Exposure to genistein during gestation and lactation demasculinizes the reproductive system in rats

Amy B. Wisniewski, Sabra L Klein, Yegappan Lakshmanan, John Phillip Gearhart

Research output: Contribution to journalArticle

Abstract

Purpose: Exposure to the phytoestrogen genistein (Indofine Chemical Co., Somerville, New Jersey) can disrupt normal male sexual differentiation. To determine if perinatal (that is gestation and lactation) genistein exposure at doses common in human diets alters masculinization we examined the development of the external genitalia, testes, wolffian ducts and sexual behavior in male rats exposed to genistein supplemented diets during early development. Materials and Methods: Female rats were fed a phytoestrogen-free diet supplemented with no genistein (free), a low genistein dose (low) or a high genistein dose (high) throughout gestation and lactation. Anogenital distance of male offspring was measured weekly from postnatal days 2 to 21. At puberty (postnatal day 40 to 45) preputial separation, and testis length and width of male offspring were measured. At age 70 days reproductive organ masses, plasma testosterone concentration, sperm counts and sexual behavior were assessed in male offspring. Results: Exposure to genistein resulted in temporary, prepubertal urogenital abnormalities at postnatal days 21 and 40. Males exposed to genistein had smaller anogenital distance and testis size, and delayed preputial separation. Perinatal exposure to genistein also caused long-term dysfunction in reproductive behavior, in which adult males exposed to genistein were less likely to mount, intromit and ejaculate during mating tests. Males exposed to genistein also had lower testosterone concentrations in adulthood. Conclusions: Perinatal genistein exposure results in transient and lasting alterations in masculinization of the reproductive system. These results extend our knowledge of the effects of early genistein exposure on male development and may have implications for human health in terms of potential relationships of endocrine disrupters and urogenital abnormalities thought to be increasing in incidence in boys and men.

Original languageEnglish (US)
Pages (from-to)1582-1586
Number of pages5
JournalJournal of Urology
Volume169
Issue number4
DOIs
StatePublished - Apr 1 2003
Externally publishedYes

Fingerprint

Genistein
Lactation
Pregnancy
Urogenital Abnormalities
Testis
Phytoestrogens
Diet
Sexual Behavior
Testosterone
Wolffian Ducts
Reproductive Behavior
Sex Differentiation
Sperm Count
Genitalia
Puberty

Keywords

  • Estrogens
  • Genistein
  • Male
  • Puberty, delayed
  • Urogenital abnormalities

ASJC Scopus subject areas

  • Urology

Cite this

Exposure to genistein during gestation and lactation demasculinizes the reproductive system in rats. / Wisniewski, Amy B.; Klein, Sabra L; Lakshmanan, Yegappan; Gearhart, John Phillip.

In: Journal of Urology, Vol. 169, No. 4, 01.04.2003, p. 1582-1586.

Research output: Contribution to journalArticle

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abstract = "Purpose: Exposure to the phytoestrogen genistein (Indofine Chemical Co., Somerville, New Jersey) can disrupt normal male sexual differentiation. To determine if perinatal (that is gestation and lactation) genistein exposure at doses common in human diets alters masculinization we examined the development of the external genitalia, testes, wolffian ducts and sexual behavior in male rats exposed to genistein supplemented diets during early development. Materials and Methods: Female rats were fed a phytoestrogen-free diet supplemented with no genistein (free), a low genistein dose (low) or a high genistein dose (high) throughout gestation and lactation. Anogenital distance of male offspring was measured weekly from postnatal days 2 to 21. At puberty (postnatal day 40 to 45) preputial separation, and testis length and width of male offspring were measured. At age 70 days reproductive organ masses, plasma testosterone concentration, sperm counts and sexual behavior were assessed in male offspring. Results: Exposure to genistein resulted in temporary, prepubertal urogenital abnormalities at postnatal days 21 and 40. Males exposed to genistein had smaller anogenital distance and testis size, and delayed preputial separation. Perinatal exposure to genistein also caused long-term dysfunction in reproductive behavior, in which adult males exposed to genistein were less likely to mount, intromit and ejaculate during mating tests. Males exposed to genistein also had lower testosterone concentrations in adulthood. Conclusions: Perinatal genistein exposure results in transient and lasting alterations in masculinization of the reproductive system. These results extend our knowledge of the effects of early genistein exposure on male development and may have implications for human health in terms of potential relationships of endocrine disrupters and urogenital abnormalities thought to be increasing in incidence in boys and men.",
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