首页> 外文期刊>The journal of pain: official journal of the American Pain Society >The effect of spinal and systemic administration of indomethacin on zymosan-induced edema, mechanical hyperalgesia, and thermal hyperalgesia.
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The effect of spinal and systemic administration of indomethacin on zymosan-induced edema, mechanical hyperalgesia, and thermal hyperalgesia.

机译:吲哚美辛的脊柱和全身给药对酵母聚糖诱导的水肿,机械性痛觉过敏和热痛觉过敏的影响。

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Pretreatment with intraperitoneal (i.p.) indomethacin was used to determine whether indomethacin preferentially affected the development of edema and hyperalgesia to thermal and mechanical stimuli produced by injection of zymosan in the ispsilateral hindpaw of the rat. Indomethacin also was delivered intrathecally (i.t.) either 30 minutes before or 4 hours after intraplantar zymosan to determine whether spinal prostaglandin production was important for the induction and/or maintenance of hyperalgesia. Zymosan alone produced a robust edema, a monophasic mechanical hyperalgesia, and a biphasic thermal hyperalgesia in the ipsilateral hindpaw. Systemic administration of indomethacin reduced zymosan-induced edema and increased thermal and mechanical response thresholds in the zymosan-injected paw. Systemic indomethacin did not affect thermal withdrawal response thresholds in the uninjected contralateral hindpaw of zymosan-treated rats, but significantly increased mechanical withdrawal thresholds of the uninjected contralateral paw of zymosan-treated rats. i.t. administration of indomethacin before the induction of hyperalgesia attenuated the development of zymosan-induced mechanical hyperalgesia, but did not affect the development of either zymosan-induced edema or thermal hyperalgesia. Once hyperalgesia was established, i.t. indomethacin also attenuated the mechanical hyperalgesia whereas it had no effect on thermal hyperalgesia or edema. These data suggest that peripheral, but not spinal prostaglandins contribute to the edema and development of thermal hyperalgesia produced by zymosan. In contrast, spinal prostaglandins contribute to the development and maintenance of mechanical hyperalgesia.
机译:腹膜内(i.p.)消炎痛的预处理用于确定消炎痛是否优先影响水肿和痛觉过敏的发展,而对大鼠同侧后足注射zymosan产生热和机械刺激。吲哚美辛还可以在足底内酵母聚糖的30分钟之前或之后的4小时内鞘内(即)递送,以确定脊柱前列腺素的产生对于诱导和/或维持痛觉过敏是否重要。单独的酵母聚糖在同侧后爪产生强烈的水肿,单相机械性痛觉过敏和双相热痛觉过敏。消炎痛的全身给药减少了酵母聚糖诱导的水肿,并增加了酵母聚糖注射后爪的热和机械反应阈值。全身消炎痛不会影响经zymosan治疗的大鼠的未注射对侧后爪的热戒断反应阈值,但会显着提高未受zymosan治疗的大鼠的对侧后爪的机械戒断阈值。它。在诱导痛觉过敏之前给予消炎痛可减缓zymosan诱导的机械性痛觉过敏的发展,但不影响zymosan诱导的水肿或热痛觉过敏的发展。痛觉过敏一旦建立,即消炎痛也减轻了机械性痛觉过敏,而对热痛觉过敏或水肿没有影响。这些数据表明外周但不是脊柱前列腺素有助于由酵母聚糖产生的水肿和热痛觉过敏的发展。相反,脊柱前列腺素有助于机械性痛觉过敏的发展和维持。

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