Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Mouse Imaging Centre, The Hospital for Sick Children, Toronto, Ontario, Canada.
Neuro Oncol. 2021 Sep 1;23(9):1523-1536. doi: 10.1093/neuonc/noab131.
Cranial radiation therapy (CRT) is a mainstay of treatment for malignant pediatric brain tumors and high-risk leukemia. Although CRT improves survival, it has been shown to disrupt normal brain development and result in cognitive impairments in cancer survivors. Animal studies suggest that there is potential to promote brain recovery after injury using metformin. Our aim was to evaluate whether metformin can restore brain volume outcomes in a mouse model of CRT.
C57BL/6J mice were irradiated with a whole-brain radiation dose of 7 Gy during infancy. Two weeks of metformin treatment started either on the day of or 3 days after irradiation. In vivo magnetic resonance imaging was performed prior to irradiation and at 3 subsequent time points to evaluate the effects of radiation and metformin on brain development.
Widespread volume loss in the irradiated brain appeared within 1 week of irradiation with limited subsequent recovery in volume outcomes. In many structures, metformin administration starting on the day of irradiation exacerbated radiation-induced injury, particularly in male mice. Metformin treatment starting 3 days after irradiation improved brain volume outcomes in subcortical regions, the olfactory bulbs, and structures of the brainstem and cerebellum.
Our results show that metformin treatment has the potential to improve neuroanatomical outcomes after CRT. However, both timing of metformin administration and subject sex affect structure outcomes, and metformin may also be deleterious. Our results highlight important considerations in determining the potential benefits of metformin treatment after CRT and emphasize the need for caution in repurposing metformin in clinical studies.
颅放射治疗(CRT)是治疗小儿恶性脑肿瘤和高危白血病的主要方法。尽管 CRT 提高了生存率,但它已被证明会破坏正常的大脑发育,并导致癌症幸存者认知障碍。动物研究表明,使用二甲双胍有可能促进损伤后的大脑恢复。我们的目的是评估二甲双胍是否可以恢复 CRT 小鼠模型中的脑容量。
C57BL/6J 小鼠在婴儿期接受全脑照射剂量为 7Gy。二甲双胍治疗在照射后的第 1 天或第 3 天开始,持续 2 周。在照射前和随后的 3 个时间点进行体内磁共振成像,以评估辐射和二甲双胍对大脑发育的影响。
照射后 1 周内,照射脑内出现广泛的体积损失,随后体积恢复有限。在许多结构中,照射当天开始给予二甲双胍会加剧辐射引起的损伤,尤其是在雄性小鼠中。照射后第 3 天开始给予二甲双胍治疗可改善皮质下区域、嗅球以及脑干和小脑结构的脑容量。
我们的结果表明,二甲双胍治疗有可能改善 CRT 后的神经解剖学结果。然而,二甲双胍给药的时间和对象的性别都影响结构结果,而且二甲双胍也可能有害。我们的结果强调了在确定 CRT 后使用二甲双胍治疗的潜在益处时需要考虑的重要因素,并强调在临床研究中重新使用二甲双胍时需要谨慎。