Essay On Hyperalgesia And Allodynia

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Discussion
It has been shown that intrathecal administriton of GABA receptor antagonists cause hyperalgesia and allodynia. Constitutive, the increase in the endogenous GABA activity in the spinal cord alleviate pain resulting from noxious and innoxious mechanical and thermal stimuli. Different GABA receptors have different roles in alleviating thermal and mechanical pain in different animal pain models. There is no study to date that has examined the involvement of GABA A and GABA B in sensory dimension of neuropathic pain resulting from compression of spinal cord. The current study tests the hypothesis that GABA A or GABA B receptors contributes to the allodynia and hyperalgesia observed after spinal cord injury. The results showed that the effect of GABA A and GABA B receptors on mechanical hyperalgesia is similar but these receptors have different effects on thermal hyperalgesia. While using baclofen as GABA B receptor agonist does not affect the thermal pain, thermal hyperalgesia resulting from spinal cord injury was greatly alleviated by different doses of GABA A agonist, muscimol. Both Baclofen and muscimol are able to reduce the mechanical and cold allodynia has been seen after spinal cord injury but the effect of baclofen is dose dependent with no effect in higher doses used in this study. While almost all doses of muscimol were used in this study reduce the amount of cold and mechanical allodynia. The other result obtained in this study is the short term effect of GABA agonist. The anitinociceptive effect of Baclofen and muscimol appear to be maxium at 15 min after injection and gradually diminished by time and their analgesic effect disappeared 3 hours after injection.
Currently pharmacological mechanisms affect neurop...

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...tive to intrathecal administration of morphin than tactil allodynia. Therefore, examination of both modalities is important when examining the spinal pharmacology of the nerve-injured state

Our results provide the first demonstration that GABAA but not GABA B receptor–selective agonists reverse the thermal hyperalgesia produced by spinal cord injury. In parallel, we demonstrate that in spinal cord injury similar to peripheral nerve injury, GABAA and GABAB receptor agonists reduce cold and tactile allodynia and mechanical hyperalgesia. In addition, our studies used a sensitive, reproducible test of motor function to compare the antiallodynic, antihyperalgesic, and motor effects of GABA receptor agonists. The data suggest that GABAA agonists may be efficacious in the treatment of neuropathic pain with thermal hyperalgesia without sensory or motor side effects.

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