Degeneration and regeneration in the superior cervical sympathetic ganglion afterLatrodectus venom

Brain Cell Biology - The effects of the venom of the spider Latrodectus mactans hasselti on the superior cervical ganglion were studied in the guinea pig. Under anaesthesia the ganglion was bathed...     

Spontaneous activity of the isolated rabbit superior cervical sympathetic ganglion

Investigation of spontaneous activity (mean amplitude of spikes 200–300 µV, frequency from 0.07 to 2.9 Hz) in the rabbit superior cervical sympathetic ganglion by the sucrose gap method showed that this activity was completely blocked by D-tubocurarine and hexamethonium; its frequency was increased in hypertonic solution, by an increase in the external potassium concentration, and by the addition of theophylline and ethanol. These observations suggest that the activity observed is due to spontaneous liberation of acetylcholine mediator from preganglionic nerve endings. However, addition of tetrodotoxin and an increase in the external calcium concentration to 10 mM block spontaneous activity in the ganglion. This suggests that the observed spontaneous activity consists of action potentials.     

Conducting pathways of the superior cervical sympathetic ganglion of the cat

Individual nerves of the superior cervical sympathetic ganglion were stimulated in acute experiments on cats, and action potentials (AP) were recorded from other nerves of the ganglion in order to clarify whether or not there is transmission of excitation through the ganglion from one nerve to another and to establish whether this transmission is continuous or synaptic. The method of intracellular recording from neurons of the ganglion was also used. It is established that stimulation of the cervical sympathetic nerve evokes AP in all of the peripheral nerves of the ganglion, a circumstance that is the result of synaptic transmission of excitation. There is no transmission of excitation in the reverse direction or between any of the 12 peripheral nerves of the ganglion (including the four branches of the internal carotid nerve). Orthodromic excitation is recorded intracellularly from neurons of the ganglion during stimulation of the cervical sympathetic nerve, and antidromic excitation is recorded during stimulation of a peripheral nerve (the internal carotid nerve). It follows that the pathways through the ganglion which conduct excitation from the cervical sympathetic nerve into all of the remaining nerves of the ganglion are synaptic. Analysis of EPSP latent periods indicated that preganglionic fibers that differ sharply with respect to threshold and conduction rate (groups S₂ and S₄) converge on one and the same neurons of the ganglion.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 2, No. 2, pp. 216–224, March–April, 1970.     

Ultrastructure of interneuronal connections in the superior cervical sympathetic ganglion in cats

The structure of interneuronal synapses in the superior cervical sympathetic ganglion was studied in cats under normal conditions and after division of the cervical sympathetic nerves and removal of spinal ganglia T₁₂–L₂. A definite number of dendro-dendritic and dendro-somatic junctions is observed in the ganglion and most of them remained intact after operations of both types; they are probably synapses formed by dendrites of neurons located in the ganglion. Synapses of this sort participate in the formation of nest-like complexes, consisting of consecutive junctions of one neuron with several dendrites. The formation of such complexes may provide the anatomical basis for synchronization of rhythmic neuronal activity in the cellular glomeruli of the ganglion. The results of an ultrastructural study of dendro-dendritic junctions suggests that they are synaptic in nature. Some dendro-dendritic junctions underwent degeneration after both types of operation and are probably endings of neurons in spinal ganglia. Wide club-like structures, probably receptor endings, formed by dendrites of afferent neurons of spinal ganglia, also are found in the ganglion. These structures lie freely in the stoma of the ganglion or form contacts with axon terminals and dendrites of neurons located in the ganglion; some of them degenerate after removal of spinal ganglia T₁₂–L₂.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 13, No. 3, pp. 299–306, May–June, 1981.     

Effect of ethmozine on action potentials and myocardial contraction in guinea pigs

Ethmozine decreased the maximum rate of action potential rise (Vmax) in a dose-dependent manner. Using the Scatchard plot the apparent dissociation constant was calculated to be 1.52 X 10(-5) g/ml. Ethmozine also decreased the force of contraction in the concentration range between 1 X 10(-6) and 1 X 10(-4) g/ml with the apparent dissociation constant obtained from the Scatchard plot being equal to 1.48 X 10(-5) g/ml. The linear correlation coefficient between the decrease in Vmax and the decrease in the force of contraction was found to be equal to 0.998. Negative inotropic action of ethmozine was less pronounced when the stimulation frequency had been switched from 0.8 to 0.1 Hz. The decrease in Vmax under the action of ethmozine (3 X 10(-5) g/ml) was diminished from 56 +/- 7% (0.8 Hz) to only 3 +/- 8% (0.1 Hz). This was accompanied by the decrease in the negative inotropic effect: from 58 +/- 9% (0.8 Hz) to 16 +/- 15% (0.1 Hz). It was assumed that the negative inotropic action of ethmozine was mediated by the Na--Ca exchange, which was inhibited by the decrease of the intracellular Na+ concentration due to the blockade of sodium channels by ethmozine.     

Desensitization of the muscarinic receptor controlling action potentials of sympathetic ganglion cells in bullfrogs

The desensitization of the muscarinic receptor, of which activation is known to depress the ionic K⁺ and Ca²⁺ currents generated during action potentials of bullfrog sympathetic ganglion cells, was studied. The depression of these voltage-dependent K⁺ and Ca²⁺ currents by muscarinic action of acetylcholine (ACh) was gradually restored to a certain extent when an application of ACh was sustained. After removal of ACh, the sensitivity of the muscarinic receptor was still depressed for an extended period, while resting and action potentials were apparently observed to be of normal level and size, respectively. These results indicate that desensitization of muscarinic receptors developed during a sustained application of ACh. It was suggested that the muscarinic receptor controlling these voltage-dependent currents of ganglion cells may be part of receptor-ionic channel complex (RICC) the nature of which was comparable to that of the RICC of the nicotinic receptor of the end-plate.     

Ca2+ signal summation and NFATc1 nuclear translocation in sympathetic ganglion neurons during repetitive action potentials

NFATc-mediated gene expression constitutes a critical step during neuronal development and synaptic plasticity. Although considerable information is available regarding the activation and functionality of specific NFATc isoforms, in neurons little is known about how sensitive NFAT nuclear translocation is to specific patterns of electrical activity. Here we used high-speed fluo-4 confocal imaging to monitor action potential (AP)-induced cytosolic Ca2+ transients in rat sympathetic neurons. We have recorded phasic and repetitive AP patterns, and corresponding Ca2+ transients initiated by either long (100-800 ms) current-clamp pulses, or single brief (2 ms) electrical field stimulation. We address the functional consequences of these AP and Ca2+ transient patterns, by using an adenoviral construct to express NFATc1-CFP and evaluate NFATc1-CFP nuclear translocation in response to specific patterns of electrical activity. Ten Hertz trains stimulation induced nuclear translocation of NFATc1, whereas 1 Hz trains did not. However, 1 Hz train stimulation did result in NFATc1 translocation in the presence of 2 mM Ba2+, which inhibits M-currents and promotes repetitive firing and the accompanying small (approximately 0.6 DeltaF/F0) repetitive and summating Ca2+ transients. Our results demonstrate that M-current inhibition-mediated spike frequency facilitation enhances cytosolic Ca2+ signals and NFATc1 nuclear translocation during trains of low frequency electrical stimulation.