首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Characterization of ZFOR1, a putative delta-opioid receptor from the teleost zebrafish (Danio rerio).
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Characterization of ZFOR1, a putative delta-opioid receptor from the teleost zebrafish (Danio rerio).

机译:ZFOR1的特征,推定的硬骨马斑马鱼(达尼奥·里奥)的δ-阿片样物质受体。

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摘要

ZFOR1 is a putative opioid receptor from zebrafish brain which has 66% homology with the mammalian delta-opioid receptor. When expressed in HEK293 cells ZFOR1 bound the non-selective opioid antagonist [(3)H]diprenorphine with high affinity. However, the binding of this ligand was not readily displaced by opioids selective for mu, delta or kappa opioid receptors (affinities>1000 nM). Rather non-selective ligands showed good affinity, as did the non-peptide delta-ligand BW373U86 (Ki 69 nM), the delta-antagonist naltrindole (Ki 28 nM) and the peptide beta-endorphin (Ki 37 nM). Agonist binding to the receptor encoded by ZFOR1 receptor stimulated the binding of [(35)S]GTPgammaS confirming coupling to G proteins. Study of the receptor should contribute to understanding of the evolution of the opioid system.
机译:ZFOR1是来自斑马鱼大脑的推定阿片受体,与哺乳动物的δ-阿片受体具有66%的同源性。当在HEK293细胞中表达时,ZFOR1以高亲和力结合非选择性阿片拮抗剂[(3)H] diprenorphine。然而,该配体的结合不易被对μ,δ或κ阿片受体具有选择性的阿片受体替代(亲和力> 1000nM)。相反,非选择性配体显示出良好的亲和力,非肽δ-配体BW373U86(Ki 69 nM),δ-拮抗剂纳那多尔(Ki 28 nM)和肽β-内啡肽(Ki 37 nM)也是如此。激动剂与ZFOR1受体编码的受体的结合刺激了[(35)S] GTPgammaS的结合,从而证实了与G蛋白的偶联。受体的研究应有助于了解阿片类药物系统的演变。

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