Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo 11562, Egypt.
Department of Drug Radiation Research, National Centre for Radiation Research and Technology (NCRRT)-Egyptian Atomic Energy Authority, Cairo 11787, Egypt.
Int J Mol Sci. 2022 Aug 25;23(17):9640. doi: 10.3390/ijms23179640.
The current study aims to evaluate the possible neuroprotective impact of gold nanoparticles (AuNPs) and an alpha-lipoic acid (ALA) mixture against brain damage in irradiated rats. AuNPs were synthesized and characterized using different techniques. Then, a preliminary investigation was carried out to determine the neuroprotective dose of AuNPs, where three single doses (500, 1000, and 1500 µg/kg) were orally administrated to male Wistar rats, one hour before being exposed to a single dose of 7Gy gamma radiation. One day following irradiation, the estimation of oxidative stress biomarkers (malondialdehyde, MDA; glutathione peroxidase, GPX), DNA fragmentation, and histopathological alterations were performed in brain cortical and hippocampal tissues in both normal and irradiated rats. The chosen neuroprotective dose of AuNPs (1000 µg/kg) was processed with ALA (100 mg/kg) to prepare the AuNPs-ALA mixture. The acute neuroprotective effect of AuNPs-ALA in irradiated rats was determined against valproic acid as a neuroprotective centrally acting reference drug. All drugs were orally administered one hour before the 7Gy-gamma irradiation. One day following irradiation, animals were sacrificed and exposed to examinations such as those of the preliminary experiment. Administration of AuNPs, ALA, and AuNPs-ALA mixture before irradiation significantly attenuated the radiation-induced oxidative stress through amelioration of MDA content and GPX activity along with alleviating DNA fragmentation and histopathological changes in both cortical and hippocampal tissues. Notably, the AuNPs-ALA mixture showed superior effect compared to that of AuNPs or ALA alone, as it mitigated oxidative stress, DNA damage, and histopathological injury collectively. Administration of AuNPs-ALA resulted in normalized MDA content, increased GPX activity, restored DNA content in the cortex and hippocampus besides only mild histopathological changes. The present data suggest that the AuNPs-ALA mixture may be considered a potential candidate for alleviating radiation-associated brain toxicity.
本研究旨在评估金纳米粒子(AuNPs)和α-硫辛酸(ALA)混合物对受照射大鼠脑损伤的可能神经保护作用。AuNPs 采用不同技术进行合成和表征。然后,进行了一项初步研究以确定 AuNPs 的神经保护剂量,其中三种单剂量(500、1000 和 1500µg/kg)经口给予雄性 Wistar 大鼠,在暴露于 7Gyγ射线之前 1 小时给予。照射后 1 天,在正常和照射大鼠的皮质和海马组织中评估氧化应激生物标志物(丙二醛,MDA;谷胱甘肽过氧化物酶,GPX)、DNA 片段化和组织病理学改变。选择的 AuNPs 神经保护剂量(1000µg/kg)与 ALA(100mg/kg)一起处理以制备 AuNPs-ALA 混合物。AuNPs-ALA 混合物在照射大鼠中的急性神经保护作用通过作为中枢作用的参考神经保护药物丙戊酸来确定。所有药物均在 7Gy-γ 照射前 1 小时经口给予。照射后 1 天,处死动物并进行初步实验的检查。照射前给予 AuNPs、ALA 和 AuNPs-ALA 混合物可通过改善 MDA 含量和 GPX 活性以及减轻皮质和海马组织的 DNA 片段化和组织病理学改变来显著减轻辐射引起的氧化应激。值得注意的是,AuNPs-ALA 混合物的效果优于 AuNPs 或 ALA 单独使用,因为它共同减轻了氧化应激、DNA 损伤和组织病理学损伤。给予 AuNPs-ALA 可使 MDA 含量正常化,增加 GPX 活性,恢复皮质和海马中的 DNA 含量,仅伴有轻微的组织病理学变化。这些数据表明,AuNPs-ALA 混合物可被视为缓解与辐射相关的脑毒性的潜在候选药物。