Hypertension, Vol 12, 428-433, Copyright © 1988 by American Heart Association
FB Davis, SD Blas, MM Davis and PJ Davis
Specific atrial natriuretic factor (ANF) analogues have been found to have
inhibitory activity in vitro in a calmodulin-dependent, human red blood
cell membrane Ca2+-adenosine triphosphatase (ATPase) model. Studied at
10(-8) to 10(-6) M concentrations, atriopeptin I (residues 127-147 of rat
prepro-ANF sequence) and atriopeptin III (residues 127- 150) progressively
inhibited Ca2+-ATPase activity by up to 20% (p less than 0.001). This
degree of inhibition was consistent with activities of other
(calmodulin-independent) enzyme inhibitors in this model. Therefore, the
C-terminal Phe-Arg-Tyr sequence (residues 148-150) is unnecessary for
atriopeptin action on Ca2+-ATPase. Human and rat atrial peptides with amino
acids 123-150 were inactive, indicating that the 123-126 sequence
(Ser-Leu-Arg-Arg) must be cleaved to activate atriopeptins in this system.
Human ANF fragment 129-150 also had no effect on Ca2+-ATPase, defining the
importance of residues 127-128 (Ser- Ser) proximal to the disulfide bridge
(joining 129 to 145). The addition of purified calmodulin to red blood cell
membranes in the presence of inhibitory ANF did not restore Ca2+-ATPase
activity to normal levels, indicating that the ANF effect on this enzyme is
calmodulin-independent. Atriopeptin I and atriopeptin III had no effect on
red blood cell Na+, K+-ATPase activity in vitro. Thus, the structure-
activity relationships of ANF analogues in this novel human cell membrane
model are highly specific. Although the inhibitory action of ANF analogues
on Ca2+-ATPase, a calcium pump-associated enzyme, may be unique to the red
blood cell, the calcium dependence of the gluconeogenic effects of ANF in
the kidney would be supported by inhibition of this ATPase.
ARTICLES
Analogue-specific action in vitro of atrial natriuretic factor on human red blood cell Ca2+-ATPase activity
Department of Medicine, State University of New York, Buffalo of Medicine, Buffalo.
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