Jechura, T.J. et al.: Ovarian hormones influence olfactory cue effects on reentrainment in the diurnal rodent, Octodon degus

Tammy J. Jechura, Theresa M. Lee: Ovarian hormones influence olfactory cue effects on reentrainment in the diurnal rodent, Octodon degus.
In: Hormones and Behavior 46 (2004) 349 – 355.

Link: http://www.lsa.umich.edu/psych/theresaleelab/pubs/jechura.lee.2004.pdf

Zitat :

Abstract

Octodon degus, a social hystricomorph rodent, responds to olfactory cues from a gonadally intact female entrained to a light – dark cycle (LD) by accelerating reentrainment of running wheel activity following a 6-h phase advance of the LD cycle. In this study, we examined the role of ovarian hormones in the production of and responsiveness to olfactory social cues in females. Experiment 1: intact females were sequentially phase-advanced 6 h with photic cues alone, or in the presence of an intact female donor, ovariectomized (OVX) donor, a castrated male, or a castrated male with testosterone replacement. Acceleration of reentrainment occurred only in the presence of the intact female donor while reentrainment was delayed by OVX donors. Experiment 2: OVX females undergoing a 6-h phase advance did not accelerate reentrainment in the presence of an intact female donor compared to reentrainment with photic cues alone. Thus, ovarian hormones are necessary for both the production of and responsiveness to olfactory cues. Experiment 3: OVX females implanted with estrogen-filled Silastic capsules did not accelerate reentrainment following the 6-h phase advance in the presence of an intact donor, whereas animals implanted with a combination of estrogen- and progesterone-filled capsules (Experiment 4) reduced the length of time needed to reentrain in the presence of an intact donor.
Therefore, combined progesterone and estrogen are sufficient for responsiveness to the effective olfactory cue in intact donor females. These data clarify that the sex difference in sensitivity to non-photic odor effects on circadian reentrainment is caused by both the testosterone’s inhibitory effects (Octodon degus. J. Biol. Rhythms 18 (2003) 43 – 50) and the enhancing effects of progesterone and estrogen.