首页> 外文期刊>European Journal of Pharmacology: An International Journal >Antinociceptive effects of intracerebroventricularly administered P2 purinoceptor agonists in the rat.
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Antinociceptive effects of intracerebroventricularly administered P2 purinoceptor agonists in the rat.

机译:脑室内施用的P2嘌呤受体激动剂对大鼠的镇痛作用。

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We examined the effects of adenosine 5'-triphosphate (ATP) and its analogues administered intracerebroventricularly on nociceptive thresholds in rats. Intracerebroventricular (i.c.v.) administration of ATP (10 and 100 nmol/rat), alpha,beta-methylene-ATP (1-30 nmol/rat) and 2', 3'-O-(4-benzoylbenzoyl)-ATP (1-30 nmol/rat) dose-dependently elevated the mechanical nociceptive threshold in the paw pressure test. These antinociceptive effects were rapid and short-lasting, peaking at 5 min and disappearing by 20 min after the administration. However, i.c.v. administration of beta,gamma-methylene-ATP (1-30 nmol/rat) and UTP (10 and 100 nmol/rat) had no significant effects on the mechanical nociceptive threshold. In other tests, i.c.v. administration of alpha,beta-methylene-ATP (10 and 30 nmol/rat) prolonged the thermal nociceptive latency in the hot plate test, but only a higher dose (30 nmol/rat) of alpha,beta-methylene-ATP prolonged the latency in the tail flick test. alpha,beta-Methylene-ATP produced no motor deficit in the inclined plane test. These results suggest that P2X purinoceptors play an inhibitory role in nociception at the supraspinal level.
机译:我们检查了脑室内给予腺苷5'-三磷酸腺苷(ATP)及其类似物对大鼠伤害感受性阈值的影响。脑室内(icv)施用ATP(10和100 nmol /大鼠),α,β-亚甲基-ATP(1-30 nmol /大鼠)和2',3'-O-(4-苯甲酰基苯甲酰基)-ATP(1- 30 nmol /大鼠)在爪压力测试中剂量依赖性地提高了机械伤害感受性阈值。这些抗伤害性作用迅速且持续时间短,在给药后5分钟达到高峰,在给药20分钟后消失。但是,服用β,γ-亚甲基-ATP(1-30 nmol /大鼠)和UTP(10和100 nmol /大鼠)对机械伤害阈没有明显影响。在其他测试中,在热板测试中,α,β-亚甲基-ATP(10和30 nmol /大鼠)的给药延长了热伤害感受潜伏期,但是只有较高剂量(30 nmol /大鼠)的α,β-亚甲基-ATP延长了潜伏期在甩尾测试中。在斜面试验中,α,β-亚甲基-ATP没有产生运动障碍。这些结果表明,P2X嘌呤受体在脊髓上水平上在伤害感受中起抑制作用。

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