Department of Health Laboratory Technology, School of Public Health, China Medical University, No. 77 Puhe Road, Shenyang North New Area, Shenyang 110122, China.
Laboratory of Research in Parkinson's Disease and Related Disorders, Health Sciences Institute, China Medical University, No. 77 Puhe Road, Shenyang North New Area, Shenyang 110122, China.
Nutrients. 2022 Sep 23;14(19):3958. doi: 10.3390/nu14193958.
Gastrointestinal heat retention syndrome (GHRS) often occurs in adolescents, resulting into nervous system injury. Realgar, an arsenic mineral with neuroprotective effect, has been widely used to treat GHRS. However, its mechanism of action remains unknown.
A GHRS rat model was established using a high protein and high calorie diet. We performed macroscopic characterization by assessing bowel sounds, hot/cold preference, anal temperature, and fecal features. Atomic fluorescence spectroscopy was employed to evaluate brain arsenic level while hippocampal ultrastructural changes were analyzed using transmission electron microscopy. In addition, inflammatory cytokines and BBB breakdown were analyzed by western blotting, immunofluorescence assays, and immunohistochemistry staining. We also evaluated hippocampal metabolites by LC-MS while fecal microorganisms were assessed by 16S rDNA sequencing.
Our data showed that the high protein and high calorie diet induced GHRS. The rat model depicted decreased bowel sounds, increased fecal characteristics score, preference for low temperature zone, and increased anal temperature. In addition, there was increase in inflammatory factors IL-6, Iba-1, and NF-κB p65 as well as reduced BBB structural protein Claudin-5 and Occludin. The data also showed appearance of hippocampus metabolites disorder and fecal microbial imbalance. Realgar treatment conferred a neuroprotective effect by inhibiting GHRS-specific characteristics, neuroinflammatory response, BBB impairment, metabolites disorder, and microbial imbalance in the GHRS rat model.
Taken together, our analysis demonstrated that realgar confers a neuroprotective effect in GHRS rats through modulation of the microbiota-gut-brain axis.
胃肠道蓄热综合征(GHRS)常发生于青少年,可导致神经系统损伤。具有神经保护作用的砷矿物雄黄已被广泛用于治疗 GHRS,但作用机制尚不清楚。
采用高蛋白、高热量饮食建立 GHRS 大鼠模型。通过评估肠鸣音、冷/热偏好、肛温及粪便特征进行宏观特征描述。原子荧光光谱法评估大脑砷水平,透射电镜分析海马超微结构变化。通过 Western blot、免疫荧光和免疫组化染色分析炎症细胞因子和 BBB 破坏。通过 LC-MS 评估海马代谢物,通过 16S rDNA 测序评估粪便微生物。
高蛋白、高热量饮食可诱导 GHRS,本研究数据显示该大鼠模型出现肠鸣音减弱、粪便特征评分增加、偏好低温区和肛温升高。此外,还观察到炎症因子 IL-6、Iba-1 和 NF-κB p65 增加,以及 BBB 结构蛋白 Claudin-5 和 Occludin 减少。数据还显示海马代谢物紊乱和粪便微生物失衡。雄黄治疗通过抑制 GHRS 大鼠模型的特异性特征、神经炎症反应、BBB 损伤、代谢物紊乱和微生物失衡,发挥神经保护作用。
综上所述,我们的分析表明,雄黄通过调节肠道微生物群-肠-脑轴对 GHRS 大鼠发挥神经保护作用。