The fine structure of the periaqueductal gray (PAG) of the rabbit was examined using the transmission electron microscope. On the basis of synaptic polarity, vesicle size, and the nature of the pre- and postsynaptic elements, 10 essentially different synaptic types could be discerned (6 axo-dendritic, 2 axo-somatic, 1 axo-axonic, and 1 dendro-dendritic). Synaptic contacts on the soma of PAG neurons were small and covered, on average, only 1.6% of the soma surface. The most striking feature of the synaptic structure of the PAG was that more than 94.1% of all synapses were axo-dendritic. Of these, 83.5% were of the symmetrical type. Most of these contacts occurred on buttons of small to medium size, and contained either round vesicles of medium size or pleomorphic vesicles of medium size. Boutons containing only flattened vesicles were quite rare. Boutons contacting larger dendrites were generally small-to-medium in size, made asymmetric-type synaptic contacts, and contained pleomorphic vesicles of medium-to-large size. Medium-sized dendrites were contacted principally by small boutons exhibiting either symmetrical or asymmetrical junctions containing medium-sized pleomorphic vesicles, and in addition a few of these boutons contained both large, and small, round vesicles. Dendritic spines were generally provided with only one synaptic contact, stretching the entire width of the spinous process. Boutons and the spines on dendrites were approximately the same size. Synapses between two vesicle-containing structures (axo-axonic or dendro-dendritic synapses) were rare (1.4%). They were generally asymmetric and contained round vesicles of medium size. Complex synapses, where a glial sheet enclosed the synapse, were occasionally observed. Also seen were multiple synapses, with up to 11 contacts on a single dendritic profile. Large dense-core vesicle were seen in approximately 40% of all synapses, whereas small dense-core vesicles were only found in about 3%. Data is provided on how different synaptic features relate to ventral, lateral, dorsal, and medial PAG. Principally this is in relation to neuron size, glia cell content, axonal characterization, and vesicular type.
