AXONS AND SYNAPSES MEDIATING STARTLE-LIKE RESPONSES EVOKED BY ELECTRICAL-STIMULATION OF THE RETICULAR-FORMATION IN RATS - SYMMETRICAL AND ASYMMETRIC COLLISION EFFECTS
Js. Yeomans et al., AXONS AND SYNAPSES MEDIATING STARTLE-LIKE RESPONSES EVOKED BY ELECTRICAL-STIMULATION OF THE RETICULAR-FORMATION IN RATS - SYMMETRICAL AND ASYMMETRIC COLLISION EFFECTS, Brain research, 617(2), 1993, pp. 309-319
A new method for determining the locations, directions of transmission
and transmission times of synapses mediating electrically evoked resp
onses is proposed here. Electrical stimulation of pontine or medullary
reticular formation with one 0.1-ms pulse evokes a short-latency star
tle-like response. Two pulses were delivered to single sites at variou
s interpulse intervals and the currents required to evoke a criterion
startle response were measured. The results suggest that the startle-e
voking substrates have absolute refractory periods that range from 0.2
5-0.6 ms. When one pulse was delivered to a caudal pontine site and a
second pulse was delivered to a an ipsilateral medulla site, decreases
in required current were observed as interpulse interval increased fr
om +0.4 to +0.8 ms or as interpulse interval decreased from -0.4 to -0
.8 ms. These collision-like effects, being symmetric around an interpu
lse interval of 0, suggest that electrically evoked startle is mediate
d by fast axons that pass longitudinally through medulla. When one pul
se was delivered to the rostral pons and a second pulse to the ipsilat
eral medulla, however, required currents decreased sharply as interpul
se intervals increased from +0.4 to 1.0 ms and as interpulse intervals
decreased from +0.2 to -0.2 ms. These asymmetric collision-like effec
ts suggest that strong synapses in the caudal pons, transmitting from
pons to medulla, mediate electrically evoked startle. The 0.3-ms asymm
etry suggests that the transmission time (i.e., from presynaptic stimu
lus to postsynaptic action potential) averaged 0.3 ms via monosynaptic
connections. The short duration of collision (0.7 ms) suggests that o
nly one postsynaptic action potential was produced with high probabili
ty for each presynaptic action potential. From the localization of the
se effects and the short refractory periods, we estimate that < 60 gia
nt cells on each side of the ventral pontine reticular formation media
te the startle reflex in the rat.