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丙戊酸钠、巴氯芬和百里醌三联药物组合在大鼠中表现出协同抗惊厥作用,并在人胚肾细胞293(HEK-293)中具有神经保护作用。

Trio-Drug Combination of Sodium Valproate, Baclofen and Thymoquinone Exhibits Synergistic Anticonvulsant Effects in Rats and Neuro-Protective Effects in HEK-293 Cells.

作者信息

Hyder Pottoo Faheem, Salahuddin Mohammed, Khan Firdos Alam, Albaqshi Batool Taleb, Gomaa Mohamed S, Abdulla Fatima S, AlHajri Noora, Alomary Mohammad N

机构信息

Department of Pharmacology, College of Clinical Pharmacy, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia.

Department of Clinical Pharmacy Research, Institute for Research and Medical Consultation, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia.

出版信息

Curr Issues Mol Biol. 2022 Sep 20;44(10):4350-4366. doi: 10.3390/cimb44100299.

Abstract

Epilepsy is a chronic brain disorder, with anti-epileptic drugs (AEDs) providing relief from hyper-excitability of neurons, but largely failing to restrain neurodegeneration. We investigated a progressive preclinical trial in rats, whereby the test drugs; sodium valproate (SVP; 150 and 300 mg/kg), baclofen (BFN; 5 and 10 mg/kg), and thymoquinone (THQ; 40 and 80 mg/kg) were administered (i.p, once/day for 15 days) alone, and as low dose combinations, and subsequently tested for antiseizure and neuroprotective potential using electrical stimulation of neurons by Maximal electroshock (MES). The seizure stages were monitored, and hippocampal levels of m-TOR, IL-1β, IL-6 were measured. Hippocampal histopathology was also performed. Invitro and Insilco studies were run to counter-confirm the results from rodent studies. We report the synergistic effect of trio-drug combination; SVP (150 mg/kg), BFN (5 mg/kg) and THQ (40 mg/kg) against generalized seizures. The Insilco results revealed that trio-drug combination binds the Akt active site as a supramolecular complex, which could have served as a delivery system that affects the penetration and the binding to the new target. The potential energy of the ternary complex in the Akt active site after dynamics simulation was found to be -370.426 Kcal/mol, while the supramolecular ternary complex alone was -38.732 Kcal/mol, with a potential energy difference of -331.694 Kcal/mol, which favors the supramolecular ternary complex at Akt active site binding. In addition, the said combination increased cell viability by 267% and reduced morphological changes induced by Pentylenetetrazol (PTZ) in HEK-293 cells, which indicates the neuroprotective property of said combination. To conclude, we are the first to report the anti-convulsant and neuroprotective potential of the trio-drug combination.

摘要

癫痫是一种慢性脑部疾病,抗癫痫药物(AEDs)可缓解神经元的过度兴奋,但在很大程度上无法抑制神经退行性变。我们在大鼠中进行了一项渐进性的临床前试验,单独给予试验药物丙戊酸钠(SVP;150和300mg/kg)、巴氯芬(BFN;5和10mg/kg)和百里醌(THQ;40和80mg/kg)(腹腔注射,每天一次,共15天),以及低剂量组合,随后使用最大电休克(MES)对神经元进行电刺激,测试其抗癫痫和神经保护潜力。监测癫痫发作阶段,并测量海马体中m-TOR、IL-1β、IL-6的水平。还进行了海马体组织病理学检查。进行了体外和计算机模拟研究以反证啮齿动物研究的结果。我们报告了三联药物组合SVP(150mg/kg)、BFN(5mg/kg)和THQ(40mg/kg)对全身性癫痫发作的协同作用。计算机模拟结果显示,三联药物组合作为一种超分子复合物结合Akt活性位点,这可能作为一种递送系统,影响其渗透并与新靶点结合。动力学模拟后,Akt活性位点处三元复合物的势能为-370.426千卡/摩尔,而单独的超分子三元复合物为-38.732千卡/摩尔,势能差为-331.694千卡/摩尔,这有利于超分子三元复合物在Akt活性位点的结合。此外,上述组合使HEK-293细胞的细胞活力提高了267%,并减少了戊四氮(PTZ)诱导的形态变化,这表明该组合具有神经保护特性。总之,我们首次报告了三联药物组合的抗惊厥和神经保护潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e7/9601194/b05de4658ea3/cimb-44-00299-g001.jpg

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