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鞘内注射芍药苷对蜂毒诱导的痛觉相关行为和脊髓神经元激活的抑制作用。

Suppressive effects of intrathecal paeoniflorin on bee venom-induced pain-related behaviors and spinal neuronal activation.

机构信息

Department of Emergency Medicine, Xijing Hospital, Fourth Military Medical University, Xi'an, People's Republic of China.

出版信息

Pharmacology. 2011;88(3-4):159-66. doi: 10.1159/000330456. Epub 2011 Sep 20.

Abstract

Recently, paeoniflorin (PF) administered systemically was found to have analgesic effects against inflammatory pain and hypersensitivity in a naloxone-reversible manner. In the present study, we adopted intrathecal administration to evaluate whether PF has direct antinociceptive actions at the spinal level. Pain-related behaviors and spinal c-Fos expression were induced by subcutaneous injection of bee venom (BV) into one hind paw of a rat. Intrathecal pretreatment of PF resulted in an inhibition of the BV-induced persistent spontaneous nociception and partially suppressed the occurrence of both thermal and mechanical hypersensitivity. Moreover, the PF-produced antinociception was completely reversed by naloxone. We further evaluated the intrathecal effects of the drug on the BV-induced c-Fos expression. The result showed that intrathecal PF preconditioning was effective to suppress spinal c-Fos expression in both superficial (lamina I-II) and deep (lamina IV-VI) layers of the L(4-5) dorsal spine. This result showed that PF has a direct pharmacological action in the spinal cord dorsal horn via activation of opioid receptors.

摘要

最近,发现芍药苷(PF)全身给药对炎症痛和超敏反应具有阿片类药物逆转的镇痛作用。在本研究中,我们采用鞘内给药来评估 PF 是否在脊髓水平具有直接的镇痛作用。通过向大鼠一只后足皮下注射蜂毒(BV)来诱导与疼痛相关的行为和脊髓 c-Fos 表达。鞘内预先给予 PF 可抑制 BV 诱导的持续性自发性痛觉过敏,并部分抑制热和机械性超敏反应的发生。此外,PF 产生的镇痛作用被纳洛酮完全逆转。我们进一步评估了该药物对 BV 诱导的 c-Fos 表达的鞘内作用。结果表明,鞘内 PF 预处理有效抑制了 L(4-5)背根节浅层(I-II 层)和深层(IV-VI 层)的 BV 诱导的 c-Fos 表达。该结果表明,PF 通过激活阿片受体在脊髓背角具有直接的药理学作用。

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