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Journal of Biological Rhythms, Vol. 3, No. 4, 365-384 (1988)
DOI: 10.1177/074873048800300406

Effects of Constant Darkness and Constant Light on Circadian Organization and Reproductive Responses in the Ram

Francis J. P. Ebling

MRC Reproductive Biology Unit, 37 Chalmers Street, Edinburgh, EH3 9EW, United Kingdom

Gerald A. Lincoln

MRC Reproductive Biology Unit, 37 Chalmers Street, Edinburgh, EH3 9EW, United Kingdom

Franziska Wollnik

Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208

Norah Anderson

MRC Reproductive Biology Unit, 37 Chalmers Street, Edinburgh, EH3 9EW, United Kingdom

The relationship between circadian rhythms in the blood plasma concentrations of melatonin and rhythms in locomotor activity was studied in adult male sheep (Soay rams) exposed to 16-week periods of short days (8 hr of light and 16 hr of darkness; LD 8:16) or long days (LD 16:8) followed by 16-week periods of constant darkness (dim red light; DD) or constant light (LL). Under both LD 8:16 and LD 16:8, there was a clearly defined 24-hr rhythm in plasma concentrations of melatonin, with high levels throughout the dark phase. Periodogram analysis revealed a 24-hr rhythm in locomotor activity under LD 8:16 and LD 16:8. The main bouts of activity occurred during the light phase. A change from LD 8:16 to LD 16:8 resulted in a decrease in the duration of elevated melatonin secretion (melatonin peak) and an increase in the duration of activity corresponding to the changes in the ratio of light to darkness. In all rams, a significant circadian rhythm of activity persisted over the first 2 weeks following transfer from an entraining photoperiod to DD, with a mean period of 23.77 hr. However, the activity rhythms subsequently became disorganized, as did the 24-hr melatonin rhythms. The introduction of a 1-hr light pulse every 24 hr (LD 1:23) for 2 weeks after 8 weeks under DD reinduced a rhythm in both melatonin secretion and activity: the end of the 1-hr light period acted as the dusk signal, producing a normal temporal association of the two rhythms. Under LL, the 24-hr melatonin rhythms were disrupted, though several rams still showed periods of elevated melatonin secretion. Significant activity rhythms were either absent or a weak component occurred with a period of 24 hr. The introduction of a 1-hr dark period every 24 hr for 2 weeks after 8 weeks under LL (LD 23:1) failed to induce or entrain rhythms in either of the parameters. The occurrence of 24-hr activity rhythm in some rams under LL may indicate nonphotoperiodic entrainment signals in our experimental facility. Reproductive re sponses to the changes in photoperiod were also monitored. After pretreatment with LD 8:16, the rams were sexually active; exposure to LD 16:8, DD, or LL resulted in a decline in all measures of reproductive function. The decline was slower under DD than LD 16:8 or LL. Conversely, after pretreatment with LD 16:8, the rams were sexually regressed, and exposure to LD 8:16, DD, or LL resulted in redevelopment of the reproductive axis; the rate of development was similar in all three treatments. The overall results illustrate that in the Soay ram the circadian organization of melatonin and activity rhythms is disrupted during pro longed exposure to DD and LL. Reproductive regression or recrudescence occurs under these constant conditions, apparently dictated by the immediate photoperiodic history.


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R.A. Picazo and G.A. Lincoln
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J Biol Rhythms, March 1, 1995; 10(1): 55 - 63.
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K.-I. Maeda and G.A. Lincoln
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J Biol Rhythms, June 1, 1990; 5(2): 97 - 106.
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