Induction of the P2X7 receptor in spinal microglia in a neuropathic pain model

► P2X7 mRNA in spinal cord is increased in microglia after peripheral naive injury. ► Double labeled immunohistochemistry showed the P2X7 protein increase in spinal microglia. ► Intrathecal administration of a P2X7 antagonist suppressed mechanical hypersensitivity. Peripheral nerve injury causes a p...

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Bibliographic Details
Published in:Neuroscience letters 2011-10, Vol.504 (1), p.57-61
Main Authors: Kobayashi, Kimiko, Takahashi, Emiko, Miyagawa, Yasuko, Yamanaka, Hiroki, Noguchi, Koichi
Format: Article
Language:English
Subjects:
Animals
ATP
Biological and medical sciences
Disease Models, Animal
Fundamental and applied biological sciences. Psychology
Gene Expression
Humans
Hyperalgesia - drug therapy
Male
Microglia - metabolism
Neuralgia - metabolism
Neuropathic pain
P2X7
Peripheral Nerve Injuries - metabolism
Purinergic P2X Receptor Antagonists - pharmacology
Purinergic receptor
Pyridines - pharmacology
Rats
Rats, Sprague-Dawley
Receptors, Purinergic P2X7 - biosynthesis
Spinal Cord - metabolism
Spinal microglia
Tetrazoles - pharmacology
Touch - drug effects
Vertebrates: nervous system and sense organs
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Summary:► P2X7 mRNA in spinal cord is increased in microglia after peripheral naive injury. ► Double labeled immunohistochemistry showed the P2X7 protein increase in spinal microglia. ► Intrathecal administration of a P2X7 antagonist suppressed mechanical hypersensitivity. Peripheral nerve injury causes a progressive series of morphological changes in spinal microglia, and extracellular ATP stimulates proliferation of microglia and may be involved in neuropathic pain. We defined the precise expression of P2X7 in the spinal cord following peripheral nerve injury. We found that both P2X7 mRNA and protein increased in the spinal cord, with a peak at 7 d after injury. Double labeling studies revealed that cells expressing increased P2X7 mRNA and protein after nerve injury were predominantly microglia in dorsal horn. Pharmacological blockades by intrathecal administration of a P2X7 antagonist (A 438079 hydrochloride) suppressed the development of mechanical hypersensitivity. We present distinct evidence that increases in the number of P2X7 receptors in spinal microglia may play an important role in neuropathic pain.
ISSN:0304-3940
1872-7972
DOI:10.1016/j.neulet.2011.08.058