Long-term synaptic potentiation in the superior cervical ganglion.

Brief tetanic stimulation of the preganglionic nerves to the superior cervical ganglion enhances the postganglionic response to single preganglionic stimuli for 1 to 3 hours. This long-term potentiation of transmission through the ganglion is apparently not attributable to a persistent muscarinic action of the preganglionic neurotransmitter, acetylcholine, since neither the magnitude nor the time course of the phenomenon is reduced by atropine. The decay of long-term potentiation can be described by a first-order kinetic process with a mean time constant of 80 minutes. We conclude that long-term potentiation, once considered a unique property of the hippocampus, is in fact a more general feature of synaptic function. This form of synaptic memory may significantly influence information processing and control in other regions of the nervous system, including autonomic ganglia.

[1]  R. Volle MODIFICATION BY DRUGS OF SYNAPTIC MECHANISMS IN AUTONOMIC GANGLIA , 1966 .

[2]  T. Bliss,et al.  Synaptic plasticity in the hippocampus , 1979, Trends in Neurosciences.

[3]  J. Garthwaite,et al.  MUSCARINIC RECEPTORS IN RAT SYMPATHETIC GANGLIA , 1980, British journal of pharmacology.

[4]  K. Magleby,et al.  Differential effects of Ba2+, Sr2+, and Ca2+ on stimulation-induced changes in transmitter release at the frog neuromuscular junction , 1980, The Journal of general physiology.

[5]  T. Teyler,et al.  Long-term and short-term plasticity in the CA1, CA3, and dentate regions of the rat hippocampal slice , 1976, Brain Research.

[6]  K. Koketsu,et al.  Synaptic events in sympathetic ganglia , 1978, Progress in Neurobiology.

[7]  Shin-Ho Chung Synaptic memory in the hippocampus , 1977, Nature.

[8]  B. Libet,et al.  Synaptic coupling into the production and storage of a neuronal memory trace , 1975, Nature.

[9]  G. Lynch,et al.  Intracellular responses of rat dentate granule cellsin vitro: posttetanic potentiation to perforant path stimulation , 1975, Brain Research.

[10]  W. Levy,et al.  Synapses as associative memory elements in the hippocampal formation , 1979, Brain Research.

[11]  R. Volle Enhancement of postganglionic responses to stimulating agents following repetitive preganglionic stimulation. , 1962, The Journal of pharmacology and experimental therapeutics.

[12]  Richard F. Thompson,et al.  Neuronal plasticity in the limbic system during classical conditioning of the rabbit nictitating membrane response. I. The hippocampus , 1978, Brain Research.

[13]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[14]  P. Schwartzkroin,et al.  Long-lasting facilitation of a synaptic potential following tetanization in thein vitro hippocampal slice , 1975, Brain Research.

[15]  B. McNaughton,et al.  Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents , 1978, Brain Research.

[16]  B. Libet,et al.  Orthodromic production of non‐cholinergic slow depolarizing response in the superior cervical ganglion of the rabbit , 1981, The Journal of physiology.

[17]  R. Birks Regulation by patterned preganglionic neural activity of transmitter stores in a sympathetic ganglion. , 1978, The Journal of physiology.