Direct injection of agents into the dorsal root ganglia (DRGs) offers the
opportunity to manipulate sensory neuron function at a segmental level to
explore pathophysiology of painful conditions. However, there is no described
method that has been validated in detail for such injections in adult rats. We
have found that 2 (µl of dye injected through a pulled glass pipette
directly into the distal DRG, exposed by a minimal foraminotomy, produces
complete filling of the DRG with limited extension into the spinal roots.
Injection into the spinal nerve required 3 µl to achieve comparable DRG
filling, produced preferential spread into the ventral root, and was accompanied
by substantial leakage of injected solution from the injection site. Injections
into the sciatic nerve of volumes up to 10 (µl did not reach the DRG.
Transient hypersensitivity to mechanical stimulation at threshold (von Frey) and
noxious levels (pin) developed after 2 µl saline injection directly into
the DRG that was in part attributable to the surgical exposure procedure alone.
Only minimal astrocyte activation in the spinal dorsal horn was evident after
DRG saline injections. Injection of adeno-associated virus (AAV) vector
conveying green fluorescent protein (GFP) transgene resulted in expression as
soon as 1 day after injection into the DRG, including fibers in the spinal
dorsal horn and columns. AAV injection into the DRG produced additional thermal
hypersensitivity and withdrawal from the stroke of a brush and compromised motor
performance. These findings demonstrate a method for selective injection of
agents into single DRGs for anatomically restricted actions.