Atthapan Morchang1,2, Shilu Malakar3, Siripat Aluksanasuwan1,2, Keerakarn Somsuan1,2, Narongsuk Munkong4, Kevalin Vongthoung5
1School of Medicine, Mae Fah Luang University, Chiang Rai; 2Cancer and Immunology Research Unit (CIRU), Mae Fah Luang University, Chiang Rai; 3Department of Molecular Medicine, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok; 4Department of Pathology, School of Medicine, University of Phayao, Phayao; 5Medical Technology Program, Faculty of Science and Technology, Bansomdejchaopraya Rajabhat University, Bangkok, Thailand.For correspondence:- Kevalin Vongthoung Email: kevalin.vo@bsru.ac.th
Received: 1 May 2024 Accepted: 8 October 2024 Published: 29 October 2024
Citation: Morchang A, Malakar S, Aluksanasuwan S, Somsuan K, Munkong N, Vongthoung K. Red sticky rice (Oryza sativa L.) bran extract attenuates cellular oxidative stress in human hepatocellular carcinoma cell line via Nrf-2 and HO-1 pathway. Trop J Pharm Res 2024; 23(10):1617-1622 doi: 10.4314/tjpr.v23i10.4
© 2024 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To investigate the molecular mechanism underlying the antioxidant effect of red sticky rice bran extract (RRBE; a pigmented strain of Oryza sativa L.) in human hepatocellular carcinoma cell line. Methods: Human hepatocellular carcinoma HuH-7 cells were treated with the ethanol extract of RRBE in the presence or absence of EX-537 (Sirtuin 1 inhibitor), dexamethasone (NF-κB inhibitor), brusatol (Nrf-2 inhibitor), or HO-1 inh (HO-1 inhibitor) before exposure to hydrogen peroxide-induced oxidative stress. Intracellular ROS and glutathione levels were assessed using CellROX™ green reagent and GSH-Glo™ glutathione assay, respectively. Levels of nuclear factor erythroid 2-related factor 2 (Nrf-2) and ex
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