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Influence of Genista Tinctoria L or Methylparaben on Subchronic Toxicity of Bisphenol A in Rats 被引量:2

Influence of Genista Tinctoria L or Methylparaben on Subchronic Toxicity of Bisphenol A in Rats
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摘要 Objective To evaluate the influence of an extract of Genista tinctoria L. herba (GT) or methylparaben (MP) on histopathological changes and 2 biomarkers of oxidative stress in rats subchronicly exposed to bisphenol A (BPA). Methods Adult female Wistar rats were orally exposed for 90 d to BPA (50 mg/kg), BPA+GT (35 mg isoflavones/kg) or BPA+MP (250 mg/kg). Plasma and tissue samples were taken from liver, kidney, thyroid, uterus, ovary, and mammary gland after 30, 60, and 90 d of exposure respectively. Lipid peroxidation and in vivo hydroxyl radical production were evaluated by histological analysis along with malondialdehyde and 2,3-dihydroxybenzoic acid detection. Results The severity of histopathological changes in liver and kidneys was lower after GT treatment than after BPA or BPA+MP treatment. A minimal thyroid receptor antagonist effect was only observed after BPA+MP treatment. The abnormal folliculogenesis increased in a time-dependent manner, and the number of corpus luteum decreased. No significant histological alterations were found in the uterus. The mammary gland displayed specific estrogen stimulation changes at all periods. Both MP and GT revealed antioxidant properties reducing lipid peroxidation and BPA-induced hydroxyl radical generation. Conclusion GT L. extract ameliorates the toxic effects of BPA and is proved to have antioxidant potential and antitoxic effect. MP has antioxidant properties, but has either no effect or exacerbates the BPA-induced histopathological changes. Objective To evaluate the influence of an extract of Genista tinctoria L. herba (GT) or methylparaben (MP) on histopathological changes and 2 biomarkers of oxidative stress in rats subchronicly exposed to bisphenol A (BPA). Methods Adult female Wistar rats were orally exposed for 90 d to BPA (50 mg/kg), BPA+GT (35 mg isoflavones/kg) or BPA+MP (250 mg/kg). Plasma and tissue samples were taken from liver, kidney, thyroid, uterus, ovary, and mammary gland after 30, 60, and 90 d of exposure respectively. Lipid peroxidation and in vivo hydroxyl radical production were evaluated by histological analysis along with malondialdehyde and 2,3-dihydroxybenzoic acid detection. Results The severity of histopathological changes in liver and kidneys was lower after GT treatment than after BPA or BPA+MP treatment. A minimal thyroid receptor antagonist effect was only observed after BPA+MP treatment. The abnormal folliculogenesis increased in a time-dependent manner, and the number of corpus luteum decreased. No significant histological alterations were found in the uterus. The mammary gland displayed specific estrogen stimulation changes at all periods. Both MP and GT revealed antioxidant properties reducing lipid peroxidation and BPA-induced hydroxyl radical generation. Conclusion GT L. extract ameliorates the toxic effects of BPA and is proved to have antioxidant potential and antitoxic effect. MP has antioxidant properties, but has either no effect or exacerbates the BPA-induced histopathological changes.
出处 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2014年第2期85-96,共12页 生物医学与环境科学(英文版)
基金 supported by CNCSIS-UEFISCSU Romania,project number PNII-IDEI 1337/2008
关键词 Food contaminant PHYTOESTROGEN Morphological effect Lipid peroxidation Hydroxylradical Food contaminant Phytoestrogen Morphological effect Lipid peroxidation Hydroxylradical
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  • 1Safe S. Bisphenol A and Related Endocrine Disruptors. Toxicological sciences, 2000; 56, 251-2.
  • 2Chalupka S & Chalupka AN. The impact of environmental and occupational exposures on reproductive health. Journal of Obstetric, Gynecologic, & Neonatal Nursing, 2010; 39, 84-102.
  • 3Ema M & Miyawaki E. Adverse effects on development of the reproductive system in male offspring of rats given monobutyl phthalate, a metabolite of dibutyl phthalate, during late pregnancy. Reproductive Toxicology, 2001; 15, 189 94.
  • 4Groff T. Bisphenol A: invisible pollution. Curr Opin Pediatr, 2010; 22, 524-9.
  • 5Latini G, Del Vecchio A, Massaro M, et al. In utero exposure to phthalates and fetal development. Curt Med Chem, 2006; 13, 2527-34.
  • 6Hauser R & Calafat AM. Phthalates and human health. Occup Environ Med, 2005; 62, 806-18.
  • 7Lovekamp-Swan T & Davis BJ. Mechanisms of phthalate ester toxicity in the female reproductive system. Environ HealthPerspect, 2003; 111, 139-45.
  • 8Lyche JL, Gutleb AC, Bergman Ake, et al. Reproductive and developmental toxicity of pbthalates. Journal of Toxicology and Environmental Health, Part B, 2009; 12, 225-49.
  • 9Tan BL, Kassim NM, Mohd MA. Assessment of pubertal development in juvenile male rats after sub-acute exposure to bisphenol A and nonylphenol. Toxicol Lett, 2003; 143, 261-70.
  • 10Duan Z, Zhu L, Zhu L, et al. Individual and joint toxic effects of pentachlorophenol and bisphenol A on the development of zebrafish (Danio rerio) embryo. Ecotox Environ Safe, 2008; 71, 774-80.

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  • 1May FE. Novel drugs that target the estrogen-related receptor alpha: their therapeutic potential in breast cancer [J]. Cancer management and research, 2014, 6:225-252.
  • 2Messina M. Soy foods, isoflavones, and the health of postmenopausal women [J]. American Journal Of Clinical Nutrition, 2014, 100(1): 423S-430S.
  • 3Zhang H, Sun Q. Alleviation of Plasma Homocysteine Level by Phytoestrogen alpha-Zearalanol Might Be Related to the Reduction of Cystathionine beta-Synthase Nitration [J]. Biomed Research International, 2014, 2014:143-192.
  • 4Dew TP, G Williamso. Controlled flax interventions for the improvement of menopausal symptoms and postmenopausal bone health: a systematic review [J]. Menopause-the Journal Of the North American Menopause Society, 2013, 20(11): 1207-1215.
  • 5Choi RC, Zhu JT, Yung AW, et al. Synergistic Action of Flavonoids, Baicalein, and Daidzein in Estrogenic and Neuroprotective Effects: A Development of Potential Health Products and Therapeutic Drugs against Alzheimer's Disease [J]. Evidence-based complementary and alternative medicine: eCAM, 2013, 2013:635694-635694.
  • 6Xiao Z, Huang C, Wu J, et al. The neuroprotective effects of ipriflavone against H20 and amyloid beta induced toxicity in human neuroblasto ma SH-SY5Y cells [J]. European Journal Of Pharmacology, 2013, 721(1-3): 286-293.
  • 7Strauss L, Santti R, Saarinen N, et al. Dietary phytoestrogens and their role in hormonally dependent disease [J]. Toxicology Letters, 1998, 103:349-354.
  • 8Cassidy A, B Hanley. Isoflavones, lignans and stilbenes-origins, metabolism and potential importance to human health [J]. Journal Of the Science Of Food And Agriculture, 2000, 80(7): 1044-1062.
  • 9Shim M, Bea JY, Lee YJ, et al. Tectoridin fi'om Maackia amurensis modulates both estrogen and thyroid receptors [J]. Phytomedicine, 2014, 21(5): 602-606.
  • 10Ruotolo R, Calani L, Brighenti F, et al. Glucuronidation does not suppress the estrogenic activity of quercetin in yeast and human breast cancer cell model systems [J]. Archives Of Biochemistry And Biophysics, 2014, 559:62-67.

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