P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury

Makoto Tsuda, Yukari Shigemoto-Mogami, Schuichi Koizumi, Akito Mizokoshi, Shinichi Kohsaka, Michael W. Salter and Kazuhide Inoue ()
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Makoto Tsuda: National Institute of Health Sciences
Yukari Shigemoto-Mogami: National Institute of Health Sciences
Schuichi Koizumi: National Institute of Health Sciences
Akito Mizokoshi: Kyushu University
Shinichi Kohsaka: National Institute of Neuroscience
Michael W. Salter: The Hospital for Sick Children
Kazuhide Inoue: National Institute of Health Sciences

Nature, 2003, vol. 424, issue 6950, 778-783

Abstract: Abstract Pain after nerve damage is an expression of pathological operation of the nervous system1,2, one hallmark of which is tactile allodynia—pain hypersensitivity evoked by innocuous stimuli. Effective therapy for this pain is lacking, and the underlying mechanisms are poorly understood. Here we report that pharmacological blockade of spinal P2X4 receptors (P2X4Rs)3,4,5,6,7, a subtype of ionotropic ATP receptor8, reversed tactile allodynia caused by peripheral nerve injury without affecting acute pain behaviours in naive animals. After nerve injury, P2X4R expression increased strikingly in the ipsilateral spinal cord, and P2X4Rs were induced in hyperactive microglia but not in neurons or astrocytes. Intraspinal administration of P2X4R antisense oligodeoxynucleotide decreased the induction of P2X4Rs and suppressed tactile allodynia after nerve injury. Conversely, intraspinal administration of microglia in which P2X4Rs had been induced and stimulated, produced tactile allodynia in naive rats. Taken together, our results demonstrate that activation of P2X4Rs in hyperactive microglia is necessary for tactile allodynia after nerve injury and is sufficient to produce tactile allodynia in normal animals. Thus, blocking P2X4Rs in microglia might be a new therapeutic strategy for pain induced by nerve injury.

Date: 2003
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DOI: 10.1038/nature01786

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