T. Palmgren et al., IMMUNOHISTOCHEMICAL DEMONSTRATION OF SENSORY AND AUTONOMIC NERVE-TERMINALS IN HERNIATED LUMBAR DISC TISSUE, Spine (Philadelphia, Pa. 1976), 21(11), 1996, pp. 1301-1306
Study Design. Thirty-five lumbar disc herniations removed at surgery w
ere studied by indirect immunocytochemistry. Objectives. To localize i
mmunohistochemically both sensory and autonomic nerve terminals in dis
c herniations. Summary of Background Data. Using various more or less
specific histologic and histochemical methods, investigators have repo
rted the presence of free nerve terminals in disc tissue. However, ver
y few studies have, to date, convincingly demonstrated nerve terminals
in disc tissue that morphologically resemble the tiny nerve terminals
of sensory and autonomic nerve fibers. Methods. Amplification of the
peroxidase reaction product in avidin-biotin-peroxidase complex immuno
staining by the glucose oxidase-diaminobenzidine-nickel sulfate method
was used to visualize small punctate nerve terminals at high magnific
ation. Thin frozen sections from disc herniation tissue prefixed in Za
mboni fixative were incubated with antibodies to synaptophysin to visu
alize nerve terminals in general, and with antibodies to substance P a
nd C-flanking peptide of neuropeptide Y to further characterize nerve
terminals as either sensory or sympathetic. Results. Nerve terminals c
ould be demonstrated in 29 (83%) of the 35 disc herniations. They were
observed with the synaptophysin antibody in 17 of 35 (49%) disc herni
ations, with substnace P in 16 of 35 (46%) disc herniations, and with
C-flanking peptide of neuropeptide Y in 13 of 35 (37%) disc herniation
s. Morphologically, the nerve terminals were seen as tiny immunoreacti
ve dots. Some of the nerve terminals were observed close to disc cells
, possibly suggesting direct interaction. Conclusions. Small nerve ter
minals in disc herniations, both sensory substance P endings and sympa
thetic C-flanking peptide of neuropeptide Y endings, could be involved
in mechanisms of discogenic pain, disc tissue neurogenic inflammation
, tissue repair processes after injury, and control of local blood cir
culation in the newly formed blood vessels. Disc cells may be directly
affected by the neuropeptides released from nearby nerve terminals.