Diaz Jonathan, Kuhlman Bradford M, Edenhoffer Nicholas P, Evans Angela C, Martin Kelly A, Guida Peter, Rusek Adam, Atala Anthony, Coleman Matthew A, Wilson Paul F, Almeida-Porada Graça, Porada Christopher D
Wake Forest Institute for Regenerative Medicine, Winston Salem, NC, United States.
Department of Radiation Oncology, University of California Davis School of Medicine, Sacramento, CA, United States.
Front Astron Space Sci. 2023;10. doi: 10.3389/fspas.2023.1117811. Epub 2023 May 5.
Missions beyond low Earth orbit (LEO) will expose astronauts to ionizing radiation (IR) in the form of solar energetic particles (SEP) and galactic cosmic rays (GCR) including high atomic number and energy (HZE) nuclei. The gastrointestinal (GI) system is documented to be highly radiosensitive with even relatively low dose IR exposures capable of inducing mucosal lesions and disrupting epithelial barrier function. IR is also an established risk factor for colorectal cancer (CRC) with several studies examining long-term GI effects of SEP/GCR exposure using tumor-prone APC mouse models. Studies of acute short-term effects of modeled space radiation exposures in wildtype mouse models are more limited and necessary to better define charged particle-induced GI pathologies and test novel medical countermeasures (MCMs) to promote astronaut safety.
In this study, we performed ground-based studies where male and female C57BL/6J mice were exposed to γ-rays, 50 MeV protons, or 1 GeV/n Fe-56 ions at the NASA Space Radiation Laboratory (NSRL) with histology and immunohistochemistry endpoints measured in the first 24 h post-irradiation to define immediate SEP/GCR-induced GI alterations.
Our data show that unlike matched γ-ray controls, acute exposures to protons and iron ions disrupts intestinal function and induces mucosal lesions, vascular congestion, epithelial barrier breakdown, and marked enlargement of mucosa-associated lymphoid tissue. We also measured kinetics of DNA double-strand break (DSB) repair using gamma-H2AX- specific antibodies and apoptosis via TUNEL labeling, noting the induction and disappearance of extranuclear cytoplasmic DNA marked by gamma-H2AX only in the charged particle-irradiated samples. We show that 18 h pre-treatment with curcumin-loaded nanolipoprotein particles (cNLPs) delivered via IV injection reduces DSB-associated foci levels and apoptosis and restore crypt villi lengths.
These data improve our understanding of physiological alterations in the GI tract immediately following exposures to modeled space radiations and demonstrates effectiveness of a promising space radiation MCM.
低地球轨道(LEO)以外的任务将使宇航员暴露于以太阳高能粒子(SEP)和银河宇宙射线(GCR)形式存在的电离辐射(IR)中,包括高原子序数和能量(HZE)的原子核。有文献记载,胃肠道(GI)系统对辐射高度敏感,即使相对低剂量的IR暴露也能够诱发粘膜损伤并破坏上皮屏障功能。IR也是结直肠癌(CRC)的既定风险因素,有多项研究使用易患肿瘤的APC小鼠模型研究SEP/GCR暴露对胃肠道的长期影响。在野生型小鼠模型中对模拟空间辐射暴露的急性短期影响进行的研究更为有限,但对于更好地定义带电粒子诱发的胃肠道病变以及测试促进宇航员安全的新型医学对策(MCM)而言是必要的。
在本研究中,我们进行了地面研究,将雄性和雌性C57BL/6J小鼠暴露于美国国家航空航天局空间辐射实验室(NSRL)的γ射线、50 MeV质子或1 GeV/n Fe-56离子中,并在辐照后的前24小时测量组织学和免疫组织化学终点,以确定SEP/GCR诱发的即刻胃肠道改变。
我们的数据表明,与匹配的γ射线对照组不同,急性暴露于质子和铁离子会破坏肠道功能并诱发粘膜损伤、血管充血、上皮屏障破坏以及粘膜相关淋巴组织明显肿大。我们还使用γ-H2AX特异性抗体测量了DNA双链断裂(DSB)修复的动力学,并通过TUNEL标记测量了细胞凋亡,注意到仅在带电粒子辐照的样本中,由γ-H2AX标记的核外细胞质DNA的诱导和消失。我们表明,通过静脉注射递送的载有姜黄素的纳米脂蛋白颗粒(cNLPs)进行18小时预处理可降低DSB相关灶水平和细胞凋亡,并恢复隐窝绒毛长度。
这些数据增进了我们对模拟空间辐射暴露后胃肠道立即发生的生理改变的理解,并证明了一种有前景空间辐射MCM的有效性。