首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of competitive and noncompetitive antagonists of the N-methyl-D-aspartate receptor on the analgesic action of delta 1- and delta 2-opioid receptor agonists in mice.
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Effects of competitive and noncompetitive antagonists of the N-methyl-D-aspartate receptor on the analgesic action of delta 1- and delta 2-opioid receptor agonists in mice.

机译:N-甲基-D-天冬氨酸受体的竞争性和非竞争性拮抗剂对小鼠δ1和δ2阿片类受体激动剂的镇痛作用。

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摘要

1. The effects of MK-801, a noncompetitive antagonist of the N-methyl-D-aspartate (NMDA) receptor and LY 235959, a competitive antagonists of the NMDA receptor on the analgesic actions of [D-Pen2,D-Pen5]enkephalin (DPDPE) and [D-Ala2, Glu4] deltorphin II (deltorphin II), the putative delta 1- and delta 2-opioid receptor agonists, respectively, were determined in the male Swiss-Webster mice. 2. Intracerebroventricular administration of DPDPE or deltorphin II produced analgesia. MK-801 administered intraperitoneally 10 min before the injection of DPDPE or deltorphin II, dose-dependently antagonized the analgesic actions of both drugs. 3. LY 235959 also dose-dependently antagonized the analgesic actions of DPDPE and deltorphin II. 4. The effects of MK-801 and LY 235959 on the binding of [3H]-DPDPE to mouse brain membranes were also determined. Neither of the NMDA receptor antagonists had any effect on the binding of [3H]-DPDPE. 5. It is concluded that competitive and noncompetitive antagonists of the NMDA receptor antagonize the analgesic action of delta 1- and delta 2-opioid receptor agonists and that such effects are not mediated via a direct interaction with brain delta-opioid receptors.
机译:1. N-甲基-D-天门冬氨酸(NMDA)受体的非竞争性拮抗剂MK-801和NMDA受体的竞争性拮抗剂LY 235959对[D-Pen2,D-Pen5]的镇痛作用的影响在雄性Swiss-Webster小鼠中分别确定了脑啡肽(DPDPE)和[D-Ala2,Glu4]德尔托芬II(deltorphin II),即假定的delta 1和delta 2阿片样物质受体激动剂。 2.脑室内施用DPDPE或deltorphin II可产生镇痛作用。在注射DPDPE或deltorphin II前10分钟腹膜内施用MK-801,剂量依赖性拮抗两种药物的镇痛作用。 3. LY 235959也剂量依赖性地拮抗DPDPE和deltorphin II的镇痛作用。 4.还确定了MK-801和LY 235959对[3H] -DPDPE与小鼠脑膜结合的影响。两种NMDA受体拮抗剂均未对[3H] -DPDPE的结合产生任何影响。 5.结论是,NMDA受体的竞争性和非竞争性拮抗剂拮抗δ1和δ2阿片受体激动剂的镇痛作用,并且这种作用不是通过与脑δ阿片受体的直接相互作用来介导的。

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