首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Mode of antinociceptive action of flupirtine in the rat.
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Mode of antinociceptive action of flupirtine in the rat.

机译:氟吡汀在大鼠中的镇痛作用模式。

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摘要

1. Flupirtine is a novel, centrally acting, non-opioid analgesic agent. The present investigation was undertaken to ascertain which neuronal systems might be responsible for its antinociceptive effect in rodents. The antinociceptive responses to the test compounds were examined in the tail-flick test. 2. The selective destruction of noradrenergic pathways by 6-hydroxydopamine considerably reduced the flupirtine-induced inhibition of nociceptive responses but not the clonidine-induced antinociception which was significantly enhanced. Depletion of spinal 5-hydroxytryptaminergic pathways by pretreatment with 5,7-dihydroxytryptamine failed to affect the action of flupirtine and clonidine. 3. The depletion of neurotransmitters by reserpine totally abolished the antinociceptive action of flupirtine. By contrast, clonidine-induced inhibition of nociceptive responses remained unchanged. 4. Inhibition of the synthesis of noradrenaline by alpha-methyl-L-p-tyrosine attenuated the antinociception induced by flupirtine. In contrast, inhibition of the synthesis of 5-hydroxytryptamine by (+/-)-6-fluorotryptophan did not influence the antinociceptive activity of flupirtine. 5. Inhibition of noradrenaline uptake by imipramine led to a significant augmentation of flupirtine-induced antinociception. 6. Selective antagonists at alpha-adrenoceptors significantly decreased the antinociceptive action of flupirtine. Antinociception induced by clonidine was significantly diminished by idazoxan but not by prazosin. 7. The 5-hydroxytryptamine (5-HT) antagonist, ketanserin diminished the antinociceptive activity of flupirtine, probably due to its additional alpha 1-adrenoceptor antagonist activity. The antinociceptive effect of clonidine was not influenced by ketanserin. 8. Cholinoceptor antagonists such as mecamylamine and pirenzepine did not alter the antinociceptive action of flupirtine. Flupirtine-induced antinociception also remained unchanged after pretreatment with haloperidol.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:氟吡汀是一种新型的中枢性非阿片类镇痛药。进行本研究以确定哪些神经元系统可能对其啮齿动物的抗伤害感受作用负责。在甩尾测试中检查对测试化合物的镇痛反应。 2.通过6-羟基多巴胺选择性破坏去甲肾上腺素能途径大大降低了氟吡汀诱导的伤害感受抑制,但未显着增强可乐定诱导的镇痛作用。通过用5,7-二羟基色胺预处理对脊髓5-羟基色胺能途径的消耗未能影响氟吡汀和可乐定的作用。 3.利血平对神经递质的消耗完全消除了氟吡汀的镇痛作用。相比之下,可乐定诱导的伤害感受抑制作用保持不变。 4.α-甲基-L-对-酪氨酸抑制去甲肾上腺素的合成减弱了氟吡汀诱导的抗伤害感受。相反,(+/-)-6-氟色氨酸抑制5-羟色胺的合成不会影响氟吡汀的抗伤害感受活性。 5.丙咪嗪抑制去甲肾上腺素的摄取导致氟吡汀诱导的抗伤害感受显着增加。 6.α-肾上腺素受体的选择性拮抗剂显着降低了氟吡汀的抗伤害感受作用。可乐定诱导的抗伤害感受作用被伊达沙生显着降低,而哌唑嗪则没有。 7. 5-羟色胺(5-HT)拮抗剂酮色林降低了氟吡汀的抗伤害感受活性,这可能是由于其附加的α1-肾上腺素能受体拮抗剂活性。可乐定的抗伤害感受作用不受酮色林的影响。 8.诸如美加明胺和哌仑西平之类的受体受体拮抗剂不会改变氟吡汀的镇痛作用。氟哌汀引起的镇痛作用在氟哌啶醇预处理后也保持不变。(摘要截断为250字)

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