A. Hiura et H. Ishizuka, EARLY MORPHOLOGICAL-CHANGES OF PRIMARY AFFERENT NEURONS AND THEIR PROCESSES IN NEWBORN MICE AFTER TREATMENT WITH CAPSAICIN, Experimental Brain Research, 101(2), 1994, pp. 203-215
Degenerating figures of dorsal root ganglion (DRG) neurons and their c
entral and peripheral processes (dorsal root and saphenous nerve) and
terminals (central terminals in the superficial dorsal horn and cutane
ous nerve of the hind paw dorsal skin) of neonatal mice were examined
30 min, 1, 2 and 5 h, and 2, 3, 5, and 10 days after subcutaneous inje
ction of capsaicin on post-natal day 2. Many small DRG neurons showed
degeneration Ih after treatment. Scarcely any features of degeneration
were seen in the DRG and dorsal root 10 days after treatment. The deg
enerating aspects of terminal axons in the marginal layer of the super
ficial dorsal horn were characterized by enlarged round axons with clo
sely packed osmiophilic materials, lamellar bodies, and loss of axopla
smic organelles. Two types of central terminals (C-terminals) showed d
egeneration in the substantia gelatinosa from 30 min after treatment o
nward. One type consisted of small, round, sinuous or slender dark ter
minals (CI-terminals), and the other of large, pale, round or angular
terminals (CII-terminals). Those that degenerated markedly had homogen
eously electron-dense axoplasm with dilated synaptic vesicles and incl
usion bodies. Extensive degeneration of terminal axons in the marginal
layer occurred 5 h after treatment, whereas conspicuous degeneration
of C-terminals occurred from 30 min to 10 days after treatment in the
substantia gelatinosa. CI-terminals showed marked degeneration during
the first 3 days, whereas marked degeneration of CII-terminals occurre
d between 5 and 10 days after treatment. This time difference between
the peaks of degeneration of CI- and CII-terminals indicates an import
ant difference in the origins of these two types of capsaicin-sensitiv
e, nociceptive fibers in the superficial dorsal horn; CI-terminals are
derived from small DRG cells, whereas CII-terminals are derived from
larger DRG cells. Unmyelinated axons in the dorsal root, saphenous ner
ve, and dorsal skin of the hind paw showed similar degeneration patter
ns 2 h after treatment to those of terminal axons in the marginal laye
r. Thus, the degenerating profiles in the marginal layer suggest that
these axons arose from collaterals of unmyelinated primary axons desce
nding or ascending within the marginal layer. Numerous enlarged degene
rating axons showing vacuolation were conspicuous in the dorsal skin 3
days after treatment. The synchronous degeneration of the smaller DRG
neurons, their central and peripheral processes, and their CI-termina
ls in the substantia gelatinosa supports the idea that the smaller DRG
neurons are directly influenced by capsaicin, and that their degenera
tion is followed by centrifugal degeneration.