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Título

Oleanolic acid bioavailability in human serum

AutorGarcía-González, Aída CSIC; Espinosa, Juan M.; Cerrillo, Isabel; Montero Romero, Emilio; Rivas-Melo, Juan José; Romero-Báez, Andrea; Jiménez-Andreu, María Dolores; Ruíz-Trillo, Carmen Amelia; Rodríguez-Rodríguez, Ana; Martínez-Ortega, Antonio Jesús; Roque-Cuellar, María Del Carmen; García-Rey, Silvia; Jiménez-Sánchez, Andrés; Mangas-Cruz, Miguel Ángel; Pereira-Cunill, José Luis; Perona, Javier S. CSIC ORCID ; García-Luna, Pedro Pablo CSIC; Castellano, José María CSIC ORCID
Palabras claveOleanolic acid
Bioavailability in humans
Pharmacokinetics
NCT05529953
Postprandial trial
Human serum proteins
Human triglyceride-rich lipoproteins
Fecha de publicación22-sep-2023
EditorDIGITAL.CSIC
CitaciónGarcía-González, Aída; Espinosa, Juan M.; Cerrillo, Isabel; Montero Romero, Emilio; Rivas-Melo, Juan José; Romero-Báez, Andrea; Jiménez-Andreu, María Dolores; Ruíz-Trillo, Carmen Amelia; Rodríguez-Rodríguez, Ana; Martínez-Ortega, Antonio Jesús; Roque-Cuellar, María Del Carmen; García-Rey, Silvia; Mangas-Cruz, Miguel Ángel; Pereira-Cunill, José Luis; Perona, Javier S.; García-Luna, Pedro Pablo; Castellano, José María; 2023; Oleanolic acid bioavailability in human serum [Dataset]; DIGITAL.CSIC; https://doi.org/10.20350/digitalCSIC/15571
ResumenEvidence of the pharmacological activity of oleanolic acid (OA) suggests its potential therapeutic application. However, its use in functional foods, dietary supplements, or nutraceuticals is hindered by limited human bioavailability studies. The BIO-OLTRAD trial is a double-blind, randomized controlled study with 22 participants that received a single dose of 30 mg OA formulated as a functional olive oil. The study revealed that the maximum serum concentration of OA ranged from 500 to 600 ng/mL, with an AUC0–∞ value of 2862.50 ± 174.50 ng·h/mL. Furthermore, we discovered a physiological association of OA with serum albumin and triglyceride-rich lipoproteins (TRL). UV absorption spectra showed conformational changes in serum albumin due to the formation of an adduct with OA. Additionally, we demonstrated that TRL incorporate OA, reaching a maximum concentration of 140 ng/mL after 2-4 hours. We conjecture that both are efficient carriers to reach target tissues and to yield high bioavailability. This dataset includes the raw data used in the elaboration of the results reported in the article (DOI).
Descripción[Description of methods used for collection/generation of data] 1. Extraction and GC-MS determination (DOI 10.1002/bmc.3480); 2. UV Spectrophotometry method for OA-HSA association (DOI 10.1021/jf1039537); 3. Enzymatic methods were used to determine serum glucose, total cholesterol, HDL and triglycerides, whereas LDL was estimated by the Friedewald formula (14). Total lipoprotein Apo B (Apo B48 + Apo B100) was quantified by an immunoturbidimetric assay (Tinaquant; Roche Diagnostics, Mannheim, Germany), and serum insulin using an ELISA kit (Diaclone, Besançon, France).
[Methods for processing the data] The variables were expressed as mean ± standard deviation (SD), unless otherwise stated. Differences between the study groups were evaluated by one- or two-way ANOVA, following by Bonferroni´s multiple-comparison test or Kruskal-Wallis test.
URIhttp://hdl.handle.net/10261/335582
DOIhttps://doi.org/10.20350/digitalCSIC/15571
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1. Raw data OA pharmacokinetics in human serum.xlsx44,15 kBMicrosoft Excel XMLEmbargoed until 22 de septiembre de 2024    Petición de una copia
2. Raw data OA-HSA association.xlsx44,9 kBMicrosoft Excel XMLEmbargoed until 22 de septiembre de 2024    Petición de una copia
3. Raw data OA in TRL.xlsx28,7 kBMicrosoft Excel XMLEmbargoed until 22 de septiembre de 2024    Petición de una copia
4. Raw data blood biochemistry.xlsx28,59 kBMicrosoft Excel XMLEmbargoed until 22 de septiembre de 2024    Petición de una copia
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