Effect of bisphenol A on blood glucose, lipid profile and oxidative stress indices in adult male mice

References

• Aebi H. (1984). Catalane in vitro. Method Enzymol 105:121–26
   PubMed Web of Science ®Google Scholar
• Alonso-Magdalena P, Ropero AB, Soriano S, et al. (2010a). Bisphenol-A: a new diabetogenic factor? Hormones 9:118–26
   PubMedGoogle Scholar
• Alonso-Magdalena P, Vieira E, Soriano S, et al. (2010b). Bisphenol A exposure during pregnancy disrupts glucose homeostasis in mothers and adult male offspring. Environ Health Perspect 118:1243–50
   PubMed Web of Science ®Google Scholar
• Aydogan M, Korkmaz A, Barlas N, Kolankaya D. (2008). The effect of vitamin C on bisphenol A, nonylphenol and octylphenol induced brain damages of male rats. Toxicology 249:35–9
   PubMed Web of Science ®Google Scholar
• Batista TM, Alonso-Magdalena P, Viera E, et al. (2012). Short-term treatment with bisphenol-A leads to metabolic abnormalities in adult male rats. PLoS One 7:e33814
   PubMed Web of Science ®Google Scholar
• Benachour N, Aris A. (2009). Toxic effects of low doses of Bisphenol-A on human placental cells. Toxicol Appl Pharmacol 241:322–8
   PubMed Web of Science ®Google Scholar
• Benzie IF, Strain JJ. (1996). The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 239:70–76
   PubMed Web of Science ®Google Scholar
• Beutler E, Duron O, Kelly BM. (1963). Improved method for the determination of blood glutathione. J Lab Clin Med 61:882–8
   PubMed Web of Science ®Google Scholar
• Bradford MM. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 72:248–54
   PubMed Web of Science ®Google Scholar
• Budin S, Othman F, Louis SA, et al. (2009). The effects of palm oil to cotrienol-rich fraction supplementation on biochemical parameters, oxidative stress and the vascular wall of streptozotocin-induced diabetic rats. Clinics 64:235–44
   PubMed Web of Science ®Google Scholar
• Carwile JL, Michels KB. (2011). Urinary bisphenol A and obesity: NHANES 2003–2006. Environ Res 111:825–30
   PubMed Web of Science ®Google Scholar
• Cox DA, Cohen ML. (1996). Effects of oxidized low density lipoproteins on vascular contraction and relaxation: clinical and pharmacological implications in atherosclerosis. Pharmacol Rev 48:3–9
   PubMed Web of Science ®Google Scholar
• Demuro A, Mina E, Kayed R, et al. (2005). Calcium dysregulation and membrane disruption as a ubiquitous neurotoxic mechanism of soluble amyloid oligomers. J Biol Chem 280:17294–300
   PubMed Web of Science ®Google Scholar
• Dodge JA, Glasebrook AL, Magee DE, et al. (1996). Environmental estrogens: effects on cholesterol lowering and bone in the ovariectomized rat. J Steroid Biochem Mol Biol 59:155–61
   PubMed Web of Science ®Google Scholar
• El-Missiry MA. (1999). Enhanced testicular antioxidant system by ascorbic acid in alloxan diabetic rats. Comp Biochem Physiol C 124:233–7
   PubMed Web of Science ®Google Scholar
• Gharibi S, Dilmaghanian A, Sadighara P, et al. (2013). The effect of bisphenol A on oxidative stress indices and pathological changes in the brain of chicken embryos. World Appl Sci J 26:345–51
   Google Scholar
• Gleichmann M, Mattson MP. (2011). Neuronal calcium homeostasis and dysregulation. Antioxid Redox Signal 14:1261–73
   PubMed Web of Science ®Google Scholar
• Groff T. (2010). Bisphenol A: invisible pollution. Curr Opin Pediatr 22:524–9
   PubMed Web of Science ®Google Scholar
• Grune T, Siems WG, Petras T. (1997). Identification of metabolic pathways of the lipid peroxidation product 4-hydroxynonenal in in situ perfused rat kidney. J Lipid Res 38:1660–5
   PubMed Web of Science ®Google Scholar
• Hassan ZK, Elobeid MA, Virk P, et al. (2012). Bisphenol A induces hepatotoxicity through oxidative stress in rat model. Oxid Med Cell Longev 2012:194829
   PubMed Web of Science ®Google Scholar
• Indumathi D, Jayashree S, Selvaraj J, et al. (2013). Effect of bisphenol A on insulin signal transduction and glucose oxidation in skeletal muscle of adult male albino rat. Hum Exp Toxicol 32:960–71
   PubMed Web of Science ®Google Scholar
• Johansen JS, Harris AK, Rychly DJ, Ergul A. (2005). Oxidative stress and the use of antioxidants in diabetes: linking basic science to clinical practice. Cardiovasc Diabetol 4:5
   PubMed Web of Science ®Google Scholar
• Kabuto H, Amakawa M, Shishibori T. (2004). Exposure to bisphenol A during embryonic/fetal life and infancy increases oxidative injury and causes underdevelopment of the brain and testis in mice. Life Sci 74:2931–40
   PubMed Web of Science ®Google Scholar
• Kim K, Park H. (2013). Association between urinary concentrations of bisphenol A and type 2 diabetes in Korean adults: a population-based cross-sectional study. Int J Hyg Environ Health 216:467–71
   PubMed Web of Science ®Google Scholar
• Lacoste L, Lam JY, Hung J, et al. (1995). Hyperlipidemia and coronary disease: correction of the increased thrombo-genic potential with cholesterol reduction. Circulation 92:3172–7
   PubMed Web of Science ®Google Scholar
• Liu J, Yu P, Qian W, et al. (2013). Perinatal bisphenol A exposure and adult glucose homeostasis: identifying critical windows of exposure. PLoS One 8:e64143
   Google Scholar
• Lorber D. (2014). Importance of cardiovascular disease risk management in patients with type 2 diabetes mellitus. Diabetes Metab Syndr Obes 7:169–83
   PubMedGoogle Scholar
• Lorenzo A, Razzaboni B, Weir GC, Yankner BA. (1994). Pancreatic islet cell toxicity of amylin associated with type-2 diabetes mellitus. Nature 368:756–60
   PubMed Web of Science ®Google Scholar
• Marklund S, Marklund G. (1979). Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 47:469–74
   Google Scholar
• Marmugi A, Ducheix S, Lasserre F, et al. (2012). Low doses of bisphenol A induce gene expression related to lipid synthesis and trigger triglyceride accumulation in adult mouse liver. Hepatology 55:395–407
   PubMed Web of Science ®Google Scholar
• Marmugi A, Lasserre F, Beuzelin D, et al. (2014). Adverse effects of long-term exposure to bisphenol A during adulthood leading to hyperglycaemia and hypercholesterolemia in mice. Toxicology 325:133–43
   PubMed Web of Science ®Google Scholar
• Miyawaki J, Sakayama K, Kato H, et al. (2007). Perinatal and postnatal exposure to bisphenol A increases adipose tissue mass and serum cholesterol level in mice. J Atheroscler Thromb 14:245–52
   PubMed Web of Science ®Google Scholar
• Pieper GM, Jordan M, Dondlinger LA, et al. (1995). Peroxidative stress in diabetic blood vessels. Reversal by pancreatic islet transplantation. Diabetes 44:884–9
   Google Scholar
• Ryan KK, Haller AM, Sorrell JE, et al. (2010). Perinatal exposure to Bisphenol-A and the development of metabolic syndrome in CD-1 mice. Endocrinology 151:2603–12
   PubMed Web of Science ®Google Scholar
• Samarghandian S, Afshari R, Sadati A. (2014a). Evaluation of lung and bronchoalveolar lavage fluid oxidative stress indices for assessing the preventing effects of safranal on respiratory distress in diabetic rats. Sci World J 2014:251378
   Web of Science ®Google Scholar
• Samarghandian S, Azimi-Nezhad M, Samini F. (2014b). Ameliorative effect of saffron aqueous extract on hyperglycemia, hyperlipidemia, and oxidative stress on diabetic encephalopathy in streptozotocin induced experimental diabetes mellitus. Biomed Res Int 2014:920857
   Web of Science ®Google Scholar
• Samarghandian S, Azimi-Nezhad M, Samini F, Farkhondeh T. (2015). Chrysin treatment improves diabetes and its complications in streptozotocin-induced diabetic rats. Can J Physil Pharmacol. [Epub ahead of print]. doi:10.1139/cjpp
   Google Scholar
• Samarghandian S, Borji A, Delkhosh MB, Samini F. (2013a). Safranal treatment improves hyperglycemia, hyperlipidemia and oxidative stress in streptozotocin-induced diabetic rats. J Pharm Pharm Sci 16:352–62
   PubMed Web of Science ®Google Scholar
• Samarghandian S, Borji A, Tabasi SH. (2013b). Effects of Cichorium intybus linn on blood glucose, lipid constituents and selected oxidative stress parameters in streptozotocin-induced diabetic rats. Cardiovasc Hematol Disord Drug Targets 13:231–6
   PubMedGoogle Scholar
• Samarghandian S, Hadjzadeh MA, Amin Nya F, Davoodi S. (2012). Antihyperglycemic and antihyperlipidemic effects of guar gum on streptozotocin-induced diabetes in male rats. Pharmacogn Mag 8:65–72
   PubMed Web of Science ®Google Scholar
• Seidlová-Wuttke D, Jarry H, Christoffel J, et al. (2005). Effects of bisphenol-A (BPA), dibutylphtalate (DBP), benzophenone-2 (BP2), procymidone (Proc), and linurone (Lin) on fat tissue, a variety of hormones and metabolic parameters: a 3 months comparison with effects of estradiol (E2) in ovariectomized (ovx) rats. Toxicology 213:13–24
   PubMed Web of Science ®Google Scholar
• Selvaraju V, Joshi M, Suresh S, et al. (2012). Diabetes, oxidative stress, molecular mechanism, and cardiovascular disease – an overview. Toxicol Mech Methods 22:330–5
   PubMed Web of Science ®Google Scholar
• Shahady E. (1995). Hyperlipidemia in diabetes – etiology, consequences and treatment Adapted from Libby P. Circulation 9:2844–50
   Google Scholar
• Siddiqui MR, Taha A, Moorthy K, et al. (2005). Amelioration of altered antioxidant status and membrane linked functions by vanadium and Trigonella in alloxan diabetic rat brains. J Biosci 30:483–90
   PubMed Web of Science ®Google Scholar
• Song S, Zhang L, Zhang H, et al. (2014). Perinatal BPA exposure induces hyperglycemia, oxidative stress and decreased adiponectin production in later life of male rat offspring. Int J Environ Res Public Health 11:3728–42
   PubMed Web of Science ®Google Scholar
• Sparr E, Engel MF, Sakharov DV, et al. (2004). Islet amyloid polypeptide-induced membrane leakage involves uptake of lipids by forming amyloid fibers. FEBS Lett 577:117–20
   PubMed Web of Science ®Google Scholar
• Vom Saal FS, Nagel SC, Coe BL, et al. (2012). The estrogenic endocrine disrupting chemical bisphenol A (BPA) and obesity. Mol Cell Endocrinol 354:74–84
   PubMed Web of Science ®Google Scholar
• Watson CS, Jeng YJ, Kochukov MY. (2010). Nongenomic signaling pathways of estrogen toxicity. Toxicol Sci 115:1–11
   PubMed Web of Science ®Google Scholar
• Wei J, Lin Y, Li Y, et al. (2011). Perinatal exposure to bisphenol A at reference dose predisposes offspring to metabolic syndrome in adult rats on a high-fat diet. Endocrinology 152:3049–61
   PubMed Web of Science ®Google Scholar
• Wiernsperger NF. (2003). Oxidative stress as a therapeutic target in diabetes: revisiting the controversy. Diabete Metab 29:579–85
   PubMed Web of Science ®Google Scholar
• Yagi K. (1984). Assay for blood plasma or serum lipid peroxides. Methods Enzymol 105:28–31
   Google Scholar
• Zraika S, Hull RL, Udayasankar J, et al. (2009). Oxidative stress is induced by islet amyloid formation and time dependently mediates amyloid-induced beta cell apoptosis. Diabetologia 52:626–35
   PubMed Web of Science ®Google Scholar