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DOI 10.1073/pnas.93.20.11208

Медицинская библиотека · Proceedings of the National Academy of Sciences of the United States of America · 1996

Diurnal variation of the adenylyl cyclase type 1 in the rat pineal gland.

Tzavara E T, Pouille Y, Defer N, Hanoune J

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Nocturnal melatonin production in the pineal gland is under the control of norepinephrine released from superior cervical ganglia afferents in a rhythmic manner, and of cyclic AMP. Cyclic AMP increases the expression of serotonin N-acetyltransferase and of inducible cAMP early repressor that undergo circadian oscillations crucial for the maintenance and regulation of the biological clock. In the present study, we demonstrate a circadian pattern of expression of the calcium/calmodulin activated adenylyl cyclase type 1 (AC1) mRNA in the rat pineal gland. In situ hybridization revealed that maximal AC1 mRNA expression occurred at midday (12:00-15:00), with a very low signal at night (0:00-3:00). We established that this rhythmic pattern was controlled by the noradrenergic innervation of the pineal gland and by the environmental light conditions. Finally, we observed a circadian responsiveness of the pineal AC activity to calcium/calmodulin, with a lag due to the processing of the protein. At midday, AC activity was inhibited by calcium (40%) either in the presence or absence of calmodulin, while at night the enzyme was markedly (3-fold) activated by the calcium-calmodulin complex. These findings suggest (i) the involvement of AC1 acting as the center of a gating mechanism, between cyclic AMP and calcium signals, important for the fine tuning of the pineal circadian rhythm; and (ii) a possible regulation of cyclic AMP on the expression of AC1 in the rat pineal gland.

Для цитирования: Tzavara E T, Pouille Y, Defer N, Hanoune J. Diurnal variation of the adenylyl cyclase type 1 in the rat pineal gland.. Proceedings of the National Academy of Sciences of the United States of America. 1996. DOI: 10.1073/pnas.93.20.11208.

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