Inhibition of endothelin A receptor by a novel, selective receptor antagonist enhances morphine-induced analgesia: Possible functional interaction of dimerized endothelin A and μ-opioid receptors.
第一作者:
Yui,Kuroda
第一单位:
Department of Anesthesiology and Pain Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Pain Control Research, The Jikei University School of Medicine, Tokyo, Japan.
作者:
关键词
AnalgesicBQ-123 sodium salt (PubChem CID: 52943236)BQ-788 sodium salt (PubChem CID: 23693553)Endothelin A receptor antagonistG protein-coupled receptorMorphinePainReceptor heterodimerizationand Bosentan Monohydrate (PubChem CID: 185462)included endothelin-1 (PubChem CID: 16212950)morphine hydrochloride (PubChem CID: 5464110)
主题词
镇痛药, 阿片类(Analgesics, Opioid);动物(Animals);剂量效应关系, 药物(Dose-Response Relationship, Drug);HEK293细胞(HEK293 Cells);人类(Humans);男(雄)性(Male);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL);吗啡(Morphine);疼痛测定(Pain Measurement);肽类, 环(Peptides, Cyclic);蛋白质多聚化(Protein Multimerization);受体, 内皮素A(Receptor, Endothelin A);受体, 阿片样, μ(Receptors, Opioid, mu)
DOI
10.1016/j.biopha.2021.111800
PMID
34175819
发布时间
2021-12-15
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