高级检索

    阿司匹林、甘氨酸和利多卡因对小鼠急性内脏痛的调节作用

    Effects of aspirin, glycine and lidocaine on acute visceral pain in mice

    • 摘要: 目的 探讨阿司匹林、甘氨酸和利多卡因对小鼠急性内脏痛的镇痛作用,为临床合理用药提供理论依据。方法 将36只小鼠随机分为6组(n=6):生理盐水组(NS组)、乙酸模型组(AA组)、吗啡+乙酸组(AA+Morphine组)、阿司匹林+乙酸组(AA+Aspirin组)、甘氨酸+乙酸组(AA+Gly组)、利多卡因+乙酸组(AA+Lidocaine组)。小鼠腹腔注射0.6%乙酸建立急性内脏痛模型,观察乙酸致小鼠扭体潜伏期、扭体次数。结果 腹腔注射乙酸明显导致小鼠急性内脏痛。与AA组比较,AA+Aspirin组、AA+Gly组小鼠扭体潜伏期明显延长,差异有统计学意义(P<0.05);AA+Aspirin组、AA+Gly组、AA+Lidocaine组小鼠的扭体次数明显减少,差异有统计学意义(P<0.05)。结论 阿司匹林、利多卡因、甘氨酸对乙酸致急性内脏痛发挥镇痛作用。

       

      Abstract: Objective To investigate the effects of aspirin, glycine and lidocaine on acute visceral pain in mice, so as to provide theoretical evidence for rational clinical use. Methods A total of 36 Kunming mice were randomly divided into 6 groups (n=6): a normal saline group (Group NS), an acetic acid model group (Group AA), a morphine + AA group (Group AA+Morphine), an aspirin + AA group (Group AA+Aspirin), a glycine + AA group (Group AA+Gly) and a lidocaine+ AA group (Group AA+Lidocaine). Then, a mouse model of acute visceral pain was established by intraperitoneal injection of 0.6% acetic acid. The latency and counts of acetic acid-induced writhing response were recorded. Results Intraperitoneal injection of acetic acid significantly induced acute visceral pain in mice. Compared with Group AA, mice in Groups AA+Aspirin and AA+Glycine showed significantly prolonged latency (P<0.05); mice in Groups AA+Aspirin, AA+Glycine and AA+Lidocaine showed remarkably decreased counts of writhing response (P<0.05). Conclusions Aspirin, glycine and lidocaine exert an analgesic effect against acute visceral pain in mice induced by acetic acid.

       

    /

    返回文章
    返回