Differential accumulation of BPA in some tissues of offspring of Balb-C mice exposed to different BPA doses

Environmental Toxicology and Pharmacology

Volumn 33, Issue 1, 2012, Pages 9-15

  Mita, L ^a,b   Baldi, A ^a,b,c   Diano, N ^a,b,d   Viggiano, E ^a,b   Portaccio, M ^a,b   Nicolucci, C ^a,d   Grumiro, L ^a,b   Menale, C ^a,b   Mita, D G ^a,b,d   Spugnini, E P ^e   Viceconte, R ^c   Citro, G ^e   Pierantoni, R ^a,b   Sica, V ^a,b   Marino, M ^a,f   Signorile, P G ^c   Bianco, M ^a,b  

^a NATIONAL INSTITUTE OF BIOSTRUCTURES AND BIOSYSTEMS   (Italy)

^b SECOND UNIVERSITY OF NAPLES   (Italy)

^c Fondazione Italiana Endometriosi   (Italy)

^d INSTITUTE OF GENETICS AND BIOPHYSICS ADRIANO BUZZATI TRAVERSO   (Italy)

^e REGINA ELENA NATIONAL CANCER INSTITUTE   (Italy)

^f ROMA TRE UNIVERSITY   (Italy)

Author keywords

BPA; Endocrine disruptors; Gender difference; Mice

Indexed keywords

4,4' ISOPROPYLIDENEDIPHENOL;

ADULT ANIMAL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOACCUMULATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DELIVERY; DRUG EXPOSURE; FEMALE; FOREBRAIN; GESTATION PERIOD; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; LIVER; MALE; MOUSE; MUSCLE; NONHUMAN; PREGNANCY; PRIORITY JOURNAL; PROGENY; RHOMBENCEPHALON; SEX DIFFERENCE;

ANIMALS; ESTROGENS, NON-STEROIDAL; FEMALE; HUMANS; MALE; MICE; MICE, INBRED BALB C; PHENOLS; PREGNANCY; TISSUE DISTRIBUTION;

MUS;

EID: 80055025170     PISSN: 13826689     EISSN: 18727077     Source Type: Journal    
DOI: 10.1016/j.etap.2011.09.008     Document Type: Article

References (31)

1. Bakker J., De Mees C., Douhard Q., Balthazart J., Gabant P., Szpirer J., Szpirer C. Alpha-fetoprotein protects the developing female mouse brain from masculinization and defeminization by estrogens. Nat. Neurosci. 2006, 9(2):220-226.
2. Bakker J., Baum M.J. Role for estradiol in female-typical brain and behavioral sexual differentiation. Front. Neuroendocrinol. 2008, 29(1):1-16.
3. Bianco M., Mita L., Portaccio M., Diano N., Sica V., De Luca B., Mita D.G., Romano Carratelli C., Viggiano E. Differential accumulation levels in the brain of rats exposed to the endocrine disruptor 4-tert-octylphenol (OP). Environ. Toxicol. Pharmacol. 2011, 31:198-204.
4. Cox K.H., Gatewood J.D., Howeth C., Rissman E.F. Gestational exposure to bisphenol A and cross-fostering affect behaviours in juvenile mice. Horm. Behav. 2010, 58(5):754-761.
5. Diano N., Grano V., Fraconte L., Caputo P., Ricupito A., Attanasio A., Bianco M., Bencivenga U., Rossi S., Manco I., et al. Nonisothermal bioreactors in enzymatic remediation of waters polluted by endocrine disruptors: the BPA as model of pollutant. Appl. Catal. B: Environ. 2007, 69:252-261.
6. Fenton S.E. Endocrine-disrupting compounds and mammary gland development: early exposure and later life consequences. Endocrinology 2006, 147(6 Suppl.):S18-S24.
7. Georgieva S., Godjevargova T., Mita D.G., Diano N., Menale C., Nicolucci C., Romano Carratelli C., Mita L., Golovinsky E. Non-isothermal bioremediation of waters polluted by phenol and some of its derivatives by laccase covalently immobilized on polypropylene membranes. J. Mol. Catal. B: Enzym. 2010, 66:210-218.
8. Georgieva S., Godjevargova T., Portaccio M., Lepore M., Mita D.G. Advantages in using non-isotermal bioreactors in bioremediation of water polluted by phenol by means of immobilized laccase from Rhus vernicifera. J. Mol. Catal. B: Enzym. 2008, 55:177-184.
9. Gioiosa L., Fissore E., Ghirardelli G., Parmigiani S., Palanza P. Developmental exposure to low-dose estrogenic endocrine disruptors alters sex differences in exploration and emotional responses in mice. Horm. Behav. 2007, 52(3):307-316.
10. Howdeshell K.L., Hotchkiss A.K., Thayer K.A., Vandenbergh J.G., vom Saal F.S. Exposure to bisphenol A advances puberty. Nature 1999, 401(6755):763-764.
11. Keller M., Pawluski J.L., Brock O., Douhard Q., Bakker J. The α-fetoprotein knock-out mouse model suggests that parental behavior is sexually differentiated under the influence of prenatal estradiol. Horm. Behav. 2010, 57(4-5):434-440.
12. Kubo K., Arai O., Omura M., Watanabe R., Ogata R., Aou S. Low dose effects of bisphenol A on sexual differentiation of the brain and behavior in rats. Neurosci. Res. 2003, 45:345-356.
13. Mita D.G., Diano N., Grano V., Portaccio M., Rossi S., Bencivenga U., Manco I., Nicolucci C., Bianco M., Grimaldi T., et al. The process of thermodialysis in bioremediation of waters polluted by endocrine disruptors. J. Mol. Catal. B: Enzym. 2009, 58:199-2007.
14. Mita L., Bianco M., Viggiano E., Zollo F., Bencivenga U., Sica V., Monaco G., Portaccio M., Diano N., Colonna A., et al. Bisphenol A content in fish caught in two different sites of the Tyrrhenian Sea (Italy). Chemosphere 2011, 82:405-410.
15. Nishikawa M., Iwano H., Yanagisawa R., Koike N., Inoue H., Yokota H. Placental transfer of conjugated bisphenol A and subsequent reactivation in the rat fetus. Environ. Health Perspect. 2010, 118:1196-1203.
16. Okada H., Tokunaga T., Liu X., Takayanagi S., Matsushima A., Shimohigashi Y. Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma. Environ. Health Perspect. 2008, 116:32-38.
17. Palanza P.L., Howdeshell K.L., Parmigiani S., vom Saal F.S. Exposure to a low dose of bisphenol A during fetal life or in adulthood alters maternal behavior in mice. Environ. Health Perspect. 2002, 110:415-422.
18. Ramos J.G., Varayoud J., Sonnenschein C., Soto A.M., Munoz De Toro M., Luque E.H. Prenatal exposure to low doses of bisphenol A alters the periductal stroma and glandular cell function in the rat ventral prostate. Biol. Reprod. 2001, 65:1271-1277.
19. Richter C.A., Birnbaum L.S., Farabollini F., Newbold R.R., Rubin B.S., Talsness C.E., Vandenbergh J.G., Walser-Kuntz D.R., vom Saal F.S. In vivo effects of bisphenol A in laboratory rodent studies. Reprod. Toxicol. 2007, 24:199-224.
20. Ricupito A., Del Pozzo G., Diano N., Grano V., Portaccio M., Marino M., Bolli A., Galluzzo P., Bontempo P., Mita L., et al. Effect of bisphenol A with or without enzyme treatment on the proliferation and viability of MCF-7 cells. Environ. Int. 2009, 35:21-26.
21. Rubin B.S., Lenkowski J.R., Schaeberle C.M., Vandenberg L.N., Ronsheim P.M., Soto A.M. Evidence of altered brain sexual differentiation in mice exposed perinatally to low, environmentally relevant levels of bisphenol A. Endocrinology 2006, 147(8):3681-3691.
22. Schonfelder G., Wittfoht W., Hopp H., Talsness C.E., Paul M., Chahoud I. Parent bisphenol A accumulation in the human maternal-fetal-placental unit. Environ. Health Perspect. 2002, 110(11):A703-A707.
23. Selevan S.G., Kimmel C.A., Mendola P. Identifying critical windows of exposure for children's health. Environ. Health Perspect. 2000, 108:451-455.
24. Signorile P.G., Spugnini E.P., Mita L., Mellone P., D'Avino A., Bianco M., Diano N., Caputo L., Rea F., Viceconte R., et al. Pre-natal exposure of mice to bisphenol A elicits an endometriosis-like phenotype in female offspring. Gen. Comp. Endocrinol. 2010, 168:318-325.
25. Takahashi O., Oishi S. Disposition of orally administered 2,2-bis(4-hydroxyphenyl)propane (Bisphenol A) in pregnant rats and the placental transfer to fetuses. Environ. Health Perspect. 2000, 108:931-935.
26. Timms B.G., Howdeshell K.L., Barton L., Bradley S., Richter C.A., vom Saal F.S. Estrogenic chemicals in plastic and oral contraceptives disrupt development of the fetal mouse prostate and urethra. Proc. Natl. Acad. Sci. U. S. A. 2005, 102:7014-7019.
27. Vivacqua A., Recchia A.G., Fasanella G., Gabriele S., Carpino A., Rago V., Di Gioia M.L., Leggio A., Bonofiglio D., Liguori A., et al. The food contaminants bisphenol A and 4-nonylphenol act as agonists for estrogen receptor alpha in MCF7 breast cancer cells. Endocrine 2003, 22:275-284.
28. Volkel W., Kiranoglu M., Fromme H. Determination of free and total bisphenol A in human urine to assess daily uptake as a basis for a valid risk assessment. Toxicol. Lett. 2008, 179:155-162.
29. Welshons W.V., Nagel S.C., vom Saal F.S. Large effects from small exposures. III. Endocrine mechanisms mediating effects of bisphenol A at levels of human exposure. Endocrinology 2006, 147:S56-S69.
30. Xu L.C., Sun H., Chen J.F., Bian Q., Qian J., Song L., Wang X.R. Evaluation of androgen receptor transcriptional activities of bisphenol A, octylphenol and nonylphenol in vitro. Toxicology 2005, 216:197-203.
31. Yokota H., Iwano H., Endo M., Kobayashi T., Inoue H., Ikushiro S., Yuasa A. Glucuronidation of the environmental oestrogen bisphenol A by an isoform of UDP-glucuronosyltransferase, UGT2B1, in the rat liver. Biochem. J. 1999, 340:405-409.