Xu Yiran, Sun Yanyan, Zhou Kai, Li Tao, Xie Cuicui, Zhang Yaodong, Rodriguez Juan, Wu Yanling, Hu Min, Shao Linus R, Wang Xiaoyang, Zhu Changlian
Henan Key Laboratory of Child Brain Injury, Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Centre for Brain Repair and Rehabilitation, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Dev Neurosci. 2018;40(2):120-133. doi: 10.1159/000487923. Epub 2018 Apr 10.
Cranial radiotherapy is one of the most effective tools for treating children with brain tumors. However, radiotherapy-induced late-onset side effects have a significant impact on patients' quality of life. The purpose of this study was to investigate the effects of irradiation on metabolism and the possible molecular and cellular mechanisms behind such effects. Female Wistar rats were subjected to a single dose of 6-Gy whole-brain irradiation on postnatal day 11. The animals were sacrificed 6 h or 20 weeks after irradiation. Cell death and proliferation, microglial activation, and inflammation were analyzed and RNA sequencing was performed. We found that irradiation led to a significantly increased body weight from 15 weeks (p < 0.05) along with white adipose tissue accumulation and adipocyte hypertrophy at 20 weeks, and these changes were accompanied by glucose and lipid metabolic disturbances as indicated by reduced glucose tolerance, increased insulin resistance, increased serum triglycerides, and an increased leptin/adiponectin ratio. Furthermore, irradiation induced cell death, microglial activation, inflammation, and persistent astrocyte reactivity in the hypothalamus. Hypothalamic transcriptome analysis showed that 865 genes were downregulated and 290 genes were upregulated in the irradiated group 20 weeks after irradiation, and further pathway analysis showed that the insulin resistance-related PI3K-Akt signaling pathway and the energy expenditure-related adipocytokine signaling pathway were downregulated. Gene Ontology enrichment analysis showed that the expression of fatty acid metabolism-related proteins and effector proteins was significantly different in the irradiation group. This study demonstrates that ionizing radiation to the juvenile female brain induces hypothalamic damage that is likely to be associated with delayed metabolic abnormalities, and this critical vulnerability of the hypothalamus to irradiation should be taken into consideration in the development of future protective strategies for radiotherapy.
颅脑放疗是治疗儿童脑肿瘤最有效的手段之一。然而,放疗引起的迟发性副作用对患者的生活质量有重大影响。本研究的目的是调查辐射对代谢的影响以及这种影响背后可能的分子和细胞机制。在出生后第11天,对雌性Wistar大鼠进行单次6 Gy全脑照射。在照射后6小时或20周处死动物。分析细胞死亡和增殖、小胶质细胞活化及炎症情况,并进行RNA测序。我们发现,照射导致体重从15周起显著增加(p < 0.05),同时在20周时出现白色脂肪组织堆积和脂肪细胞肥大,这些变化伴随着葡萄糖和脂质代谢紊乱,表现为葡萄糖耐量降低、胰岛素抵抗增加、血清甘油三酯升高以及瘦素/脂联素比值升高。此外,照射诱导下丘脑细胞死亡、小胶质细胞活化、炎症以及星形胶质细胞持续反应。下丘脑转录组分析显示,照射后20周,照射组中有865个基因下调,290个基因上调,进一步的通路分析表明,与胰岛素抵抗相关的PI3K - Akt信号通路和与能量消耗相关的脂肪细胞因子信号通路下调。基因本体富集分析显示,照射组中脂肪酸代谢相关蛋白和效应蛋白的表达存在显著差异。本研究表明,对幼年雌性大脑进行电离辐射会导致下丘脑损伤,这可能与延迟的代谢异常有关,在未来放疗保护策略的制定中应考虑下丘脑对辐射的这种关键易损性。