Liu Jin-Bian, Jiang Wei, Wang Ai-Zhong
Department of Anesthesiology, Shanghai Sixth People's Hospital, Shanghai Jiaotong University, Shanghai 200233, China.
Zhonghua Yi Xue Za Zhi. 2009 Aug 18;89(31):2221-4.
To investigate the expression of metabotropic glutamate receptor 5 (mGluRS) in spinal cord of morphine tolerant rats and understand the influence of mGluR5 antagonist MPEP upon the expression of mGluRS.
Male Sprague-Dawley rats were randomly divided into four groups with 8 rats each:control group (NS), morphine group, morphine plus MPEP group and MPEP group. A morphine tolerance model of rat was established by repeated administration of 10 microg morphine intrathecally twice daily for 7 days. The effects of morphine co-administrated with MPEP upon the thermal pain threshold were examined by tail flick test. Tail flick latency (TFL) was measured at 30 min pre- and postdosing. MPE% (percentage of maximal possible effect) was calculated by the equation: MPE (%) = [(test response time-basal response time)/(cut-off time-basal response time)] x 100%. The rats were sacrificed and L4-5 spinal cord tissue was removed. The expression of mGluR5 in every group was examined by immunofluorescence and Western blot.
MPE% of morphine group decreased gradually after chronic administration of morphine intrathecally. There was no significant difference between morphine group and control group at Day 7 (P > 0.05). Morphine plus MPEP group had significant analgesic effect as compared with morphine group at Day 7 (P < 0.05). The expression of mGluR5 was up-regulated in the dorsal horn of spinal cord in morphine tolerant rats. The protein level of mGluRS in morphine plus MPEP group was lower than that in morphine group (P < 0.05), but higher than control group (P < 0.05).
The mGluR5 antagonist MPEP can prevent the development of morphine tolerance. The expression of mGluR5 protein increases in the spinal cord of morphine tolerant rats. MPEP plays its role in morphine tolerance by partly inhibiting the expression of mGluRS.
研究代谢型谷氨酸受体5(mGluR5)在吗啡耐受大鼠脊髓中的表达情况,并了解mGluR5拮抗剂2-甲基-6-(苯乙炔基)吡啶(MPEP)对mGluR5表达的影响。
雄性Sprague-Dawley大鼠随机分为四组,每组8只:对照组(生理盐水)、吗啡组、吗啡加MPEP组和MPEP组。通过每日两次鞘内注射10微克吗啡,连续7天建立大鼠吗啡耐受模型。采用甩尾试验检测吗啡与MPEP联合应用对热痛阈的影响。在给药前和给药后30分钟测量甩尾潜伏期(TFL)。最大可能效应百分比(MPE%)通过以下公式计算:MPE(%)=[(测试反应时间-基础反应时间)/(截止时间-基础反应时间)]×100%。处死大鼠,取出L4-5脊髓组织。通过免疫荧光和蛋白质印迹法检测每组中mGluR5的表达。
鞘内慢性给予吗啡后,吗啡组的MPE%逐渐降低。第7天时,吗啡组与对照组之间无显著差异(P>0.05)。第7天时,吗啡加MPEP组与吗啡组相比具有显著镇痛作用(P<0.05)。吗啡耐受大鼠脊髓背角中mGluR5的表达上调。吗啡加MPEP组中mGluR5的蛋白水平低于吗啡组(P<0.05),但高于对照组(P<0.05)。
mGluR5拮抗剂MPEP可防止吗啡耐受的形成。吗啡耐受大鼠脊髓中mGluR5蛋白表达增加。MPEP通过部分抑制mGluR5的表达在吗啡耐受中发挥作用。