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Am J Physiol Regul Integr Comp Physiol (August 26, 2004). doi:10.1152/ajpregu.00272.2004
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Submitted on April 27, 2004
Accepted on August 20, 2004

Inhibiting Cortisol Response Accelerates Recovery from a Photic Phase Shift

Jennifer A Mohawk1, Katherine Cashen1, and Theresa M Lee1*

1 Department of Psychology, University of Michigan, Ann Arbor, MI, USA

* To whom correspondence should be addressed. E-mail: terrilee{at}umich.edu.

Jetlag results when a temporary loss of circadian entrainment alters phase relationships among internal rhythms and between an organism and the outside world. After a large shift in the light:dark (LD) cycle, rapid recovery of entrainment minimizes the negative effects of internal circadian disorganization. There is evidence in the existing literature for an activation of the hypothalamic-pituitary-adrenal (HPA) axis following a photic phase shift, and it is possible that the degree of HPA-axis response is a determining factor of reentrainment time. This study utilized a diurnal rodent, Octodon degus, to test the prediction that altering cortisol levels would affect the reentrainment rate of circadian locomotor rhythms. In Experiment 1 we examined the effect of decreased cortisol (using metyrapone, an 11-{beta} hydroxylase inhibitor) on the rate of running-wheel rhythm recovery following a 6 h photic phase advance. Metyrapone treatment significantly shortened the length of time it took animals to entrain to the new LD cycle (11.5% acceleration). In Experiment 2 we examined the effects of increased cortisol on the rate of reentrainment following a 6 h photic phase advance. Increasing plasma cortisol levels increased the number of days (8%) animals took to reentrain running-wheel activity rhythms, but this effect did not reach significance. A third experiment replicated the results of Experiment 1 and also demonstrated that suppression of HPA activity via dexamethasone injection is capable of accelerating reentrainment rates by approximately 33%. These studies provide support for an interaction between the stress axis and circadian rhythms in determining the rate of recovery from a phase shift of the LD cycle.




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