K. Parham et Do. Kim, SPONTANEOUS AND SOUND-EVOKED DISCHARGE CHARACTERISTICS OF COMPLEX-SPIKING NEURONS IN THE DORSAL COCHLEAR NUCLEUS OF THE UNANESTHETIZED DECEREBRATE CAT, Journal of neurophysiology, 73(2), 1995, pp. 550-561
1. We examined the spontaneous and sound-evoked discharge characterist
ics of 20 complex-spiking units recorded in the dorsal cochlear nucleu
s (DCN) of 15 unanesthetized, decerebrate cats. 2. The extracellularly
recorded complex spikes consisted of bursts of two to five action pot
entials whose size gradually decreased during the burst. Complex spike
s were observed both in the spontaneous and sound-evoked activity of t
he units in our sample. 3. The spontaneous rates (SRs) of DCN complex-
spiking units ranged from 0 to 30 spikes/s. Spontaneous activity consi
sted of complex and simple (i.e., the common single neuronal action po
tential) spikes. Comparison of the SR distributions of the DCN complex
-spiking units with that of a total sample of 194 DCN units (from 9 ca
ts) suggests that the complex-spiking units tended to be in the lower
half of the DCN SR distribution. 4. Sound-evoked discharges could cons
ist of both complex and simple spikes. On the basis of their sound-dri
ven responses, we divided the DCN complex-spiking units into two group
s. The majority (15 of 20, 75%) were weakly driven by pure tones and i
nhibited by broadband noise. They tended to have broad response areas.
Their response latencies to pure tone and noise stimuli were relative
ly long (10-20 ms). The recording depths of these units tended to be s
uperficial (i.e., 10 of 15 units were located within 400 mu m of the d
orsal surface of the DCN). A minority (5 of 20, 25%) of the complex-sp
iking units were strongly driven by pure tone and broadband noise stim
uli. These units had more clearly defined excitatory regions of respon
se areas than the weakly driven units. Their response latencies to pur
e tone and noise stimuli were short (< 10 ms). The recording depths of
these units tended to be deeper (i.e., 4 of 5 units were located at 4
00-700 mu m) than those of the weakly driven units. 5. Intracellular r
ecording and labeling studies of in vitro DCN slice preparations have
correlated complex spikes with the superficially located cartwheel cel
ls. Given the complex spikes of the units, many of which were located
superficially, we suggest that our sample, particularly the weakly dri
ven group of neurons, corresponds to the cartwheel cells. 6. Cartwheel
cells are putative inhibitory interneurons whose axons primarily cont
act on the main projection neurons of DCN, the fusiform cells. The pre
sent finding of sound-evoked discharges by the superficially located c
omplex-spiking units suggests that cartwheel cells should play a role
in modifying the sound-evoked responses of the fusiform cells.