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中枢神经系统对电离辐射暴露的反应:细胞、生化和分子视角

Central Nervous System Response Against Ionizing Radiation Exposure: Cellular, Biochemical, and Molecular Perspectives.

作者信息

Kumar Ravi, Kumari Pratibha, Kumar Raj

机构信息

Radiation Biotechnology Department, Institute of Nuclear Medicine and Allied Sciences (INMAS), Defence Research and Development Organization (DRDO), Brig. S.K. Mazumdar Road, Timarpur, Delhi, 110054, India.

出版信息

Mol Neurobiol. 2025 Jun;62(6):7268-7295. doi: 10.1007/s12035-025-04712-z. Epub 2025 Jan 28.

Abstract

Gamma radiation is known to induce several detrimental effects on the nervous system. The hippocampus region, specifically the dentate gyrus (DG) and subventricular zone (SVZ), have been identified as a radiation-sensitive neurogenic niche. Radiation alters the endogenous redox status of neural stem cells (NSCs) and other proliferative cells, especially in the hippocampus region, leading to oxidative stress, neuroinflammation, and cell death. Planned (i.e., radiotherapy of brain tumor patients) or unplanned radiation exposure (i.e., accidental radiation exposure) can induce nonspecific damage to neuronal tissues, resulting in chronic or acute radiation syndrome. Although anatomical alterations in the neuronal tissues have been reported at higher doses of gamma radiation, biochemical and molecular perturbations may be evident even at much lower radiation doses. They may manifest in the form of neuronal deficits and cognitive impairment. In the present review, several molecular events and signaling pathways, such as oxidative stress, neuroinflammation, apoptosis, cognition, neuroplasticity, and neurotoxicity induced in neuronal cells upon ionizing radiation exposure, are reviewed. Furthermore, brain-specific radioprotectors and mitigators that protect normal neuronal cells and tissues against ionizing radiation during radiotherapy of cancer patients or nuclear emergencies are also discussed.

摘要

已知γ辐射会对神经系统产生多种有害影响。海马区,特别是齿状回(DG)和脑室下区(SVZ),已被确定为对辐射敏感的神经发生微环境。辐射会改变神经干细胞(NSCs)和其他增殖细胞的内源性氧化还原状态,尤其是在海马区,从而导致氧化应激、神经炎症和细胞死亡。计划性(即脑肿瘤患者的放射治疗)或非计划性辐射暴露(即意外辐射暴露)可对神经元组织造成非特异性损伤,导致慢性或急性放射综合征。尽管在较高剂量的γ辐射下已报道了神经元组织的解剖学改变,但即使在低得多的辐射剂量下,生化和分子扰动也可能很明显。它们可能表现为神经元缺陷和认知障碍。在本综述中,对电离辐射暴露后神经元细胞中诱导的几种分子事件和信号通路,如氧化应激、神经炎症、细胞凋亡、认知、神经可塑性和神经毒性进行了综述。此外,还讨论了在癌症患者放疗或核紧急情况下保护正常神经元细胞和组织免受电离辐射的脑特异性辐射防护剂和缓解剂。

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