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脑损伤及电离辐射后神经血管紊乱模式。放射治疗和辐射复合伤的并发症。

Brain Damage and Patterns of Neurovascular Disorder after Ionizing Irradiation. Complications in Radiotherapy and Radiation Combined Injury.

机构信息

MCG, Rockville, Maryland.

Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, Maryland.

出版信息

Radiat Res. 2021 Jul 1;196(1):1-16. doi: 10.1667/RADE-20-00147.1.

Abstract

Exposure to ionizing radiation, mechanical trauma, toxic chemicals or infections, or combinations thereof (i.e., combined injury) can induce organic injury to brain tissues, the structural disarrangement of interactive networks of neurovascular and glial cells, as well as on arrays of the paracrine and systemic destruction. This leads to subsequent decline in cognitive capacity and decompensation of mental health. There is an ongoing need for improvement in mitigating and treating radiation- or combined injury-induced brain injury. Cranial irradiation per se can cause a multifactorial encephalopathy that occurs in a radiation dose- and time-dependent manner due to differences in radiosensitivity among the various constituents of brain parenchyma and vasculature. Of particular concern are the radiosensitivity and inflammation susceptibility of: 1. the neurogenic and oligodendrogenic niches in the subependymal and hippocampal domains; and 2. the microvascular endothelium. Thus, cranial or total-body irradiation can cause a plethora of biochemical and cellular disorders in brain tissues, including: 1. decline in neurogenesis and oligodendrogenesis; 2. impairment of the blood-brain barrier; and 3. ablation of vascular capillary. These changes, along with cerebrovascular inflammation, underlie different stages of encephalopathy, from the early protracted stage to the late delayed stage. It is evident that ionizing radiation combined with other traumatic insults such as penetrating wound, burn, blast, systemic infection and chemotherapy, among others, can exacerbate the radiation sequelae (and vice versa) with increasing severity of neurogenic and microvascular patterns of radiation brain damage.

摘要

电离辐射、机械创伤、有毒化学物质或感染,或其组合(即联合损伤)可导致脑组织的器质性损伤、神经血管和神经胶质细胞相互作用网络的结构紊乱,以及旁分泌和全身破坏的排列紊乱。这会导致随后的认知能力下降和心理健康失调。因此,需要不断改进减轻和治疗辐射或联合损伤引起的脑损伤的方法。颅照射本身可引起多因素脑病,其发生方式为辐射剂量和时间依赖性,这是由于脑实质和脉管系统的各种成分之间的放射敏感性存在差异。特别值得关注的是:1. 室管膜下和海马区的神经发生和少突胶质细胞发生龛;2. 微血管内皮。因此,颅照射或全身照射可导致脑组织发生大量的生化和细胞紊乱,包括:1. 神经发生和少突胶质细胞发生减少;2. 血脑屏障受损;3. 血管毛细血管消融。这些变化,以及脑血管炎症,是脑病不同阶段的基础,从早期迁延阶段到晚期延迟阶段。显然,电离辐射与其他创伤性损伤(如穿透性伤口、烧伤、爆炸、全身感染和化疗等)相结合,可使辐射后遗症恶化(反之亦然),导致神经发生和微血管辐射脑损伤模式的严重程度增加。

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