Moselhy Omnia A, Abdel-Aziz Nahed, El-Bahkery Azza, Moselhy Said S, Ibrahim Ehab A
Biochemistry Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
Radiation Biology Research Department, National Center for Radiation Research & Technology, Egyptian Atomic Energy Authority, Cairo, Egypt.
Sci Rep. 2025 Jan 31;15(1):3857. doi: 10.1038/s41598-025-87635-y.
Despite the diverse applications of γ radiation in radiotherapy, industrial processes, and sterilization, it causes hazardous effects on living organisms, such as cellular senescence, persistent cell cycle arrest, and mitochondrial dysfunction. This study evaluated the efficacy of curcumin nanoparticles (CNPs) in mitigating mitochondrial dysfunction and cellular senescence induced by γ radiation in rat brain tissues. Four groups of male Wistar albino rats (n = 8 per group) were included: (Gr1) the control group; (Gr2) the CNPs group (healthy rats receiving oral administration of curcumin nanoparticles at a dose of 10 mg/kg/day, three times per week for eight weeks); (Gr3) the irradiated group (rats exposed to a single dose of 10 Gy head γ irradiation); and (Gr4) the irradiated + CNPs group (irradiated rats treated with CNPs). The data obtained demonstrated that oral administration of CNPs for eight weeks attenuated oxidative stress in γ-irradiated rats by lowering the brain's lipid peroxidation level [malondialdehyde (MDA)] and enhancing antioxidant markers [superoxide dismutase (SOD), reduced glutathione (GSH), and total antioxidant capacity (TAC)] (P < 0.05). In addition, CNPs significantly increased mitochondrial function by improving complex I, complex II, and ATP production levels compared to the irradiated group. In irradiated rats, CNPs also showed anti-neuroinflammatory effects by reducing brain interleukin 6 (IL-6), tumor necrosis factor-alpha (TNF-α), and nuclear factor-kappa B (NF-ĸB) levels (P < 0.05). Moreover, CNPs administered to irradiated rats significantly reduced brain β-galactosidase activity and the expression levels of p53, p21, and p16 genes (P < 0.05) while concurrently inducing a significant increase in AMPK mRNA expression compared to the irradiated group. In conclusion, CNPs ameliorated the neurotoxicity of γ radiation and hold promise as a novel agent to delay cellular senescence via their combined antioxidant, anti-inflammatory, and mitochondrial-enhancing properties.
尽管γ辐射在放射治疗、工业生产过程和灭菌等方面有多种应用,但它会对生物体造成有害影响,如细胞衰老、持续的细胞周期停滞和线粒体功能障碍。本研究评估了姜黄素纳米颗粒(CNPs)减轻γ辐射诱导的大鼠脑组织线粒体功能障碍和细胞衰老的效果。将雄性Wistar白化大鼠分为四组(每组n = 8):(Gr1)对照组;(Gr2)CNPs组(健康大鼠口服剂量为10 mg/kg/天的姜黄素纳米颗粒,每周三次,共八周);(Gr3)辐照组(大鼠接受单次10 Gy头部γ辐射);(Gr4)辐照+CNPs组(接受辐照的大鼠用CNPs治疗)。获得的数据表明,连续八周口服CNPs可通过降低大脑脂质过氧化水平[丙二醛(MDA)]和增强抗氧化标志物[超氧化物歧化酶(SOD)、还原型谷胱甘肽(GSH)和总抗氧化能力(TAC)]来减轻γ辐照大鼠的氧化应激(P < 0.05)。此外,与辐照组相比,CNPs通过改善复合物I、复合物II和ATP生成水平,显著提高了线粒体功能。在辐照大鼠中,CNPs还通过降低大脑白细胞介素6(IL-6)、肿瘤坏死因子-α(TNF-α)和核因子-κB(NF-κB)水平显示出抗神经炎症作用(P < 0.05)。此外,与辐照组相比,给辐照大鼠施用CNPs可显著降低大脑β-半乳糖苷酶活性以及p53、p21和p16基因的表达水平(P < 0.05),同时诱导AMPK mRNA表达显著增加。总之,CNPs改善了γ辐射的神经毒性,并有望作为一种新型药物,通过其抗氧化、抗炎和增强线粒体功能的综合特性来延缓细胞衰老。