Abstract
Modulation of sensory afferent inputs to the spinal cord by GABA appears to be an important physiological mechanism and may provide an antinociceptive control system. In the present study we have evaluated the antinociceptive activity of the GABA B receptor agonist, (±)-baclofen, in rats with unilateral chronic inflammatory or neuropathic hyperalgesia. (±)-Baclofen was antinociceptive in untreated control animals and both animal models. In the neuropathic model the sensitivity to (±)-baclofen was significantly increased by 3-fold in the ipsilateral limb. By contrast, in animals with chronic inflammation no difference in sensitivity between ipsilateral and contralateral limbs to (±)-baclofen was observed. Receptor autoradiographic analysis in spinal cord sections revealed no increase in the density of GABA B receptor binding sites and no change in receptor affinity in the neuropathic model.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have