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Serotonin produces long-term changes in the excitability of Aplysia sensory neurons in culture that depend on new protein synthesis

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Dale, N, Kandel, ER, Schacher, S·1987·The Journal of Neuroscience

Abstract

When isolated and grown in cell culture, the sensory and motor neurons of the gill withdrawal reflex of Aplysia readily form synaptic connections. Repeated exposures to 5-HT cause facilitation of the synaptic connections between co-cultured sensory and motor neurons lasting at least 24 hr. As a first step toward understanding the locus and the mechanisms underlying this long-term synaptic facilitation, we have examined the membrane excitability of the isolated presynaptic sensory neurons grown alone in dissociated cell culture. Four repeated applications of 1 microM 5-HT caused a significant increase in the excitability of sensory neurons, lasting at least 24 hr. This resembles the short-term changes in excitability seen in response to a single application of 5-HT. Unlike the short-term effect, this long-lasting change was blocked by exposure of the cells during the 5-HT treatment to 10 microM anisomycin, an inhibitor of protein synthesis. Thus, like the synaptic facilitation, the long-term change in excitability of the isolated presynaptic neurons differs from the short-term in requiring the synthesis of new protein. This finding suggests that the sensory neuron uses gene products to modulate membrane currents in its long- term response to repeated external stimuli that are not required in its short-term response to a single stimulus.

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Crossref · 10.1523/jneurosci.07-07-02232.1987

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Figures

Figure 1 Repeated application of 5-HT causes a long-term change in the excitability of sensory neurons in synaptic contact with L7 motor neurons. The excitability of a sensory neuron recorded before and 24 hr after 5-HT treatment.
Figure 1 Repeated application of 5-HT causes a long-term change in the excitability of sensory neurons in synaptic contact with L7 motor neurons. The excitability of a sensory neuron recorded before and 24 hr after 5-HT treatment.CC-BY-NC-SA · From the PDF
'-ens L- () ee e e ei o s es a o n " y s e o ei- set nt A2, Examples of the spike trains evoked by current injection corresponding to the numbered points on the graph. B, In a control sensory neuron, the excitability declines over 24 hr. Figure 2.
'-ens L- () ee e e ei o s es a o n " y s e o ei- set nt A2, Examples of the spike trains evoked by current injection corresponding to the numbered points on the graph. B, In a control sensory neuron, the excitability declines over 24 hr. Figure 2.CC-BY-NC-SA · From the PDF
Image 3
CC-BY-NC-SA · From the PDF
Figure 4 Long-term changes in excitability are blocked by the protein synthesis inhibitor anisomycin. A, In the presence of 10 μM anisomycin, 5-HT cannot evoke a long-ter change iette o id s e s e e o a e ey ie te o sto rn ie e rs s s n and 24 hr later ().
Figure 4 Long-term changes in excitability are blocked by the protein synthesis inhibitor anisomycin. A, In the presence of 10 μM anisomycin, 5-HT cannot evoke a long-ter change iette o id s e s e e o a e ey ie te o sto rn ie e rs s s n and 24 hr later ().CC-BY-NC-SA · From the PDF
Figure 5 Neither 5-HT plus anisomycin nor anisomycin alone causes significant long-term changes in the excitability of sensory neurons at any of the interpolated current levels.
Figure 5 Neither 5-HT plus anisomycin nor anisomycin alone causes significant long-term changes in the excitability of sensory neurons at any of the interpolated current levels.CC-BY-NC-SA · From the PDF
Figure 6 Short-term changes in excitability do not require protein synthesis. A, Recording from an isolated sensory neuron that has been exposed to 10 μm anisomycin for 2 hr. The injection of depolarizing current (bottom trace) evokes 2 action potentials. B, One minute after the application of 1 μM 5-HT, the same current pulse evokes a continuous train of pulses. Note how the afterpotentials following the depolarizing pulse have been altered by the 5-HT. C, After 2 min of washing, the same current pulse evokes only 3 action potentials. The membrane potential of the cell and the amplitude of the injected current pulse shown in D are the same as in A-C.
Figure 6 Short-term changes in excitability do not require protein synthesis. A, Recording from an isolated sensory neuron that has been exposed to 10 μm anisomycin for 2 hr. The injection of depolarizing current (bottom trace) evokes 2 action potentials. B, One minute after the application of 1 μM 5-HT, the same current pulse evokes a continuous train of pulses. Note how the afterpotentials following the depolarizing pulse have been altered by the 5-HT. C, After 2 min of washing, the same current pulse evokes only 3 action potentials. The membrane potential of the cell and the amplitude of the injected current pulse shown in D are the same as in A-C.CC-BY-NC-SA · From the PDF
Figure 7 Summary bar chart showing the mean difference in the maximum number of spikes before and 24 hr after the 4 treatments. Bars represent 1 SEM.
Figure 7 Summary bar chart showing the mean difference in the maximum number of spikes before and 24 hr after the 4 treatments. Bars represent 1 SEM.CC-BY-NC-SA · From the PDF

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Cites

Research works printed but not linked: 1

  1. Frost, W. N., V. F. Castellucci, R. D. Hawkins, and E. R. Kandel (1985) The monosynaptic connections from the sensory neurons participate in the storage of long-term memory for sensitization of the gill-and siphon-withdrawal reflex in Aplysia. Proc. Natl. Acad. Sci. USA 82: 8266-8269.

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Metadata

Authors
Dale, N., Kandel, E., & Schacher, S.
Affiliations
Howard Hughes Medical Institute (US)
Venue
The Journal of Neuroscience
Published
1987-07-01
Volume
7
Issue
7
Pages
2232-2238
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W1625157937
Cited by
118
References
9
Citations by year
2026: 1 · 2024: 1 · 2023: 2 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2014: 5 · 2013: 2 · 2012: 2
FWCI
3.06
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
Keywords
serotonin, sensory neuron excitability, Aplysia, gill-withdrawal reflex, synaptic facilitation, long-term synaptic plasticity, anisomycin, presynaptic neurons, membrane currents, sensory-motor synapses
MeSH terms
Action Potentials, Animals, Anisomycin, Aplysia, Cells, Cultured, Gills, Nerve Tissue Proteins, Neurons, Afferent, Serotonin

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