Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

The Chemical BPA - a Threat to Human Life?


Affiliations
1 Birla Institute of Technology, Mesra, Ranchi, India
2 Institute of Post Graduate Medical Education & Research, Kolkata, India
3 Institute of Post Graduate Medical Education & Research, Kolkata, India
     

   Subscribe/Renew Journal


Bisphenol A (BPA) is a monomer used to manufacture polycarbonate plastics, the resin of cans and other products with global capacity in excess of 6.4 billion pounds per year. Because ester bonds in these BPA based polymers are subjected to hydrolysis, leaching of BPA has wide spread human exposure. A recent report prepared by Harvard Center for Risk and funded by the American Plastic Council concluded that evidence for low dose effect of BPA is weak on the basis of a review of only 19 studies; the report was issued after a delay of 2.5 years. A current comprehensive literature review reveals that the opposite is true of December'2004, there were 115 published in vivo studies of low dose effect of BPA, and 94 of these report significant effects. In 31 publications of vertebrate and invertebrate animals, significant effect occurred below the predicted "safe" or Reference 50microgram/kg/day BPA. An oestrogenic mode of action of BPA is confirmed by an in vitro study which describes disruption of cell function at.23ppt. nonetheless, chemical manufacturer continue to discount these published findings because no industry funded have reported significant effects of low doses of BPA, although more than 90% of Government funded reports have noted significant effects.

Keywords

Bisphenol A, Endocrine Disruption, Plastic, Low Dose Effects, Toxicities
Subscription Login to verify subscription
User
Notifications
Font Size


  • Environmemtal Health Perspect 113:926-93, 2005.
  • Purchase IFH 2004. Fraud, errors and gamesmanship in experimental toxicology.Toxic 202:1-20.
  • Gray G M et al 2004. Weight of the Evidence Evaluation of Low Dose Reproductive and Developmental Effects of BPA, Human and Ecological Risk Assessment.10(5):875- 921.
  • Gupta C.2000. Reproductive malformation of the male off-springs following maternal exposure to oestrogenic chemicals. Proc Sco Exp Biol Med 224:61-68.
  • Timms B G, Howshedell K L, Barton L, Bradley S, Richter C A, Vom Saal F S.2005. Estrogen chemicals in plastic and oral contraceptives disrupt development of the mouse prostate and urethra. Proc Nat L Acad Sci USA 102:7014- 7019.
  • Negal S C, Vom Saal F S, Thayer K A, Dhar M G, Boecheler M, Welshon W V. Relative Binding Affinity – Serum Modified Access (RBASMA) Assay predicts the Relative In- Vivo Bio-activity of the xenoestrogen BPA and Octylphenol. Environmental Health Perspective. 1997;105:70-76.
  • Wade V Welshons. Low Dose Bioactivity of Xenoestrogens in animals: fetal exposure to low doses of methoxychlor and other xenoestrogens increases adult prostate size in mice. Toxicology and Industrial Health;Vol.15.1-2,12- 25(1999).
  • Pottinger L H et al.2000. The Relative Bioavailability and Metabolism of BPA in Rats is Dependent upon Route of Administration. Toxicol.Sci.54(1):3-18.
  • Ashby J, Odum J.2001.Gene expression changes in the immature rat uterus:effects of uterotrophic and subuterotrophic doses of BPA.Toxicol Sci 82:458-467.
  • Ashby J, Tinwell H, Haseman J.1999.Lack of effects for low dose levels of bisphenol A and Diethyl stibesterol (DES) on the prostate gland of CF1 mice exposed in utero:Regular Pharmacol 30:156-166.
  • Cagen S Z,Waechter J M, Diamond S S, Breslin W J, Butala J H, Jekat F W et al 1999.Non-reproductive organ development in CF-1 mice following prenatal exposure to bisphenol A:Toxicol Sci.11:15-29.
  • Honma S., Suzuki A., Buchanan DL., Katsu Y., Watanabe H., Iguchi T. 2002. Low dose effects of utero exposure to bisphenol A and Diethylstibesterol on female mice reproduction. Repro Toxicol.16:117-122.
  • Takai Y., Tsutsumi O., Ikezuki Y., Kaemi Y., Osuga Y., Yanot et al.2000. Preimplantation exposure to bisphenol A advances post natal development. Reprod Toxicol 15:71-74.
  • Honma S., Suzuki A., Buchanan DL., Katsu Y., Watanabe H., Iguchi T. 2002. Low dose effects of utero exposure to bisphenol A and Diethylstibesterol on female mice reproduction. Repro Toxicol.16:117-122.
  • Nikaido Y., Yoshizawa K., Danbara N., Tsujita Kyutoku M., Yuri T., Vehera N., et al.2004. Effects of maternal xenoestrogen exposure on development of reproductive tract and mammary gland in female CD – 1 mouse offspring. Reprod Toxicol 18:803-811.
  • Akingbemi BT., Sottas CM., Koulova AL., Klinefelter GR., Hardy MP.2004. Inhibition of testicular steroidogenesis by the xenoestrogen bisphenol A is associated with reduced pituitary luteininzing hormone secretion and decreased steroidogenic enzyme gene expression in rat testicular cells. Endocrinology 145:592-603.
  • Akingbemi BT., Sottas CM., Koulova AL., Klinefelter GR., Hardy MP.2004. Inhibition of testicular steroidogenesis by the xenoestrogen bisphenol A is associated with reduced pituitary luteininzing hormone secretion and decreased steroidogenic enzyme gene expression in rat testicular cells. Endocrinology 145:592-603.
  • Kawai K., Takehiro N., Nishikata H., Takaii M., Kuboc.2003. Aggressive behaviour in serum testosterone concentration during the maturation process of male mice: the effects of exposure to bisphenol A. Environ Health Perspect 111:175-178.
  • Al-hiyasat AS., Darmani H., Elbeticha AM.2002.Effects of bisphenol A on adult male mice fertility.Eur J Oral Sci 110:163-167.
  • Chitra KC., Latchoumycandanc C., Mathur PP.2003. Induction of oxidative stress by bisphenolA in the epididymal sperm in rats. Toxicology 185:119-127.
  • Vom Saal FS., Cooke PS., Buchanan DL., Palaza P., Thayer KA., Nagel SC., et al.1998. A physiologically based approach to the study of bisphenol A and other estrogenic chemicals in the size of reproductive organs, daily sperm production and behaviour. Toxicol Ind Health 14:239-260.
  • Markey CM., Lugue EH., Munoz D Toro M., Sonnensehein C., Soto AM.2001. In utero exposure to bisphenol A alters the developmenmt and tissue organization of the mouse mammary gland. Biol Reprod 65:1215-1223.
  • Hunt PA., Koehler KE., Susiarjo M., Hodges CM., Hogan A., Voigt RC., et al. 2003. Bisphenol A causes meiotic aneuploidy in the female mouse. Current Biol 13:546-553.
  • Al-hiyasat AS., Darmani H., Elbeticha AM.2004. Leached components from dental composites and their effects on fertility of female mice. Eur J Oral Sci 112:267-272.
  • Nikaido Y., Yoshizawa K., Danbara N., Tsujita Kyutoku M., Yuri T., Vehera N., et al.2004. Effects of maternal xenoestrogen exposure on development of reproductive tract and mammary gland in female CD – 1 mouse offspring. Reprod Toxicol 18:803-811.
  • Sawai C., Anderson K., Walser-Kuntz D.2003. Effects of bisphenol A on murine immune function: modification of Interferon alpha, IgG2a and disease symptoms in NZB NZWF.Environ Health Perspect 111:1883-1887.
  • Yoshino S., Yamaki K., Yanagisawa R., Takano H., Hayashi H., Mori Y.2003. Effects of bisphenol A on antigen specific antibody production, proliferative responses of lymphoid cells and TH2 immune responses in mice. Br J.Pharmacol:1271-1276.
  • Aloishi AM., Della Setta D., Ceccarelli I., Farabollini F.2001. Bisphenol A differently affects estrogen receptors alpha in estrous cycling and lactating female rats. NeuroSci Lett 310.
  • Ishido M., masuo Y., Kunimoto M., Oka S., Morito M. 2004. Bisphenol A causes hyperactivity in the rat concomitantly with impairment of Tyrosine Hydroxylase immunoreactivity. J Neuro Res 76:423-433.
  • Farabollini F., Porrinni S., Della Setta D, Bianchi F., Dessi Fulgheri F.2002. Effects of perineal exposure to bisphenol A on sociosexual behaviour of female and male rats. Environ Health Perspect 110(Supple3): 409-414.
  • Kubo K., Arai O., Omura M., Watanabe R., Ogata R., Aou S.2003. Low dose effects of bisphenol a on sexual differentiation of the brain and behaviour in rats. Neurosci Res 45:345-356.
  • Wozniak A L, Bulayena N N, Waison C S.2005. Xenoestrogens at picometer concentrations trigger membrane oestrogen receptor – alpha medicated ca2++ fluxes and prolactin release in GH3/B6 pitutary tumor cells. Environmental Health Perspective. 113(4):431-9.
  • Wetherill Y B, Petra C E, Monk K R, Puga A, Kmedsen K E.2002. The xenoestrogen bisphenol A induces inappropriate androgen receptor activation and mitogenesis in prostate adenocarcinomatous cells. Mol Cancer Ther 7:515-524.
  • Maclusky N J, Hajszan T, Leranth C.2005. The environmental oestrogen bisphenol A in oestrogen induced hippocampal synaptogenesis. Environmental Health Perspective. 113:675-679; doi 10.1289/Chp.7633 (onliner 24th Feb 2005).
  • Endocrine Disruptors Group.2005.BisphenolA references. Columbia, MO : Curators of University of Missouri. 37. Raloff J.1999. Food for thought: What’s coming out of babys bottle; Science News Online 156:1-4.
  • Takeuchi T, Tsutsumi O, Idezuki Y, Takai Y, Taketani Y.2004. Positive relationship between androgen and the endocrine disruptor BPA in normal women and women with ovarian dysfunction, Endocrine Journal 51(2):165-9.
  • Vom Saal F, Hughes C.2005. An extensive new literature concerning Low Dose Effects of BPA shows the need for new risk assessment. Environmental Health Perspective. 113(8):926-33.
  • Vom Saal F S, Sheehan D M.1998. Challenging Risk assessment. Forum Appl Res Public 13:11-18.
  • Vom Saal F, et al.2007. Chappel Hill BPA Expert Panel consensus Statement: Integration of mechanisms, effects in animals and potential to effect human health at current levels of exposures. Reproductive Toxicology 24(2):131-8.
  • NTP(US National Toxicology Program). 1982.”Carcinogenesis Bioassay of BPA(CAS No.80-05-7) in F344 Rats and B6C3F1 Mice (Feed Study). Technical Report Series No.215.” NTP Research Triangle Park.N.C.
  • Huff J.2002. Carcinogenecity of Bisphenol A revisited. Toxicol Sci 70:281-283.
  • Calafat A M, Yex, Wong L Y, Reidy J A, Needham L L. 2007.Exposure of the US population to bisphenol a and 4-tertiary octylphenol: 2003-2004. Environmental Health Perspective. Advance copy, online 24th October 2007.
  • CERHR Expert Panel Report for Bisphenol a (http:// cerhr.niehs.nih.gov/chemi cals/bisphenol A/BPA Final EPVF 112607.pdf.”) Retrieved on 2007-12-07.
  • MatsumotoA, Kitagawa K, Isse T, Oyama T, Foureman G L, Morita M, Kawamoto T. 2003. bisphenol A levels in human urine. Environmental Health Perspectives 111(1):101-4
  • and 37. Howshedel K, A K Hotchkiss, K A Thayer, J G Vandenbergh and F S Vom Saal. 1999. Plastic bisphenol A speeds growth and puberty. Nature 401:762-764.
  • E.C.Rodds and W.Lawson. “Synthetic Oestrogenic Agents without the Phenanthrene Nucleus.” Nature 137(1936), 996.
  • Morrissey et al 1987, George et al 1985, Reel et al 1984, 1987 – A series of studies from the NTP examining the teratogenic potential of BPA in rats and mice.

Abstract Views: 294

PDF Views: 0




  • The Chemical BPA - a Threat to Human Life?

Abstract Views: 294  |  PDF Views: 0

Authors

Chandan Datta
Birla Institute of Technology, Mesra, Ranchi, India
Suparna Datta
Institute of Post Graduate Medical Education & Research, Kolkata, India
U. B. RoyChowdhury
Institute of Post Graduate Medical Education & Research, Kolkata, India

Abstract


Bisphenol A (BPA) is a monomer used to manufacture polycarbonate plastics, the resin of cans and other products with global capacity in excess of 6.4 billion pounds per year. Because ester bonds in these BPA based polymers are subjected to hydrolysis, leaching of BPA has wide spread human exposure. A recent report prepared by Harvard Center for Risk and funded by the American Plastic Council concluded that evidence for low dose effect of BPA is weak on the basis of a review of only 19 studies; the report was issued after a delay of 2.5 years. A current comprehensive literature review reveals that the opposite is true of December'2004, there were 115 published in vivo studies of low dose effect of BPA, and 94 of these report significant effects. In 31 publications of vertebrate and invertebrate animals, significant effect occurred below the predicted "safe" or Reference 50microgram/kg/day BPA. An oestrogenic mode of action of BPA is confirmed by an in vitro study which describes disruption of cell function at.23ppt. nonetheless, chemical manufacturer continue to discount these published findings because no industry funded have reported significant effects of low doses of BPA, although more than 90% of Government funded reports have noted significant effects.

Keywords


Bisphenol A, Endocrine Disruption, Plastic, Low Dose Effects, Toxicities

References