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Involvement of serotonergic, noradrenergic and GABAergic systems in the antinociceptive effect of a ketamine-magnesium sulfate combination in acute pain

机译:血清素,去甲肾上腺素能和GABA能系统参与氯胺酮-硫酸镁联合用药在急性疼痛中的镇痛作用

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Ketamine and magnesium can interact in additive, supra-additive and antagonistic manners in analgesia or anesthesia. Ketamine is a non-competitive NMDA receptor antagonist. Magnesium is an endogenous non-competitive NMDA antagonist that causes anion channel blockade in a dose-dependent manner. It has been established that ketamine and magnesium interact synergistically in the tail-immersion test in rats.To determine the role of serotonergic, GABAergic and noradrenergic systems in analgesia induced by the ketamine-magnesium sulfate combination.Experiments were performed on male Wistar albino rats (200-250 g). Antinociception was evaluated by the tail-immersion test.Methysergide (0.5 and 1 mg/kg, sc) administered alone did not affect nociception in rats. Methysergide (0.5 and 1 mg/kg, sc) antagonized the antinociceptive effect of the ketamine (5 mg/kg)-magnesium sulfate (5mg/kg) combination. Bicuculline (0.5 and 1 mg/kg, sc) given alone did not change the threshold to thermal stimuli in rats. Bicuculline (0.5 and 1 mg/kg, sc) antagonized the antinociceptive effect of the ketamine (5 mg/kg)-magnesium sulfate (5 mg/kg) combination. Yohimbine (0.5, 1 and 3 mg/kg, sc) applied alone did not change nociception. Yohimbine at a dose of 0.5 mg/kg did not influence the effect of ketamine (5 mg/kg)-magnesium sulfate (5 mg/kg), while yohimbine at doses of 1 and 3 mg/kg antagonized the antinociceptive effect of this combination.Serotonergic, noradrenergic and GABAergic systems participate, at least in part, in the antinociceptive effect of the ketamine-magnesium sulfate combination in acute pain in rats.
机译:氯胺酮和镁可以在镇痛或麻醉中以加性,超加性和拮抗性的方式相互作用。氯胺酮是一种非竞争性NMDA受体拮抗剂。镁是一种内源性非竞争性NMDA拮抗剂,它以剂量依赖的方式引起阴离子通道阻滞。已经确定氯胺酮和镁在大鼠的尾部浸入试验中具有协同作用。确定氯胺酮-硫酸镁联合诱导的血清素能,GABA能和去甲肾上腺素能系统在镇痛中的作用。 200-250克)。通过尾巴浸没试验评估抗伤害感受。单独服用美塞麦肽(0.5和1 mg / kg,皮下注射)不会影响大鼠的伤害感受。甲基麦角乙二胺(0.5和1 mg / kg,sc)拮抗氯胺酮(5 mg / kg)-硫酸镁(5mg / kg)组合的镇痛作用。单用双cuculline(0.5和1 mg / kg,皮下注射)不会改变大鼠的热刺激阈值。 Bicuculline(0.5和1 mg / kg,sc)拮抗氯胺酮(5 mg / kg)-硫酸镁(5 mg / kg)组合的镇痛作用。单独施用育亨宾(0.5、1和3 mg / kg,皮下注射)不会改变伤害感受。育亨宾的剂量为0.5 mg / kg不会影响氯胺酮(5 mg / kg)-硫酸镁(5 mg / kg)的作用,而育亨宾的剂量为1和3 mg / kg则拮抗该组合的镇痛作用5-羟色胺能,去甲肾上腺素能和GABA能系统至少部分参与氯胺酮-硫酸镁组合在大鼠急性疼痛中的镇痛作用。

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