The ventral nerve cord of crayfish contains axons of five pairs of exc
itatory interneurons, each of which can activate the swimmeret system.
Perfusion of the ventral nerve cord with the neuropeptide proctolin a
lso activates the swimmeret system. The experiments reported here were
conducted to test the hypothesis that one or more of these excitatory
interneurons uses proctolin as a transmitter. Each of the five excita
tory axons was located and stimulated separately in an individual cray
fish, and similar motor activity was elicited by stimulating each of t
hem. Quantitative comparison of spontaneous swimmeret motor patterns w
ith activity caused by stimulating one of these excitatory axons, E(C)
, or by perfusing with proctolin solutions showed that the motor patte
rns produced under these three conditions were not significantly diffe
rent (P > 0.05). By using a new, affinity-purified proctolin antiserum
, we labeled axons in the connective tissue between the last thoracic
and first abdominal ganglion and compared the positions of labeled axo
ns with the previously described positions of the excitatory axons. Ab
out 0.3% of the axons in these connective tissues showed proctolin-lik
e immunoreactivity, but heavily labeled pairs of axons did occur bilat
erally in the regions of excitatory swimmeret axons. The projections o
f these labeled axons into the abdominal ganglia were traced in serial
plastic sections. Labeled processes were abundant in the lateral neur
opils, the loci of the swimmeret pattern-generating circuitry. From th
is evidence, we propose that three of these excitatory swimmeret inter
neurons use proctolin as a transmitter, but that a fourth does not. Th
e evidence for the fifth axon is ambiguous. (C) 1994 Wiley-Liss, Inc.