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首页> 外文期刊>Canadian Journal of Physiology and Pharmacology >CB1 and CB2 contribute to antinociceptive and anti-inflammatory effects of electroacupuncture on experimental arthritis of the rat temporomandibular joint
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CB1 and CB2 contribute to antinociceptive and anti-inflammatory effects of electroacupuncture on experimental arthritis of the rat temporomandibular joint

机译:CB1和CB2有助于电针对大鼠颞下颌关节实验性关节炎的镇痛和抗炎作用

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摘要

Electroacupuncture (EA) and cannabinoids have been reported to have anti-inflammatory and antinociceptive effects in animal models of arthritis. Male Wistar rats were injected with saline or zymosan (2 mg) into the temporomandibular joint (TMJ). EA (10 Hz, 30 min) was performed 2 h after or 1 h before zymosan administration. AM251 or AM630 (3 mg/kg, i.p.)were administered before EA treatment. Mechanical hypernociception was accessed after zymosan administration. Rats were sacrificed 6 h after zymosan administration and the joint was removed for histopathological analysis. The gene expression of CB1 and CB2 receptors was assessed after sacrifice of the TMJ arthritic animals. EA inhibited zymosan-induced hypernociception (p 0.05). AM251 reversed significantly the antinociceptive effect of EA, suggesting that the CB1 receptor is involved in this effect. AM630 reversed the anti-inflammatory effect of EA. CB1 and CB2 receptor gene expression was upregulated 6 h after zymosan-induced arthritis in the EA-treated group. We observed downregulation of CB2 receptor gene expression in the EA group at the 24th hour compared with the 6th hour. Higher CB1 receptor gene expression was also found compared with the 6th hour. EA produced antinociceptive and anti-inflammatory effects, and these effects appeared to be mediated through CB1 and CB2 receptor activation.
机译:据报道,电针(EA)和大麻素在关节炎的动物模型中具有抗炎和镇痛作用。将雄性Wistar大鼠生理盐水或酵母聚糖(2 mg)注射入颞下颌关节(TMJ)。给予酵母聚糖后2小时或之前1小时进行EA(10 Hz,30分钟)。在EA治疗前先服用AM251或AM630(3 mg / kg,腹膜内)。给予酵母聚糖后,出现机械性神经痛。给予酵母聚糖后6 h处死大鼠,取出关节进行组织病理学分析。处死TMJ关节炎动物后评估CB1和CB2受体的基因表达。 EA抑制酵母聚糖诱导的痛觉过敏(p <0.05)。 AM251显着逆转了EA的抗伤害感受作用,表明CB1受体参与了该作用。 AM630逆转了EA的抗炎作用。在EA治疗组中,酵母聚糖诱导的关节炎后6小时,CB1和CB2受体基因表达被上调。我们观察到,与第6小时相比,EA组在第24小时的CB2受体基因表达下调。与第6小时相比,还发现了更高的CB1受体基因表达。 EA产生抗伤害和抗炎作用,这些作用似乎是通过CB1和CB2受体激活介导的。

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