首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Delta-1 opioid receptor-mediated antinociceptive properties of a nonpeptidic delta opioid receptor agonist, (-)TAN-67, in the mouse spinal cord.
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Delta-1 opioid receptor-mediated antinociceptive properties of a nonpeptidic delta opioid receptor agonist, (-)TAN-67, in the mouse spinal cord.

机译:Delta-1阿片受体介导的非肽δ阿片受体激动剂(-)TAN-67在小鼠脊髓中的镇痛特性。

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摘要

The effects of enantiomorphs of TAN-67 (2-methyl-4a alpha-(3-hydroxyphenyl)-1,2,3,4,4a,5,12,12a alpha-octahydro-quinolino[2,3,3-g]isoquinoline), (-)TAN-67 and (+)TAN-67, given intrathecally (i.t.) on antinociceptive response with the tail-flick test were studied in male ICR mice. (-)TAN-67 at doses from 17.9 to 89.4 nmol given i.t. produced a dose- and time-dependent inhibition of the tail-flick response, whereas its enantiomer (+)TAN-67 even at smaller doses (1.8, 4.5 and 8.9 nmol) given i.t. decreased the latencies of the tail-flick response. In addition, (+)TAN-67 at higher doses (17.9-89.4 nmol) given i.t. produced scratching and biting pain-like responses. The antinociceptive response induced by i.t.-administered (-)TAN-67 was mediated by the stimulation of delta-1 but not by delta-2, mu or kappa opioid receptors, because the effect was blocked by the i.t. pretreatment with BNTX, but not by naltriben, [D-Phe-Cys-Tyr-[D-Try-Orn-Thr-Pen-Thr-NH2 or nor-binaltorphimine dihydrochloride. Pretreatment with (-)TAN-67 given i.t. 3 hr earlier attenuated the tail-flick inhibition induced by subsequent i.t. administration of (-)TAN-67 and by [D-Pen2,5]enkephalin (DPDPE). However, the tail-flick inhibition induced by [D-Ala2]deltorphin II, [D-Ala2,NMePhe4,Gly5-ol]enkephalin and U50,488H were not affected by (-)TAN-67 pretreatment. Conversely, pretreatment with DPDPE given i.t. 3 hr earlier attenuated the tail-flick inhibition induced by subsequent i.t. administration of (-)TAN-67 and by DPDPE. However, the tail-flick inhibition induced by [D-Ala2]deltorphin II was not affected by i.t. DPDPE pretreatment. It is concluded that (-)TAN-67 given i.t. produces delta-1 opioid receptor-mediated antinociception; on the other hand, its enantiomer (+)TAN-67 produces hyperalgesia. Present studies provide other evidence that delta-1 opioid receptors exist separated from delta-2 opioid receptor.
机译:TAN-67(2-甲基-4aα-(3-羟苯基)-1,2,3,4,4a,5,12,12a对映体的影响α-八氢喹啉[2,3,3-g在雄性ICR小鼠中研究了鞘内(it)的甩尾试验对(i)异喹啉),(-)TAN-67和(+)TAN-67的镇痛作用。腹膜内给予(-)TAN-67,剂量为17.9至89.4 nmol。产生对甩尾反应的剂量和时间依赖性抑制,而它的对映异构体(+)TAN-67甚至在i.t.给予较小剂量(1.8、4.5和8.9 nmol)时也是如此。减少了甩尾反应的延迟。另外,以更高剂量(17.9-89.4 nmol)给予(+)TAN-67。产生抓挠和咬痛般的反应。 i.t.(-)TAN-67诱导的镇痛反应是通过刺激delta-1介导的,而不是通过delta-2,mu或kappa类阿片受体刺激的,因为这种作用被i.t.阻断。用BNTX预处理,但不使用纳曲本,[D-Phe-Cys-Tyr- [D-Try-Orn-Thr-Pen-Thr-NH2]或去甲双萘酚盐酸盐预处理。给予(-)TAN-67预处理3小时之前减弱了随后的i.t.引起的甩尾抑制。 (-)TAN-67和[D-Pen2,5]脑啡肽(DPDPE)给药。但是,[D-Ala2] deltorphin II,[D-Ala2,NMePhe4,Gly5-ol]脑啡肽和U50,488H诱导的甩尾抑制不受(-)TAN-67预处理的影响。相反地​​,用DPDPE进行i.t.预处理。 3小时之前减弱了随后的i.t.引起的甩尾抑制。 (-)TAN-67和DPDPE的使用。但是,[D-Ala2] deltorphin II诱导的甩尾抑制不受i.t.的影响。 DPDPE预处理。结论是(-)TAN-67给定i.t.产生delta-1阿片受体介导的镇痛作用;另一方面,其对映体(+)TAN-67产生痛觉过敏。目前的研究提供了其他证据,表明存在delta-1阿片受体与delta-2阿片受体分离。

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