Oral CoQ10 attenuates high salt-induced hypertension by restoring neurotransmitters and cytokines in the hypothalamic paraventricular nucleus

Sci Rep. 2016 Jul 25:6:30301. doi: 10.1038/srep30301.

Abstract

High salt intake leads to an increase in some proinflammatory cytokines and neurotransmitters involved in the pathogenesis of hypertension. The purpose of this work was to know if oral administration of anti-oxidant and free-radical scavenger CoQ10 may attenuate high salt-induced hypertension via regulating neurotransmitters and cytokines in the hypothalamic paraventricular nucleus (PVN). Adult male Sprague-Dawley (SD) rats were fed with a normal salt diet (NS, 0.3% NaCl) or a high salt diet (HS, 8% NaCl) for 15 weeks to induce hypertension. These rats received CoQ10 (10 mg/kg/day) dissolved in olive oil was given by gavage (10 mg/kg/day) for 15 weeks. HS resulted in higher mean arterial pressure (MAP) and the sympathetic nerve activity (RSNA). These HS rats had higher PVN levels of norepinephrine (NE), tyrosine hydroxylase (TH), interleukin (IL)-1β, NOX2 and NOX4, lower PVN levels of gamma-aminobutyric acid (GABA), IL-10, copper/zinc superoxide dismutase (Cu/Zn-SOD) and the 67-kDa isoform of glutamate decarboxylase (GAD67), as compared with NS group. CoQ10 supplementation reduced NE, TH, IL-1β, NOX2 and NOX4 in the PVN, and induced IL-10, Cu/Zn-SOD and GAD67 in the PVN. These findings suggest that CoQ10 supplementation restores neurotransmitters and cytokines in the PVN, thereby attenuating high salt-induced hypertension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / administration & dosage*
  • Free Radical Scavengers / administration & dosage*
  • Gene Expression Regulation / drug effects
  • Humans
  • Hypertension / chemically induced
  • Hypertension / drug therapy*
  • Hypertension / metabolism
  • Hypertension / pathology
  • Interleukin-1beta / metabolism
  • NADPH Oxidase 2 / metabolism
  • Neurotransmitter Agents / metabolism
  • Norepinephrine / metabolism
  • Paraventricular Hypothalamic Nucleus / drug effects
  • Paraventricular Hypothalamic Nucleus / metabolism*
  • Rats
  • Salts / toxicity
  • Superoxide Dismutase-1 / metabolism
  • Tyrosine 3-Monooxygenase / metabolism
  • Ubiquinone / administration & dosage
  • Ubiquinone / analogs & derivatives*

Substances

  • Antioxidants
  • Free Radical Scavengers
  • IL1B protein, rat
  • Interleukin-1beta
  • Neurotransmitter Agents
  • Salts
  • Ubiquinone
  • Tyrosine 3-Monooxygenase
  • Superoxide Dismutase-1
  • Cybb protein, rat
  • NADPH Oxidase 2
  • coenzyme Q10
  • Norepinephrine