Control of a central pattern generator by an identified modulatory interneurone in crustacea. II. Induction and modification of plateau properties in pyloric neurones.

In the isolated stomatogastric nervous system of the lobster Fasus lalandii, the strong modifications of the pyloric motor pattern induced by firing of the single anterior pyloric modulator neurone (APM) are due primarily to modulation by APM activity of the regenerative membrane properties which are responsible for the 'burstiness' of all the pyloric neurones and particularly of the non-pacemaker neurones (constrictor motoneurones). This modulation has been studied under experimental conditions where the main extrinsic influences usually received by the pyloric constrictor neurones (intra-network synaptic interactions, activity of pacemaker neurones, and phasic central inputs from two premotor centres) are minimal. Under these conditions a brief discharge of neurone APM induces long plateaus of firing in all of the pyloric neurones. The non-pacemaker neurones of the pyloric network are not simply passive follower neurones, but can produce regenerative depolarizations (plateau potentials) during which the neurones fire spikes. The ability of the pyloric constrictor neurones to produce plateau potentials (plateau properties) contributes greatly to the generation of the rhythmical pyloric motor pattern. When these neurones spontaneously express their plateau properties, firing of neurone APM amplifies these properties. When most of the central inputs usually received by the pyloric constrictor neurones are experimentally suppressed, these neurones can no longer produce plateau potentials. In such conditions, firing of the single modulatory neurone APM can reinduce plateau properties of the pyloric constrictor neurones. In addition, firing in APM neurone slows down the active repolarization phase which terminates the plateau potentials of pyloric constrictor neurones. This effect is long-lasting and voltage-dependent. Modulation by APM of the plateau properties of the pyloric neurones also changes the sensitivity of these neurones to synaptic inputs. This effect can explain the strong modifications that an APM discharge exerts on a current pyloric motor pattern. Moreover, it might render the motoneurones of the pyloric pattern generator more sensitive to inputs from a command oscillator, and contribute to switching on the pyloric motor pattern.

[1]  A. Watanabe,et al.  Acceleratory Synapses on Pacemaker Neurons in the Heart Ganglion of a Stomatopod, Squilla oratoria , 1968, The Journal of general physiology.

[2]  D. Maynard,et al.  SIMPLER NETWORKS * , 1972, Annals of the New York Academy of Sciences.

[3]  I. Parnas,et al.  Prolonged excitatory and inhibitory synaptic modulation of a bursting pacemaker neuron. , 1974, Journal of neurophysiology.

[4]  E. Kandel,et al.  Neural control of circulation in Aplysia. I. Motoneurons. , 1974, Journal of neurophysiology.

[5]  E. Kandel,et al.  Neural control of circulation in Aplysia. II. Interneurons. , 1974, Journal of neurophysiology.

[6]  H. Reuter Localization of beta adrenergic receptors, and effects of noradrenaline and cyclic nucleotides on action potentials, ionic currents and tension in mammalian cardiac muscle , 1974, The Journal of physiology.

[7]  W. Davis,et al.  Motor organization and generation of rhythmic feeding output in buccal ganglion of Pleurobranchaea. , 1974, Journal of neurophysiology.

[8]  D. Hartline,et al.  Neurohormonal alteration of integrative properties of the cardiac ganglion of the lobster Homarus americanus. , 1975, The Journal of experimental biology.

[9]  H. Gainer,et al.  Studies on bursting pacemaker potential activity in molluscan neurons. III. Effects of hormones , 1975, Brain Research.

[10]  H. Gainer,et al.  Peptide factor extracted from molluscan ganglia that modulates bursting pacemaker activity , 1975, Nature.

[11]  Meissner Hp Electrical characteristics of the beta-cells in pancreatic islets. , 1976 .

[12]  H. Meissner Electrical characteristics of the beta-cells in pancreatic islets. , 1976, Journal de physiologie.

[13]  A. Selverston,et al.  The stomatogastric nervous system: Structure and function of a small neural network , 1976, Progress in Neurobiology.

[14]  W. Giles,et al.  Changes in membrane currents in bullfrog atrium produced by acetylcholine. , 1976, The Journal of physiology.

[15]  E. Marder,et al.  The pharmacological properties of some crustacean neuronal acetylcholine, gamma‐aminobutyric acid, and L‐glutamate responses. , 1978, The Journal of physiology.

[16]  D. F. Russell,et al.  Bursting neural networks: a reexamination. , 1978, Science.

[17]  K. Tazaki,et al.  Ionic bases of slow, depolarizing responses of cardiac ganglion neurons in the crab, Portunus sanguinolentus. , 1979, Journal of neurophysiology.

[18]  K Tazaki,et al.  Spontaneous electrical activity and interaction of large and small cells in cardiac ganglion of the crab, Portunus sanguinolentus. , 1979, Journal of neurophysiology.

[19]  M. Vassalle Electrogenesis of the plateau and pacemaker potential. , 1979, Annual review of physiology.

[20]  K. Tazaki,et al.  Isolation and characterization of slow, depolarizing responses of cardiac ganglion neurons in the crab, Portunus sanguinolentus. , 1979, Journal of neurophysiology.

[21]  D. F. Russell CNS control of pattern generators in the lobster stomatogastric ganglion , 1979, Brain Research.

[22]  E. Mayeri,et al.  Multiple, prolonged actions of neuroendocrine bag cells on neurons in Aplysia. I. Effects on bursting pacemaker neurons. , 1979, Journal of neurophysiology.

[23]  M Bidaut,et al.  Pharmacological dissection of pyloric network of the lobster stomatogastric ganglion using picrotoxin. , 1980, Journal of neurophysiology.

[24]  W. Crill,et al.  Plateau potentials in pancreatic islet cells are voltage-dependent action potentials , 1980, Nature.

[25]  J. Miller,et al.  Mechanisms underlying pattern generation in lobster stomatogastric ganglion as determined by selective inactivation of identified neurons. I. Pyloric system. , 1980, Journal of neurophysiology.

[26]  O. Oscarsson,et al.  Prolonged depolarization elicited in Purkinje cell dendrites by climbing fibre impulses in the cat. , 1981, The Journal of physiology.

[27]  A. Berlind,et al.  Cyclic Adenosine Monophosphate Mediation of Peptide Neurohormone Effects on the Lobster Cardiac Ganglion , 1981 .

[28]  D. F. Russell,et al.  A multiaction synapse evoking both EPSPs and enhancement of endogenous bursting , 1981, Brain Research.

[29]  M. Moulins,et al.  Participation of an Unpaired Motor Neurone in the Bilaterally Organized Oesophageal Rhythm in the Lobsters Jasus Lalandii and Palinurus Vulgaris , 1981 .

[30]  M. Moulins,et al.  All-or-none control of the bursting properties of the pacemaker neurons of the lobster pyloric pattern generator. , 1982, Journal of neurobiology.

[31]  P. S. Dickinson,et al.  Control of a central pattern generator by an identified modulatory interneurone in crustacea. I. Modulation of the pyloric motor output. , 1983, The Journal of experimental biology.

[32]  R. Robertson,et al.  Oscillatory command input to the motor pattern generators of the crustacean stomatogastric ganglion , 1981, Journal of comparative physiology.

[33]  Allen Selverston,et al.  Ionic requirements for bursting activity in lobster stomatogastric neurons , 1981, Journal of comparative physiology.

[34]  R. Robertson,et al.  Oscillatory command input to the motor pattern generators of the crustacean stomatogastric ganglion , 2004, Journal of Comparative Physiology A.

[35]  Gunther S. Stent,et al.  Neuronal control of heartbeat in the medicinal leech , 2004, Journal of comparative physiology.

[36]  A. Selverston,et al.  Organization of the stomatogastric ganglion of the spiny lobster , 2004, Journal of comparative physiology.