共 71 条
Thymoquinone Potentiates the Effect of Phenytoin against Electroshock-Induced Convulsions in Rats by Reducing the Hyperactivation of m-TOR Pathway and Neuroinflammation: Evidence from In Vivo, In Vitro and Computational Studies
被引:9
作者:
Pottoo, Faheem Hyder
[1
]
Salahuddin, Mohammed
[2
]
Khan, Firdos Alam
[3
]
Alomar, Fadhel
[1
]
AL Dhamen, Marwa Abdullah
[1
]
Alhashim, Abrar Fouad
[1
]
Alqattan, Hawra Hussain
[1
]
Gomaa, Mohamed S.
[4
]
Alomary, Mohammad N.
[5
]
机构:
[1] Imam Abdulrahman Bin Faisal Univ, Dept Pharmacol, Coll Clin Pharm, POB 1982, Dammam 31441, Saudi Arabia
[2] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Dept Clin Pharm Res, POB 1982, Dammam 31441, Saudi Arabia
[3] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Dept Stem Cell Res, POB 1982, Dammam 31441, Saudi Arabia
[4] Imam Abdulrahman Bin Faisal Univ, Dept Pharmaceut Chem, Coll Clin Pharm, POB 1982, Dammam 31441, Saudi Arabia
[5] Kind Abdulaziz City Sci & Technol KACST, Natl Biotechnol Ctr, POB 1982, Riyadh 11442, Saudi Arabia
关键词:
phenytoin;
thymoquinone;
PI3K/Akt/m-TOR signaling;
grand mal seizures;
neuronal inflammation;
convulsions;
molecular docking;
neuroprotection;
cooperative binding;
NIGELLA-SATIVA SEEDS;
MAJOR CONSTITUENT;
COMBINATION THERAPY;
STATUS EPILEPTICUS;
OXIDATIVE STRESS;
MAMMALIAN TARGET;
CELL-DEATH;
EPILEPSY;
MTOR;
NEURODEGENERATION;
D O I:
10.3390/ph14111132
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Epilepsy is a chronic neurodegenerative disease characterized by multiple seizures, hereto 35% of patients remain poor responders. Phenytoin (PHT; 20 and 40 mg/kg) and thymoquinone (THQ; 40 and 80 mg/kg) were given alone and as a low dose combination for 14 days (p.o), prior to challenge with maximal electroshock (MES; 180 mA, 220 V, 0.2 s). Apart from observing convulsions, hippocampal mTOR, IL-1 beta, IL-6 and TNF-alpha levels were measured. Hippocampal histomorphological analysis was also conducted. In vitro cell line studies and molecular docking studies were run in parallel. The results revealed the synergistic potential of the novel duo-drug combination regimen: PHT (20 mg/kg) and THQ (40 mg/kg) against MES-induced convulsions. MES amplified signaling through mTOR, and inflated the levels of proinflammatory markers (IL-1 beta, IL-6 and TNF-alpha), which was significantly averted (p < 0.001) with the said drug combination. The computational studies revealed that PHT and THQ cooperatively bind the active site on Akt (upstream target of m-TOR) and establish a good network of intermolecular interactions, which indicates the sequential inhibition of PI3K/Akt/m-TOR signaling with the combination. The combination also increased cell viability by 242.81% compared to 85.66% viability from the the toxic control. The results suggest that the PHT and THQ in combination possesses excellent anticonvulsant and neuroprotective effects.
引用
收藏
页数:18
相关论文