Department of Nutrition and Food Hygiene, Public Health College, Harbin Medical University, 194 Xuefu Road, Harbin, Heilongjiang, 150081, China.
Environ Sci Pollut Res Int. 2018 Feb;25(4):3765-3774. doi: 10.1007/s11356-017-0774-8. Epub 2017 Nov 22.
This study aimed to assess the toxic effect of chronic exposure to cadmium through a metabolomic approach based on ultra-performance liquid chromatography/mass spectrometry (UPLC-MS). Forty male Sprague-Dawley rats were randomly assigned to the following groups: control, low-dose cadmium chloride (CdCl) (0.13 mg/kg body weight (bw)), middle-dose CdCl (0.8/kg bw), and high-dose CdCl (4.9 mg/kg bw). The rats continuously received CdCl via drinking water for 24 weeks. Rat urine samples were then collected at different time points to establish the metabolomic profiles. Multiple statistical analyses with principal component analysis and partial least squares-discriminant analysis were used to investigate the metabolomic profile changes in the urine samples and screen for potential biomarkers. Thirteen metabolites were identified from the metabolomic profiles of rat urine after treatment. Compared with the control group, the treated groups showed significantly increased intensities of phenylacetylglycine, guanidinosuccinic acid, 4-pyridoxic acid, 4-aminohippuric acid, 4-guanidinobutanoic acid, allantoic acid, dopamine, LysoPC(18:2(9Z,12Z)), and L-urobilinogen. By contrast, the intensities of creatinine, L-carnitine, taurine, and pantothenic acid in the treated groups were significantly decreased. These results indicated that Cd disrupts energy and lipid metabolism. Meanwhile, Cd causes liver and kidney damage via induction of oxidative stress; serum biochemical indices (e.g., creatinine and urea nitrogen) also support the aforementioned results.
本研究旨在通过基于超高效液相色谱/质谱 (UPLC-MS) 的代谢组学方法评估镉慢性暴露的毒性作用。40 只雄性 Sprague-Dawley 大鼠被随机分为以下几组:对照组、低剂量氯化镉 (CdCl)(0.13mg/kg 体重(bw))、中剂量 CdCl(0.8/kg bw)和高剂量 CdCl(4.9mg/kg bw)。大鼠通过饮用水连续接受 CdCl 处理 24 周。然后收集不同时间点的大鼠尿液样本以建立代谢组学图谱。采用主成分分析和偏最小二乘判别分析等多种统计分析方法,研究尿液样本中的代谢组学图谱变化,并筛选潜在生物标志物。从大鼠尿液的代谢组学图谱中鉴定出 13 种代谢物。与对照组相比,处理组的苯乙酰甘氨酸、胍基琥珀酸、4-吡啶酸、4-氨基马尿酸、4-胍基丁酸、尿刊酸、多巴胺、LysoPC(18:2(9Z,12Z))和 L-尿胆素原的强度明显增加。相比之下,处理组的肌酐、L-肉碱、牛磺酸和泛酸的强度明显降低。这些结果表明 Cd 破坏了能量和脂质代谢。同时,Cd 通过诱导氧化应激导致肝和肾损伤;血清生化指标(如肌酐和尿素氮)也支持上述结果。