The role of nerve growth factor (NGF) and glial-derived neurotrophic factor
(GDNF) in sympathetic sprouting within the dorsal root ganglion was invest
igated. In nerve-intact rats, intrathecal NGF (1 mg/ml, 14 days) but not GD
NF (1 mg/ml, 14 days) induced extensive sprouting of tyrosine hydroxylase i
mmunoreactive (TH-IR) fibres and formation of pericellular TH-IR baskets wi
thin lumbar DRGs. TH-LR baskets were distributed equally to trkA-expressing
and trkA-negative neuronal profiles. Sciatic nerve transection (14-21 days
) induced TH-IR baskets within lumbar DRG's around neuronal profiles with b
oth intact and lesioned axons. The percentage of neuronal profiles surround
ed by TH-IR baskets following sciatic transection was unaffected following
peripheral application of the NGF sequestering antibody, trkA-IgG (1 mg/ml,
14 days), Intracellular responses were recorded from sensory neurons in an
in vitro DRG/peripheral nerve preparation following bath application of no
radrenaline. In preparations from animals treated 14 days previously with i
ntrathecal NGF, 69% of neurons responded with depolarizing responses whilst
18% of neurons responded to bath applied noradrenaline in tissue prepared
from naive animals. Our data indicate that sympathetic neurons sprout into
the DRG in response to sciatic nerve injury and intrathecal NGF but not GDN
F. Distribution of sympathetic sprouts within the DRG is independent of whe
ther target neurons are injured or express trkA. Sequestration of NGF at th
e peripheral injury site does not influence basket formation within the DRG
. It is likely that functional noradrenergic connections exist between symp
athetic sprouts and sensory neuron cell bodies following exogenous NGF. (C)
1999 International Association for the Study of Pain. Published by Elsevie
r Science B.V.