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Melatonin accelerates reentrainment of the circadian rhythm of its own production after an 8-h advance of the light-dark cycle

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Summary

The rhythm in melatonin production in the rat is driven by a circadian rhythm in the pineal N-acetyltransferase (NAT) activity. Rats adapted to an artificial lighting regime of 12 h of light and 12 h of darkness per day were exposed to an 8-h advance of the light-dark regime accomplished by the shortening of one dark period; the effect of melatonin, triazolam and fluoxetine, together with 5-hydroxytryptophan, on the reentrainment of the NAT rhythm was studied.

In control rats, the NAT rhythm was abolished during the first 3 cycles following the advance shift. It reappeared during the 4th cycle; however, the phase relationship between the evening rise in activity and the morning decline was still compressed.

Melatonin accelerated the NAT rhythm reentrainment. In rats treated chronically with melatonin at the new dark onset, the rhythm had already reappeared during the 3rd cycle, in the middle of the advanced night, and during the 4th cycle, the phase relationship between the evening onset and the morning decline of the NAT activity was the same as before the advance shift. In rats treated chronically with melatonin at the old dark onset or in those treated with melatonin 8 h, 5 h and 2 h after the new dark onset during the 1st, 2nd and 3rd cycle, respectively, following the advance shift, the NAT rhythm reappeared during the 3rd cycle as well but in the last third of the advanced night only.

Neither triazolam nor fluoxetine together with 5-hydroxytryptophan administered around the new dark onset facilitated NAT rhythm reentrainment after the 8-h advance of the light-dark cycle.

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Abbreviations

NAT :

N-acetyltransferase

LD cycle :

light-dark cycle

CT :

circadian time

LD x∶y :

light dark cycle comprising x h of light and y h of darkness

References

  • Arendt J, Aldhous M, Marks V (1986) Alleviation of jet-lag by melatonin: preliminary results of controlled double trial. Brit Med J 292:1170

    Google Scholar 

  • Arendt J, Aldhous M, English J, Marks V, Arendt JH (1987) Some effects of jet-lag and their alleviation by melatonin. Ergonomics 30:1379–1393

    Google Scholar 

  • Armstrong SM, Chesworth MJ (1987) Melatonin phase-shifts a mammalian circadian clock. In: Trentini GP, De Gaetani C, Pévet P (eds) Fundamentals and clinics in pineal research. Sereno Symposia 44, Raven Press, New York, pp 195–198

    Google Scholar 

  • Brownstein M, Axelrod J (1974) Pineal gland: 24-hour rhythm in norepinephrine turnover. Science 184:163–165

    Google Scholar 

  • Carter DS, Goldman BD (1983) Antigonadal effects of timed melatonin infusion in pinealectomized male Djungarian hamsters (Phodopus sungorus sungorus): Duration is the critical parameter. Endocrinology 113:1261–1267

    Google Scholar 

  • Cassone VM, Menaker M (1984) Is the avian circadian system a neuroendocrine loop? J Exp Zool 232:539–549

    Google Scholar 

  • Cassone VM, Chesworth MJ, Armstrong SM (1986) Dose-dependent entrainment of rat circadian rhythms by daily injections of melatonin. J Biol Rhythms 1:219–229

    Google Scholar 

  • Cassone VM, Roberts MH, Moore RY (1987) Melatonin inhibits metabolic activity in the rat suprachiasmatic nuclei. Neurosci Let 81:29–34

    Google Scholar 

  • Corrent G, Eskin A (1982) Transmitter action of serotonin in phase shifting a rhythm from the Aplysia eye. Am J Physiol 242:R333-R338

    Google Scholar 

  • Deguchi T, Axelrod J (1972) Sensitive assay for serotonin N-acetyltransferase activity in rat pineal. Anal Biochem 50:174–179

    Google Scholar 

  • Finkelstein JS, Baum Fr, Cambell CS (1978) Entrainment of the female hamster to reversed photoperiod: Role of the pineal. Physiol Behav 21:105–111

    Google Scholar 

  • Gwinner E, Benzinger J (1978) Synchronization of a circadian rhythm in pinealectomized European starlings by daily injections of melatonin. J Comp Physiol 127:209–213

    Google Scholar 

  • Hoffmann K, Illnerová H, Vaněček J (1981) Effect of photoperiod and of one minute light at night-time on the pineal rhythm in N-acetyltransferase activity in the Djungarian hamster Phodopus sungorus. Biol Reprod 24:551–556

    Google Scholar 

  • Illnerová H (1986) Circadian rhythms in the mammalian pineal gland. Rozpravy Československé Akademie Věd 96 (1), Academia, Prague

    Google Scholar 

  • Illnerová H, Vaněček J (1980) Pineal rhythm in N-acetyltransferase activity in rats under different artificial photoperiods and in natural daylight in the course of a year. Neuroendocrinology 31:321–326

    Google Scholar 

  • Illnerová H, Vaněček J (1982) Two-oscillator structure of the pacemaker controlling the circadian rhythm of N-acetyltransferase in the rat pineal gland. J Comp Physiol 145:539–548

    Google Scholar 

  • Illnerová H, Vaněček J (1985) Entrainment of the circadian rhythm in rat pineal N-acetyltransferase activity under extremely long and short photoperiods. J Pineal Res 2:67–78

    Google Scholar 

  • Illnerová H, Vaněček J (1987a) Dynamics of discrete entrainment of the circadian rhythm in the rat pineal N-acetyltransferase activity during transient cycles. J Biol Rhythms 2:95–108

    Google Scholar 

  • Illnerová H, Vaněček J (1987b) Entrainment of the circadian rhythm in the rat pineal N-acetyltransferase activity by prolonged periods of light. J Comp Physiol A 161:495–510

    Google Scholar 

  • Illnerová H, Vaněček J, Hoffmann K (1983) Regulation of the pineal melatonin concentration in the rat (Rattus norvegicus) and in the Djungarian hamster (Phodopus sungorus). Comp Biochem Physiol 74:155–159

    Google Scholar 

  • Illnerová H, Hoffmann K, Vanček J (1986) Adjustment of the rat pineal N-acetyltransferase rhythm to change from long to short photoperiod depends on the direction of extension of the dark period. Brain Res 362:403–408

    Google Scholar 

  • Illnerová H, Vaněček J, Hoffmann K (1987) Adjustment of the rat pineal N-acetyltransferase rhythm to eight-hour shifts of the light-dark cycle: advance of the cycle disturbs the rhythm more than delay. Brain Res 417:167–171

    Google Scholar 

  • Kincl FA, Chang CC, Zbuzkova V (1970) Observation on the influence of changing photoperiod on spontaneous wheel-running activity of neonatally pinealectomized rats. Endocrinology 87:38–42

    Google Scholar 

  • Klein DC (1978) The pineal gland: A model of neuroendocrine regulation. In: Reichlin S, Baldessarini RR, Martin JB (eds) The hypothalamus. Raven Press, New York, pp 303–327

    Google Scholar 

  • Klein DC, Moore RJ (1979) Pineal N-acetyltransferase and hydroxyindole-O-methyltransferase: Control by the retinal hypothalamic tract and the suprachiasmatic nucleus. Brain Res 174:245–262

    Google Scholar 

  • Klein DC, Weller JL (1970) Indole methabolism in the pineal gland: A circadian rhythm in N-acetyltransferase activity. Science 169:1093–1095

    Google Scholar 

  • Mrosovski N (1988) Phase response curves for social entrainment. J Comp Physiol A 162:35–46

    Google Scholar 

  • Mrosovski N, Salmon PA (1988) A behavioral method for accelerating re-entrainment of rhythms to new light-dark cycles. Nature 330:372–373

    Google Scholar 

  • Murakami N, Hayafuji C, Sasaki Y, Yamazaki J, Takahashi K (1983) Melatonin accelerates the reentrainment of the circadian adreno-cortical rhythm in inverted illumination cycle. Neuroendocrinology 36:385–391

    Google Scholar 

  • Parfitt A, Weller JL, Klein DC, Sakai KK, Marks BH (1975) Blockade by oubain or elevated potassium ion concentration of the adrenergic and adenosine cyclic 3′,5′-monophosphate induced stimulation of pineal serotonin N-acetyltransferase activity. Mol Pharmacol 11:241–255

    Google Scholar 

  • Quay WB (1970) Physiological significance of the pineal during adaptation of shifts in photoperiod. Physiol Behav 5:353–360

    Google Scholar 

  • Quay WB (1972) Pineal homeostatic regulation of shifts in the circadian activity rhythm during maturation and aging. Trans NY Acad Sci 34:239–254

    Google Scholar 

  • Ralph MR, Menaker M (1985) Bicuculline blocks circadian phase delays but not phase advances. Brain Res 325:362–365

    Google Scholar 

  • Redman JR, Armstrong SM (1988) Reentrainment of rat circadian activity rhythms: Effects of melatonin. J Pineal Res 5:203–215

    Google Scholar 

  • Redman JS, Armstrong SM, Ng KT (1983) Free-running activity rhythms in the rat: Entrainment by melatonin. Science 219:1089–1091

    Google Scholar 

  • Reppert SM, Weaver DR, Rivkees SA, Stopa EG (1988) Putative melatonin receptors in a human biological clock. Science 242:78–81

    Google Scholar 

  • Rusak B, Zucker J (1979) Neural regulation of circadian rhythms. Physiol Rev 59:449–526

    Google Scholar 

  • Turek FW, Losee-Olson S (1986) A benzodiazepine used in the treatment of insomnia phase-shifts the mammalian circadian clock. Nature 321:167–168

    Google Scholar 

  • Underwood H, Harless M (1985) Entrainment of the circadian activity rhythm of a lizard to melatonin injections. Physiol Behav 35:267–270

    Google Scholar 

  • Van Reeth O, Turek FW (1987) Adaptation of circadian rhythmicity to shift in light-dark cycle accelerated by a benzodiazepine. Am J Physiol 253:R204-R207

    Google Scholar 

  • Vaněček J, Pavlík A, Illnerová H (1987) Hypothalamic melatonin receptor sites revealed by autoradiography. Brain Res 435:359–362

    Google Scholar 

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Illnerová, H., Trentini, G.P. & Maslova, L. Melatonin accelerates reentrainment of the circadian rhythm of its own production after an 8-h advance of the light-dark cycle. J Comp Physiol A 166, 97–102 (1989). https://doi.org/10.1007/BF00190214

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