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Science 20 January 1978:
Vol. 199. no. 4326, pp. 309 - 311
DOI: 10.1126/science.202027

Articles

Science, Vol 199, Issue 4326, 309-311
Copyright © 1978 by American Association for the Advancement of Science


articles

Pineal serotonin N-acetyltransferase activity: abrupt decrease in adenosine 3',5'-monophosphate may be signal for "turnoff"

DC Klein, MJ Buda, CL Kapoor, and G Krishna

Dispersed pinealocytes have been used to study the role of adenosine 3',5'-monophosphate (cyclic AMP) in the "turnoff" of N-acetyltransferace activity. Activity was first stimulated 100-fold by treating cells with 1-norepinephrine. 1-Propranolol acted stereospecifically to rapidly reverse this, resulting in a 70 percent loss of enzyme activity within 15 minutes. An even more rapid 1-propranolol-induced decreased in cyclic AMP also occurred. This together with the observation that the inhibitory effect of 1-propranolol on N-acetyltransferase was blocked by dibutyryl cyclic AMP and phosphodiesterase inhibitors indicate that an abrupt decrease in cyclic AMP may be the signal for the rapid decrease in pineal N-acetyltransferase activity.


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The Vascular Smooth Muscle Type I Angiotensin II Receptor mRNA Is Destabilized by Cyclic AMP-Elevating Agents.
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Pineal Serotonin N-Acetyltransferase: Expression Cloning and Molecular Analysis.
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Vertebrate Circadian and Photoperiodic Systems: Role of the Pineal Gland and Melatonin.
H. Underwood and B. D. Goldman (1987)
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The psychopharmacology of the human pineal.
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Pineal N-acetyltransferase is inactivated by disulfide-containing peptides: insulin is the most potent.
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