Antiestrogens were used to test the hypothesis that estrogen exerts a "maintenance," as well as a "priming," effect on rat and hamster sexual receptivity as it apparently does for guinea pigs. MER-25 (75 or 150 mg/kg) significantly reduced rat LQ when given-2 hr OI 8 hr after EB injection. MER-25 given at 34 hr (2 hr prior to I') failed to diminish rat LQ. With hamsters, MER-25 in large doses (7.50 mg/kg) given either at-2 hr or 34 hr reduced lordosis duration to 40% of controls, but this effect was confounded by severe illness among the MER-25 injected animals. Lower doses failed to block behavior, but still produced some toxicity. CI 628 (50 mg/kg) greatly reduced hamster lordosis duration and increased lordosis latency when given 0 hr, but not 34 hr, after EB. The results are consistent with similar previous work on rats and do not support the concept of estrogen "maintenance" in either rats or hamsters. Among ovariectomized rats, hamsters, and guinea pigs, lordosis can be induced by the sequential administration of estrogen and progesterone (Boling and Blandau, 1939; Frank and Fraps, 1945; Dempsey, Hertz, and Young, 1936). Several lines of evidence suggest that estrogen must be available for a number of hours before progesterone is administered in order that the animal be "primed" for a synergistic action of the facilitatory hormones. If the interval between the two hormones is too short, sexual behavior is absent or inadequate (