Loading…
Serotonergic and Peptidergic Modulation of the Buccal Mass Protractor Muscle (I2) in Aplysia
1 Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York, New York 10029; 2 Department of Life Sciences, Bar-Ilan University, Ramat-Gan 52 900, Israel; and 3 Center for Neurobiology and Behavior, College of Physicians and Surgeons, Columbia University, New York, New...
Saved in:
Published in: | Journal of neurophysiology 2000-12, Vol.84 (6), p.2810-2820 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | 1 Department of Physiology and Biophysics,
Mount Sinai School of Medicine, New York, New York 10029;
2 Department of Life Sciences, Bar-Ilan
University, Ramat-Gan 52 900, Israel; and
3 Center for Neurobiology and Behavior, College
of Physicians and Surgeons, Columbia University, New York, New York
10032
Hurwitz, I.,
E. C. Cropper,
F. S. Vilim,
V. Alexeeva,
A. J. Susswein,
I. Kupfermann, and
K. R. Weiss.
Serotonergic and Peptidergic Modulation of the Buccal Mass
Protractor Muscle (I2) in Aplysia . J. Neurophysiol. 84: 2810-2820, 2000. Plasticity of
Aplysia feeding has largely been measured by noting changes
in radula protraction. On the basis of previous work, it has been
suggested that peripheral modulation may contribute to behavioral
plasticity. However, peripheral plasticity has not been demonstrated in
the neuromuscular systems that participate in radula protraction.
Therefore in this study we investigated whether contractions of a major
radula protraction muscle (I2) are subject to modulation. We
demonstrate, first, that an increase in the firing frequency of the
cholinergic I2 motoneurons will increase the amplitude of the resulting
muscle contraction but will not modulate its relaxation rate. We show,
second, that neuronal processes on the I2 muscle are immunoreactive to
myomodulin (MM), RFamide, and serotonin (5-HT), but not to small
cardioactive peptide (SCP) or buccalin. The I2 motoneurons B31, B32,
B61, and B62 are not immunoreactive to RFamide, 5-HT, SCP, or buccalin.
However, all four cells are MM immunoreactive and are capable of
synthesizing MMa. Third, we show that the bioactivity of the different
modulators is somewhat different; while the MMs (i.e., MMa and MMb) and
5-HT increase I2 muscle relaxation rate, and potentiate muscle
contraction amplitude, MMa, at high concentrations, depresses muscle
contractions. Fourth, our data suggest that cAMP at least partially
mediates effects of modulators on contraction amplitude and relaxation rate. |
---|---|
ISSN: | 0022-3077 1522-1598 |
DOI: | 10.1152/jn.2000.84.6.2810 |