Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2415
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dc.contributor.authorUsta, Julnaren_US
dc.contributor.authorShatha, Sen_US
dc.contributor.authorRacha, Ken_US
dc.contributor.authorBou-Moughlabey, Yollaen_US
dc.contributor.authorRifai, Omar Alen_US
dc.contributor.authorK, Sawsanen_US
dc.contributor.authorEchtay, Karimen_US
dc.date.accessioned2020-12-23T09:12:48Z-
dc.date.available2020-12-23T09:12:48Z-
dc.date.issued2011-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2415-
dc.description.abstractLinalool is the major component of coriander-sativum seeds. We have recently reported (1) a 100%-decrease in the viability of HepG2 treated with 2µM linalool. No effect was observed with other cell lines. Linalool resulted in a decrease in the ATP and GSH levels; increase in ROS; and inhibition of ETC-complexes I and II. ROS are known to affect level of UCP2 and ANT. Recent report showed Leukemias cells treated with linalool induced apoptosis mediated by P-53 up-regulation (2). We investigate the effect of linalool on 10ry -hepatocytes, variation in UCP2, ANT and P53 expression in HepG2 and 10ry-hepatocytes. Viability of 1ory- hepatocytes (3), treated with varying concentration of linalool was determined using MTT assay. Expression of P53, ANT, & UCP2 in 10ry- hepatocytes was compared to those of HepG2 cells, using western blotting and was expressed relative to GAPDH. We report that: a) 10ry-hepatocytes were not sensitive to linalool treatment; Comparing 1ory-hepatocytes to HepG2 cells, a 250 fold of linalool concentration was needed to demonstrate a 100% b) Increase in P53 expression was obtained in HepG-2 cells whereas P53 was not detected in 10ry- hepatocytes; c) Down regulated of the expression of ANT and UCP-2 in HepG-2 cells. Linalool effect is specific to HepG2 cells but had no significant effect on 10ry- hepatocytes. There is a role of P53, and the mitochondrial proteins ANT and UCP2 in rendering HepG2 cells more sensitive. Biotransformation into toxic metabolites of linalool by HepG2 cells, but not 10ry -hepatocytes, may not be disregarded. Acknowledgement: Medical Practice Plan and University research Board at the American University of Beirut References: 1. Usta J et al. (2009) Chem- Biol Interact 180: 39–46 2. Gu Y et al. (2010) Toxicology 268:19–24 3. Schaffner I et al. (2005) Assay Drug Dev Technol 3(1)27–38.en_US
dc.language.isoengen_US
dc.titlePossible mediators underlying Linalool effect on HepG-2 but not primary hepatocytesen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume2011en_US
dc.date.catalogued2017-12-14-
dc.description.statusPublisheden_US
dc.identifier.OlibID175597-
dc.relation.ispartoftextJournal of planta medicaen_US
dc.provenance.recordsourceOliben_US
Appears in Collections:Faculty of Medicine
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