Vaseghi Golnaz, Rashidi Nastaran, Zare Nasrin, Ghasemi Fahimeh, Pourhadi Marjan, Rafiee Laleh, Javanmard Shaghayegh Haghjooy
Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2022 Dec 26;11:122. doi: 10.4103/abr.abr_97_21. eCollection 2022.
In this study, the effects of methadone and naloxone on the expression of toll-like receptor 4 () gene have been evaluated in human non-small cell lung carcinoma A549 cell line migration using and techniques.
Lung cancer A549 cell cultures were stimulated for 24 h with methadone (5, 10, and 20 μM) and naloxone (20 and 40 μM) concentrations. The level of expression was determined by the quantitative real-time polymerase chain reaction. Migration of the A549 cells was investigated after a 4-h incubation period with methadone using the Boyden Chamber assay.
Migration rate of the A549 cells treated with 5 ( < 0.05) and 20 ( < 0.01) μM methadone was, respectively, increased and decreased with 20 μM naloxone ( < 0.05). Furthermore, the expression was enhanced with 5 ( < 0.05) and 20 ( < 0.01) μM methadone and decreased with 20 ( < 0.05) and 40 μM naloxone ( < 0.01). In addition, docking analysis revealed docking of methadone to MD-2 and .
According to the present DATA, methadone affects the expression. It may however cause adverse consequences by increasing the expression. Therefore, the useful analgesic properties of methadone should be separated from the unwanted -mediated side effects.
在本研究中,已使用[具体技术1]和[具体技术2]技术评估了美沙酮和纳洛酮对人非小细胞肺癌A549细胞系迁移中Toll样受体4(TLR4)基因表达的影响。
用美沙酮(5、10和20μM)和纳洛酮(20和40μM)浓度刺激肺癌A549细胞培养物24小时。通过定量实时聚合酶链反应测定TLR4表达水平。使用Boyden小室分析法在与美沙酮孵育4小时后研究A549细胞的迁移。
用5μM(P<0.05)和20μM(P<0.01)美沙酮处理的A549细胞迁移率分别增加,而用20μM纳洛酮处理后迁移率降低(P<0.05)。此外,5μM(P<0.05)和20μM(P<0.01)美沙酮可增强TLR4表达,而20μM(P<0.05)和40μM纳洛酮可降低TLR4表达(P<0.01)。此外,[分子对接]分析显示美沙酮与MD-2和[另一受体名称]对接。
根据目前的数据,美沙酮影响TLR4表达。然而,它可能通过增加TLR4表达而导致不良后果。因此,应将美沙酮的有效镇痛特性与不需要的TLR4介导的副作用区分开来。