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5-甲氧基黄酮对小鼠的镇静催眠样作用及体内和计算机模拟方法对可能机制的研究

Sedative-hypnotic like effect of 5-methoxyflavone in mice and investigation on possible mechanisms by in vivo and in silico methods.

作者信息

Shanmugasundaram Jaikumar, Subramanian Viswanathan, Nadipelly Jagan S, Kathirvelu Parimala, Sayeli Vijaykumar, Cheriyan Binoy Varghese

机构信息

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.

出版信息

Biomed Pharmacother. 2018 Dec;108:85-94. doi: 10.1016/j.biopha.2018.08.117. Epub 2018 Sep 12.

Abstract

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.

摘要

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。

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