【摘 要】
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Previous work has demonstrated that the sensitization of spinal neurons and microglia is important in the development of pain behaviors induced by BmK Ⅰ,a Na+ channel activator and a major peptide component of the venom of the scorpion Buthus martensi Kar
【机 构】
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Laboratory of Neuropharmacology and Neurotoxicology,Shanghai University, Shanghai 200444, China;Depa
论文部分内容阅读
Previous work has demonstrated that the sensitization of spinal neurons and microglia is important in the development of pain behaviors induced by BmK Ⅰ,a Na+ channel activator and a major peptide component of the venom of the scorpion Buthus martensi Karsch (BmK).We found that the expression of P2X7 receptors (P2X7Rs) was up-regulated in the ipsilateral spinal dorsal horn after BmK Ⅰ injection in rats.P2X7R was selectively localized in microglia but not astrocytes or neurons.Similarly,interleukin 1β (IL-1β) was selectively up-regulated in microglia in the spinal dorsal horn after BmK Ⅰ injection.Intrathecal injection of P2X7R antagonists largely reduced BmK Ⅰ-induced spontaneous and evoked pain behaviors,and the up-regulation of P2X7R and IL-1β in the spinal cord.These data suggested that the up-regulation of P2X7Rs mediates microglial activation in the spinal dorsal horn,and therefore contributes to the development of BmK I-induced pain.
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