In the frog, unitary electrophysiological recordings have been extensi
vely used to investigate odor processing along the olfactory pathways.
From the responses of primary second-order neurons, neuroreceptor and
mitral cells, odor stimuli could be classified in qualitative groups,
revealing that neuronal discriminative mechanisms are partly based on
the structure of odor molecule. In the olfactory bulb, thanks both to
the anatomical convergence of primary afferences and intrinsic networ
k properties, mitral cells have been demonstrated to gain in odor disc
rimination and detection power abilities. GABAergic bulbar interneuron
s were found to be involved in the control of mitral cell excitability
, adjusting response thresholds and duration and promoting a progressi
ve increase of burst discharges with stimulus concentration. Otherwise
, dopamine was observed to shunt off mitral cell spontaneous activity
without altering their odor responsivity properties. Dopamine was demo
nstrated to act through D2 receptors. Matching anatomical and electrop
hysiological data, D2 receptors are assumed to be localized on mitral
cells. The frog olfactory cortex neurons, silent at rest, could be seg
regated in two functional groups basing on their odor response propert
ies. The first group shared most intensity coding properties with mitr
al cells while showing a lower discriminative power, similar to that o
f neuroreceptor cells. By contrast, the second group provided only min
imal intensity coding and, basing on its high discrimination power, wa
s assumed to be mainly devoted to odor discrimination. Thus, along the
olfactory pathways, intensity and quality odor parameters which are s
imultaneously encoded by a neuroreceptor or mitral cell, become specif
ied by two distinct populations in the cortex. (C) 1997 Elsevier Scien
ce Ltd.