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Untargeted Metabolomics Analysis Reveals Toxicity Based on the Sex and Sexual Maturity of Single Low-Dose DEHP Exposure.
Lee, Hyeon-Jeong; Jin, Jonghwa; Seo, Yoondam; Kang, Inseon; Son, Junghyun; Yi, Eugene C; Min, Hophil.
Afiliación
  • Lee HJ; Doping Control Center, Korea Institute of Science and Technology, Seongbuk-gu, Seoul 02792, Republic of Korea.
  • Jin J; Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Jongno-gu, Seoul 03080, Republic of Korea.
  • Seo Y; New Drug Development Center, Heungdeok-gu, Cheongju-si, Chungbuk 28160, Republic of Korea.
  • Kang I; Doping Control Center, Korea Institute of Science and Technology, Seongbuk-gu, Seoul 02792, Republic of Korea.
  • Son J; Doping Control Center, Korea Institute of Science and Technology, Seongbuk-gu, Seoul 02792, Republic of Korea.
  • Yi EC; Doping Control Center, Korea Institute of Science and Technology, Seongbuk-gu, Seoul 02792, Republic of Korea.
  • Min H; Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Jongno-gu, Seoul 03080, Republic of Korea.
Toxics ; 11(9)2023 Sep 20.
Article en En | MEDLINE | ID: mdl-37755804
Di-(2-Ethylhexyl) phthalate (DEHP) is a prevalent environmental endocrine disruptor that affects homeostasis, reproduction, and developmental processes. The effects of DEHP have been shown to differ based on sex and sexual maturity. This study examines the metabolic profiles of mature adult rats from both sexes, aged 10 weeks, and adolescent female rats, aged 6 weeks, following a single 5 mg/kg of body weight DEHP oral administration. An untargeted metabolomic analysis was conducted on urine samples collected at multiple times to discern potential sex- and maturity-specific DEHP toxicities. Various multivariate statistical analyses were employed to identify the relevant metabolites. The findings revealed disruptions to the steroid hormone and primary bile acid biosynthesis. Notably, DEHP exposure increased hyocholic, muricholic, and ketodeoxycholic acids in male rats. Moreover, DEHP exposure was linked to heart, liver, and kidney damage, as indicated by increased plasma GOT1 levels when compared to the levels before DEHP exposure. This study provides detailed insights into the unique mechanisms triggered by DEHP exposure concerning sex and sexual maturity, emphasizing significant distinctions in lipid metabolic profiles across the different groups. This study results deepens our understanding of the health risks linked to DEHP, informing future risk assessments and policy decisions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Toxics Año: 2023 Tipo del documento: Article Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Toxics Año: 2023 Tipo del documento: Article Pais de publicación: Suiza