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在小鼠输精管和豚鼠回肠中缺乏δ-阿片样激动剂对μ-阿片样激动剂作用调节的证据。

Evidence for lack of modulation of mu-opioid agonist action by delta-opioid agonists in the mouse vas deferens and guinea-pig ileum.

作者信息

Elliott J, Traynor J R

机构信息

Department of Chemistry, Loughborough University of Technology, Leics.

出版信息

Br J Pharmacol. 1995 Mar;114(5):1064-8. doi: 10.1111/j.1476-5381.1995.tb13314.x.

Abstract
  1. There is evidence from in vivo studies for an interaction of mu- and delta-opioid ligands. In the present work this concept has been investigated using the mouse vas deferens and guinea-pig ileum myenteric plexus-longitudinal preparations. 2. In field stimulated vasa deferentia of the mouse, co-administration of sub-effective concentrations of the delta-opioid agonist [D-Pen2,D-Pen5]enkephalin (DPDPE) and [Met5]- or [Leu5]enkephalin had no effect on the dose-response curves of the mu-agonists [D-Ala2,MePhe4, Gly-ol5]enkephalin (DAMGO) and morphine. Similarly, the delta-opioid agonists did not alter the potency of morphine and DAMGO when added at different times prior to the mu-opioid agonists, or when EC50 concentrations of delta-opioid ligands were co-administered. Compounds with preferred activity for the putative delta 1-(DPDPE) or delta 2-([D-Ala2,Glu4]deltorphin II (Delt II)) opioid receptors were ineffective in this respect. 3. The guinea-pig ileum contains delta-opioid receptors. No function of these receptors in mediating blockage of field-stimulated contractions was observed with ligands having affinity for the putative delta 1 or delta 2 subtypes nor were the agonists able to modulate responses to mu-opioid ligands in this tissue. 4. The results demonstrate the modulation of mu-opioid agonists by delta-opioid agonists does not occur in the isolated peripheral tissues examined. Thus the findings do not support the concept of a functional coupling of opioid receptors, though the results may be explained by differences between opioid systems in the brain and peripheral tissues examined.
摘要
  1. 体内研究有证据表明μ和δ阿片样物质配体之间存在相互作用。在本研究中,使用小鼠输精管和豚鼠回肠肌间神经丛-纵肌制备物对这一概念进行了研究。2. 在小鼠输精管的场刺激实验中,联合给予亚有效浓度的δ阿片样物质激动剂[D-青霉胺2,D-青霉胺5]脑啡肽(DPDPE)与[Met5]-或[Leu5]脑啡肽,对μ激动剂[D-丙氨酸2,甲基苯丙氨酸4,甘氨醇5]脑啡肽(DAMGO)和吗啡的剂量反应曲线没有影响。同样,当在μ阿片样物质激动剂之前的不同时间添加δ阿片样物质激动剂时,或者当联合给予δ阿片样物质配体的半数有效浓度(EC50)时,δ阿片样物质激动剂也不会改变吗啡和DAMGO的效力。对假定的δ1-(DPDPE)或δ2-([D-丙氨酸2,谷氨酸4]强啡肽II(Delt II))阿片样物质受体具有优先活性的化合物在这方面无效。3. 豚鼠回肠含有δ阿片样物质受体。对于假定的δ1或δ2亚型具有亲和力的配体,未观察到这些受体在介导场刺激收缩的阻断中发挥作用,并且这些激动剂也无法调节该组织中对μ阿片样物质配体的反应。4. 结果表明,在所检测的离体外周组织中,δ阿片样物质激动剂对μ阿片样物质激动剂不存在调节作用。因此,这些发现不支持阿片样物质受体功能偶联的概念,尽管这些结果可能由所检测的脑内和外周组织阿片样物质系统之间的差异来解释。

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