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The Journal of Neurophysiology Vol. 81 No. 5 May 1999, pp. 2437-2450
Copyright ©1999 by the American Physiological Society
Neurobiology, Physiology, and Behavior, University of California, Davis, California 95616-8519
Namba, Hisaaki and
Brian Mulloney.
Coordination of Limb Movements: Three Types of Intersegmental
Interneurons in the Swimmeret System and Their Responses to Changes in
Excitation. J. Neurophysiol. 81: 2437-2450, 1999.
Coordination of limb movements: three types of intersegmental
interneurons in the swimmeret system and their responses to changes in
excitation. During forward locomotion, the movements of
swimmerets on different segments of the crayfish abdomen are coordinated so that more posterior swimmerets lead their anterior neighbors by ~25%. This coordination is accomplished by mechanisms within the abdominal nerve cord. Here we describe three different types
of intersegmental swimmeret interneurons that are necessary and
sufficient to accomplish this coordination. These interneurons could be
identified both by their structures within their home ganglion and by
their physiological properties. These interneurons occur as bilateral
pairs in each ganglion that innervates swimmerets, and their axons
traverse the minuscule tract (MnT) of their home ganglion before
leaving to project to neighboring ganglia. Two types, ASCE
and ASCL, projected an axon anteriorly; the third type,
DSC, projected posteriorly. Each type fires a burst of impulses starting at a different phase of the swimmeret cycle in its home ganglion. In active preparations, excitation of individual
ASCE or DSC interneurons at different phases in the cycle
affected the timing of the next cycle in the interneuron's target
ganglion. The axons of these interneurons that projected between two
ganglia ran close together, and their firing often could be recorded by the same electrode. Experiments in which either this tract or the rest
of the intersegmental connectives was cut bilaterally showed that these
interneurons were both necessary and sufficient for coordination of
neighboring swimmerets. When the level of excitation of the swimmeret
system was increased by bath application of carbachol, the period of
the system's cycle shortened, but the characteristic phase difference
within and between ganglia was preserved. Each of these interneurons
responded to this increase in excitation by increasing the frequency of
impulses within each burst, but the phases and relative durations of
their bursts did not change, and their activity remained coordinated
with the cycle in their home ganglion. The decrease in duration of each
burst was matched to the increase in impulse frequency within the burst so that the mean numbers of impulses per burst did not change significantly despite a threefold change in period. These three types
of interneurons appear to form a concatenated intersegmental coordinating circuit that imposes a particular intersegmental phase on
the local pattern generating modules innervating each swimmeret. This
circuit is asymmetric, and forces posterior segments to lead each cycle
of output.
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