Biosynthesized Selenium Nanoparticles Using Epigallocatechin Gallate Protect against Pentylenetetrazole-Induced Acute Epileptic Seizures in Mice via Antioxidative, Anti-Inflammatory, and Anti-Apoptotic Activities

被引:6
|
作者
Alrashdi, Barakat M. [1 ]
Fehaid, Alaa [2 ]
Kassab, Rami B. [3 ]
Rizk, Sara [4 ]
Habotta, Ola A. [2 ]
Moneim, Ahmed Abdel E. [5 ]
机构
[1] Jouf Univ, Coll Sci, Biol Dept, Sakaka 41412, Saudi Arabia
[2] Mansoura Univ, Fac Vet Med, Dept Forens Med & Toxicol, Mansoura 35516, Egypt
[3] Al Baha Univ, Fac Sci & Arts, Dept Biol, Al Baha 65799, Saudi Arabia
[4] Hadayek Helwan Med Ctr Family Hlth, Dept Immunizat & Vaccines, Cairo, Egypt
[5] Helwan Univ, Fac Sci, Zool & Entomol Dept, Cairo 11792, Egypt
关键词
epigallocatechin gallate; selenium nanoparticles; epilepsy; oxidative stress; inflammation; apoptosis; mice; OXIDATIVE STRESS; GREEN-SYNTHESIS; NANO-SELENIUM; MOUSE MODEL; ASSAY; TEA;
D O I
10.3390/biomedicines11071955
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several negative outcomes are associated with current anti-epileptic medications. Epigallocatechin gallate (EGCG) is a plant-derived compound called catechin and has many medicinal activities, such as anti-inflammatory and antioxidant activities. Biosynthesized selenium nanoparticles are also showing their neuroprotective effect. The anti-epileptic effect of EGCG, alone or with SeNPs, is still debated. Here, we aimed to investigate the potential anti-seizure effect of biosynthesized SeNPs using EGCG (EGCG-SeNPs) against epileptic seizures and hippocampal damage, which is enhanced by pentylenetetrazole (PTZ) injection in mice. Mice were grouped as follows: control; PTZ-exposed group (epileptic model); EGCG + PTZ-treated group; sodium selenite (Na2SeO3) + PTZ-treated group; EGCG-SeNPs + PTZ-treated group; and valproic acid (VPA) + PTZ-treated group. EGCG-SeNPs administration showed anti-epileptic activity by increasing the latency time and reducing the seizure duration following the PTZ injection. Additionally, EGCG-SeNPs counteracted the PTZ-induced changes in oxidants and antioxidants. Moreover, EGCG-SeNPs inhibited the inflammatory response by suppressing the release of pro-inflammatory cytokines and decreasing the immunoreactivity of the glial fibrillary acidic protein and mRNA expression of glutamate receptor subunit zeta-1 (NMDAR; Grin1), showing their inhibitory effect on epilepsy-associated inflammation. Moreover, EGCG-SeNPs reduced PTZ-induced neuronal apoptosis, as indicated by a reduction in the levels of pro-apoptotic proteins and an elevation of the anti-apoptotic protein. Moreover, EGCG-SeNPs administration significantly modulated the PTZ-induced changes in monoamine levels and acetylcholinesterase activity in the hippocampal tissue. The obtained findings suggest the anti-seizure activity of EGCG-SeNPs via their antioxidant, anti-inflammatory, and anti-apoptotic effects, along with their neuromodulatory effect.
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页数:16
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