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The Journal of Neurophysiology Vol. 84 No. 1 July 2000, pp. 596-599
Copyright ©2000 by the American Physiological Society
RAPID COMMUNICATION
Laboratoire de Neurobiologie des Réseaux, Université Bordeaux I and Centre National de la Recherche Scientifique- Unité Mixte de Recherche 5816, 33405 Talence, France
Thoby-Brisson, Muriel and
John Simmers.
Transition to Endogenous Bursting After Long-Term
Decentralization Requires De Novo Transcription in a Critical Time
Window. J. Neurophysiol. 84: 596-599, 2000. Rhythmic motor pattern generation by the pyloric
network in the lobster stomatogastric ganglion (STG) requires
neuromodulatory inputs from adjacent ganglia. However, although
suppression of these inputs by cutting the stomatogastric nerve (stn)
causes the pyloric network to fall silent, network output similar to that expressed when the stn is intact returns after 3-4 days in organ
culture. Intracellular recordings from identified pyloric dilator (PD) neurons indicate that the fundamental change underlying rhythm recovery resides with the intrinsic excitability of pyloric neurons themselves, since the prolonged absence of extrinsic modulatory inputs allows the expression of an endogenous oscillatory capability that is maintained in a strictly conditional state when these inputs
are present. To examine whether gene transcription was involved in this
change in neuronal behavior, we performed in vitro experiments in which
the STG was exposed to the RNA-synthesis inhibitor actinomycin D (ACD).
ACD (50 µM) incubation at the time of decentralization prevented
subsequent reacquisition of PD neuron bursting, but the inhibitor was
much less effective when applied at later postdecentralization times,
suggesting that the recovery process arises from new protein synthesis
triggered when modulatory inputs are first removed. Moreover, in the
nondecentralized STG, trans-synaptic modulatory instruction may sustain
the conditional pyloric network phenotype by continuously regulating
expression of genes responsible for intrinsic neuronal rhythmogenesis.
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