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Environ Sci Pollut Res Int. 2019 Jun;26(18):18181-18190. doi: 10.1007/s11356-019-05075-4. Epub 2019 Apr 29.

Metabonomic analysis of the hepatic injury suffer from hexavalent chromium poisoning in broilers.

Author information

1
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, P.R. China.
2
College of Veterinary Medicine, Cornell University, Ithaca, NY, 14853, USA.
3
University College of Veterinary and Animal Sciences, Islamia University of Bahawalpur, Bahawalpur, 63100, Pakistan.
4
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, P.R. China. bigdefoot@163.com.

Abstract

Chromium is used in daily life and has a wide range of functions. It plays an important role in protein synthesis and carbohydrate and lipid metabolism. Chromium is found in trivalent Cr(III) and hexavalent Cr(VI) form; Cr(III) is relatively stable and intimately participates with many phenomena of metabolisms. Whereas, Cr(VI) is toxic, which results in growth inhibition and leading to changes in components of antioxidant systems as well as secondary metabolites. However, the molecular mechanism that is involved in Cr (VI)-induced hepatotoxicity is still unclear. For this purpose, 40 chickens were randomly assigned into two groups: the normal group (feeding the basic diet and clear water), the chromium group (16%LD50, 74.24 mg/kg/day K2Cr2O7 ). The samples were subjected to pathological examination and UHPLC-QE-MS non-target metabolomics method for metabolomics analysis of broiler liver using principal component analysis (PCA) and partial least squares discriminant analysis (OPLS-DA). The central venous cells of the broiler liver in the chromium poisoning group showed turbidity and flaky necrosis, nuclear condensation, nuclear rupture, and even nuclear dissolution. The differential metabolite analysis between the chromium poisoning and the control group showed that 32 differential metabolites were upregulated and 15 were downregulated in positive ion mode. Whereas,17 differential metabolites were downregulated, and 35 were downregulated in negative ion mode (P ≤ 0.05). The potential marker substances are oleic acidamide, farnesylacetone, betaine, taurine, choline, and galactinol. Additionally, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways showed that the lipid metabolism, carbohydrate metabolism, nucleotide metabolism, amino acid metabolism, energy metabolism, membrane transport, digestive system, and nervous system were the most important metabolic pathways in the liver. This study provides a theoretical basis for the future understanding of the pathogenesis of chromium poisoning and a new insight of the subsequent molecular mechanism of chromium hepatotoxicity.

KEYWORDS:

Chromium poisoning; Differential metabolites; Hepatotoxicity; Metabolites; UHPLC-QE-MS metabolomics

PMID:
31037529
DOI:
10.1007/s11356-019-05075-4

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