Faculty of Science, Mansoura University, Mansoura, Egypt.
Environ Sci Pollut Res Int. 2021 Jun;28(24):31108-31121. doi: 10.1007/s11356-021-12951-5. Epub 2021 Feb 17.
The current study aimed to investigate the ameliorative effect of melatonin (MLT) against brain injury in rats undergoing whole-body exposure to γ-radiation. Male Wistar rats were whole-body exposed to 4-Gy γ-radiation from a cesium-137 source. MLT (10 mg/kg) was orally administrated 30 minutes before irradiation and continued once daily for 1 and 7 days after exposure. In the irradiated rats, the plasma levels of glutamate were increased, while the gamma-aminobutyric acid (GABA) levels were decreased, and MLT improved the disturbed glutamate and GABA levels. These effects paralleled an increase in pro-inflammatory cytokines (IL-1b, IL-6, and TNF-a) and C-reactive protein as well as a decrease in IL-10 in the plasma of the irradiated rats. MLT treatment markedly reduced these effects, indicating its anti-inflammatory impact. Immunohistochemical studies demonstrated a remarkable upregulation of caspase-3 and P53 expression, indicating the increased apoptosis in the brain of irradiated rats. MLT significantly downregulated the expression of these parameters compared with that in the irradiated rats, indicating its anti-apoptotic effect. Oxidative stress is developed in the brain as evidenced by increased levels of malondialdehyde; decreased activities of superoxide dismutase, catalase, and glutathione peroxidase; and decreased content of glutathione in the brain. MLT remarkably ameliorated the development of oxidative stress in the brain of the irradiated rats indicating its antioxidant impact. The histopathological results were consistent with the biochemical and immunohistochemical results and showed that MLT remarkably protected the histological structure of brain tissue compared with that in the irradiated rats. In conclusion, MLT showed potential neuroprotective properties by increasing the release of neurotransmitters, antioxidants, and anti-inflammatory factors and reducing pro-inflammatory cytokines and apoptosis in the brain of irradiated rats. MLT can be beneficial in clinical and occupational settings requiring radiation exposure; however, additional studies are required to elucidate its neuroprotective effect in humans.
本研究旨在探讨褪黑素(MLT)对全身 γ 射线照射大鼠脑损伤的改善作用。雄性 Wistar 大鼠全身接受来自铯-137 源的 4-Gy γ 射线照射。照射前 30 分钟给予 MLT(10mg/kg)口服,并在照射后 1 天和 7 天每天一次继续给药。在照射大鼠中,血浆谷氨酸水平升高,而γ-氨基丁酸(GABA)水平降低,MLT 改善了谷氨酸和 GABA 水平的紊乱。这些作用与血浆中促炎细胞因子(IL-1b、IL-6 和 TNF-a)和 C 反应蛋白的增加以及 IL-10 的减少相一致。MLT 治疗显著降低了这些效应,表明其具有抗炎作用。免疫组织化学研究表明,caspase-3 和 P53 表达显著上调,表明照射大鼠脑内凋亡增加。与照射大鼠相比,MLT 显著下调了这些参数的表达,表明其具有抗凋亡作用。氧化应激在大脑中发展,表现为丙二醛水平升高;超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性降低;大脑中谷胱甘肽含量降低。MLT 显著改善了照射大鼠脑内氧化应激的发展,表明其具有抗氧化作用。组织病理学结果与生化和免疫组织化学结果一致,表明 MLT 与照射大鼠相比,显著保护了脑组织的组织结构。总之,MLT 通过增加神经递质、抗氧化剂和抗炎因子的释放,减少促炎细胞因子和凋亡,显示出对照射大鼠脑的潜在神经保护特性。MLT 在需要辐射暴露的临床和职业环境中可能有益,但需要进一步研究以阐明其在人类中的神经保护作用。