Qi Luming, Li Yao, Chen Zhixuan, Wei Changhong, Wen Xue, Hu Shuangyan, Wu Hang, Lv Zhuoheng, Xu Zhangmeng, Xia Lina
School of Health Preservation and Rehabilitation, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Jiangxi Province Key Laboratory of Traditional Chinese Medicine Pharmacology, Institute of Traditional Chinese Medicine Health Industry, China Academy of Chinese Medical Sciences, Nanchang, China.
Front Nutr. 2024 Sep 24;11:1408778. doi: 10.3389/fnut.2024.1408778. eCollection 2024.
The present study examined the effect of two dietary regimens with elevated salt concentrations (4% and 8% salt) on hemorheological functions of SD rats, and explored the underlying mechanisms mainly through microbiome-metabolome analysis. An 8% HSD substantially altered the hemorheological parameters, and compromised intestinal barrier integrity and reduced the short-chain fatty acid levels. The microbiome-metabolome analysis revealed that 49 genus-specific microorganisms and 156 metabolites showed a consistent trend after exposure to both 4% and 8% HSDs. Pathway analysis identified significant alterations in key metabolites within bile acid and arachidonic acid metabolism pathways. A two-sample Mendelian randomization (MR) analysis verified the link between high dietary salt intake and hemorheology. It also suggested that some key microbes and metabolites (such as _UCG-005, _NK4A136, _6, and _UCG-010, TXB-2, 11,12-diHETrE, glycochenodeoxycholate) may involve in abnormalities in blood rheology caused by high salt intake. Collectively, our findings underscored the adverse effects of high dietary salt on hemorheological functions and provide new insight into the underlying mechanism based on microbiome-metabolome analysis.
本研究考察了两种高盐浓度(4%和8%盐)饮食方案对SD大鼠血液流变学功能的影响,并主要通过微生物组-代谢组分析探索其潜在机制。8%的高盐饮食显著改变了血液流变学参数,损害了肠道屏障完整性并降低了短链脂肪酸水平。微生物组-代谢组分析显示,在暴露于4%和8%的高盐饮食后,49种属特异性微生物和156种代谢物呈现出一致的趋势。通路分析确定了胆汁酸和花生四烯酸代谢途径中关键代谢物的显著变化。两样本孟德尔随机化(MR)分析验证了高盐饮食摄入与血液流变学之间的联系。研究还表明,一些关键微生物和代谢物(如_UCG-005、_NK4A136、_6和_UCG-010、TXB-2、11,12-二氢二十碳四烯酸、甘氨鹅脱氧胆酸)可能与高盐摄入引起的血液流变学异常有关。总的来说,我们的研究结果强调了高盐饮食对血液流变学功能的不利影响,并基于微生物组-代谢组分析为潜在机制提供了新的见解。