To develop the BALB/c mouse strain as an animal model for the study of
progressive sensorineural hearing loss, mice ranging in age from youn
g adult through middle age were studied. Auditory brainstem response t
hresholds, histopathology [cytocochleograms for hair cells, the packin
g density of spiral ganglion cells (SGCs), the number of neurons and o
verall size of the anterior ventral cochlear nucleus (AVCN)], and beha
vioral paradigms (prepulse inhibition. fear-potentiated startle) were
compared with previous data from C57BL/6J (C57) and DBA/2J (DBA) mouse
strains. Progressive high frequency hearing loss in BALB/c mice was g
enerally more rapid than C57 and slower than DBA (e.g. mean thresholds
for 16 kHz: 10-month-old BALB/c mice = 71 dB SPL; 55-day-old DBA mice
= 79 dB SPL: 12-month-old C57 mice = 50 dB SPL). Like the other strai
ns, BALB/c exhibited a progressive loss of hair cells and SGCs that wa
s most severe in the cochlear base and least severe in the middle turn
s; however, BALB/c mice had relatively more SGC loss in the apex. Unli
ke C57 and DBA, no loss of neurons was observed in the AVCN following
cochlear pathology (although AVCN volume was reduced). Like the other
strains, successful fear conditioning was obtained with a 12 kHz condi
tioned stimulus. Prepulse inhibition showed that middle and low freque
ncy tones (4-12 kHz) became more salient as high frequency hearing dec
lined. Similar results had been previously obtained with C57 and DBA m
ice and were interpreted as reflecting hearing-loss-induced plasticity
in the central auditory system. (C) 1998 Elsevier Science B.V.