Abstract

Sexual behavior was assessed in castrated adult CD-1 male mice given exogenous steroids under various treatment regimens. Castrated mice maintained on 20 μg testosterone (T) daily for 1 week, but given 250 μg testosterone propionate (TP) on the day of testing showed higher levels of copulatory activity than intact mice or the males receiving an additional dose of 20 μg T on the test day, although plasma testosterone levels were not different at the time of behavioral testing. Castrated males given 50, 125, or 250 μg TP for 1 week including the day of testing showed higher levels of sexual behavior than males receiving the same doses of TP only once, on the test day. A single injection of 17β-estradiol (E 2) completely restored the male copulatory pattern, including ejaculation, in castrated mice under every condition examined. Testosterone and dihydrotestosterone (DHT) were less effective than E 2, as was the combination of E 2 and DHT. The relative efficacy of a single dose of T, DHT, and E 2 plus DHT was dependent upon factors such as the delay between steroid administration and testing, as well as whether or not the castrated mice received androgen replacement prior to testing. Estradiol benzoate (E 2B) was not capable of restoring sexual behavior in castrated mice in this study. The comparison of results obtained with TP, T, E 2, and E 2B suggests that an appreciable, but not necessarily sustained, elevation of E 2 levels in the brain may be critical in the facilitation of male copulatory behavior in mice.

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