P. Fort et al., PHARMACOLOGICAL CHARACTERIZATION AND DIFFERENTIATION OF NONCHOLINERGIC NUCLEUS BASALIS NEURONS IN-VITRO, NeuroReport, 9(1), 1998, pp. 61-65
USING intracellular recordings in guinea pig brain slices, the pharmac
ology of electrophysiologically identified and immunohistochemically c
onfirmed non-cholinergic nucleus basalis neurons was studied to determ
ine their response to the major neurotransmitters of the subcortical a
fferents to this region. The cells were differentiated into three type
s: Type A cells (similar to 44%) were depolarized by noradrenaline (NA
) and muscarine, Type B cells (similar to 23%) were depolarized by NA
but hyperpolarized by muscarine, and Type C cells (similar to 15%) wer
e hyperpolarized by both agonists. These cell types were also differen
tially responsive to serotonin (hyperpolarizing B, C) and histamine (d
epolarizing A, B). Accordingly, the non-cholinergic neurons share cert
ain discharge properties but appear nonetheless to comprise distinct t
ypes which respond differentially to the major modulatory neurotransmi
tters and thus play potentially different roles in cortical modulation
across the sleep-wake cycle.