Val-Tyr as a natural antihypertensive dipeptide can be absorbed into the human circulatory blood system

Clin Exp Pharmacol Physiol. 2002 Mar;29(3):204-8. doi: 10.1046/j.1440-1681.2002.03628.x.

Abstract

1. Intact absorption of the bioactive dipeptide Val-Tyr (VY), with in vivo antihypertensive ability in normotensive human subjects, was investigated. 2. As a result of a single oral administration of VY, the VY absorption curve occurred maximally over the second hour postprandially; a greater than 10-fold higher increment of VY following a dose of 12 mg was observed in the plasma at 2 h compared with the baseline concentration of VY at 0 h (1934 +/- 145 vs 159 +/- 11 fmol/mL plasma, respectively). 3. Plasma VY levels increased with dose administered (3, 6 and 12 mg), suggesting that exogenous VY could be absorbed intact into the human blood depending on the dose. The elimination half time (t1/2) of VY was estimated to be 3.1 h. The area under the curve for the 12 mg VY dose was 9185 +/- 688 fmol small middle doth/mL plasma.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorption
  • Administration, Oral
  • Adult
  • Aldosterone / blood
  • Angiotensin I / blood
  • Angiotensin II / blood
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / blood
  • Antihypertensive Agents / pharmacokinetics*
  • Blood Circulation / drug effects
  • Blood Circulation / physiology*
  • Dipeptides / administration & dosage
  • Dipeptides / blood*
  • Dose-Response Relationship, Drug
  • Humans
  • Male

Substances

  • Antihypertensive Agents
  • Dipeptides
  • valyltyrosine
  • Angiotensin II
  • Aldosterone
  • Angiotensin I