Identification of lead-produced lipid hydroperoxides in human HepG2 cells and protection using rosmarinic and ascorbic acids with a reference to their regulatory roles on Nrf2-Keap1 antioxidant pathway. (1st December 2019)

• Record Type: Journal Article
• Authors: Li, Yonghan; Darwish, Wageh Sobhy; Chen, Zhen; Hui, Tan; Wu, Yue; Hirotaka, Suzuki; Chiba, Hitoshi; Hui, Shu-Ping
• Is Part Of: Chemico-biological interactions. Volume 314(2019)
• Publication Date: 2019-12-01
• Subjects: Lead -- HepG2 cells -- Lipid hydroperoxides -- Rosmarinic acid -- Ascorbic acid -- Nrf2; Biochemistry -- Periodicals; Toxicological chemistry -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biochimie -- Périodiques; Toxicologie biochimique -- Périodiques; 572
• DOI: 10.1016/j.cbi.2019.108847
• Languages: English
• ISSNs: 0009-2797

Abstract

Abstract: Lead (Pb) is one of the toxic heavy metals that have several toxicological implications including cytotoxicities and oxidative stress. The release of reactive oxygen species (ROS) usually initiates lipid peroxidation and resulting in inflammation and tissue injury. However, the detailed identification of the Pb-produced lipid hydroperoxides has received little attention. Furthermore, the mechanisms behind such effects are less informed. Therefore, this study firstly investigated Pb-produced lipid hydroperoxides in human HepG2 cells using LC/MS. The effects of Pb on the antioxidant enzymes were additionally examined using qPCR and their dependent activities. As a protection trial, the ameliorative effects of rosmarinic (RMA) and ascorbic (ASA) acids on Pb-induced cytotoxicity and oxidative stress and their regulatory effects on Nrf2/Keap1 pathway were investigated. The achieved results confirmed cytotoxicity and oxidative damage of Pb on HepG2 cells. In addition, 20 lipid hydroperoxides (LOOH) were identified including 11 phosphatidylcholine hydroperoxides (PCOOH), 5 triacylglycerol hydroperoxides (TGOOH) and 4 cholesteryl ester hydroperoxides (CEOOH). The most dominant LOOH species were PCOOH 34:2, PCOOH 34:3, PCOOH 38:7, TGOOH 60:14, TGOOH 60:15, CEOOH 18:3 and CEOOH 20:4. Pb significantly downregulated Nrf2-regulated antioxidant enzymes at both the pretranscriptional and functional levels. Co-exposure of HepG2 cells to RMA and ASA significantly reduced Pb-produced adverse outcomes. This protection occurred via activation Nrf2-Keap1 antioxidant pathway. Graphical abstract: Image 1 Highlights: Lead (Pb) induced cytotoxicity and oxidative stress production in HepG2 cells. Lead produced 20 lipid hydroperoxides including TGOOH, CEOOH and PCOOH. Lead downregulated antioxidant enzymes. Ascorbic and Rosmarinic acids reduced Pb-induced cytotoxicity and oxidative stress. Ascorbic and Rosmarinic acids enhanced antioxidant enzymes via Nrf2 activation.