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作 者:黄思婷[1] 姬宁宁 杜雷[1] 章功良[2] 张咏梅[1]
机构地区:[1]徐州医学院江苏省麻醉学重点实验室,江苏省麻醉与镇痛应用技术重点实验室,山东徐州221002 [2]安徽医科大学基础医学院,安徽合肥230032
出 处:《中国药理学通报》2017年第2期223-227,共5页Chinese Pharmacological Bulletin
基 金:国家自然科学基金资助项目(No81171041,81271217);江苏省高校自然科学基金重点项目(No13KJA320001);江苏省自然科学基金资助项目(NoBK20161171)
摘 要:目的探讨5-羟色胺(5-hydroxytryptamine,5-HT)2A受体拮抗剂MDL11939在急性乙酸内脏痛、急性切口痛和坐骨神经慢性缩窄性损伤(chronic constrictive injury,CCI)模型中发挥的作用及意义。方法选用♂昆明小鼠,建立急性乙酸内脏痛、急性切口痛和CCI神经病理性痛模型,通过腹腔注射给药,观察乙酸致小鼠扭体反应次数变化、切口痛和CCI痛患侧热缩足反射潜伏期(thermal withdrawal latency,TWL)变化。结果在小鼠急性乙酸内脏痛模型中,与溶剂对照组相比,MDL11939(0.25、0.5、1.0 mg·kg^(-1),i.p.)呈剂量依赖性地减轻乙酸内脏痛,扭体反应次数明显减少。在急性切口痛和CCI模型中,与模型组和自身给药前相比,MDL11939(0.5 mg·kg^(-1),i.p.)可以明显提高小鼠患侧的热缩足阈值,减轻疼痛。结论 MDL11939通过腹腔系统性给药可以有效地减轻急性乙酸内脏痛、急性切口痛和CCI慢性神经病理性痛。Aim To investigate the effects and signifi-cance of 5-HT2A receptor antagonist MDL1 1 939 on a-mice.Methods Kunming male mice were suffered a-cute acetic acid visceral pain,acute incision pain and CCI neuropathic pain.After each animal model was es-tablished,MDL1 1 939 was injected intraperitoneally. The writhing reaction was used to assess acute acetic acid visceral pain,while the thermal withdrawal laten-cy (TWL)was used to evaluate the acute incision pain and CCI neuropathic pain.Results Compared with the control group,MDL1 1 939 (0.25,0.5,1 .0 mg·kg^ -1 ,i.p.)relieved acetic acid visceral pain signifi-cantly in a dose-dependent manner in mice,as re-vealed by the significant reduction of the number of twisting.In acute incision pain and CCI neuropathic pain,MDL1 1 939 (0.5 mg·kg^-1 ,i.p.)significantly increased TWL level.Conclusion 5-HT2A receptor antagonist MDL1 1 939 has analgesic effects on visceral pain,acute pain and neuropathic pain,which might be a novel therapeutic target to treat different pain in clini-cal situations.
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