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Volume 16, Number 24,
Issue of December 15, 1996
pp. 8105-8114
Copyright ©1996 Society for Neuroscience
Release of Peptide Cotransmitters in Aplysia:
Regulation and Functional Implications
Received June 24, 1996; revised Sept. 20, 1996; accepted Sept. 24, 1996.
F. S. Vilim1, 3,
E. C. Cropper3,
D. A. Price2,
I. Kupfermann1, and
K. R. Weiss3
1 Center for Neurobiology and Behavior, College of
Physicians and Surgeons, Columbia University, New York, New York 10032, 2 C. V. Whitney Laboratories, University of Florida, St.
Augustine, Florida 32086, and 3 Department of Physiology
and Biophysics, Mount Sinai School of Medicine, New York, New York
10029
To gain insights into the physiological role of cotransmission, we
measured peptide release from cell B15, a motorneuron that utilizes ACh
as its primary transmitter but also contains putative peptide
cotransmitters, the small cardioactive peptides (SCPs) and the
buccalins (BUCs). All stimulation parameters used were in the range in
which B15 fires in freely moving animals. We stimulated neuron B15 in
bursts and systematically varied the interburst interval, the
intraburst frequency, and burst duration. Both peptides were
preferentially released when B15 was stimulated at higher intra- or
interburst frequencies or with longer burst durations. Across
stimulation patterns, the amount of peptide released depended on the
mean frequency of stimulation and was independent of the specific
pattern of stimulation. The parameters of stimulation that produce a
larger release of peptides correspond to those that evoke larger
contractions. Large and frequent contractions are likely to fuse or
summate, thus disrupting the rhythmic behavior mediated by the muscle
innervated by motorneuron B15. Because the combined effect of the SCPs
and BUCs is to accelerate the relaxation and shorten the duration of
muscle contractions, these peptides reduce the probability of the
disruptive fusion or summation of muscle contractions. Because these
cotransmitters regulate an aspect of muscle contractions that is not
controlled by acetylcholine (ACh), the primary transmitter of B15, we
suggest that peptides and ACh form parallel but functionally distinct
lines of transmission at the neuromuscular junction. Both types of
transmission may be necessary to ensure that behavior remains efficient
over a wide range of conditions.
Key words:
neuropeptides;
dense-core vesicles;
peptide
release;
Aplysia;
cotransmission;
confocal
immunocytochemistry;
motorneuron;
modulation;
muscle contractions;
feeding
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