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μ-和δ-阿片样物质激动剂在MOR基因缺陷小鼠输精管中的活性。

Activity of mu- and delta-opioid agonists in vas deferens from mice deficient in MOR gene.

作者信息

Maldonado R, Severini C, Matthes H W, Kieffer B L, Melchiorri P, Negri L

机构信息

Laboratori de Neurofarmacologia, Facultat de Ciences de la Salut i de la Vida, Universitat Pompeu Fabra, c/Dr Aiguader 80, 08003 Barcelona, Spain.

出版信息

Br J Pharmacol. 2001 Apr;132(7):1485-92. doi: 10.1038/sj.bjp.0703966.

Abstract
  1. Mice lacking the mu-opioid receptor have been recently generated. Centrally mediated responses of mu-opioid agonists are suppressed whereas some of the delta-opioid responses are preserved in these mutant mice. 2. The vas deferens bioassay has been used in this study to investigate the functional activity at a peripheral level of mu- and delta-opioid agonists in mice lacking mu-opioid receptors. 3. The different mu-opioid agonists evaluated, morphine, DAMGO, dermorphin and [Lys(7)]-dermorphin produced an inhibitory response in vas deferens from wild-type mice but had no relevant activity on vas deferens from mutant mice. 4. The selective delta-opioid agonists DPDPE, BUBU, deltorphin I, deltorphin II and [D-Met(2)]-deltorphin induced inhibitory effects in vas deferens from both wild-type and mutant mice. However, the biological activities of these ligands were slightly reduced in preparations from mutant mice. The inhibitory responses of all these delta-opioid agonists were prevented by the administration of the selective delta-opioid antagonist naltrindole. 5. These data indicate that delta-opioid agonists, but not mu-opioid agonists, are biologically active in vas deferens from mice lacking mu-opioid receptors. The decreased response of delta-agonists in mutant mice suggests that some cooperativity may exist between mu- and delta-opioid receptors in these vas deferens preparations.
摘要
  1. 最近已培育出缺乏μ-阿片受体的小鼠。在这些突变小鼠中,μ-阿片激动剂的中枢介导反应受到抑制,而一些δ-阿片反应得以保留。2. 本研究采用输精管生物测定法来研究缺乏μ-阿片受体的小鼠外周水平上μ-和δ-阿片激动剂的功能活性。3. 所评估的不同μ-阿片激动剂,吗啡、DAMGO、皮啡肽和[Lys(7)]-皮啡肽在野生型小鼠的输精管中产生抑制反应,但对突变小鼠的输精管无相关活性。4. 选择性δ-阿片激动剂DPDPE、BUBU、δ-内啡肽I、δ-内啡肽II和[D-Met(2)]-δ-内啡肽在野生型和突变型小鼠的输精管中均诱导抑制作用。然而,这些配体在突变小鼠的制剂中的生物活性略有降低。所有这些δ-阿片激动剂的抑制反应都可通过给予选择性δ-阿片拮抗剂纳曲吲哚来阻断。5. 这些数据表明,δ-阿片激动剂而非μ-阿片激动剂在缺乏μ-阿片受体的小鼠的输精管中具有生物活性。突变小鼠中δ-激动剂反应的降低表明在这些输精管制剂中μ-和δ-阿片受体之间可能存在某种协同作用。

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Opioids: first lessons from knockout mice.阿片类药物:基因敲除小鼠带来的初步启示。
Trends Pharmacol Sci. 1999 Jan;20(1):19-26. doi: 10.1016/s0165-6147(98)01279-6.
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The dermorphin peptide family.皮啡肽肽家族。
Gen Pharmacol. 1996 Oct;27(7):1099-107. doi: 10.1016/0306-3623(95)02149-3.

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