Salt-Responsive Metabolite, β-Hydroxybutyrate, Attenuates Hypertension Article (Faculty180)

cited authors

  • Chakraborty, Saroj; Galla, Sarah; Cheng, Xi; Yeo, Ji- Y; Mell, Blair; Singh, Vishal; Yeoh, BengSan; Saha, Piu; Mathew, Anna V; Vijay-Kumar, Matam; Joe, Bina

description

  • 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.

publication date

  • 2018

published in

start page

  • 677

end page

  • 689.e4

volume

  • 25