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http://dx.doi.org/10.4062/biomolther.2020.062

Fumonisin B1-Induced Toxicity Was Not Exacerbated in Glutathione Peroxidase-1/Catalase Double Knock Out Mice  

Yayeh, Taddesse (Department of Veterinary Science, College of Agriculture and Environmental Sciences, Bahir Dar University)
Jeong, Ha Ram (St. Louis College of Pharmacy)
Park, Yoon Soo (St. Louis College of Pharmacy)
Moon, Sohyeon (Department of Molecular Medicine, School of Medicine, Ewha Womans University)
Sur, Bongjun (Department of Molecular Medicine, School of Medicine, Ewha Womans University)
Yoo, Hwan-Soo (College of Pharmacy, Chungbuk National University)
Oh, Seikwan (Department of Molecular Medicine, School of Medicine, Ewha Womans University)
Publication Information
Biomolecules & Therapeutics / v.29, no.1, 2021 , pp. 52-57 More about this Journal
Abstract
Fumonisin B1 (FB1) structurally resembles sphingolipids and interferes with their metabolism leading to sphingolipid dysregulation. We questioned if FB1 could exacerbate liver or kidney toxicities in glutathione peroxidase 1 (Gpx1) and catalase (Cat) knockout mice. While higher serum levels of thiobarbituric acid reactive substances (TBARS) and sphinganine (Sa) were measured in Gpx1/Cat knockout mice (Gpx1/Cat KO) than wild type mice after 5 days of FB1 treatment, serum levels of alanine aminotransferase (ALT), sphingosine-1 phosphate (So-1-P), and sphinganine-1 phosphate (Sa-1-P) were found to be relatively low. Although Sa was highly elevated in Gpx1/Cat KO mice and wild mice, lower levels of So and Sa were found in both the kidney and liver tissues of Gpx/Cat KO mice than wild type mice after FB1 treatment. Paradoxically, FB1-induced cellular apoptosis and necrosis were hastened under oxidative stress in Gpx1/Cat KO mice.
Keywords
Fumonisin B1; Catalase; Glutathione peroxidase1; Sphingosine; Sphinganine;
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