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首页> 外文期刊>Japanese Journal of Pharmacology >Involvement of beta2-adrenergic and mu-opioid receptors in antinociception produced by intracerebroventricular administration of alpha,beta-methylene-ATP.
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Involvement of beta2-adrenergic and mu-opioid receptors in antinociception produced by intracerebroventricular administration of alpha,beta-methylene-ATP.

机译:β2-肾上腺素能和μ阿片受体参与脑室内给予α,β-亚甲基-ATP产生的抗伤害感受。

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摘要

The present study examined what kind of receptors are involved in the antinociception produced by intracerebroventricular (i.c.v.) administration of a,beta-methylene-ATP using antagonists at adrenergic, serotonin or opioid receptors. Antinociceptive effect of alpha,beta-methylene-ATP (10 nmol/rat) was significantly attenuated by subcutaneous pretreatment with propranolol and naloxone, but not phentolamine or methysergide, at a dose of 10 mg/kg. I.c.v. pretreatment with propranolol (100 nmol/rat), butoxamine (100 nmol/rat), ICI-I 18,551 (100 nmol/rat) and naloxone (30 nmol/rat) significantly attenuated the antinociceptive effect of alpha,beta-methylene-ATP. However, i.c.v. pretreatment with atenolol (100 nmol/rat), naltrindole (30 nmol/rat) or nor-binaltorphimine (30 nmol/rat) did not show any significant effects. These results suggest that supraspinal beta2-adrenergic and mu-opioid receptors are involved in the antinociceptive effect of i.c.v. administered alpha,beta-methylene-ATP.
机译:本研究研究了使用肾上腺素能,5-羟色胺或阿片受体的拮抗剂,通过脑室内(i.c.v.)给予α,β-亚甲基-ATP产生的抗伤害感受涉及哪种受体。通过以10 mg / kg的剂量使用普萘洛尔和纳洛酮而不是苯妥拉明或美塞麦肽进行皮下预处理,可显着减弱α,β-亚甲基-ATP(10 nmol /大鼠)的抗伤害感受作用。 I.c.v.用普萘洛尔(100 nmol /大鼠),丁氧胺(100 nmol /大鼠),ICI-I 18,551(100 nmol /大鼠)和纳洛酮(30 nmol /大鼠)预处理显着减弱了α,β-亚甲基-ATP的抗伤害感受作用。但是,用阿替洛尔(100 nmol /大鼠),纳曲酮(30 nmol /大鼠)或去甲倍他芬胺(30 nmol /大鼠)预处理未显示任何显着效果。这些结果表明,脊髓上β2-肾上腺素和μ阿片样物质受体参与了i.c.v.的抗伤害性作用。施用α,β-亚甲基-ATP。

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