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• W2553518529 abstract "Painful diabetic neuropathy causes allodynia and does not respond to commonly used analgesics such as non‑steroidal anti‑infl ammatory drugs or opioids at doses below those producing disruptive side eff ects. In the present study we examined the effect of P2X receptor antagonists which are known to modulate the pain pathway on mechanical allodynia in streptozotocin (STZ) ‑induced diabetic mice. The paw withdrawal frequency measured by von Frey fi laments began to signifi cantly increase 5 days after STZ injection and was maintained for more than 14 days. Intrathecal administration of P2X receptor antagonists (PPADS and TNP‑ATP) inhibited the mechanical allodynia in diabetic mice. Next the levels of mRNA for the P2X receptors in DRG in diabetic mice were measured using quantitative real‑time PCR. The levels of P2X2 and P2X3 receptors mRNA were signifi cantly increased in diabetic mice at 14 days after the intravenous injection of STZ. Furthermore we investigate the localization of glial cells and neuron in spinal cord of diabetic mice. However microglia astrocyte and neuron were not changed in spinal cord. These results suggest that the upregulation of P2X2 P2X3 and/or P2X2/3 receptor in DRG neurons is associated with mechanical allodynia in STZ‑induced diabetic mice. Hirosaki Med.J.　61 Supplement:S255―S261,2010" @default.
• W2553518529 created "2016-11-30" @default.
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• W2553518529 date "2010-01-01" @default.
• W2553518529 modified "2023-09-26" @default.
• W2553518529 title "＜Poster＞Involvement of P2X2 and P2X3 receptors in dorsal root ganglion neurons of streptozotocin-induced diabetic neuropathy" @default.
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