Ultrastructure of bombesin-like immunoreactive nerve terminals in the nucleus of the solitary tract and the dorsal motor nucleus.

Bombesin (gastrin-releasing peptide 14-27) inhibits gastric function and feeding when microinjected into the nucleus of the solitary tract (NTS)/dorsal motor nucleus of the vagus (DMV) complex. We performed a preembedding immunoelectron microscopic study in rats to describe the bombesin containing nerve terminals and to characterize their postsynaptic structures. 228 bombesin-L1 nerve terminals which made synaptic contacts in the NTS/DMV complex were studied. Labeling was heaviest over dense core vesicles and lighter over small clear vesicles. The dense core vesicles were typically located along the plasmalemma away from the synaptic face, a finding that is typical of neuropeptide containing nerve terminals. The postsynaptic structures were most often medium sized dendrites (56%) and small sized dendrites (27%), with similar percentages in the NTS and DMV. In the DMV, synapses on cell bodies (8%) were more frequent than in the NTS (1%). In the NTS, synapses on dendritic spines (10%) were more frequent than in the DMV (4%). Only a single axo-axonal contact was identified. These findings add to the increasing body of evidence that bombesin is a neurotransmitter/neuromodulator in the NTS/DMV complex. Bombesin rarely makes presynaptic (axo-axonal) contacts that might inhibit the release of excitatory neurotransmitters, but rather makes postsynaptic contacts potentially effecting vagal motoneurons.