Program in Physiological Genomics, Microbiome Consortium, Center for Hypertension and Personalized Medicine, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Department of Internal Medicine-Nephrology, University of Michigan, Ann Arbor, MI, USA.
Cell Rep. 2018 Oct 16;25(3):677-689.e4. doi: 10.1016/j.celrep.2018.09.058.
Dietary salt reduction and exercise are lifestyle modifications for salt-sensitive hypertensives. While exercise has prominent metabolic effects, salt has an adverse effect on metabolic syndrome, of which hypertension is a hallmark. We hypothesized that dietary salt impacts metabolism in a salt-sensitive model of hypertension. An untargeted metabolomic approach demonstrates lower circulating levels of the ketone body, beta-hydroxybutyrate (βOHB), in high salt-fed hypertensive rats. Despite the high salt intake, specific rescue of βOHB levels by nutritional supplementation of its precursor, 1,3-butanediol, attenuates hypertension and protects kidney function. This beneficial effect of βOHB was likely independent of gut-microbiotal and Th17-mediated effects of salt and instead facilitated by βOHB inhibiting the renal Nlrp3 inflammasome. The juxtaposed effects of dietary salt and exercise on salt-sensitive hypertension, which decrease and increase βOHB respectively, indicate that nutritional supplementation of a precursor of βOHB provides a similar benefit to salt-sensitive hypertension as exercise.
饮食中减少盐的摄入和进行锻炼是针对盐敏感型高血压患者的生活方式调整措施。尽管锻炼对代谢有显著的影响,但盐对代谢综合征有不良影响,而高血压是代谢综合征的一个标志。我们假设饮食中的盐会影响盐敏感型高血压模型中的代谢。一种非靶向代谢组学方法表明,高盐饮食会导致高血压大鼠循环中的酮体β-羟丁酸(βOHB)水平降低。尽管盐摄入量很高,但通过补充其前体 1,3-丁二醇进行特定的βOHB 水平的补救,可减轻高血压并保护肾功能。βOHB 的这种有益作用可能与盐的肠道微生物群和 Th17 介导的作用无关,而是通过βOHB 抑制肾脏 NLRP3 炎性小体来实现的。饮食中盐和运动对盐敏感型高血压的相反作用,分别降低和增加βOHB,表明βOHB 前体的营养补充与运动对盐敏感型高血压具有相似的益处。