Abstract
The study was conducted to assess the effect of vanadium (V) in high-fat diet on the liver and kidney of rats in a 5-week trial. Seventy-two female Wistar rats (BW = 95 ± 5 g) were randomly allotted into eight groups. Groups I, II, III, and IV obtained low-fat diet containing 0, 3, 15, and 30 mg/kg V, and V, VI, VII, and VIII groups received the respective vanadium doses with high-fat diet, respectively. There were lesions in the liver and kidney of V, VI, VII, and VIII groups, granular degeneration and vacuolar degeneration were observed in the renal tubular and glomerulus epithelial cells, and hepatocytes showed granular degeneration and vacuolar degeneration. Supplemented high-fat diet with vanadium was shown to decrease (P < 0.05) activities of superoxide dismutase, total antioxidant capacity, glutathione-S transferase, and NAD(P)H/quinone oxidoreductase 1 (NQO1) and increase malondialdehyde content in the liver and kidney. The relative expression of hepatic nuclear factor erythroid 2-related factor 2 (Nrf-2) and NQO1 mRNA was downregulated by V addition and high-fat diet, and the effect of V was more pronounced in high-fat diet (interaction, P < 0.05), with VIII group having the lowest mRNA expression of Nrf-2 and NQO1 in the liver and kidney. In conclusion, it suggested that dietary vanadium ranging from 15 to 30 mg/kg could lead to oxidative damage and vanadium accumulation in the liver and kidney, which caused renal and hepatic toxicity. The high-fat diet enhanced vanadium-induced hepatic and renal damage, and the mechanism was related to the modulation of the hepatic and renal mRNA expression of Nrf-2 and NQO1.
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Abbreviations
- ALT:
-
Alanine aminotransferase
- AST:
-
Aspartate aminotransferase
- MDA:
-
Malondialdehyde
- SOD:
-
Superoxide dismutase
- T-AOC:
-
Total antioxidant capacity
- GST:
-
Glutathione-S transferase
- GSH:
-
Glutathione
- NQO1:
-
NAD(P)H/quinone oxidoreductase 1
- Nrf-2:
-
Nuclear factor erythroid 2-related factor 2
References
Léonard A, Gerber GB (1994) Mutagenicity, carcinogenicity and teratogenicity of vanadium compounds. Mut Res/Rev GenetToxicol 317:81–88
Cortizo AM, Bruzzone L, Molinuevo S, et al (2000) A possible role of oxidative stress in the vanadium-induced cytotoxicity in the MC3T3E1 osteoblast and UMR106 osteosarcoma cell lines. Toxicol 147:89–99
Huang HC, Nguyen T, Pickett CB (2002) Phosphorylation of Nrf2 at Ser-40 by protein kinase C regulates antioxidant response element-mediated transcription. J Biol Chem 277:42769–42774
Liu J, Cui H, Liu X et al (2012) Dietary high vanadium causes oxidative damage-induced renal and hepatic toxicity in broilers. Biol Trace Elem Res145:189–200.
Fang YZ, Yang S, Wu G (2002) Free radicals, antioxidants, and nutrition. Nutrition 18:872–879
Zhe S, Hui YL, Xiao DY (2011) Vanadium stimulates mitochondrial ROS production in different ways. J Chinese Pharm Sci 5:498–495
Anwar-Mohamed A, El-Kadi AO (2009) Down-regulation of the detoxifying enzyme NAD(P)H:quinone oxidoreductase 1 by vanadium in Hepa 1c1c7 cells. Toxic Appl Pharm 236:261–269
Boden G, Chen XH, Riuz J, et al (1996) Effects of vanadyl sulfate on carbohydrate and lipid metabolism in patients with non-insulin-dependent diabetes mellitus. Metabolism 45:1130–1136
Mukherjee B, Patra B, Mahapatra S, et al (2004) Vanadium—an element of atypical biological significance. Toxicol Letters 150:135–143
Imura H, Shimada A, Naota M, et al (2013) Vanadium toxicity in mice: possible impairment of lipid metabolism and mucosal epithelial cell necrosis in the small intestine. Toxicol Path 41:842–856
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analyt Biochem 72:248–254
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods 25:402–408
Shukla R, Barve V, Padhye S, et al (2006) Reduction of oxidative stress induced vanadium toxicity by complexing with a flavonoid, quercetin: a pragmatic therapeutic approach for diabetes. Biometals 19:685–693
Nriagu, JP (1998) Vanadium in the environment, part 2: health effects, John Wiley and sons, New York, Chichester, Weinheim, Brisbane, Singapore, Toronto.
Poucheret P, Verma S, Grynpas MD, McNeill JH (1998) Vanadium and diabetes. Mol Cell Biochem 188:73–80
Hirano S, Suzuki KT (1996) Exposure metabolism and toxicity for rare earths and related compounds. Environ Health Perspect 104:85–95
Beaulieu M, Costantini D (2014) Biomarkers of oxidative status: missing tools in conservation physiology. Conservaton Physio 2. doi:10.1093/conphys/cou014
Russanov E, Zaporowska H, Ivancheva E et al. (1994) Lipid peroxidation and antioxidant enzymes in vanadate-treated rats. Comparative biochemistry and physiology part C: pharmacology, toxicology and endocrinology 107: 415–421.
Borges G, Mendonça P, Joaquim N, et al (2003) Acute effects of vanadate oligomers on heart, kidney, and liver histology in the Lusitanian toadfish (Halobatrachus didactylus). Arch Environ Contam Toxicol 45:415–422
Scibor A (2005) Some selected blood parameters in rats exposed to vanadium and chromium via drinking water. Trace Elem Electro 22:40–46
Aydin ASA, Sayin S, Erdem O (2005) An investigation on the relationship between vanadium and antioxidative enzyme system in rats. Turkish J Pharm Sci 2:17–24
Mahmoud KST, Deraz S, Umbayev B (2011) Combined effect of vanadium and nickel on lipid peroxidation and selected parameters of antioxidant system in liver and kidney of male rat. Afr J Biotech 10:18319–18325
Gaweł SWM, Niedworok E, Wardas P (2004) Malondialdehyde (MDA) as a lipid peroxidation marker. Wiadomosci Lekarskie 57:453–455
Limon-Pacheco J, Gonsebatt ME (2009) The role of antioxidants and antioxidant-related enzymes in protective responses to environmentally induced oxidative stress. Mut Res/Rev Genet Toxicol 674:137–147
Hosseini MJ, Shaki F, Ghazi-Khansari M, Pourahmad J (2013) Toxicity of vanadium on isolated rat liver mitochondria: a new mechanistic approach. Metallomics 5:152–166
Francik R, Krośniak M, Barlik M, et al (2011) Impact of vanadium complexes treatment on the oxidative stress factors in Wistar rats plasma. Bioinorg Chem Appl 2011:206316
Nanji AA, Griniuviene B, Sadrzadeh SM (1995) Effect of type of dietary fat and ethanol on antioxidant enzyme mRNA induction in rat liver. J Lipid Res 36:736–744
Shyamala MP, Venukumar MR, Latha MS (2003) Antioxidant of the Syzygium aromaticum (Gaertn..) Linn. (CLOVES) in rats fed with high fat diet. Indian J Pharm 35:99–103.
Abdelhamid G, Anwar-Mohamed A, Badary OA, et al (2010) Transcriptional and posttranscriptional regulation of CYP1A1 by vanadium in human hepatoma HepG2 cells. Cell Biol Toxicol 26:421–434
Kim AD, Zhang R, Kang KA, et al (2011) Increased glutathione synthesis following Nrf2 activation by vanadyl sulfate in human chang liver cells. Int J Mol Sci 12:8878–8894
Acknowledgments
This project was fanatically supported by the Ministry of Science and Technology Support Program (2014BAD13B04), National Natural Science Foundation of China (31402031), Sichuan Provincial Department of Education Project (13ZB0290), and Sichuan Provincial Department of Science and Technology Project (2014NZ0043, 2014NZ0002, 2013NZ0054).
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J. P. Wang and R. Y. Cui contributed to the work equally and should be regarded as co-first authors.
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Wang, J.P., Cui, R.Y., Zhang, K.Y. et al. High-Fat Diet Increased Renal and Hepatic Oxidative Stress Induced by Vanadium of Wistar Rat. Biol Trace Elem Res 170, 415–423 (2016). https://doi.org/10.1007/s12011-015-0475-4
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DOI: https://doi.org/10.1007/s12011-015-0475-4