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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Increased cold allodynia following intrathecal N-methyl-D-aspartate in rats with a mononeuropathy.

NMDA receptors are involved in the modulation of neuropathic pain behavior and central sensitization. In vivo, this is mostly demonstrated by the use of specific antagonists such as MK801. Because studies evaluating the direct impact of spinal NMDA in neuropathic pain models are lacking, we performed a series of experiments to study the role of spinal NMDA injection on existing cold allodynia, as a measurement of neuropathic pain behavior in rodents. Intrathecal injection of NMDA resulted in an enhanced neuropathic pain behavior in CCI rats on a cold plate. The activity was present from a dose of 5 ng/rat onward and could selectively be reversed by intraperitoneal injections of doses of > or = 0.01 mg/kg MK801. These results support the regulatory role of NMDA receptors in the hypersensitivity to cold observed in neuropathic pain behavior in rodents.[1]

References

  1. Increased cold allodynia following intrathecal N-methyl-D-aspartate in rats with a mononeuropathy. Vissers, K.C., Hoffmann, V.L., Adriaensen, H.F., Heylen, R.J., Meert, T.F. Life Sci. (2005) [Pubmed]
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