吉佳慧, 苗龙, 万柳, 孙蓉丽, 张娟, 尹立红, 浦跃朴. 噪声暴露对大鼠代谢组学的影响[J]. 环境与职业医学, 2020, 37(5): 433-439. DOI: 10.13213/j.cnki.jeom.2020.20059
引用本文: 吉佳慧, 苗龙, 万柳, 孙蓉丽, 张娟, 尹立红, 浦跃朴. 噪声暴露对大鼠代谢组学的影响[J]. 环境与职业医学, 2020, 37(5): 433-439. DOI: 10.13213/j.cnki.jeom.2020.20059
JI Jia-hui, MIAO Long, WAN Liu, SUN Rong-li, ZHANG Juan, YIN Li-hong, PU Yue-pu. Metabolomic effects of noise exposure on rats[J]. Journal of Environmental and Occupational Medicine, 2020, 37(5): 433-439. DOI: 10.13213/j.cnki.jeom.2020.20059
Citation: JI Jia-hui, MIAO Long, WAN Liu, SUN Rong-li, ZHANG Juan, YIN Li-hong, PU Yue-pu. Metabolomic effects of noise exposure on rats[J]. Journal of Environmental and Occupational Medicine, 2020, 37(5): 433-439. DOI: 10.13213/j.cnki.jeom.2020.20059

噪声暴露对大鼠代谢组学的影响

Metabolomic effects of noise exposure on rats

  • 摘要: 背景

    诸多研究证实噪声暴露与听力损失、高血压等健康损害相关,而目前关于噪声暴露的代谢组学研究鲜有报道。

    目的

    探索噪声暴露对Wistar大鼠的健康效应以及噪声暴露相关的大鼠血清及尿液代谢产物的改变。

    方法

    8周龄雄性Wistar大鼠随机分为噪声暴露组(10只)和对照组(8只)。暴露组大鼠给予85 dB声压级的宽带噪声暴露,每天8 h,每周5 d,共计6周。暴露周期结束后,分别测量大鼠的体重、脏器质量和血压,通过听性脑干反应(ABR)测定大鼠的听力状况,并进行血生化检查。收集两组大鼠的血清和尿液,应用高分辨四级杆飞行时间质谱仪进行非靶向代谢组学研究,分析噪声暴露引起的小分子代谢产物表达的变化及相关代谢通路。

    结果

    噪声暴露对大鼠的体重、脏器系数和血压无明显影响(P>0.05)。暴露组大鼠在32 kHz处的ABR阈值为(74.00±5.48)dB,高于对照组(55.00±3.54)dB(P < 0.05)。暴露组大鼠的甘油三酯、总胆固醇和高密度脂蛋白浓度分别为(1.14±0.20)、(1.90±0.33)、(1.34±0.25)mmol·L-1,均高于对照组(0.75±0.28)、(1.58±0.25)、(1.11±0.16)mmol·L-1(均P < 0.05),而低密度脂蛋白无明显改变(P>0.05)。血清代谢组学研究筛选并鉴定了27种噪声暴露相关的差异代谢物,涉及甘油磷脂代谢、亚油酸代谢和类固醇代谢等通路。尿液代谢组学研究筛选并鉴定了18种差异代谢物,涉及脂类代谢、苯丙氨酸代谢和色氨酸代谢等通路。

    结论

    噪声暴露可影响大鼠听力阈值和血脂水平,同时可引起血清和尿液中小分子代谢物表达改变,干扰甘油磷脂代谢、亚油酸代谢、苯丙氨酸代谢等代谢通路。

     

    Abstract: Background

    Many studies have proven that noise exposure is associated with hearing loss, hypertension, and other adverse health effects. However, few studies on the metabolomic effects of noise exposure have been reported.

    Objective

    This study investigates the health effects of noise exposure on Wistar rats, and related changes of selected metabolites in serum and urine.

    Methods

    Male Wistar rats aged eight weeks were randomly divided into a noise exposure group (n=10) and a control group (n=8). The rats in the exposure group were given 85 dB sound pressure level (SPL) broadband noise exposure for 8 h per day, 5 d per week, and lasting for 6 weeks. After the exposure, body weight, organ weight, and blood pressure of rats were measured respectively, hearing threshold was measured by auditory brainstem response (ABR), and selected blood biochemical indicators were detected. After the serum and urine samples of the two groups of rats were collected, the changes in the expressions of small molecule metabolites associated with noise exposure and related pathways were analyzed by untargeted metabolomics analysis using high-resolution quadrupole coupled with time-of-flight mass spectrometer.

    Results

    Noise exposure had no obvious effects on the body weight, organ coefficient, and blood pressure of the rats (P>0.05). The ABR threshold at 32 kHz was (74.00±5.48) dB in the exposure group, higher than that in the control group(55.00±3.54) dB (P < 0.05). The concentrations of triglyceride, total cholesterol, and high-density lipoprotein in the exposure group were (1.14±0.20), (1.90±0.33), and (1.34±0.25) mmol·L-1, respectively, all higher than those in the control group(0.75±0.28), (1.58±0.25), and (1.11±0.16) mmol·L-1, respectively (P < 0.05). However, there was no significant change in low-density lipoprotein concentration between the two groups (P>0.05). The serum metabolomics analysis screened and identified 27 differential metabolites associated with noise exposure, and these metabolites participated in glycerophospholipid metabolism, linoleic acid metabolism, and steroid metabolism. The urine metabolomics analysis screened and identified 18 noise exposure-related differential metabolites which were involved in lipid metabolism, phenylalanine metabolism, and tryptophan metabolism.

    Conclusion

    Noise exposure can affect the hearing threshold and blood lipid level of rats. In addition, it can also interfere expressions of small molecule metabolites in serum and urine, and disturb glycerophospholipid metabolism, linoleic acid metabolism, phenylalanine metabolism, and other metabolic pathways.

     

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