A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
RoyChowdhury, U. B.
- The Chemical BPA - a Threat to Human Life?
Authors
1 Birla Institute of Technology, Mesra, Ranchi, IN
2 Institute of Post Graduate Medical Education & Research, Kolkata, IN
3 Institute of Post Graduate Medical Education & Research, Kolkata, IN
Source
Indian Journal of Forensic Medicine & Toxicology, Vol 3, No 1 (2009), Pagination: 21-25Abstract
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, ToxicitiesReferences
- 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.
- Surrogacy—The Bless or Curse of Technological Advancement
Authors
1 Dept of Forensic and State Medicine, IPGMER, 244, AJC Bose Road, Kolkata 700020, IN
2 Dept of Forensic and State Medicine, Institute of Post Graduate Medical Education and Research (IPGMER)
3 Senior Lecturer, Dept of Polymer Science and Technology, Birla Institute of Technology, Mesra, Ranchi, IN
Source
Indian Science Cruiser, Vol 24, No 1 (2010), Pagination: 8-11Abstract
The word Surrogate is derived from the latin Subrogare means to substitute. The procedure of surrogacy is the Brain Child of ART or Assisted Reproductive Techniques which is considered as one of the bless of modem technological advancement that has given smiles to the faces of many infertile couples.
According to this technique, a surrogate mother is a woman agreeing to have an embryo generated from the sperm of a man who is not her husband and the oocyte of another woman implanted in her womb to carry the pregnancy to full term and deliver the child to its biological parents.
Unfortunately the curtain raising incidence that produced much hue and cry among the social activists about the necessity of this procedure is the delivery of a surrogate baby at Apollo Gleneagles Hospital, Kolkata on 25th of Sept'2008, where contrary to the guidelines given in the Surrogate Bill to be passed by the Parliament, the surrogate mother was a 46 years old Indian woman who was provided with Rs.3000/- per month as maintenance charge during pregnancy and Rs.3 lakhs on successful delivery of the baby and handing it over to the biological parents who were US citizens. Thus came into view out of a sudden oblivion about a nexus of Medical Tourism and surrogacy, spreading rapidly in the whole society in the name of technological advancement.
- The Chill Thrill
Authors
1 IPGMR&R, Kolkata, IN
Source
Indian Science Cruiser, Vol 23, No 1 (2009), Pagination: 17-20Abstract
This article is about one of the most toxic herbicide, the Paraquat, in the beverage Cola which resembles it in appearance. Although the sale of cola has been banned in some areas eg. in Kerala of India by a Government Order No. (Rt)No. 2396/06/II&FWD dated 10.08.2006 because of its residues of organochlorine pesticides like Chloropyrophos and Malathion, one of the most dangerous quarternary ammonium compound, the Paraquat that resembles cola has not been much mentioned. The cola is a carbonated soU drink sold in stores throughout the world after its recipe was first invented by John Pemberton originally in the name of coca wine in 1885. He intended it as a patent medicine but the patent was bought out by a businessman Asa Griggs Candler, whose marketing tactics led this cola to its dominance of the world of soft drink market throughout the 20th and now the 21st century. In acute toxicity studies using laboratory animals, Paraquat has been shown to be highly toxic by the inhalation route and has been placed in Toxicity Category I (the highest of four levels). However the p]PA has determined that particles used in agricultural practices (400-800 nanomicron) are well beyond the respirable range. It shows category II toxicity in the oral route and moderately toxic that is category III by the dermal route. Paraquat will cause moderate to severe eye irritation and minimal dermal irritation, and has been placed in toxicity categories II and IV (slightly toxic) for these effects.- Criminal Profiling: the reality behind the myth
Authors
1 Dept. of Forensic and State Medicine, Institute of Postgraduate Medical Education and Research, 244, AJC Bose Road, Kolkata- 700 020, IN
2 Dept. of Forensic and State Medicine, Institute of Postgraduate Medical Education and Research, Kolkata, IN
3 Dept. of Forensic and State Medicine, N.R.S. Medical College, Kolkata, IN
4 Dept. of Pathology, Midnapore Medical College, Paschim Mediuipur, West Bengal, IN
Source
Indian Science Cruiser, Vol 23, No 5 (2009), Pagination: 54-57Abstract
In contemporary criminology, with the advent of Criminal Profiling, criminal investigative procedure has changed dramatically. Various theories and methodologies of criminal profiling have been proposed e.g., FBI's Crime Scene Analysis, Brent Turve^s Behavioral Evidence Analysis, Canter's Profiling Technique etc. It is certain that in near fiiture, Criminal Profiling will play a decisive role in modem criminal investigation.Keywords
criminal profiling, crime, behaviour, victim.- Virtual Autopsy - The future of Forensic Medicine
Authors
1 Department of Forensic and State Medicine, Institute of Postgraduate Medical Education & Research, 244 A .J.C. Bose Road, Kolkata-20 W.B., IN
2 Department of Pathology, Midnapore Medical College, Paschim Medinipur, W.B., IN