Actions of dibutyryl cyclic adenosine monophosphate, papaverine and isoprenaline on the intestinal smooth muscle.
نویسندگان
چکیده
It is known that papaverine and isoprenaline stop the spontaneous spike discharge, usually with some hyperpolarization (1-6). The action of fl-adrenergic stimulants is thought to be related to the ability of these drugs to increase the intracellular level of cyclic 3', 5'-adenosine monophosphate (cyclic 3', 5'-AMP) in the smooth muscles. In the iso lated smooth muscle, catecholamine-induced relaxation is thought to be preceded by a rapid rise in cyclic 3', 5'-AMP concentration. Although exogeneously applied cyclic 3', 5'-AMP does not gain access to the intracellular fluid in significant amount (7), the N6, 2'-0-dibutyryl derivative, dibutyryl cyclic adenosine monophosphate (dibutyryl cyclic AMP) has a clear action on the rat intestinal smooth muscle (8). The different effects of the nucleotides may be due to possibly increased entry into cells and a greater resistance to hydrolysis by addition of dibutyryl groups to cyclic AMP. In this paper, mode of ac tion of isoprenaline, dibutyryl cyclic AMP and papaverine has been compared with each other.
منابع مشابه
Actions of papaverine on intestinal smooth muscle and its inhibition of cyclic AMP and cyclic GMP phosphodiesterases.
Papaverine, a nonspecific smooth muscle relaxant, is well known to be a potent cyclic AMP phosphodiesterase inhibitor (1, 2). In recent papers (3-8) it has been reported that smooth muscle relaxing action of papaverine is likely to be mediated through an increase of cyclic AMP due to its phosphodiesterase inhibition. Recently attention has drawn to the role of cyclic GMP, which often presents p...
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ورودعنوان ژورنال:
- Japanese journal of pharmacology
دوره 21 4 شماره
صفحات -
تاریخ انتشار 1971