Xiong Yi, Guo Jianguo, Yu Wenchen, Zeng Deyong, Song Chenchen, Zhou Li, Anatolyevna Nadtochii Liudmila, Baranenko Denis, Xiao Dan, Zhou Yingyu, Lu Weihong
School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, China.
National and Local Joint Engineering Laboratory for Synthesis, Harbin Institute of Technology, Harbin 150001, China.
Int J Mol Sci. 2025 Mar 27;26(7):3094. doi: 10.3390/ijms26073094.
Space flight has many adverse effects on the physiological functions of astronauts. Certain similarities have been observed in some physiological processes of rodents and astronauts in space, although there are also differences. These similarities make rodents helpful models for initial investigations into space-induced physiological changes. This study uses a 3D-Clinostat to simulate microgravity and explores the role of microgravity in space flight-induced liver and brain abnormalities by comparing changes in the gut microbiota, serum metabolites, and the function and physiological biochemistry of liver and brain tissues between the simulated microgravity (SMG) group mice and the wild type (WT) group mice. The study, based on hematoxylin-eosin (HE) staining, 16S sequencing technology, and non-targeted metabolomics analysis, shows that the gut tissue morphology of the SMG group mice is abnormal, and the structure of the gut microbiota and the serum metabolite profile are imbalanced. Furthermore, using PICRUST 2 technology, we have predicted the functions of the gut microbiota and serum metabolites, and the results indicate that the liver metabolism and functions (including lipid metabolism, amino acid metabolism, and sugar metabolism, etc.) of the SMG group mice are disrupted, and the brain tissue metabolism and functions (including neurotransmitters and hormone secretion, etc.) are abnormal, suggesting a close relationship between microgravity and liver metabolic dysfunction and brain dysfunction. Additionally, the high similarity in the structure of the gut microbiota and serum metabolite profile between the fecal microbiota transplant (FMT) group mice and the SMG group mice, and the physiological and biochemical differences in liver and brain tissues compared to the WT group mice, suggest that microgravity induces imbalances in the gut microbiota, which in turn triggers abnormalities in liver and brain metabolism and function. Finally, through MetaMapp analysis and Pearson correlation analysis, we found that valeric acid, a metabolite of gut microbiota, is more likely to be the key metabolite that relates to microgravity-induced gut microbiota abnormalities, disorders of amino acid and lipid metabolism, and further induced metabolic or functional disorders in the liver and brain. This study has significant practical application value for deepening the understanding of the adaptability of living organisms in the space environment.
太空飞行对宇航员的生理功能有许多不利影响。尽管啮齿动物和太空中的宇航员在某些生理过程中存在差异,但也观察到了一些相似之处。这些相似之处使啮齿动物成为初步研究太空引起的生理变化的有用模型。本研究使用三维回转器模拟微重力,并通过比较模拟微重力(SMG)组小鼠和野生型(WT)组小鼠的肠道微生物群、血清代谢物以及肝脏和脑组织的功能及生理生化变化,探讨微重力在太空飞行引起的肝脏和大脑异常中的作用。该研究基于苏木精-伊红(HE)染色、16S测序技术和非靶向代谢组学分析,结果表明,SMG组小鼠的肠道组织形态异常,肠道微生物群结构和血清代谢物谱失衡。此外,我们使用PICRUST 2技术预测了肠道微生物群和血清代谢物的功能,结果表明,SMG组小鼠的肝脏代谢和功能(包括脂质代谢、氨基酸代谢和糖代谢等)受到干扰,脑组织代谢和功能(包括神经递质和激素分泌等)异常,这表明微重力与肝脏代谢功能障碍和脑功能障碍之间存在密切关系。此外,粪便微生物群移植(FMT)组小鼠与SMG组小鼠的肠道微生物群结构和血清代谢物谱高度相似,与WT组小鼠相比,肝脏和脑组织的生理生化存在差异,这表明微重力会导致肠道微生物群失衡,进而引发肝脏和大脑代谢及功能异常。最后,通过MetaMapp分析和Pearson相关性分析,我们发现肠道微生物群的代谢物戊酸更有可能是与微重力引起的肠道微生物群异常、氨基酸和脂质代谢紊乱以及进一步诱导的肝脏和大脑代谢或功能紊乱相关的关键代谢物。本研究对于深化对生物体在太空环境中适应性的理解具有重要的实际应用价值。