METABOLISM OF ENDOTHELIN-1 AND BIG ENDOTHELIN-1 BY RECOMBINANT NEUTRAL ENDOPEPTIDASE EC.3.4.24.11

Citation
Za. Abassi et al., METABOLISM OF ENDOTHELIN-1 AND BIG ENDOTHELIN-1 BY RECOMBINANT NEUTRAL ENDOPEPTIDASE EC.3.4.24.11, British Journal of Pharmacology, 109(4), 1993, pp. 1024-1028
Citations number
37
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00071188
Volume
109
Issue
4
Year of publication
1993
Pages
1024 - 1028
Database
ISI
SICI code
0007-1188(1993)109:4<1024:MOEABE>2.0.ZU;2-8
Abstract
1 Inhibitors of neutral endopeptidase EC.3.4.24.11 (NEP) have been sho wn to attenuate the hypertensive effect of big-endothelin-1 (BET-1) in rats. To determine whether NEP converts BET-1 to endothelin-1 (ET-1), the effect of a recombinant NEP (rNEP) on BET-1 and on ET-1 was asses sed in vitro. 2 Incubation of [I-125]-ET-1 with 1 mug ml-1 of rNEP res ulted in degradation of the peptide within minutes. Increase in the am ount of rNEP to 10 mug ml-1 led to total cleavage of [I-125]-ET-1 with in seconds. 3 Phosphoramidon (10 muM) or SQ-28,603 (100 muM) totally s uppressed the degradation of [I-125]-ET-1 by rNEP. 4 The degradation o f [I-125]-BET-1 by either 1 or 10 mug ml-1 of rNEP was much slower tha n that of [I-125]-ET-1. Again, both phosphoramidon and SQ 28,603 prote cted the peptide from degradation. 5 Intact [I-125]-ET-1 was not obser ved when [I-125]-BET-1 was incubated with rNEP. 6 These data show that neutral endopeptidase EC.3.4.24.11 is not an endothelin convertin enz yme.