IDEAS home Printed from https://ideas.repec.org/a/gam/jijerp/v13y2016i5p501-d70089.html
   My bibliography  Save this article

Nonylphenol Toxicity Evaluation and Discovery of Biomarkers in Rat Urine by a Metabolomics Strategy through HPLC-QTOF-MS

Author

Listed:
  • Yan-Xin Zhang

    (School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150090, China)

  • Xin Yang

    (School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150090, China)

  • Pan Zou

    (School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150090, China)

  • Peng-Fei Du

    (Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standard & Testing Technology for Agro-Product, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    Key Laboratory of Agro-Product Safety and Quality, Ministry of Agriculture, Beijing 100081, China)

  • Jing Wang

    (Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standard & Testing Technology for Agro-Product, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    Key Laboratory of Agro-Product Safety and Quality, Ministry of Agriculture, Beijing 100081, China)

  • Fen Jin

    (Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standard & Testing Technology for Agro-Product, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    Key Laboratory of Agro-Product Safety and Quality, Ministry of Agriculture, Beijing 100081, China)

  • Mao-Jun Jin

    (Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standard & Testing Technology for Agro-Product, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    Key Laboratory of Agro-Product Safety and Quality, Ministry of Agriculture, Beijing 100081, China)

  • Yong-Xin She

    (Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standard & Testing Technology for Agro-Product, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    Key Laboratory of Agro-Product Safety and Quality, Ministry of Agriculture, Beijing 100081, China)

Abstract

Nonylphenol (NP) was quantified using liquid chromatography tandem mass spectrometry (LC-MS/MS) in the urine and plasma of rats treated with 0, 50, and 250 mg/kg/day of NP for four consecutive days. A urinary metabolomic strategy was originally implemented by high performance liquid chromatography time of flight mass spectrometry (HPLC-QTOF-MS) to explore the toxicological effects of NP and determine the overall alterations in the metabolite profiles so as to find potential biomarkers. It is essential to point out that from the observation, the metabolic data were clearly clustered and separated for the three groups. To further identify differentiated metabolites, multivariate analysis, including principal component analysis (PCA), orthogonal partial least-squares discriminant analysis (OPLS-DA), high-resolution MS/MS analysis, as well as searches of Metlin and Massbank databases, were conducted on a series of metabolites between the control and dose groups. Finally, five metabolites, including glycine, glycerophosphocholine, 5-hydroxytryptamine, malonaldehyde (showing an upward trend), and tryptophan (showing a downward trend), were identified as the potential urinary biomarkers of NP-induced toxicity. In order to validate the reliability of these potential biomarkers, an independent validation was performed by using the multiple reaction monitoring (MRM)-based targeted approach. The oxidative stress reflected by urinary 8-oxo-deoxyguanosine (8-oxodG) levels was elevated in individuals highly exposed to NP, supporting the hypothesis that mitochondrial dysfunction was a result of xenoestrogen accumulation. This study reveals a promising approach to find biomarkers to assist researchers in monitoring NP.

Suggested Citation

  • Yan-Xin Zhang & Xin Yang & Pan Zou & Peng-Fei Du & Jing Wang & Fen Jin & Mao-Jun Jin & Yong-Xin She, 2016. "Nonylphenol Toxicity Evaluation and Discovery of Biomarkers in Rat Urine by a Metabolomics Strategy through HPLC-QTOF-MS," IJERPH, MDPI, vol. 13(5), pages 1-17, May.
  • Handle: RePEc:gam:jijerp:v:13:y:2016:i:5:p:501-:d:70089
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/1660-4601/13/5/501/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/1660-4601/13/5/501/
    Download Restriction: no
    ---><---

    References listed on IDEAS

    as
    1. Tatsuo Hashimoto & Thomas Perlot & Ateequr Rehman & Jean Trichereau & Hiroaki Ishiguro & Magdalena Paolino & Verena Sigl & Toshikatsu Hanada & Reiko Hanada & Simone Lipinski & Birgit Wild & Simone M. , 2012. "ACE2 links amino acid malnutrition to microbial ecology and intestinal inflammation," Nature, Nature, vol. 487(7408), pages 477-481, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Mouna Chajadine & Ludivine Laurans & Tobias Radecke & Nirmala Mouttoulingam & Rida Al-Rifai & Emilie Bacquer & Clara Delaroque & Héloïse Rytter & Marius Bredon & Camille Knosp & José Vilar & Coralie F, 2024. "Harnessing intestinal tryptophan catabolism to relieve atherosclerosis in mice," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    2. Guanlan Hu & Catriona Ling & Lijun Chi & Mehakpreet K. Thind & Samuel Furse & Albert Koulman & Jonathan R. Swann & Dorothy Lee & Marjolein M. Calon & Celine Bourdon & Christian J. Versloot & Barbara M, 2022. "The role of the tryptophan-NAD + pathway in a mouse model of severe malnutrition induced liver dysfunction," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    3. Nguyen T. Van & Karen Zhang & Rachel M. Wigmore & Anne I. Kennedy & Carolina R. DaSilva & Jialing Huang & Manju Ambelil & Jose H. Villagomez & Gerald J. O’Connor & Randy S. Longman & Miao Cao & Adam E, 2023. "Dietary L-Tryptophan consumption determines the number of colonic regulatory T cells and susceptibility to colitis via GPR15," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:13:y:2016:i:5:p:501-:d:70089. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.