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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >NAN-190, a possible specific antagonist for methamphetamine.
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NAN-190, a possible specific antagonist for methamphetamine.

机译:NAN-190,可能是甲基苯丙胺的特异性拮抗剂。

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Effect of NAN-190, a selective 5-HT(1A) receptor antagonist, on methamphetamine-induced locomotor activity, anorexia, analgesia, and hyperthermia was investigated in male mice. Methamphetamine (1.5 mg/kg, i.p) produced a significant increase in locomotor activity, which was significantly antagonized by NAN-190 at a dose of 4 mg/kg, i.p. NAN-190 did not alter the antinociceptive activity of mice when it was administered alone. Methamphetamine (2 mg/kg, i.p) produced a significant decrease in food intake of mice, which were deprived of food during the previous 24h. This anorectic activity of methamphetamine was significantly antagonized by NAN-190 at a dose of 2 mg/kg, i.p. NAN-190 did not alter the food intake of mice when it was administered alone. Methamphetamine (2 mg/kg, i.p) also produced a significant increase in body temperature of mice, which was significantly antagonized by NAN-190 at a dose of 0.5 mg/kg, i.p. NAN-190 did not alter the body temperature of mice when it was administered alone. Inthe writhing test, methamphetamine (1 mg/kg, i.p) produced a significant antinociceptive effect in mice. This was significantly antagonized by NAN-190 at a dose of 1 mg/kg, i.p. NAN-190 did not alter the antinociceptive activity of mice when it was administered alone. The results of the present study indicate a possible role for serotonergic mechanisms, in addition to the catecholaminergic systems, in the above-studied activities of methamphetamine in mice. This role is possibly mediated through direct stimulation of the 5-HT(1A) receptor subtype. All of the above-studied activities of methamphetamine were antagonized by NAN-190, which may indicate that NAN-190 is a possible antagonist for methamphetamine.
机译:在雄性小鼠中研究了选择性5-HT(1A)受体拮抗剂NAN-190对甲基苯丙胺诱导的自发活动,厌食,镇痛和热疗的影响。甲基安非他明(1.5 mg / kg,i.p)使运动活性显着增加,NAN-190在4 mg / kg,i.p.的剂量下明显拮抗。单独使用NAN-190不会改变小鼠的抗伤害感受活性。甲基苯丙胺(2 mg / kg,i.p)使小鼠的食物摄入显着减少,而在之前的24小时内,小鼠的食物被剥夺了。甲基苯丙胺的这种厌食活性被NAN-190以2 mg / kg的剂量显着拮抗。单独使用NAN-190不会改变小鼠的食物摄入量。甲基苯丙胺(2 mg / kg,i.p.)也使小鼠的体温显着升高,而NAN-190在0.5 mg / kg(i.p.)时明显拮抗。单独使用NAN-190不会改变小鼠的体温。在扭体试验中,甲基苯丙胺(1 mg / kg,i.p)对小鼠产生明显的镇痛作用。 NAN-190以1 mg / kg的剂量腹腔注射明显拮抗。单独使用NAN-190不会改变小鼠的抗伤害感受活性。本研究的结果表明,除儿茶酚胺能系统外,血清素能机制在上述甲基苯丙胺在小鼠中的活性中可能发挥作用。此作用可能是通过直接刺激5-HT(1A)受体亚型介导的。上述所有甲基苯丙胺的活性均被NAN-190拮抗,这可能表明NAN-190是甲基苯丙胺的可能拮抗剂。

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