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Specific inhibition of renin by an angiotensinogen analog: studies in sodium depletion and renin-dependent hypertension.

Abstract
The angiotensin substrate analog Pro-His-Pro-Phe-His-Phe-Phe-Val-Tyr-Lys has no significant effect on blood pressure in sodium-replete monkeys (Macaca fascicularis) but blocks the pressor response to infused human renin. Pressor responses to angiotensin I and angiotensin II are not attenuated. In five studies in sodium-depleted monkeys, an infusion of 2 mg of the peptide per kg of body weight resulted in a reduction of mean arterial pressure (MAP) from 105 +/- 4 to 79 +/- 3 mm Hg, which is not significantly different from the response to 1 mg of the angiotensin I-converting enzyme inhibitor teprotide per kg. In uninephrectomized monkeys, inflation of a suprarenal aortic cuff caused an increase in MAP from 107 +/- 3 to 131 +/- 3 mm Hg. Infusion of 0.6 mg of the renin-inhibitory peptide per kg was followed by a return of blood pressure to 107 +/- 4 mm Hg--a depressor response similar to that observed with teprotide. This specific in vivo inhibitor of renin can now be applied to a wide variety of physiologic studies.
AuthorsJ Burton, R J Cody Jr, J A Herd, E Haber
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 77 Issue 9 Pg. 5476-9 (Sep 1980) ISSN: 0027-8424 [Print] United States
PMID6159648 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Oligopeptides
  • Angiotensinogen
  • Angiotensin II
  • renin inhibitory peptide
  • Angiotensin I
  • Sodium
  • Teprotide
  • Peptidyl-Dipeptidase A
  • Renin
Topics
  • Angiotensin I (pharmacology)
  • Angiotensin II (pharmacology)
  • Angiotensinogen
  • Animals
  • Blood Pressure (drug effects)
  • Hypertension (physiopathology)
  • Macaca fascicularis (physiology)
  • Male
  • Oligopeptides (pharmacology)
  • Peptidyl-Dipeptidase A (metabolism)
  • Renin (antagonists & inhibitors, pharmacology)
  • Sodium (metabolism)
  • Teprotide (pharmacology)

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