In utero effects of maternal phthalate exposure on male genital development

2019 ◽  
Vol 39 (3) ◽  
pp. 209-218 ◽  
Author(s):  
Rebecca J. Wineland ◽  
Michael S. Bloom ◽  
Lori Cruze ◽  
Celeste D. Butts ◽  
Abby G. Wenzel ◽  
...  
2017 ◽  
Vol 216 (1) ◽  
pp. S282-S283
Author(s):  
Rebecca J. Wineland ◽  
Michael S. Bloom ◽  
Lori Cruze ◽  
Celeste D. Butts ◽  
Abby G. Wenzel ◽  
...  

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

2016 ◽  
Vol 46 (5) ◽  
pp. 236
Author(s):  
Ida Bagus Andhita ◽  
Wayan Bikin Suryawan

5-alpha-reductase (5-ARD) type 2 deficiencyis an autosomal sex-linked disorder, resulting inthe inability to convert testosterone to the morephysiological active dihydrotestosterone (DHT).DHT is the most potent androgen, bound selec-tively to the androgen receptors in genital skin andfibroblasts, making its action necessary for the de-velopment of normal male genital anatomy. SinceDHT is required for normal masculinizaton of theexternal genitalia in utero, genetic males with 5-ARD are usually born with ambiguous genitalia(male pseudohermaphroditism). The hallmarkof 5-ARD is elevated ratio of serum testosteroneto DHT. In healthy prepubertal children, thebaseline testosterone-to-DHT ratio is 1:2. Thispaper reports a 20-month old patient with malepseudohermaphroditism due to 5-alpha reductasetype-2 deficiency.


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

FEBS Letters ◽  
2005 ◽  
Vol 579 (19) ◽  
pp. 4131-4137 ◽  
Author(s):  
Noriko Hamada ◽  
Carl-Magnus Bäckesjö ◽  
C.I. Edvard Smith ◽  
Daisuke Yamamoto

2012 ◽  
Vol 2012 ◽  
pp. 1-15 ◽  
Author(s):  
K. A. Mooslehner ◽  
J. D. Davies ◽  
I. A. Hughes

Partial androgen insensitivity syndrome (PAIS) is associated with impaired male genital development and can be transmitted through mutations in the androgen receptor (AR). The aim of this study is to develop a cell model suitable for studying the impact AR mutations might have on AR interacting proteins. For this purpose, male genital development relevant mouse cell lines were genetically modified to express a tagged version of wild-type AR, allowing copurification of multiprotein complexes under native conditions followed by mass spectrometry. We report 57 known wild-type AR-interacting proteins identified in cells grown under proliferating and 65 under nonproliferating conditions. Of those, 47 were common to both samples suggesting different AR protein complex components in proliferating and proliferation-inhibited cells from the mouse proximal caput epididymus. These preliminary results now allow future studies to focus on replacing wild-type AR with mutant AR to uncover differences in protein interactions caused by AR mutations involved in PAIS.


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 ◽  
...  

2017 ◽  
Vol 102 (6) ◽  
pp. 1870-1878 ◽  
Author(s):  
Sheela Sathyanarayana ◽  
Samantha Butts ◽  
Christina Wang ◽  
Emily Barrett ◽  
Ruby Nguyen ◽  
...  

Abstract Context: Adequate sex steroid hormone concentrations are essential for normal fetal genital development in early pregnancy. Our previous study demonstrated an inverse relationship between third-trimester di-2-ethyl hexyl phthalate exposure and total testosterone (TT) concentrations. Here, we examine early-pregnancy phthalates, sex steroid hormone concentrations, and newborn reproductive outcomes. Design: We examined associations between urinary phthalate metabolite concentrations in early pregnancy and serum free testosterone (FT), TT, estrone (E1), and estradiol (E2) in 591 woman/infant dyads in The Infant Development and Environment Study; we also examined relationships between hormones and newborn genital outcomes using multiple regression models with covariate adjustment. Results: E1 and E2 concentrations were 15% to 30% higher in relation to 1-unit increases in log monoisobutyl phthalate (MiBP), mono-2-ethyl hexyl phthalate, and mono-2-ethyl-5-oxy-hexyl phthalate concentrations, and E2 was 15% higher in relation to increased log monobenzyl phthalate (MBzP). FT concentrations were 12% lower in relation to 1-unit increases in log mono(carboxynonyl) phthalate (MCNP) and mono-2-ethyl-5-carboxypentyl phthalate concentrations. Higher maternal FT was associated with a 25% lower prevalence of having a male genital abnormality at birth. Conclusions: The positive relationships between MiBP, MBzP, and DEHP metabolites and E1/E2 are unique and suggest a positive estrogenic effect in early pregnancy. The inverse relationship between MCNP and DEHP metabolites and serum FT supports previous work examining phthalate/testosterone relationships later in pregnancy. Higher FT in relation to a 25% lower prevalence of male genital abnormalities confirms the importance of testosterone in early fetal development.


2004 ◽  
Vol 172 (4 Part 2) ◽  
pp. 1725-1730 ◽  
Author(s):  
SELCUK YUCEL ◽  
ANTONIO DESOUZA ◽  
LAURENCE S. BASKIN
Keyword(s):  
In Utero ◽  

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