Summary
Vagal effects on the mammalian ventricular myocardium vary greatly in different species and depend on sympathetic influences. After chemical sympathectomy it can be demonstrated that acetylcholine antagonizes the positive inotropic action of catecholamines on cat papillary muscles in a noncompetitive way. It is generally accepted that adenosine-3′5′-monophosphate mediates the effects of catecholamines in the myocardial cell.George et al. (1970) suggested guanosine-3′5′-monophosphate to be a mediator of negative inotropic effects, because perfusion of rat hearts with acetylcholine causes an elevated content of this cyclic nucleotide. There are various findings in the literature, which lead to the supposition that the myocardial contractility may be regulated in an antagonistic manner by the two cyclic nucleotides, whereas a possible central role of the adenosine-3′5′-monophosphate phosphodiesterase must be discussed.
Zusammenfassung
Im Säugerventrikelmyokard sind vagale Effekte abhängig von sympathischen Einflüssen und variieren stark bei verschiedenen Spezies. Nach chemischer Sympathektomie läßt sich zeigen, daß die positiv inotrope Wirkung von Katecholaminen am Katzenpapillarmuskel in nichtkompetitiver Weise von Acetylcholin gehemmt wird. Es wird allgemein angenommen, daß Katecholamine ihre Wirkung an der Myokardzelle über zyklisches Adenosin-3′5′-monophosphat ausüben. VonGeorge u. a. (1970) wurde vermutet, daß negativ inotrope Effekte von Acetylcholin über zyklisches Guanosin-3′5′-monophosphat vermittelt werden, da der Gehalt dieses zyklischen Nukleotids in Rattenherzen nach Perfusion mit Acetylcholin erhöht ist. Es werden verschiedene Beispiele aus der Literatur angeführt, die die Annahme nahelegen, daß die Myokardkontraktilität in gegenwobei eine zentrale Rolle der Adenosin-3′5′-monophosphat-phosphodiesterase zu diskutieren ist.
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Schwegler, M. Sympathetic-parasympathetic interactions on the ventricular myocardium: possible role of cyclic nucleotides. Basic Res Cardiol 69, 215–221 (1974). https://doi.org/10.1007/BF01906202
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DOI: https://doi.org/10.1007/BF01906202