Program in Physiological Genomics, Microbiome Consortium and Center for Hypertension and Precision Medicine Department of Physiology and Pharmacology University of Toledo College of Medicine and Life Sciences Toledo OH.
J Am Heart Assoc. 2020 Jan 21;9(2):e014373. doi: 10.1161/JAHA.119.014373. Epub 2020 Jan 11.
Background Pediatric hypertension is recognized as an emerging global health concern. Although new guidelines are developed for facilitating clinical management, the reasons for the prevalence of hypertension in children remain unknown. Genetics and environmental factors do not fully account for the growing incidence of pediatric hypertension. Because stable bacterial flora in early life are linked with health outcomes later in life, we hypothesized that reshaping of gut microbiota in early life affects blood pressure (BP) of pediatric subjects. Methods and Results To test this hypothesis, we administered amoxicillin, the most commonly prescribed pediatric antibiotic, to alter gut microbiota of young, genetically hypertensive rats (study 1) and dams during gestation and lactation (study 2) and recorded their BP. Reshaping of microbiota with reductions in Firmicutes/Bacteriodetes ratio were observed. Amoxicillin treated rats had lower BP compared with untreated rats. In young rats treated with amoxicillin, the lowering effect on BP persisted even after antibiotics were discontinued. Similarly, offspring from dams treated with amoxicillin showed lower systolic BP compared with control rats. Remarkably, in all cases, a decrease in BP was associated with lowering of Veillonellaceae, which are succinate-producing bacteria. Elevated plasma succinate is reported in hypertension. Accordingly, serum succinate was measured and found lower in animals treated with amoxicillin. Conclusions Our results demonstrate a direct correlation between succinate-producing gut microbiota and early development of hypertension and indicate that reshaping gut microbiota, especially by depleting succinate-producing microbiota early in life, may have long-term benefits for hypertension-prone individuals.
儿科高血压被认为是一个新出现的全球健康问题。尽管新的指南已经制定以促进临床管理,但儿童高血压的流行原因仍不清楚。遗传和环境因素不能完全解释儿科高血压发病率的上升。由于早期稳定的细菌菌群与以后的健康结果有关,我们假设早期生活中肠道微生物群的重塑会影响儿科患者的血压(BP)。
为了验证这一假设,我们给年轻的遗传性高血压大鼠(研究 1)和孕哺期的母鼠(研究 2)施用了最常被用于儿科的抗生素阿莫西林,以改变肠道微生物群,并记录它们的 BP。观察到微生物群的重塑与厚壁菌门/拟杆菌门比例降低有关。与未治疗的大鼠相比,用阿莫西林处理的大鼠的 BP 较低。在接受阿莫西林治疗的年轻大鼠中,即使停止使用抗生素,其对 BP 的降低作用仍然持续。同样,来自接受阿莫西林治疗的母鼠的后代的收缩压也低于对照大鼠。值得注意的是,在所有情况下,BP 的降低与产琥珀酸的韦荣氏球菌科(Veillonellaceae)的降低有关,而高血压患者的血浆琥珀酸水平升高。因此,测量了血清琥珀酸,发现用阿莫西林治疗的动物的血清琥珀酸水平较低。
我们的研究结果表明,产琥珀酸的肠道微生物群与高血压的早期发展之间存在直接相关性,并表明重塑肠道微生物群,特别是通过早期减少生活中产生琥珀酸的微生物群,可能对易患高血压的个体有长期益处。