The Hoover-Drickamer effect occurs when adult female mice are exposed to the urine of pregnant and lactating adult female mice, resulting in a longer than typical oestrus period. The effect was first noted by J. E. Hoover and L. C. Drickamer in their 1979 study wherein they randomly assigned adult female mice to one of four treatment conditions: a control group where the subjects were exposed to water, a group that was exposed to the urine of pregnant mice, a group that was exposed to the urine of lactating mice and a group that was exposed to the urine of a singly caged female mouse.
The results of their study demonstrated that the adult female mice exposed to urine of pregnant or lactating females exhibited significantly longer mean periods of oestrus than adult females mice that had been in the control group or exposed to the urine of the singly caged female mouse. The female mice exposed to the urine of the pregnant and lactating mice were also found to ovulate during this atypical, longer oestrus period and successfully conceived and bore litters when mated with male mice. Hoover and Drickamer also found that while their initial method had been to psychically paint their subjects with the urine used, when mice were exposed to the urine by a capsule containing a soaked cotton ball, the effect still occurred, demonstrating the airborne nature of the pheromones in the urine of the pregnant and lactating mice.
Discovery
The Hoover-Drickamer effect was initially demonstrated in J.E. Hoover and L.C. Drickamer's 1979 study. The researchers noted that while other studies had examined the effect of urine from pregnant and/or lactating females on the onset of puberty in young female mice, no work had been done to examine what urine from pregnant and/or lactating females would do to oestrous cycles in already matured female mice. Their research utilized two different experiments to demonstrate that female mouse oestrus cycles were effected upon exposure to urine from pregnant and/or lactating mice, and that pheromones were involved in this process.
In their first experiment of the study, Hoover and Drickamer randomly assigned 80 adult female rats to four treatment groups, a control group where subjects were exposed to water, a group where the subjects were exposed to the urine of pregnant mice, a group where the subjects were exposed to the urine of lactating mice and finally a group where subjects were exposed to the urine of a singly caged female mouse. Their findings were that subjects exposed to the urine of pregnant and lactating mice were in oestrus for significantly more days relative to the female mice in the control group or when exposed to the urine of the singly caged female mouse.
Their second experiment of the study utilized the same four subject groups, but they changed their method of exposing their subjects. Rather than painting the mice with the urine, they housed their subjects were capsules that contained soaked cotton balls (varied between water, urine from pregnant mice, urine from lactating mice and urine from a singly caged female, like experiment one). Parallel to the results of their first experiment, subjects housed with the capsules injected with the urine of pregnant and lactating mice demonstrated significantly more total oestrus smears over a twenty one day period, more complete oestrus cycles and a longer total duration of oestrus cycles relative to the subjects in the control group and the group that was exposed to the urine of the singly caged female.
Hypothesized mechanisms
Hoover and Drickamer's original study did not delve into any specific mechanisms of action for the effect on female oestrus cycles beyond stating that the results of their work support the conclusion that some factor in the urine of the pregnant and lactating mice used did act to affect the oestrus cycles of the subjects used. Their conclusions suggested exploring the excretory components of the urine of pregnant and lactating mice to explore whether any substances in it constituted a pheromone that could impact mice on a physiological level such that oestrus cycles could be affected.