TY - JOUR
T1 - Perinatal exposure to genistein alters reproductive development and aggressive behavior in male mice
AU - Wisniewski, Amy B.
AU - Cernetich, Amy
AU - Gearhart, John P.
AU - Klein, Sabra L.
N1 - Funding Information:
We thank Dr. Patrick C. Walsh, Professor and Director of the Brady Urological Institute, Mr. Robert D. Carl III and Ms. Anne Currie for their generous support of this project. We also thank Benjamin Graff, Peter Klein, Jocelyn Reider and Tom Novak for assistance with data collection and Randy Nelson, Andrew Hotchkiss and Michelle Gatien for assistance with the radioimmunoassay. This research was supported by NIH HD 37940 (ABW), NIH AI 054995 (SLK) and in part by NIH MH 57535 (RJN).
PY - 2005/2/15
Y1 - 2005/2/15
N2 - Exposure to endocrine disrupting chemicals adversely affects reproductive development and behavior in males. The goal of this study was to determine if exposure to genistein, an isoflavone found in soy, during early periods of sex differentiation alters reproductive development and behavior in male mice. Female C57BL/6 mice were fed a phytoestrogen-free diet supplemented with 0, 5 or 300 mg/kg of genistein throughout gestation and lactation. Anogenital distance (AGD) and body mass of male offspring was measured weekly from postnatal days 2-21, timing of preputial separation was assessed at puberty, and in adulthood, reproductive organ masses, sperm and testosterone production, and reproductive and aggressive behaviors were assessed. Exposure to genistein resulted in smaller AGD are reduced body mass, with the low-dose diet exerting a greater effect. Timing of preputial separation, adult reproductive behavior, sperm concentrations and testosterone production were not influenced by genistein treatment at either dose. Aggressive behaviors were decreased, whereas defensive behaviors were increased, in males that received the low-dose genistein diet. Exposure to genistein during critical periods of sex differentiation results in concurrent and persistent demasculinization in male mice. Phenotypic and behavioral abnormalities induced by genistein showed a non-monotonic response, where treatment with a low dose exerted a greater effect than treatment with a high dose of genistein. Given the popularity of soy infant formulas, the influence isoflavone exposure on reproductive and behavioral health in boys and men should be considered.
AB - Exposure to endocrine disrupting chemicals adversely affects reproductive development and behavior in males. The goal of this study was to determine if exposure to genistein, an isoflavone found in soy, during early periods of sex differentiation alters reproductive development and behavior in male mice. Female C57BL/6 mice were fed a phytoestrogen-free diet supplemented with 0, 5 or 300 mg/kg of genistein throughout gestation and lactation. Anogenital distance (AGD) and body mass of male offspring was measured weekly from postnatal days 2-21, timing of preputial separation was assessed at puberty, and in adulthood, reproductive organ masses, sperm and testosterone production, and reproductive and aggressive behaviors were assessed. Exposure to genistein resulted in smaller AGD are reduced body mass, with the low-dose diet exerting a greater effect. Timing of preputial separation, adult reproductive behavior, sperm concentrations and testosterone production were not influenced by genistein treatment at either dose. Aggressive behaviors were decreased, whereas defensive behaviors were increased, in males that received the low-dose genistein diet. Exposure to genistein during critical periods of sex differentiation results in concurrent and persistent demasculinization in male mice. Phenotypic and behavioral abnormalities induced by genistein showed a non-monotonic response, where treatment with a low dose exerted a greater effect than treatment with a high dose of genistein. Given the popularity of soy infant formulas, the influence isoflavone exposure on reproductive and behavioral health in boys and men should be considered.
KW - Demasculinization
KW - Endocrine disruption
KW - Phytoestrogens
KW - Sexual dysfunction
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U2 - 10.1016/j.physbeh.2004.12.008
DO - 10.1016/j.physbeh.2004.12.008
M3 - Article
C2 - 15708785
AN - SCOPUS:13544271676
SN - 0031-9384
VL - 84
SP - 327
EP - 334
JO - Physiology and Behavior
JF - Physiology and Behavior
IS - 2
ER -