scholarly journals The orl Rat with Inherited Cryptorchidism Has Increased Susceptibility to the Testicular Effects of In Utero Dibutyl Phthalate Exposure

2008 ◽  
Vol 105 (2) ◽  
pp. 360-367 ◽  
Author(s):  
Kamin J. Johnson ◽  
Suzanne M. McCahan ◽  
Xiaoli Si ◽  
Liam Campion ◽  
Revital Herrmann ◽  
...  
Chemosphere ◽  
2022 ◽  
Vol 287 ◽  
pp. 132046
Author(s):  
Tongtong Zhang ◽  
Xiang Zhou ◽  
Xu Zhang ◽  
Xiaohan Ren ◽  
Jiajin Wu ◽  
...  

2019 ◽  
Vol 3 ◽  
pp. 428-429
Author(s):  
Watkins D ◽  
Zimmerman E ◽  
Manjourides J ◽  
Hines M ◽  
Huerta-Montañez G ◽  
...  
Keyword(s):  
In Utero ◽  

2019 ◽  
Vol 37 (21) ◽  
pp. 1800-1809 ◽  
Author(s):  
Thomas P. Ahern ◽  
Anne Broe ◽  
Timothy L. Lash ◽  
Deirdre P. Cronin-Fenton ◽  
Sinna Pilgaard Ulrichsen ◽  
...  

PURPOSE Phthalate exposure is ubiquitous and especially high among users of drug products formulated with phthalates. Some phthalates mimic estradiol and may promote breast cancer. Existing epidemiologic studies on this topic are small, mostly not prospective, and have given inconsistent results. We estimated associations between longitudinal phthalate exposures and breast cancer risk in a Danish nationwide cohort, using redeemed prescriptions for phthalate-containing drug products to measure exposure. METHODS We ascertained the phthalate content of drugs marketed in Denmark using an internal Danish Medicines Agency ingredient database. We enrolled a Danish nationwide cohort of 1.12 million women at risk for a first cancer diagnosis on January 1, 2005. By combining drug ingredient data with the Danish National Prescription registry, we characterized annual, cumulative phthalate exposure through redeemed prescriptions. We then fit multivariable Cox regression models to estimate associations between phthalate exposures and incident invasive breast carcinoma according to tumor estrogen receptor status. RESULTS Over 9.99 million woman-years of follow-up, most phthalate exposures were not associated with breast cancer incidence. High-level dibutyl phthalate exposure (≥ 10,000 cumulative mg) was associated with an approximately two-fold increase in the rate of estrogen receptor–positive breast cancer (hazard ratio, 1.9; 95% CI, 1.1 to 3.5), consistent with in vitro evidence for an estrogenic effect of this compound. Lower levels of dibutyl phthalate exposure were not associated with breast cancer incidence. CONCLUSION Our results suggest that women should avoid high-level exposure to dibutyl phthalate, such as through long-term treatment with pharmaceuticals formulated with dibutyl phthalate.


2019 ◽  
Vol 222 (1) ◽  
pp. 101-110 ◽  
Author(s):  
Feiby L. Nassan ◽  
Tim I.M. Korevaar ◽  
Brent A. Coull ◽  
Niels E. Skakkebæk ◽  
Stephen A. Krawetz ◽  
...  

2016 ◽  
Vol 2016 (1) ◽  
Author(s):  
Deborah J. Watkins* ◽  
Karen E. Peterson ◽  
Alejandra Cantoral ◽  
Maritsa Solano-Gonzalez ◽  
Martha-Maria Tellez-Rojo ◽  
...  

2019 ◽  
Vol 38 (8) ◽  
pp. 899-913 ◽  
Author(s):  
NP de Souza ◽  
AP Ferragut Cardoso ◽  
LMM Gomide ◽  
TRR Lima ◽  
HA Miot ◽  
...  

Cryptorchidism (CPT), the most common male congenital abnormality, is variably associated with other male reproductive tract problems. We evaluated if cryptorchid rats develop enhanced testicular susceptibility to dibutyl phthalate (DBP) or acrylamide (AA) after extended exposure. Three studies with rats were performed: (1) in utero and postnatal exposure to DBP or AA; (2) establishment of CPT and orchiopexy; and (3) in utero and postnatal exposures to DBP or AA associated with CPT/orchiopexy. Seminiferous tubules were histologically scored according to the severity of lesions: (1) Rats exposed to DBP (score 1.5) or AA (score 1.1) presented mostly preserved spermatogenesis. Some seminiferous tubules showed vacuolated germinative epithelium, germ cell apoptosis, and a Sertoli cell-only (SCO) pattern. (2) CPT (score 3.3) resulted in decreased absolute testes weights, degenerated and SCO tubules, and spermatogenesis arrest that were reversed by orchiopexy (score 1.1). (3) Exposure to DBP or AA with CPT/orchiopexy led to atrophic testes, spermatogenesis arrest, germ cell exfoliation/multinucleation, and SCO tubules (both chemicals score 2.5). Exposure to chemicals such as DBP or AA prevented the recovery of cryptorchid testes by orchiopexy. The possible role of environmental contaminants should be considered when looking for factors that modulate human testicular disorders associated with CPT.


2013 ◽  
Vol 2013 (1) ◽  
pp. 5894
Author(s):  
John D. Meeker ◽  
Kelly K. Ferguson ◽  
Alejandra Cantoral Preciado ◽  
Karen E. Peterson ◽  
Martha Maria Tellez-Rojo Solis

2016 ◽  
Vol 2016 (1) ◽  
Author(s):  
Deborah J. Watkins* ◽  
John D. Meeker ◽  
Lourdes Schnaas ◽  
Maritsa Solano-Gonzalez ◽  
Erika Osorio-Valencia ◽  
...  

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