Excretion and binding of tritium-labelled oestradiol in mice (Mus musculus): implications for the Bruce effect.

Male mouse urine contains 17beta-oestradiol (E(2)) and other steroids. Given that males actively direct urine at proximate females and intrauterine implantation of blastocysts is vulnerable to minute amounts of exogenous oestrogens, males' capacity to disrupt early pregnancy could be mediated by steroids in their urine. When male mice were implanted with osmotic pumps containing tritium-labelled E(2) ((3)H-E(2)) or injected i.p. with (3)H-E(2), radioactivity was reliably detected in their urine. Following intranasal administration of (3)H-E(2) to inseminated females, radioactivity was detected in diverse tissue samples, with there being significantly more in reproductive tissues than in brain tissues. When urine was taken from males injected with (3)H-E(2), and then intranasally administered to inseminated females, radioactivity was detected in the uterus, olfactory bulbs, and mesencephalon and diencephalon (MC+DC). When inseminated and ovariectomised females were perfused at the point of killing to remove blood from tissues, more radioactivity was detected in the uterus than in muscle, olfactory bulbs, MC+DC and cerebral cortex. Pre-treatment with unlabelled E(2) significantly reduced the uptake of (3)H-E(2) in the uterus. Taken with evidence that males deliver their urine to the nasal area of females, these results indicate that male urinary E(2) arrives in tissues, including the uterus, where it could lead to the disruption of blastocyst implantation.