Dorsal unpaired median ( DUM ) neurons are bilaterally symmetrical. A single primary neurite arises from the soma and runs anteriorly through the neuropil before dividing into two lateral neurites which pass to the nerve roots on each side of the ganglion. The primary neurite runs in one of two tracts, one of which lies further from the surface of the ganglion than the other. The primary neurites in the deeper tract belong to DUM1 , DUM5 and DUM3 ,4,5 neurons, and those in the more superficial tract, to DUM3 , DUM3 ,4 and DUM3 ,4,5 neurons. Previous studies have shown that in the developing embryonic nervous system the primary neurites of DUM neurons can also be observed to lie in one of two tracts, but these do not appear to correspond to those seen in the adult. The results described here differ further from those of other investigations of adult and embryonic locusts in that no DUM4 ,5 neurons were seen, but DUM3 ,4 neurons, not found in previous studies, were frequently stained. The secondary neurites of DUM neurons characteristically give rise to fine 0.2-0.5 micron diameter processes which may run for hundreds of microns through the neuropil with very little branching. The problems this may pose for signal transmission along such processes is discussed. Presynaptic processes of several types make inputs on to spines on the lateral neurites of DUM neurons and on to branches from secondary neurites. Output synapses were rarely observed and were found only on lateral neurite spines. It therefore appears unlikely that the DUM neurons examined play a major central role within the metathoracic ganglion. A novel structure, with the appearance of a presynaptic density but which was not associated with synaptic vesicles, was found in certain regions of the neurons.

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gamma-Aminobutyric acid (GABA) and glycine have been implicated in the inhibition of sensory pathways in the dorsal horn of the spinal cord. The object of this study is to investigate the interactions between neurones immunoreactive for GABA and/or glycine and hair follicle afferent terminals labelled by intracellular injection with neurobiotin. GABA and glycine-like immunoreactivity in axons and dendrites in synaptic contact with the afferent terminals was demonstrated by using a postembedding immunogold method, and serial section reconstruction was used to show the distribution and nature of these interactions in lamina III of the dorsal horn. Most afferent boutons (94%) were postsynaptic at axo-axonic synapses: 67% of presynaptic boutons presynaptic to the afferent terminals were immunoreactive for GABA and glycine, 24% for GABA alone, and 7% for glycine alone. Only a small percentage of dendrites postsynaptic to afferent boutons appeared to belong to inhibitory interneurones: 3% were immunoreactive for GABA and glycine, 10% for glycine alone, but 87% were immunoreactive for neither antibody. Many afferent boutons were the central terminals of what appeared to be type IIb glomeruli and were involved triadic synaptic arrangements at which boutons presynaptic to an afferent terminal also made axodendritic contacts with dendrites postsynaptic to the afferent. Many of the presynaptic boutons involved in the triads were immunoreactive for GABA and glycine. Because afferent terminals do not themselves express glycine receptors (Mitchell et al. [1993] J. Neurosci. 13:2371-2381), glycine may therefore act on dendrites postsynaptic to hair follicle afferent terminals at these triads.