Morphine and oxycodone, but not fentanyl, exhibit antinociceptive effects mediated by G-protein inwardly rectifying potassium (GIRK) channels in an oxaliplatin-induced neuropathy rat model.
第一作者:
Tomoe,Kanbara
第一单位:
Pain & Neurology, Discovery Research Laboratories, SHIONOGI Co., Ltd., 1-1, 3-chome, Futaba-cho, Toyonaka 561-0825, Osaka, Japan; Department of Toxicology, Hoshi University School of Pharmacy and Pharmaceutical Sciences, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan.
作者:
主题词
镇痛药, 阿片类(Analgesics, Opioid);动物(Animals);抗肿瘤药(Antineoplastic Agents);芬太尼(Fentanyl);G蛋白偶联内向整流钾通道(G Protein-Coupled Inwardly-Rectifying Potassium Channels);男(雄)性(Male);吗啡(Morphine);神经痛(Neuralgia);有机铂化合物(Organoplatinum Compounds);羟可酮(Oxycodone);大鼠, Sprague-Dawley(Rats, Sprague-Dawley);受体, 阿片样, μ(Receptors, Opioid, mu)
DOI
10.1016/j.neulet.2014.08.005
PMID
25128218
发布时间
2018-12-02
- 浏览20
Neuroscience letters
119-24页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文