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Cyclic Nucleotides - Part II: Physiology and Pharmacology (Paperback, Softcover reprint of the original 1st ed. 1982)
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Cyclic Nucleotides - Part II: Physiology and Pharmacology (Paperback, Softcover reprint of the original 1st ed. 1982)
Series: Handbook of Experimental Pharmacology, 58 / 2
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Cyclic nucleotides are intimately involved in the consequences of
either stimulation or blockade of receptors; therefore, an
understanding of the biochemistry of cyclic nucleotides ought to be
important for pharmacologists. Pharmacology is a science that among
other things investigates chemical compounds that affect the
physiology of cells, tissues and organs. Frequently pharmacologists
account for the effect of low concentrations of a drug upon a
tissue by invoking the presence of a receptor upon the surface of
the cell. Traditional pharmacologists excelled at identifying and
classifying the properties of receptors. A. J. CLARK'S monograph in
the earlier series of the Handbook of Experimental Pharmacology
(CLARK 1937) summarized the mathematics underlying the traditional
pharmacological approach towards receptors. By its nature, however,
classic pharmacology provided little useful information about the
intracellular events occurring as a consequence of occupying a
receptor; for example, ALQUIST (1948) identified the beta-adrenocep
tor, but he did not provide any insight into how stimulation of the
receptor produces tissue-specific physiological responses. The
discovery of cyclic AMP by RALL and SUTHERLAND (see RALL, Vol. I)
led to biochemical investigations of many different receptors
(including ALQUIST'S beta-adrenoceptor) that share a cyclic
nucleotide as a common factor in the biochemical mechanisms that
translate the occupancy of receptors into physiological effects.
Ten years ago, in the introduction to their monograph on cyclic
nucleotides, ROBISON et al. (1971) commented on the rapid growth of
interest in cyclic nucleotides over the preceding years."
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