The cockroach escape response begins with a turn away from a wind puff such as that generated by an approaching predator. The presence and direction of that wind is detected by hairs on the animal's cerci, and this information is conducted to the thoracic ganglia via two populations of giant interneurons. In the thoracic ganglia, the giant interneurons excite a number of interneurons, at least some of which in turn excite motor neurons that control leg movement. In this paper we examine response properties of various thoracic neurons to wind stimuli originating from different directions. Three sets of thoracic neurons were distinguished on the basis of latency. Type A interneurons had short latencies to wind stimuli (1.3-2.25 ms). Type B interneurons had longer latencies (4-6 ms), and motor neurons had the longest latencies (5.6-17.0 ms). Individual type A interneurons either responded equally to wind from all directions or were biased in their response. Directionality was related to the presence of ventral branches near one or both sides of the midline of the ganglion. Cells with ventral median (VM) branches on either side tended to be omnidirectional or front-rear biased, whereas cells with VM branches on only one side were biased to that side. Although several type B interneurons had strong wind responses and were directionally sensitive, they did not have VM branches. We hypothesize that the presence of VM branches in type A interneurons permits connection with ventral giant interneurons, and this connection accounts for their short latency and directional properties. This hypothesis will be tested in the companion paper.
Dorsal unpaired median (DUM) cells in orthopteran insects are known to contain the neuromodulatory substance octopamine, and DUM cells with peripheral axons augment synaptic activity at neuromuscular junctions. One of the most studied systems in the cockroach is the giant interneuron (GI) system which controls the initial movements of a wind-mediated escape response. Our data demonstrate that DUM cells that are restricted to the central nervous system (DUM interneurons) receive inputs from ventral giant interneurons (vGIs) but not from dorsal giant interneurons (dGIs). In contrast, DUM cells that have peripheral axons consistently fail to be excited by any giant interneurons. The DUM interneurons are excited by vGIs on both sides of the CNS and, when the vGIs are excited in pairs, summation occurs. Wind fields that have been generated for two of the DUM interneurons are omnidirectional. These data, taken along with the known association of DUM cells with the neuromodulatory substance octopamine, suggest that the DUM interneurons may act to modulate central synapses.
In order to determine the contribution of individual giant interneurons (GIs) to wind-evoked motor outputs, responses were recorded from depressor and levator motor neurons in the cockroach Periplaneta americana to wind puffs of different directions. The depressor response was generally stronger to wind from the ipsilateral rear than to wind from the contralateral rear. The levator response was more variable but was more often stronger to wind from the contralateral rear than to wind from the ipsilateral rear. These results are as expected based on behavioral responses to wind puffs. (Camhi and Tom, 1978). The depressor response was nearly or totally abolished by severing the ipsilateral connective of the nerve cord but was little affected by severing the contralateral connective. The levator response was greatly reduced for some angles by severing the ipsilateral connective and for other angles by severing the contralateral connective. Blocking conduction in the ipsilateral GI 5 nearly or completely abolished the depressor response to wind from the ipsilateral rear. This is the first time that a GI has been shown to be necessary, not just sufficient, for a given motor output.
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