Tissue plasminogen activator release in vivo in response to vasoactive agents

D Smith, M Gilbert, WG Owen - 1985 - ashpublications.org
D Smith, M Gilbert, WG Owen
1985ashpublications.org
Release of tissue plasminogen activator into the circulation of rats in response to
intravascular injections of vasoactive agents is studied by using a sensitive and specific clot
lysis assay. Intra-arterial bradykinin elicits a rapid and transient rise in circulating
plasminogen activator, which is maximum within one minute and is cleared within four to
eight minutes. The plasminogen activator is fibrin dependent and is neutralized by an
antiserum to human tissue-type plasminogen activator. Bradykinin is 1,000-fold more potent …
Abstract
Release of tissue plasminogen activator into the circulation of rats in response to intravascular injections of vasoactive agents is studied by using a sensitive and specific clot lysis assay. Intra-arterial bradykinin elicits a rapid and transient rise in circulating plasminogen activator, which is maximum within one minute and is cleared within four to eight minutes. The plasminogen activator is fibrin dependent and is neutralized by an antiserum to human tissue- type plasminogen activator. Bradykinin is 1,000-fold more potent than the other agonists tested, which include histamine, norepinephrine, epinephrine, eledoisin-related peptide, arginine-vasopressin, lysine- vasopressin, desmopressin acetate, carbachol, and acetylcholine. Potency of bradykinin is related to its amino acid sequence. Sequential infusions of bradykinin produce a tachyphylactoid response that could be overcome by increasing the dose of the sequential bradykinin challenge. It is concluded that the characteristics of the responses to bradykinin and other agents in vivo differ significantly from those observed in isolated tissue preparations.
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