Post-synaptic inhibition of bulbar inspiratory neurones in the cat.

Stable intracellular recordings from thirty-six bulbar inspiratory neurones revealed three centrally originating, rhythmic patterns of synaptic inhibition (i.p.s.p.s). (i) A declining pattern of i.p.s.p.s accompanying the early stages of inspiration (early inspiratory inhibition) was identified in a total of twenty neurones representing examples of each of the functional classes of bulbar neurones examined, i.e. six R alpha- and two R beta-neurones of the dorsal respiratory group and twelve R alpha-neurones of the ventral respiratory group. (ii) A transient pattern of i.p.s.p.s just preceding or coinciding with the cessation of inspiration (late inspiratory inhibition) was present in the remaining sixteen neurones which were tested, representing six R alpha-neurones and three R beta-neurones of the dorsal respiratory group and seven R alpha-neurones of the ventral respiratory group. (iii) An augmenting pattern of expiratory i.p.s.p.s was present in all thirty-six neurones. Late inspiratory and expiratory i.p.s.p.s in the same neurones showed a similar time course of reversal when chloride was injected or allowed to diffuse into the cells and were associated with similar increases in input conductance. Both patterns of i.p.s.p.s appear to arise at or close to the cell soma. Early inspiratory i.p.s.p.s required a relatively longer period of chloride injection for reversal to be accomplished. Input conductance changes were either absent or smaller than those associated with late inspiratory or expiratory inhibition. These i.p.s.p.s appear to arise at more distal dendritic sites. These patterns of i.p.s.p.s are discussed in relation to the mechanisms shaping the growth of central inspiratory activity, bringing this activity to an end, and suppressing its redevelopment during expiration.