Abstract
Cyclic AMP [(cAMP) cyclic adenosine 3′,5′-monophosphate] was initially discovered by Sutherland and Rall31 in 1958. Further investigations have led to the concept that cAMP may be involved as the intracellular mediator of the actions of other hormones and of various putative synaptic transmitters. According to this concept, first messengers, the hormones or transmitters themselves, move from their cells of origin and induce the synthesis of cAMP in their target cells. Thereby, cAMP, by activating an appropriate sequence of enzymes, can evoke the specific response of a target cell to the hormone.33 During the course of research on cAMP, a second cyclic nucleotide, cyclic guanosine 3′,5′-monophosphate (cGMP), was discovered1 and is now thought to act as a second messenger for the actions of various neurotransmitters, including acetylcholine.
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© 1980 Plenum Press, New York
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Fleischer, A.S., Tindall, G.T. (1980). Cerebrospinal Fluid Cyclic Nucleotide Alterations in Traumatic Coma. In: Wood, J.H. (eds) Neurobiology of Cerebrospinal Fluid 1. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1039-6_25
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DOI: https://doi.org/10.1007/978-1-4684-1039-6_25
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