Cadmium influence on lipid metabolism in Sprague–Dawley rats through linoleic acid and glycerophospholipid metabolism pathways

Author:

Chen Mengyuan1,Dong Jingjing1,Zhao Xiaole1,Yin Xiaoyao1,Wu Kejia1,Wang Qiao1,Liu Xin1,Wu Yongning12,Gong Zhiyong1ORCID

Affiliation:

1. Key Laboratory for Deep Processing of Major Grain and Oil (The Chinese Ministry of Education), Hubei Key Laboratory for Processing and Transformation of Agricultural Products, Food Safety Research Center, Key Research Institute of Humanities and Social Sciences of Hubei Province, College of Food Science and Engineering Wuhan Polytechnic University Wuhan Hubei China

2. NHC Key Laboratory of Food Safety Risk Assessment, Food Safety Research Unit (2019RU014) of Chinese Academy of Medical Science China National Center for Food Safety Risk Assessment Beijing China

Abstract

AbstractCadmium (Cd) is widely distributed in the environment and easy adsorbed by living organisms with adverse effects. Exposure to Cd‐contaminated food may disrupt lipid metabolism and increase human health risk. To study the perturbation effect of Cd on lipid metabolism in vivo, 24 male Sprague–Dawley (SD) rats were randomly assigned four groups and treated by Cd chloride solution (0, 1.375 mg/kg, 5.5 mg/kg, 22 mg/kg) for 14 days. The characteristic indexes of serum lipid metabolism were analyzed. Afterwards, untargeted metabolomics analysis was applied to explore the adverse effects of Cd on rats by liquid chromatography coupled with mass spectrometry (LC‐MS). The results revealed that Cd exposure obviously decreased the average serum of triglycerides (TG) and low‐density lipoprotein cholesterol (LDL‐C) and caused an imbalance of endogenous compounds in the 22 mg/kg Cd‐exposed group. Compared with the control group, 30 metabolites with significant differences were identified in the serum. Our results indicated that Cd caused lipid metabolic disorders in rats by disrupting linoleic acid and glycerophospholipid metabolism pathways. Furthermore, there were three kinds of remarkable differential metabolites—9Z,12Z‐octadecadienoic acid, PC(20:4(8Z,11Z,14Z,17Z)/0:0), and PC(15:0/18:2(9Z,12Z)), which enriched the two significant metabolism pathways and could be the potential biomarkers.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

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