This study examined the nature of spontaneous discharge patterns in cochlea
r ganglion cells in embryonic day 13 (E13) to early E17 chicken embryos (st
ages 39-43). Neural recordings were made with glass micropipettes. No sound
-driven activity was seen for the youngest embryos (maximum intensity 107 d
B sound pressure level). Ganglion cells were labeled with biotinylated dext
ran amine in four embryos. In two animals, primary afferents projected to h
air cells in the middle region along the length of the basilar papilla in w
hich, in one cell, the terminals occupied a neural transverse position and,
in the other, a more abneural location. Statoacoustic ganglion cells showi
ng no spontaneous activity were seen for the first time in the chicken. The
proportion of "silent" cells was largest at the youngest stages (stage 39,
67%). In active cells, mean spontaneous discharge rates [9.4 +/- 10.4 spik
es (Sp)/sec; n = 44] were lower than rates for older embryos (19 +/- 17 Sp/
sec) (Jones and Jones, 2000). Embryos at stages 39-41 evidenced even lower
rates (4.2 +/- 5.0 Sp/sec). The most salient feature of spontaneous activit
y for stages 39-43 was a bursting discharge pattern in >75% of active neuro
ns (33 of 44). Moreover, in 55% of these cells, there was a clear, slow, rh
ythmic bursting pattern. The proportion of cells showing rhythmic bursting
was greatest at the youngest stages (39-42) and decreased to <30% at stage
43. Rate of bursting ranged from 1 to 54 bursts per minute. The presence of
rhythmic bursting in cochlear ganglion cells at E13-E17 provides an explan
ation for the existence of such patterns in central auditory relays. The bu
rsting patterns may serve as a patterning signal for central synaptic refin
ements in the auditory system during development.