The effects of novel cathepsin E inhibitors on the big endothelin pressor response in conscious rats

Biochem Biophys Res Commun. 1992 Jan 15;182(1):224-31. doi: 10.1016/s0006-291x(05)80134-2.

Abstract

The aspartic protease, cathepsin E, has been shown to specifically cleave big endothelin (big ET-1) at the Trp21-Val22 bond to produce endothelin (ET-1) and the corresponding C-terminal fragment. To determine whether cathepsin E is a physiologically relevant endothelin converting enzyme (ECE), three novel and potent inhibitors of cathepsin E were administered to conscious rats prior to a pressor challenge with big ET-1. One of the inhibitors of cathepsin E, SQ 32,056 (3 mg/kg i.v.), blocked the big ET-1 response. However, this dose of SQ 32,056 also blocked the pressor response to ET-1. Phosphoramidon specifically inhibited the Big ET-1 pressor response. These results suggest that ECE is not cathepsin E.

MeSH terms

  • Amino Acid Sequence
  • Angiotensin I / pharmacology
  • Animals
  • Blood Pressure / drug effects*
  • Cathepsin E
  • Cathepsins / antagonists & inhibitors*
  • Cathepsins / metabolism
  • Endothelins / metabolism
  • Endothelins / pharmacology*
  • Glycopeptides / pharmacology*
  • Humans
  • Male
  • Molecular Sequence Data
  • Molecular Structure
  • Norepinephrine / pharmacology
  • Oligopeptides / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Reference Values

Substances

  • Endothelins
  • Glycopeptides
  • Oligopeptides
  • SQ 32602
  • SQ 32056
  • Angiotensin I
  • Cathepsins
  • Cathepsin E
  • phosphoramidon
  • Norepinephrine