期刊文献+

围生期暴露双酚A对青春期子代雌性大鼠糖代谢和血清炎症因子的影响 被引量:2

Effects of perinatal exposure to bisphenol A on glucose metabolism and inflammatory factors in adolescent female offspring rats
原文传递
导出
摘要 目的探讨围生期暴露双酚A(bispheno1 A,BPA)对青春期雌性子代大鼠体重、糖代谢及细胞炎症因子的影响。方法将21只清洁级SD妊娠大鼠分为3组,分别为对照(含1%无水乙醇的水)组和低(1μg/ml)、高(10μg/ml)浓度BPA暴露组,每组7只。从妊娠第6天至哺乳期(出生后20 d),母鼠采用自由饮水方式进行染毒;断乳后,雌性仔鼠采用自由饮水(不含BPA)方式继续喂养30 d。测定雌性仔鼠体重、空腹血糖、胰岛素水平及血清肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)和白介素6(interleukin-6,IL-6)水平,并计算胰岛素抵抗指数。结果各浓度BPA暴露组雌性仔鼠体重、空腹血糖、血清胰岛素水平和胰岛素抵抗指数、TNF-α、IL-6水平均明显高于对照组,差异有统计学意义(P<0.05,P<0.01)。结论围生期暴露BPA可引起子代雌性大鼠体重增高和胰岛素抵抗,并可诱发机体炎症反应。 Objective To explore the effects of perinatal exposure to bisphenol A(BPA) on body weight and inflammatory factors in adolescent female offspring rats. Methods A total of 21 pregnant Sprague-Dawley rats were randomly divided into three groups, seven rats in each group, the control group (1% of anhydrous alcohol with water),low dose (1 μg/ml) and high dose (10 μg/ml) groups of BPA exposed through drinking water,from gestation day 6 to the end of lactation respectively. Female offspring drank water without BPA for 30 days after weaning. Body weight,fasting serum glucose,insulin,necrosis factor-α (TNF-α) and interleukin-6 (IL-6) levels were determined, and insulin resistance index was calculated in female offspring after postnatal day 50. Results There were significantly higher body weight,serum glucose,insulin,and insulin resistance index,TNF-α and IL-6 levels in BPA-exposed female rats compared with the controls (P〈0.05 or P〈0.01). Conclusion Perinatal exposure to BPA may result in body weight gain and insulin resistance,and induce inflammatory response in female offspring.
出处 《环境与健康杂志》 CAS CSCD 北大核心 2013年第8期665-667,共3页 Journal of Environment and Health
基金 国家自然科学基金(81072311)
关键词 双酚A 肥胖 胰岛素抵抗 肿瘤坏死因子-α 白介素6 Bisphenol A Obesity Insulin resistance Tumor necrosis faetor-α Interleukin-6
  • 相关文献

参考文献4

二级参考文献122

  • 1Cani PD, Delzenne NM, Amar J, Burcelin R. Role of gut microflora in the development of obesity and insulin resistance following high-fat diet feeding. Pathol Biol (Paris) 2008; 56(5): 305-9.
  • 2Sun L, Yu Z, Ye X, Zou S, Li H, Yu D, et al. A marker of endotoxemia isassociated with obesity and related metabolic disorders in apparently healthy Chinese. Diabetes Care 2010; 33(9): 1925-32.
  • 3Bluestone JA, Herold K, Eisenbarth G. Genetics, pathogenesis and clinical interventions in type 1 diabetes. Nature 2010; 464(7293): 1293-300.
  • 4Nishimura S, Manabe I, Nagasakil M, Eto K, Yamashita H, Ohsugi M, et al. CD8+ effector T cells contribute to macrophage recruitment and adipose tissue inflammation in obesity. Nat Med 2009; 15(8): 914-20.
  • 5Kurokawa J, Arai S, Nakashima K, Nagano H, Nishijima A, Miyata K, et al. Macrophage-derived AIM is endocytosed into adipocytes and decreases lipid droplets via inhibition of fatty acid synthase activity. Cell Metab 2010; 11(6): 479-92.
  • 6Maury E, Noel L, Detry R, Brichard SM. in vitro hyper-responsiveness to TNF- {alpha} contributes to adipokine dysregulation in omental adipocytes of obese subjects. J Clin Endocrinol Metab 2009; 94(4): 1393-400.
  • 7Jiao P, Chen Q, Shah S, Du J, Tao B, Tzameli I, et al. Obesityrelated upregulation of monocyte chemotactic factors in adipocytes: involvement ofNF-{kappa} B and JNK pathways. Diabetes 2009; 58(1): 104-15.
  • 8Maury E, Brichard SM. Adipokine dysregulation, adipose tissue inflammation and metabolic syndrome. Mol Cell Endocrinol 2010; 314(1): 1-16.
  • 9Yang RZ, Lee M J, Hu H, Pray J, Wu HB, Hansen BC, et al. Identification of omentin as a novel depotspecific adipokine in human adipose tissue: possible role in modulating insulin action. Am J Physiol Endocrinol Metab 2006; 290(6): E 1253-61.
  • 10El-Mesallamy HO, Kassem DH, Ebtehal Demerdash, Amin AI. Vaspin and visfatin/Nampt are interesting interrelated adipokines playing a role in the pathogenesis of type 2 diabetes mellitus. Metabolism 2010; 60(1): 63-70.

共引文献50

同被引文献25

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部