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
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.