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This study investigated the pattern of autonomic innervation of the heart of the fat-tailed dunnart (Sminthopsis crassicaudata) using isolated cardiac preparations. While the pattern of autonomic innervation of the atria was consistent with that found in other mammals, the ventricles displayed an unusual pattern of mammalian cardiac innervation. Transmural stimulation of the intramural nerves of isolated right ventricular preparations caused a decrease in the force of contraction of 46.8+/-3.2% followed by a rebound increase in the force of contraction beyond basal levels of 40.9+/-6.9%. These responses could be blocked independently by the application of the muscarinic receptor antagonist hyoscine and beta-adrenoreceptor antagonist propranolol respectively and could also be mimicked by the application of the agonists acetylcholine (Ach) and noradrenaline (NA). These findings indicated the presence of a functional cholinergic innervation of the ventricles that was capable of reducing the force of contraction below basal levels. This pattern of innervation has only been found previously in one other mammal, the bent-winged bat (Miniopterus schreibersii). Given that both of these species are heterotherms, it is possible that such a pattern of innervation may relate to the control of cardiac output during torpor. These findings are the first that demonstrate the homogeneity of a physiological control mechanism in a so-called 'shallow, daily torpidator' (S. crassicaudata) and a 'deep hibernator' (M. schreibersii) that is absent in mammalian homeotherms. These findings are consistent with recent work suggesting that there may be little difference between these types of heterothermy.

The adrenergic innervation of the heart of the bat (Miniopterus schreibersii) was studied with a fluorescence histochemical technique. The appearance and distribution pattern of the terminal adrenergic nerve fibers demonstrated in the atria, sinoatrial and atrioventricular nodes, and ventricles is typically mammalian. Fine varicose adrenergic fibers run in and parallel to the ventricular muscle where they are common and uniformly distributed. Indian ink perfusion of the coronary vasculature demonstrates the high density of vessels in the ventricles, but obscures the terminal innervation of the ventricular muscle. This alone, or in combination with the apparent seasonal change in the terminal innervation of the ventricles, may explain the inability of previous workers to identify an adrenergic ventricular innervation in the bat Nyctalus noctula. The adrenergic ventricular innervation might be involved in the large increases in cardiac output associated with the commencement of flight and in the massive sympathetic activation that mediates arousal from torpor.

Adult Miniopterus schreibersii were anesthetized with chloroform, and in vitro preparations of cardiac chambers were prepared. Stimulation of intramural nerves in right ventricles paced at 6 Hz caused an inhibition (56.3 +/- 3.5% decrease on basal force) mediated by cholinergic nerves and an excitation (91.5 +/- 9.9% increase on basal force) mediated by adrenergic nerves. Mean pD2s (-log effective concentration, 50%) for ventricular beta-adrenoceptors and muscarinic cholinoceptors were 6.99 +/- 0.03 and 6.42 +/- 0.07, respectively. The inhibition of ventricular contractility, by nerve stimulation or exogenous acetylcholine, occurred even after blockade of beta-adrenoceptors. The results were comparable to those obtained on atria. In some experiments, the heart was perfused in situ and paced via electrodes on the ventricle: stimulation of the right vagus nerve decreased right ventricular contractility by up to 90%. The results show that, at least in this hibernating mammal, there is an adrenergic innervation of the ventricle. The presence of a cholinergic vagal innervation capable of inhibiting the basal force of ventricular contraction has not been shown in any other mammal.

1. The effects of vagal stimulation and applied acetylcholine were compared on the isolated sinus venosus preparation of the toad, Bufo marinus. 2. The effects of applied acetylcholine and of low-frequency, or short bursts of high-frequency vagal stimulation were abolished by hyoscine. 3. When intracellular recordings were made from muscle cells of the sinus venosus, it was found that applied acetylcholine caused bradycardia and a cessation of the heart beat which was associated with membrane hyperpolarization and a reduction in the duration of the action potentials. Much of the effect of acetylcholine can be attributed to it causing an increase in potassium conductance, gK. 4. When slowing was produced by low-frequency vagal stimulation, only a small increase in maximum diastolic potential was detected. During vagal arrest the membrane potential settled to a potential positive of the control maximum diastolic potential. 5. In the presence of barium, much of the bradycardia associated with vagal stimulation persisted. Although the bradycardia produced by added acetylcholine also persisted in the presence of barium, the effects of acetylcholine that could be attributed to an increase in gK were abolished. 6. Addition of caesium ions produced bradycardia with membrane potential changes similar to those seen during vagal stimulation. 7. The results are discussed in relation to the idea that neuronally released acetylcholine reduces inward current flow during diastole. In contrast applied acetylcholine as well as reducing inward current flow during diastole also increases outward current flow by increasing gK.

1. Intracellular recordings were made from pacemaker cells lying in the sino-atrial node of guinea-pigs. 2. Low-frequency vagal stimulation slowed the rate of generation of pacemaker action potentials; high-frequency stimulation stopped the generation of action potentials. 3. During vagal stimulation the rate of diastolic depolarization was reduced with the action potential otherwise unchanged: when the heart stopped the membrane potential of pacemaker cells settled to a value positive of the maximum diastolic potential. 4. In contrast, added acetylcholine caused membrane hyperpolarization and shortened the duration of action potentials. 5. The effects of both added acetylcholine and vagally released acetylcholine were abolished by hyoscine. 6. It is suggested that neurally released acetylcholine acts to change the balance between inward and outward current flow during diastole by modifying the properties of existing voltage-dependent channels. In contrast added acetylcholine appears to activate a different set of receptors which increase the potassium conductance of pacemaker cells.