Timing of activity of B7 and evidence that the activity of B7 corresponds to the
third largest unit on BN3. A, B7 is activated before
and during the retraction phase of a feeding-like motor program induced by
carbachol. Extracellular recordings from RN, BN2, and BN3 were made simultaneously
with an intracellular recording from B7. A schematic bar above the traces indicates
the protraction phase (open bars) and the retraction phase (filled bars). Note that
large-unit extracellular activity in RN and BN2 occurs at essentially the same time,
which is characteristic of an ingestion pattern (Morton and Chiel, 1993a,b). Neuron
B7 becomes active just before the onset of the retraction phase and remains active
throughout the retraction phase (as judged by activity in BN2). Action potentials in
B7 correspond to the third largest extracellular unit on BN3 (line labeled 3
pointing to the BN3 trace; second largest and largest units are indicated with lines
labeled 2 and 1, respectively). Between the first and second ingestive-like
patterns, B7 was injected with strong hyperpolarizing current (marked with a bar
labeled B). This blocked action potentials in B7 and abolished the third largest
extracellular units in BN3. The hyperpolarizing artifact has been suppressed so that
the voltage trace from B7 is visible; note that B7 is not generating action
potentials. B, Expanded timescale excerpt of the data
marked with a bar and the “B” in A. Note
the one-to-one correspondence between action potentials in B7 and extracellular
units in BN3. During hyperpolarization of B7, the third largest extracellular units
on BN3 are completely abolished and only return when B7 is released from
hyperpolarization. The hyperpolarizing artifact has again been suppressed so that
the voltage trace from B7 can be shown.