Shanmugasundaram Jaikumar, Subramanian Viswanathan, Nadipelly Jagan S, Kathirvelu Parimala, Sayeli Vijaykumar, Cheriyan Binoy Varghese
Department of Pharmacology, Meenakshi Medical College & Research Institute, Meenakshi Academy of Higher Education and Research, Kanchipuram, 631552, India.
Faculty of Medicine, Department of Pharmacology, Texila American University, Georgetown, Guyana.
Biomed Pharmacother. 2018 Dec;108:85-94. doi: 10.1016/j.biopha.2018.08.117. Epub 2018 Sep 12.
Flavonoids have been shown to possess central nervous system (CNS) depressant effect mediated through the ionotropic GABA receptors. In the present study, 5-methoxyflavone was evaluated for sedative-hypnotic like activity in mice and the mechanisms involved by employing a battery of tests including molecular docking studies. In the open field test, 5-methoxyflavone in various doses (50, 100 and 150 mg/kg, i.p) exhibited a significant and dose-dependent reduction in the spontaneous locomotor activity (F (530) = 87.17 P < 0.001). Pretreatment with 5-methoxyflavone decreased the latency to sleep induction after pentobarbitone or ether administration and also significantly increased the duration of sleep (p < 0.001). A significant and dose-dependent myorelaxant effect was observed with 5-methoxyflavone in the inclined plane, horizontal wire test and rota rod test. Pretreatment with picrotoxin, bicuculline, glycine, caffeine or NMDA either decreased or completely abolished the hypnotic effect of 5-methoxyflavone in mice. The above results revealed the involvement of GABA, adenosine, glycine and NMDA receptors in the hypnotic effect of 5-methoxyflavone. The results of in silico studies indicated that, 5-methoxyflavone exhibits good binding affinity towards these receptors by H-bond interactions. In conclusion, the present study identified a novel and potential sedative-hypnotic like effect of 5-methoxyflavone involving multiple mechanisms.
黄酮类化合物已被证明具有通过离子型GABA受体介导的中枢神经系统(CNS)抑制作用。在本研究中,通过一系列测试(包括分子对接研究)评估了5-甲氧基黄酮在小鼠中的镇静催眠样活性及其相关机制。在旷场试验中,不同剂量(50、100和150mg/kg,腹腔注射)的5-甲氧基黄酮均显著且剂量依赖性地降低了自发运动活性(F(5,30)=87.17,P<0.001)。预先给予5-甲氧基黄酮可缩短戊巴比妥或乙醚给药后诱导睡眠的潜伏期,并且显著增加睡眠时间(p<0.001)。在倾斜平面试验、水平钢丝试验和转棒试验中观察到5-甲氧基黄酮具有显著且剂量依赖性的肌松作用。预先给予印防己毒素、荷包牡丹碱、甘氨酸、咖啡因或NMDA可降低或完全消除5-甲氧基黄酮对小鼠的催眠作用。上述结果揭示了GABA、腺苷、甘氨酸和NMDA受体参与了5-甲氧基黄酮的催眠作用。计算机模拟研究结果表明,5-甲氧基黄酮通过氢键相互作用对这些受体表现出良好的结合亲和力。总之,本研究确定了5-甲氧基黄酮具有一种涉及多种机制的新型潜在镇静催眠样作用。