Adverse effect of DEHP exposure on the serum insulin level of Balb/c mice
详细信息    查看全文
  • 作者:Jing Wang ; Jinquan Li ; Kashif Rafiq Zahid ; Kun Wang…
  • 关键词:DEHP exposure ; Diabetes ; like symptom ; Insulin ; Blood glucose ; Pancreatic cell ; Oxidative stress
  • 刊名:Molecular & Cellular Toxicology
  • 出版年:2016
  • 出版时间:March 2016
  • 年:2016
  • 卷:12
  • 期:1
  • 页码:83-91
  • 全文大小:8,115 KB
  • 参考文献:1.Bornehag, C. G. et al. Phthalates in indoor dust and their association with building characteristics [J]. Environ Health Perspect 113:1399–1404 (2005).CrossRef PubMed PubMedCentral
    2.Doull, J. et al. A cancer risk assessment of di(2-ethylhexyl) phthalate: application of the new U.S. EPA risk assessment guienlines. Regul Toxicol Pharmacol 29:327–357 (1999).CrossRef PubMed
    3.Loff, S. et al. Polyvinylchloride infusion lines expose infants to largy amounts of toxic plasticizers. J Pediatr Surg 35:1775–1781 (2000).CrossRef PubMed
    4.Huber, W. W., Grasl-Kraupp, B. & Schulte-Hermann, R. Hepatocarcinogenic potential of di(2-(ethylhexyl)) phthalate in rodents and its implications on human risk. Crit Rev Toxicol 26:365–481 (1996).CrossRef PubMed
    5.Emiko, K. et al. Role of oxidative stress in germ cell apoptosis by di(2-ethylhexyl) phthalate. Biochem J 365:849–856 (2002).CrossRef
    6.Moore, R. W. et al. Abnormalities of sexual development in male rats with in utero and lactational exposure to the antiandrogenic plasticizer di(2-ethylhexyl) Phthalate. Environ Health Persp 109:229–237 (2001).CrossRef
    7.Cobellis, L. et al. Hig Plasma Concentrations of DEHP in Women with Endometriosis. Hum Reprod 18: 1512–1515 (2003).CrossRef PubMed
    8.Li, L. H. et al. Single Dose of Di-(2-ethylhexyl) -Phthalate in Neonatal Rats Alters Gonocytes, Reduces Sertoli Cell Proliferation, and Decreases Cyclin D2 Expression. Toxicol Appl Pharmacol 166:222–229 (2000).CrossRef PubMed
    9.Yang, G. T. et al. Adjuvant effect of di-(2-ethylhexyl) phthalate on asthma-like pathological changes in ovalbumin-immunised rats. Food and Agricultural Immun 19:351–362 (2009).CrossRef
    10.Guo, J. et al. Pulmonary toxicity and adjuvant effect of di-(2-exylhexyl) phthalate in ovalbumin-immunized Balb/c mice. PLoS One 7: e39008 (2012).CrossRef PubMed PubMedCentral
    11.Lin, Y. et al. Developmental exposure to di(2-ethylhexyl) phthalate impairs endocrine pancreas and leads to long-term adverse effects on glucose homeostasis in the rat. Am J Physiol Endocrinol Metab 301: E527–E538 (2011).CrossRef PubMed
    12.Stahlhut, R. W. et al. Concentrations of urinary phthalate metabolites are associated with increased waist circumference and insulin resistance in adult US males. Environ Health Persp 115:876–882 (2007).CrossRef
    13.Srinivasan, K. et al. Combination of high-fat diet-fed and low-dose streptozotocin-treated rat: A model for type 2 diabetes and pharmacological screening. Pharmacol Res 52:313–320 (2005).CrossRef PubMed
    14.Goldstein, B. J. et al. Role of insulin induced reactive oxygen species in the insulin signaling pathway. Antioxid Redox Signal 7:1021–1030 (2005).CrossRef PubMed PubMedCentral
    15.Casals-Casas, C. & Desvergne, B. Endocrine disruptors: from endocrine to metabolic disruption. Annu Rev Physiol 73:135–162 (2010).CrossRef
    16.Selvin, E. et al. Androgens and diabetes in men: results from th Third National Health and Nutrition Examination Survey (NHANES III). Diabetes Care 30:234–238 (2007).CrossRef PubMed
    17.Silva, M. J. et al. Urinary levels of seven phthalate metabolites in the U.S. population from th National Health and Nutrition Examination Survey (NHANES) 1999–2000. Environ Health Perspect 112:331–338 (2004).CrossRef PubMed PubMedCentral
    18.Calafat, A. M., Needham, L. L., Silva, M. J. & Lambert, G. Exposure to di-(2-ethylhexyl) phthalate among premature neonates in a neonatal intensive care unit. Pediatrics 113:e429–e434 (2004).CrossRef PubMed
    19.Green, R. et al. Use of di(2-ethylhexyl) phthalate-containing medical products and urinary levels of mono (2-ethylhexyl) phthalate in neonatal intensive care unit infants. Environ Health Perspect 113:1222–1225 (2005).CrossRef PubMed PubMedCentral
    20.Kavlock, R. et al. NTP-CERH Expert Panel Update on the Reproductive and Developmental Toxicity of di (2-ethylhexyl) phthalate. Reprod Toxicol 22:291–399 (2006).CrossRef PubMed
    21.Carton, J. C. & Lapinskas, P. J. Peroxisome proliferator-activated receptors Mediators of phthalate ester-induced effect s in the male reproductive Tract. J Toxicol Sci 83:4–17 (2005).CrossRef
    22.Evans, J. L. et al. Oxidative stress and stress-activated signaling pathways: a unifying hypothesis of type2 diabetes. Endocr Rev 23:599–622 (2002).CrossRef PubMed
    23.Robertson, R. P. Oxidative stress and impaired insulin secretion in type 2 diabetes. Current Opinion in Pharmacol 6:615–619 (2006).CrossRef
    24.Nishikawa, T. et al. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 404:787–790 (2000).CrossRef PubMed
  • 作者单位:Jing Wang (1) (2)
    Jinquan Li (1)
    Kashif Rafiq Zahid (1)
    Kun Wang (3)
    Yan Qian (4)
    Ping Ma (5)
    Shumao Ding (1)
    Xu Yang (1) (5)
    Xianliang Wang (4)

    1. School of Life Sciences, Central China Normal University, Wuhan, 430079, China
    2. Hubei Center of Diseases Control and Prevention, Wuhan, 430079, China
    3. Department of Population Health, New York University, New York, 10016, USA
    4. Institute of Environmental Health and Related Product Safety, Chinese Centre for Disease Control and Prevention, Beijing, 100021, China
    5. College of Basic Medical Science, Hubei University of Science and Technology, Xianning, 437100, China
  • 刊物主题:Cell Biology; Pharmacology/Toxicology;
  • 出版者:Springer Netherlands
  • ISSN:2092-8467
文摘
Di(2-ethylhexyl) phthalate (DEHP) is a common indoor pollutant in the world, which may cause lots of harmful effects in human including diabetes according to epidemiological studies. To explore the underlying role of DEHP in diabetes-like symptoms, Balb/c mice were chose to be the experimental animals in this paper. They were separated as eight groups as follows: (1) saline+normal diet (vehicle control), (2) 10 mg/kg.day DEHP+normal diet, (3) 50 mg/kg.day DEHP+normal diet, (4) 250 mg/kg.day DEHP+normal diet, (5) streptozotocin (STZ)+high fat diet (diabetes model), (6) 10 mg/kg.day DEHP+ STZ+high fat diet, (7) 50 mg/kg.day DEHP+STZ +high fat diet, (8) 250 mg/kg.day DEHP+STZ+high fat diet. The biomarkers of this experiment include four groups: (1) general indicates: body weight and drinking water, (2) blood biomarkers: serum insulin and fasting glucose, (3) pathological examination: pancreas section and kidney section, and (4) biomarkers of oxidative stress: reactive oxygen species (ROS) and malondialdehyde (MDA) in liver cells. Our study results demonstrate that: (1) at our treatment levels DEHP cannot directly induce diabetes, but reduce serum insulin level in DEHP-exposed non-STZ-treated animals, (2) pathological examination finds that these is a dose-dependent damage in the pancreas in DEHP- exposed STZ-treated groups, and (3) the oxidative mechanism may be involved in this pathological process.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700