GABA‐immunoreactive neurons in the nematode Ascaris

Abstract γ‐Aminobutyric acid (GABA) immunoreactive neurons in the cephalic, somatic, and caudal regions of the Ascaris nervous system were visualized with serial section and whole‐mount GABA immunocytochemistry. In the ventral and dorsal nerve cords, GABA‐ like immunoreactivity (GLIR) is localized to the neurites and cell bodies of identified inhibitory motor neurons and to two fibers, one in each cord, that arise from neurons in the nerve ring. GLIR is absent from identified excitatory motor neurons and from ventral cord interneurons. In neurons containing GLIR, immunoreactivity was present throughout the cell, which argues against an exclusive localization of GABA at conventional synapses. In whole mounts, ten GABA‐immunoreactive neurons were present in the cephalic region. These include four nerve ring‐associated cells (the RME‐like cells), two bilaterally symmetrical pairs of lateral ganglia neurons (the amphid‐GABA and deirid‐GABA cells) and one bilaterally symmetrical pair of ventral ganglion cells (the VG‐GABA cells). In sections, the RME‐like cells and the VG‐GABA cells were consistently stained through the cephalic region. However, anti‐GABA staining of the lateral ganglia cells in sections was light, thus suggesting that they contain less GLIR than the other more intensely stained GABA‐immunoreactive neurons. In the caudal region, a single GABA‐immunoreactive neuron was present in the dorsal rectal ganglion. Our data suggest that these ten cephalic neurons, and a single dorsal rectal ganglion neuron, use GABA as a neurotransmitter.