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Updated: Jul 25, 2026

Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
Adrenergic-cholinergic interactions in left atria: interaction of carbachol with alpha- and beta-adrenoceptor
Abstract:
The purpose of the present investigation was to determine the nature of the functional interaction of muscarinic agonists with cAMP-generating and cAMP-independent agonists in left atria. Negative inotropic responses of rabbit isolated left atrial strips to the muscarinic agonist carbachol were measured in the absence and presence of equi-active inotropic doses of the beta-adrenoceptor stimulant isoproterenol (Iso), the mixed alpha- and beta-adrenoceptor stimulant phenylephrine (PE) plus 1 microM timolol to block the beta-receptor mediated component of its response, and elevated extracellular Ca2+. Carbachol produced dose-dependent negative inotropic responses in left atrial strips, which were much greater than control in the presence of either Iso, or PE plus timolol. However, carbachol responses were of a similar magnitude to the control in the presence of elevated extracellular Ca2+. In the presence of timolol, PE had no significant effect on cAMP levels in left atrial strips, and inotropic responses to carbachol alone and in combination with PE plus timolol were accompanied by significant increases in cGMP levels but no change in cAMP levels. Carbachol attenuated Iso-induced increases in cAMP levels, but decreases in left atrial tension were proportionally greater than the decreases in cAMP levels produced by carbachol in the presence of Iso. These results suggest that the antiadrenergic effects of muscarinic receptor stimulation may occur by a different mechanism in left atria than has been previously reported in ventricular muscle. While the nature of this mechanism is unknown, it may involve antagonism by muscarinic agents of both alpha- and beta-adrenoceptor mediated increases in Ca2+ influx.
Insights
Muscarinic agonists like carbachol reduce heart muscle contractions in rabbit left atria. This anti-adrenergic effect appears independent of cyclic AMP and may involve calcium influx antagonism.
Area of Science:
- Cardiology
- Pharmacology
- Physiology
Background:
- Muscarinic agonists modulate cardiac function through various signaling pathways.
- Understanding their interaction with adrenoceptors is crucial for cardiac drug development.
- Previous studies in ventricular muscle suggest cAMP-independent mechanisms for anti-adrenergic effects.
Purpose of the Study:
- To investigate the functional interaction of muscarinic agonists with cAMP-generating and cAMP-independent agonists in rabbit left atria.
- To elucidate the signaling mechanisms underlying the anti-adrenergic effects of muscarinic receptor stimulation in atrial tissue.
Main Methods:
- Isolated rabbit left atrial strips were used to measure negative inotropic responses.
- Experiments involved carbachol in the presence of isoproterenol, phenylephrine with timolol, and elevated extracellular calcium.
- Cyclic AMP (cAMP) and cyclic GMP (cGMP) levels were measured.
Main Results:
- Carbachol induced dose-dependent negative inotropic responses, potentiated by isoproterenol or phenylephrine/timolol, but not by elevated extracellular calcium.
- Phenylephrine did not significantly affect cAMP levels in the presence of timolol.
- Carbachol attenuated isoproterenol-induced cAMP increases, with greater negative inotropy than cAMP reduction.
Conclusions:
- The anti-adrenergic effects of muscarinic agonists in left atria differ from those in ventricular muscle.
- These effects may involve antagonism of alpha- and beta-adrenoceptor-mediated calcium influx.
- The precise mechanism remains to be fully elucidated but appears to be cAMP-independent.
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