ORPHANIN-FQ - A NEUROPEPTIDE THAT ACTIVATES AN OPIOID-LIKE G-PROTEIN-COUPLED RECEPTOR

被引:1684
作者
REINSCHEID, RK
NOTHACKER, HP
BOURSON, A
ARDATI, A
HENNINGSEN, RA
BUNZOW, JR
GRANDY, DK
LANGEN, H
MONSMA, FJ
CIVELLI, O
机构
[1] HOFFMANN LA ROCHE AG, CNS RES, DIV PHARMA, CH-4002 BASEL, SWITZERLAND
[2] OREGON HLTH SCI UNIV, VOLLUM INST ADV BIOMED RES, PORTLAND, OR 97201 USA
[3] HOFFMANN LA ROCHE AG, DIV PHARMA, GENE TECHNOL RES, CH-4002 BASEL, SWITZERLAND
关键词
D O I
10.1126/science.270.5237.792
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A heptadecapeptide was identified and purified from porcine brain tissue as a ligand for an orphan heterotrimeric GTP- binding protein (G protein)- coupled receptor (LC132) that is similar in sequence to opioid receptors. This peptide, orphanin FQ, has a primary structure reminiscent of that of opioid peptides. Nanomolar concentrations of orphanin FQ inhibited forskolin-stimulated adenylyl cyclase activity in cells transfected with LC132. This inhibitory activity was not affected by the addition of opioid ligands, nor did the peptide activate opioid receptors. Orphanin FQ bound to its receptor in a saturable manner and with high affinity. When injected intracerebroventricularly into mice, orphanin FQ caused a decrease in locomotor activity but did not induce analgesia in the hot-plate test. However, the peptide produced hyperalgesia in the tail-flick assay. Thus, orphanin FQ may act as a transmitter in the brain by modulating nociceptive and locomotor behavior.
引用
收藏
页码:792 / 794
页数:3
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