Individual and Combined Effects of Fumonisin B1, Deoxynivalenol and Zearalenone on the Hepatic and Renal Membrane Lipid Integrity of Rats

被引:33
作者
Szabo, Andras [1 ,2 ]
Szabo-Fodor, Judit [2 ]
Febel, Hedvig [3 ]
Mezes, Miklos [4 ]
Balogh, Krisztian [4 ]
Bazar, Gyorgy [5 ]
Kocso, Daniel [2 ]
Ali, Omeralfaroug [5 ]
Kovacs, Melinda [2 ]
机构
[1] Kaposvar Univ, Inst Diagnost Imaging & Radiat Oncol, H-7400 Kaposvar, Hungary
[2] Kaposvar Univ, Hungarian Acad Sci, MTA KE Mycotoxins Food Chain Res Grp, H-7400 Kaposvar, Hungary
[3] Natl Agr Res Ctr, Res Inst Anim Breeding Nutr & Meat Sci, H-2053 Herceghalom, Hungary
[4] Szent Istvan Univ, Fac Agr & Environm Sci, Dept Nutr, H-2013 Godollo, Hungary
[5] Kaposvar Univ, Fac Agr & Environm Sci, H-7400 Kaposvar, Hungary
关键词
rat; liver; kidney; fusariotoxins; multitoxic effects; phospholipids; NATURAL COOCCURRENCE; FUSARIUM TOXINS; MYCOTOXINS; EXPRESSION; TOXICITY; LIVER; ACID; MECHANISMS; NIVALENOL; GROWTH;
D O I
10.3390/toxins10010004
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
(1) Background and (2) Methods: A 14-day in vivo, multitoxic (pure mycotoxins) rat experiment was conducted with zearalenone (ZEA; 15 g/animal/day), deoxynivalenol (DON; 30 g/animal/day) and fumonisin B-1 (FB1; 150 g/animal/day), as individual mycotoxins, binary (FD, FZ and DZ) and ternary combinations (FDZ), via gavage in 1 mL water boluses. (3) Results: Body weight was unaffected, while liver (ZEA vs. DON) and kidney weight (ZEA vs. FDZ) increased. Hepatocellular membrane lipid fatty acids (FAs) referred to ceramide synthesis disturbance (C20:0, C22:0), and decreased unsaturation (C22:5 n3 and unsat. index), mainly induced by DON and to a lesser extent by ZEA. The DON-FB1 interaction was additive on C20:0 in liver lipids. In renal phospholipids, ZEA had the strongest effect on the FA profile, affecting the saturated (C18:0) and many n6 FAs; ZEA was in an antagonistic relationship with FB1 (C18:0) or DON (C18:2 n6, C20:1 n9). Hepatic oxidative stress was the most expressed in FD (reduced glutathione and glutathione peroxidase), while the nephrotoxic effect was further supported by lipid peroxidation (malondialdehyde) in the DON treatment. (4) Conclusions: In vivo study results refer to multiple mycotoxin interactions on membrane FAs, antioxidants and lipid peroxidation compounds, needing further testing.
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页数:17
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