华中科技大学学报(医学版)2024,Vol.53Issue(1) :81-85.DOI:10.3870/j.issn.1672-0741.23.04.006

柯里拉京对吗啡耐受大鼠脊髓小胶质细胞活化的作用机制

Study on the Effects of Corilagin on Microglia Activation in the Spinal Cord of Morphine-tolerant Rats

关森 王慧淼 汪冬梅 胡杰
华中科技大学学报(医学版)2024,Vol.53Issue(1) :81-85.DOI:10.3870/j.issn.1672-0741.23.04.006

柯里拉京对吗啡耐受大鼠脊髓小胶质细胞活化的作用机制

Study on the Effects of Corilagin on Microglia Activation in the Spinal Cord of Morphine-tolerant Rats

关森 1王慧淼 2汪冬梅 3胡杰1
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作者信息

  • 1. 河北省承德市中心医院麻醉科,承德 067000
  • 2. 河北省承德市中心医院检验科,承德 067000
  • 3. 河北省承德市中心医院内分泌科,承德 067000
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摘要

目的 探讨柯里拉京对吗啡耐受大鼠的影响及作用机制.方法 建立慢性吗啡镇痛大鼠耐受模型.采用水浴甩尾法检测大鼠甩尾潜伏期,利用免疫荧光检测离子化钙结合适配分子1(Iba-1)的阳性细胞率;蛋白免疫印迹法检测Iba-1和丝裂原活化蛋白激酶(MAPK)信号通路相关蛋白的表达;采用酶联免疫吸附实验(ELISA)检测白细胞介素-6(IL-6)、肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)表达;采用逆转录-聚合酶链反应(qRT-PCR)检测IL-6、TNF-α、IL-1β的mRNA表达.结果 与吗啡组相比,吗啡+柯里拉京组镇痛效果随柯里拉京浓度升高而增加.与对照组相比,吗啡组中Iba-1的阳性细胞率、Iba-1蛋白表达水平、炎性因子IL-6,TNF-α,IL-1β表达水平以及MAPK信号通路相关蛋白细胞外调节蛋白激酶(ERK)、c-Jun氨基末端激酶(JNK)和丝裂原活化蛋白激酶p38抗体(p38)的磷酸化水平显著增加,但在吗啡+柯里拉京组中随柯里拉京浓度升高而下降.吗啡和(或)柯里拉京处理对ERK、JNK和p38表达水平没有显著影响.结论 柯里拉京通过抑制MAPK通路降低大鼠吗啡耐受.

Abstract

Objective This study was designed to investigate the effects of corilagin on morphine-tolerant rats and discuss the reaction mechanism.Methods A rat model of chronic morphine analgesia tolerance was established.The tail-flick latency of rats was detected by using the water bath tail-flick method.The positive cell rate of ionized calcium binding adapter molecule-1(Iba-1)was detected by using immunofluorescence assay.The protein expressions of Iba-1 and mitogen-activated protein kinase(MAPK)pathway-related proteins were detected by Western blotting.The release of interleukin-6(IL-6),tumor necrosis factor alpha(TNF-α)and interleukin-1 beta(IL-1β)was detected by using enzyme-linked immunosorbent assay(ELISA).The mRNA levels of IL-6,TNF-α and IL-1β were detected by using quantitative reverse transcriptase polymerase chain reaction(qRT-PCR).Results Compared with the morphine(Mor)group,the analgesic effect of morphine in morphine+corilagin(Mor+Cor)group was strengthened with the increase of corilagin concentration.Compared with the Control group,the positive cell rate of Iba-1,Iba-1 protein expression level,levels of inflammatory factors IL-6,TNF-α,IL-1β,and the phosphorylated expression levels of MAPK signaling pathway-related proteins extracellular regulated protein kinases(ERK),c-Jun N-terminal kinase(JNK)and p38 were significantly increased in the Mor group,which were then decreased in Mor+Cor group with the increase of corilagin con-centration.Morphine and corilagin treatment(alone or in combination)had no significant effects on the expression levels of ERK,JNK and p38.Conclusion Corilagin reduces morphine tolerance in rats by inhibiting MAPK pathway.

关键词

柯里拉京/吗啡耐受/小胶质细胞

Key words

corilagin/morphine tolerance/microglia

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基金项目

河北省承德市科学技术研究与发展计划项目(202102A009)

出版年

2024
华中科技大学学报(医学版)
华中科技大学

华中科技大学学报(医学版)

CSTPCDCSCD北大核心
影响因子:1.443
ISSN:1672-0741
参考文献量3
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