Miyamae T, Fukushima N, Misu Y, Ueda H
Department of Pharmacology, Yokohama City University School of Medicine, Japan.
FEBS Lett. 1993 Nov 1;333(3):311-4. doi: 10.1016/0014-5793(93)80677-m.
Cloned mouse delta-subtype opioid receptor (DOR1) was expressed in Xenopus oocytes to study the signal transduction. Opioid delta-agonists evoked a calcium-dependent chloride current in oocytes injected with mRNA derived from DOR1, together with that from the alpha subunit of Gi1. The delta-agonist-induced current was blocked by naltrindol, a delta-specific antagonist. The delta-agonist evoked no or very weak currents in oocytes with the alpha subunit of Gq or G(o). These findings indicate the functional coupling between the opioid delta-receptor and phospholipase C through an activation of Gi.
克隆的小鼠δ-亚型阿片受体(DOR1)在非洲爪蟾卵母细胞中表达以研究信号转导。阿片δ-激动剂在注射了来自DOR1以及Gi1α亚基的mRNA的卵母细胞中诱发了一种钙依赖性氯离子电流。δ-激动剂诱导的电流被δ特异性拮抗剂纳曲吲哚阻断。δ-激动剂在含有Gq或G(o)α亚基的卵母细胞中未诱发电流或仅诱发非常微弱的电流。这些发现表明阿片δ-受体与磷脂酶C之间通过Gi的激活存在功能偶联。