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Updated: Oct 5, 2026

Long-term Behavioral and Reproductive Consequences of Embryonic Exposure to Low-dose Toxicants
Published on: March 6, 2018
From malformations to molecular mechanisms in the male: three decades of research on endocrine disrupters
J A McLachlan1, R R Newbold, M E Burow
1Environmental Endocrinology Laboratory, Center for Bioenvironmental Research at Tulane and Xavier Universities, New Orleans, LA 70112, USA. john.mclachlan@tulane.edu
Abstract:
For three decades, we have known that estrogens alter the development of the mammalian reproductive system in predictable ways. In mice exposed prenatally to diethylstilbestrol (DES) or other estrogens, the male offspring exhibit structural malformations including cryptorchidism, epididymal cysts and retained Mullerian ducts. The estrogen-associated alterations in the genital tract phenotype can be usefully considered as a model called Developmental Estrogenization Syndrome. While estrogen treatment during critical periods of morphogenesis of the male reproductive system has been associated with these changes, the mechanisms at the molecular level are still being discovered. Parallel findings on the hormones involved in Mullerian duct regression and testicular descent have helped guide research on the mechanisms of developmental estrogenization of the male. Cellular localization of molecular signals associated with key steps in genital tract development, use of mice with gene disruption, and knowledge of the mechanisms underlying persistent changes in gene expression are beginning to provide a blue print for both the physiological role and pathological effects of estrogens in reproductive tract development. Since many of the same biological principles underlie genital tract morphogenesis in mammals, one may expect some of the same changes in males of other species exposed to estrogen during the appropriate developmental periods.
Insights
Prenatal estrogen exposure, such as diethylstilbestrol (DES), causes male reproductive system malformations. Research is uncovering the molecular mechanisms behind this Developmental Estrogenization Syndrome in mammals.
Area of Science:
- Reproductive biology
- Developmental toxicology
- Endocrinology
Background:
- Estrogens are known to impact mammalian reproductive system development.
- Prenatal exposure to estrogens like diethylstilbestrol (DES) in mice leads to specific male offspring malformations.
Purpose of the Study:
- To explore the molecular mechanisms underlying estrogen-induced alterations in male reproductive tract development.
- To utilize the Developmental Estrogenization Syndrome model for further research.
Main Methods:
- Investigating molecular signals during critical periods of male reproductive tract morphogenesis.
- Employing genetically modified mice (gene disruption).
- Analyzing persistent changes in gene expression.
Main Results:
- Identified structural malformations in male offspring exposed prenatally to estrogens, including cryptorchidism, epididymal cysts, and retained Mullerian ducts.
- Elucidated molecular mechanisms contributing to the Developmental Estrogenization Syndrome.
- Established a blueprint for understanding estrogen's effects on reproductive tract development.
Conclusions:
- Estrogen exposure during critical developmental periods causes predictable alterations in the male reproductive system.
- Understanding these mechanisms provides insights into both physiological roles and pathological effects of estrogens.
- Similar effects are anticipated in other species exposed to estrogens during development.
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