Early short-term treatment with exogenous hydrogen sulfide postpones the transition from prehypertension to hypertension in spontaneously hypertensive rat

Clin Exp Hypertens. 2018;40(1):58-64. doi: 10.1080/10641963.2017.1313847. Epub 2017 Oct 26.

Abstract

ABSTACT Hydrogen sulfide (H2S), nitric oxide (NO), and renin-angiotensin system (RAS) are involved in hypertension. We examined whether early treatment with sodium hydrosulfide (NaHS), an exogenous H2S donor, can regulate H2S-generating pathway, NO pathway, and the RAS, to prevent the transition from prehypertension to hypertension in spontaneously hypertensive rats (SHRs). Four-week-old SHRs and control normotensive Wistar-Kyoto (WKY) rats were assigned into three groups: WKY, SHRs, and SHR + NaHS; SHRs were injected intraperitoneally with sodium hydrosulfide (14 μmol/kg/day) for 4 weeks. SHRs exhibited hypertension at 12 weeks of age, which was blocked by early sodium hydrosulfide administration. Concentrations of H2S were increased in the kidney in SHR + NaHS group versus WKY. Sodium hydrosulfide reduces mRNA expression of four H2S-generating enzymes and decreased 3-mercaptopyruvate sulphurtransferase protein level in SHRs. Early administration of sodium hydrosulfide decreases plasma NG monomethyl-l-arginine (l-NMMA, an inhibitor of NO synthase) level and increases plasma NO level in SHRs. Next, sodium hydrosulfide administration reduces renal mRNA expression of Ren, Atp6ap2, Agt, Ace, and Agtr1a in SHRs. We conclude that early short-term sodium hydrosulfide treatment increases renal H2S concentrations, restores NO bioavailability, and blocks the RAS in the kidney, in favor of vasodilatation to prevent the development of hypertension in adult SHRs.

Keywords: Hydrogen sulfide; hypertension; nitric oxide; renin–angiotensin system; spontaneously hypertensive rat.

MeSH terms

  • Angiotensinogen / genetics
  • Animals
  • Blood Pressure
  • Gene Expression / drug effects*
  • Hydrogen Sulfide / metabolism
  • Hypertension / prevention & control*
  • Kidney / metabolism
  • Male
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase / metabolism
  • Peptidyl-Dipeptidase A / genetics
  • Prehypertension / drug therapy*
  • Prehypertension / metabolism*
  • Prehypertension / physiopathology
  • Proton-Translocating ATPases / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Receptor, Angiotensin, Type 1 / genetics
  • Receptors, Cell Surface / genetics
  • Renin / genetics
  • Renin-Angiotensin System / drug effects
  • Sulfides / administration & dosage
  • Sulfides / therapeutic use*
  • Sulfurtransferases / metabolism
  • Time Factors
  • Vacuolar Proton-Translocating ATPases
  • omega-N-Methylarginine / blood

Substances

  • Agt protein, rat
  • Agtr1a protein, rat
  • RNA, Messenger
  • Receptor, Angiotensin, Type 1
  • Receptors, Cell Surface
  • Sulfides
  • Angiotensinogen
  • omega-N-Methylarginine
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Sulfurtransferases
  • 3-mercaptopyruvate sulphurtransferase
  • Peptidyl-Dipeptidase A
  • Renin
  • ATP6AP2 protein, rat
  • Vacuolar Proton-Translocating ATPases
  • Proton-Translocating ATPases
  • sodium bisulfide
  • Hydrogen Sulfide