing its cellular accumulation and induction of lipid and redox disturbances, which may impair immune function.
dc.languageeng
dc.publisherTaylor & Francis
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.tandfonline.com/doi/full/10.1080/19390211.2018.1470124
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1080/19390211.2018.1470124
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectFatty acid
dc.subjectLantana
dc.subjectSpleen
dc.subjectX-Ray Fluorescence
dc.titleEffect of the aqueous extract of Lantana grisebachii Stuck: against bioaccumulated arsenic-induced oxidative and lipid dysfunction in rat splenocytes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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