Antisense mapping DOR-1 in mice: Further support for delta receptor subtypes

被引:34
作者
Rossi, GC [1 ]
Su, W [1 ]
Leventhal, L [1 ]
Su, H [1 ]
Pasternak, GW [1 ]
机构
[1] MEM SLOAN KETTERING CANC CTR,DEPT NEUROL,COTZIAS LAB NEUROONCOL,NEW YORK,NY 10021
关键词
antisense mapping; DOR-1; delta receptor; delta(1); delta(2); analgesia;
D O I
10.1016/S0006-8993(97)00081-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In contrast to the pharmacological studies implicating delta-opioid receptor subtypes, cloning studies have identified only a single cDNA encoding a delta receptor, DOR-1. Antisense studies have established the importance of DOR-1 in delta analgesia in mice. Antisense mapping extends this approach to include oligodeoxynucleotides which are targeted against each of the exons of the gene. Five different antisense oligodeoxynucleotides based upon the three DOR-1 exons all block both spinal and supraspinal analgesic actions of the delta(2) ligand [D-Ala(2),Glu(4)]deltorphin, consistent with the suggestion that DOR-1 encodes the delta(2) receptor. At the spinal level, [D-Pen(2),D-Pen(5)]enkephalin (DPDPE) acts also acts through delta(2) receptors and all the antisense probes block spinal DPDPE analgesia. However, supraspinally only the two antisense probes targeting exon 3 block DPDPE analgesia. The remaining three antisense probes based upon exons 1 and 2 are inactive. Thus, the delta receptors responsible for spinal and supraspinal DPDPE analgesia can be discriminated at the molecular level by antisense mapping. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:176 / 179
页数:4
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