孤菲肽受体
化学
不
类阿片
药理学
止痛药
兴奋剂
受体
纳曲酮
吗啡
伤害
阿片肽
医学
生物化学
作者
Ying-Ting Hsu,Shenren Chen,Yu‐Hsin Chang,Hsiao-Fu Chang,Teng‐Kuang Yeh,Jian Ying Chuang,Horace H. Loh,Hsing‐Pang Hsieh,Shau‐Hua Ueng,Shiu‐Hwa Yeh
标识
DOI:10.1016/j.ejmech.2023.115608
摘要
The compelling demand of a consummate analgesic medication without addiction is rising due to the clinical mistreatment. Additionally, the series of severe untoward effects usually deterred the utilization while coping with serious pain. As a possible turning point, we revealed that compound 14 is a dual agonist of mu opioid receptor (MOR) and nociceptin-orphanin FQ opioid peptide (NOP) receptor in this study. More importantly, compound 14 achieves pain relieving at very small doses, meanwhile, reduces several unwanted side effects such as constipation, reward, tolerance and withdrawal effects. Here, we evaluated the antinociception and side effects of this novel compound from wild type and humanized mice to further develop a safer prescription analgesic drug.
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