(Circulation. 1995;92:2984-2994.)
© 1995 American Heart Association, Inc.
Articles |
From the Department of Laboratory Medicine (W.L.C.) and the Division of Cardiology, Department of Medicine (W.C.L., J.R.S.), University of Washington and Seattle VA Medical Center.
Correspondence to Wayne L. Chandler, MD, Department of Laboratory Medicine, SB-10, University of Washington, Seattle, WA 98195.
Background Exercise to exhaustion and infusions of isoproterenol and phenylephrine were used to study interactions between plasminogen activator regulation and the control of regional blood flow in 10 healthy males.
Methods and Results Experimental measurements of cardiac output,
heart rate, tissue plasminogen activator (TPA),
urokinase plasminogen activator (UPA),
plasminogen activator inhibitor
(PAI-1), C1-inhibitor, and TPA/C1-inhibitor
complex during the infusions and exercise were used to develop a
comprehensive fluid-phase model of the circulatory regulation of
fibrinolysis.
- and ß-adrenergic agonists
increased TPA and UPA in plasma by different mechanisms:
Phenylephrine decreased hepatic blood flow and thus
clearance while isoproterenol stimulated increased secretion of TPA and
UPA. Exercise to exhaustion increased TPA and UPA through a combination
of increased secretion and decreased clearance. The time course of UPA
and TPA release were similar, but the magnitude of their secretion
responses differed. In vivo, C1-inhibitor bound to TPA at a
rate of 553 mol-1 · s-1.
C1-inhibitor contributed equally with PAI-1 to TPA
inhibition when active PAI-1 levels were low (20 to 50 pmol/L) but was
less important when active PAI-1 levels were high.
Conclusions We conclude that secretion, inhibition, clearance, and regional blood flow effects must all be taken into account when evaluating changes in plasminogen activator levels.
Key Words: plasminogen activators exercise
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