Respiratory rhythm generation depends on a complex interaction between
synaptic and membrane properties of functionally defined neurons. To
gain a better understanding of how inhibitory and excitatory synaptic
inputs lead to the generation of the respiratory rhythm we analyzed th
e depolarization pattern of respiratory neurons that were recorded in
the transverse slice preparation of mice (P8-22) and the in vivo adult
cat. Using voltage-clamp recordings from respiratory neurons and spec
ific antagonists for inhibitory synaptic transmission we demonstrate u
nder in vitro conditions, that inspiratory (n = 7) and post-inspirator
y neurons (n = 13) received concurrent glycinergic and glutamatergic s
ynaptic input during inspiration. A similar conclusion was gained with
chloride injections into in vivo respiratory neurons. The inhibitory
input was essential not only for generating the characteristic depolar
ization pattern of respiratory neurons, but also for switching the res
piratory rhythm between inspiration and post-inspiration. The generati
on of the depolarization pattern depends also on intrinsic membrane pr
operties. Negative current injections reveal that excitatory synaptic
input was amplified by intrinsic bursting properties in some inspirato
ry neurons (n = 4) recorded in vitro. Although such properties have no
t been described,under in vivo conditions our findings suggest that wi
th respect to inspiratory, post-inspiratory and late-inspiratory neuro
ns, the principle network organization is similar under both in vitro
and in vivo conditions. (C) 1997 Elsevier Science B.V.