Abstract
The use of molluscan ganglia for neurobiological studies combines multiple technical advantages with demonstrated versatility. These benefits derive not only from the accessibility of individual neurons, and consequent ease of study, but also from the network properties of these neuronal arrays. A well-recognized advantage is that many molluscan neurons are distinct individuals. As a consequence, using criteria such as shape, size, position, electrophysiology and connectivity, molluscan neurons in several species have been identified. The use of identified cells permits incrementally assembling a library of specific information by the repeated study of the same cell in successive preparations. It further permits examination of those specific features which distinguish individual neurons, rather than studying only those general properties which are common to classes of similar cells. Similarly, specific network properties which characterize interconnections of identified cells may be used to examine or contrast particular elements, permitting analyses not available in such systems as cultured cell lines, chromaffin cells, or synaptosomes.
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References
Poulain B, Tauc L, Maisey EA, Wadsworth JDF, Mohan PM, Dolly JO. Neurotransmitter release is blocked intracellularly by botulinum neurotoxin, and this requires uptake of both toxin polypeptides by a process mediated by the larger chain. Proc Natl Acad Sci USA 1988; 85: 4090–4094.
Poulain B, Mochida S, Weller U, Högy B, Habermann E, Wadsworth JDF, Shone C, Dolly JO, Tauc L. Heterologous combinations of heavy and light chains from botulinum neurotoxin A and tetanus toxin inhibit neurotransmitter release in Aplysia. J Biol Chem 1991; 266: 9580–9585.
Strumwasser F. Types of information stored in single neurons. In: Wiersma CAG, ed. Invertebrate Nervous Systems. Chicago: University of Chicago Press, 1967: 291–319.
Gardner D. Bilateral symmetry and interneuronal organization in the buccal ganglia of Aplysia. Science 1971; 173: 550–553.
Gardner D, Kandel ER. Diphasic post-synaptic potential: a chemical synapse capable of mediating conjoint excitation and inhibition. Science 1972; 176: 675–678.
Gardner D, Kandel ER. Physiological and kinetic properties of cholinergic receptors activated by multi-action intemeurons in the buccal ganglia of Aplysia. J Neurophysiol 1977; 40: 333–348.
Tauc L, Hoffmann A, Tsuji S, Hinzen DH, Faille L. Transmission abolished on a cholinergic synapse after injection of acetylcholinesterase into the presynaptic neurone. Nature 1974; 250: 496–498.
Gardner D. Voltage-clamp analysis of a self-inhibitory synaptic potential in the buccal ganglia of Aplysia. J Physiol (London) 1977; 264: 893–920.
White RL, Gardner D. Self-inhibition alters firing patterns of neurons in Aplysia buccal ganglia. Brain Res 1981; 209: 77–83.
Baux G, Tauc L. Presynaptic actions of curare and atropine on quantal acetylcholine release at a central synapse of Aplysia. J Physiol (London) 1987; 388: 665–680.
Baux G, Fossier P, Tauc L. Histamine and FLRFamide regulate acetylcholine release at an identified synapse in Aplysia in opposite ways. J Physiol (London) 1990; 429: 147–168.
Gardner D, Stevens CF. Rate-limiting step of inhibitory post-synaptic current decay in Aplysia buccal ganglia. J Physiol (London) 1980; 304: 145–164.
Gardner D. Time integral of synaptic conductance. J Physiol (London) 1980; 304: 181–191.
Simonneau M, Tauc L, Baux G. Quantal release of acetylcholine examined by current fluctuation analysis at an identified neuro-neuronal synapse of Aplysia. Proc Natl Acad Sci USA 1980; 77: 1661 1665.
Gardner D. Paired individual and mean postsynaptic currents recorded in four-cell networks of Aplysia. J Neurophysiol 1990; 63: 1226–1240.
Gardner D. Sets of synaptic currents paired by common presynaptic or postsynaptic neurons. J Neurophysiol 1989; 61: 845–853.
Gardner D. Membrane-potential effects on an inhibitory post-synaptic conductance in Aplysia buccal ganglia. J Physiol (London) 1980; 304: 165–180.
Del Castillo J, Katz B. Quantal components of the end-plate potential. J Physiol (London) 1980; 124: 560–573.
Bekkers JM, Stevens CF. Presynaptic mechanism for long-term potentiation in the hippocampus. Nature 1990; 346: 724–729.
Malinow R, Tsien RW. Presynaptic enhancement shown by whole-cell recordings of long-term potentiation in hippocampal slices. Nature 1990; 346: 177–180.
Redman S. Quantal analysis of synaptic potentials in neurons cf the central nervous system. Physiol Rev 1990; 70: 165–198.
Gardner D. Presynaptic transmitter release is specified by postsynaptic neurons of Aplysia buccal ganglia. J Neurophysiol 1991; 66: 2150–2154.
Simonneau M, Taue L. Properties of miniature postsynaptic currents during depolarization-induced release at a cholinergic neuroneuronal synapse. Cell Molec Neurobiol 1987; 7: 175–189.
Gardner D. Static Determinants of Synaptic Strength. In: Gardner D, ed. The Neurobiology of Neural Networks. Cambridge: MIT Press, 1993 in press.
Faber DS, Korn H. Applicability of the coefficient of variation method for analyzing synaptic plasticity. Biophys J 1991; 60: 1288–1294.
Korn H, Faber DS. Quantal analysis and synaptic efficacy in the CNS. Trends in Neurosci 1991; 14: 439–445.
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Gardner, D. (1993). Transmitter Release in Aplysia: Applicability of Quantal Models and Evidence for Postsynaptic Control. In: DasGupta, B.R. (eds) Botulinum and Tetanus Neurotoxins. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9542-4_14
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DOI: https://doi.org/10.1007/978-1-4757-9542-4_14
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