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TP-9201, a glycoprotein IIb/IIIa platelet receptor antagonist, prevents rethrombosis after successful arterial thrombolysis in the dog.
Rebello, S S; Driscoll, E M; Lucchesi, B R.
Affiliation
  • Rebello SS; Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109-0632, USA.
Stroke ; 28(9): 1789-96, 1997 Sep.
Article in En | MEDLINE | ID: mdl-9303027
ABSTRACT
BACKGROUND AND

PURPOSE:

We examined the ability of TP-9201, a platelet glycoprotein IIb/IIIa receptor antagonist, to prevent carotid artery rethrombosis in the anesthetized dog.

METHODS:

Occlusive thrombosis was induced by electrolytic injury of the left carotid artery. Thirty minutes later, 0.05 U/kg of anisoylated plasminogen streptokinase activator complex (APSAC) was infused locally to achieve clot lysis. Carotid artery recanalization was followed immediately by the infusion of either saline (10 mL/h, 240 minutes; n = 9), low-dose TP-9201 (120 micrograms/kg plus 3 micrograms.kg-1.min-1, 240 minutes; n = 7), or high-dose TP-9201 (185 micrograms/kg plus 5 micrograms.kg-1.min-1, 240 minutes; n = 7). Ex vivo platelet aggregation responses to ADP or arachidonic acid were determined.

RESULTS:

TP-9201 produced complete inhibition of platelet aggregation in citrated platelet-rich plasma but a partial and dose-dependent inhibition in heparinized platelet-rich plasma. A twofold and eightfold increase in the template bleeding time was associated with the infusion of low-dose and high-dose TP-9201, respectively. There were frequent cyclic flow reductions in both the saline and low-dose TP-9201-treated groups after thrombolysis. However, the high-dose TP-9201-treated group exhibited a sustained flow with minimal evidence of cyclic flow reductions. At the conclusion of the protocol, patent vessels were found more frequently in the high-dose TP-9201 (5/7; P = .0048) than in the low-dose TP-9201 treatment group (2/7; P = .17) when compared with the saline group (0/9). Infusion of high-dose TP-9201 was associated with a significant reduction in the thrombus mass as compared with the control vessels.

CONCLUSIONS:

Administration of TP-9201 in conjunction with successful thrombolysis inhibited ex vivo platelet aggregation and prevented rethrombosis of the canine carotid artery. This study demonstrates that TP-9201, an inhibitor of the platelet GPIIb/IIIa receptor, can inhibit platelet-vessel wall interaction and thus prevent rethrombosis.
Subject(s)
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Database: MEDLINE Main subject: Peptides, Cyclic / Thrombosis / Platelet Aggregation Inhibitors / Platelet Glycoprotein GPIIb-IIIa Complex / Fibrinolytic Agents Type of study: Guideline Limits: Animals Language: En Year: 1997 Type: Article
Search on Google
Database: MEDLINE Main subject: Peptides, Cyclic / Thrombosis / Platelet Aggregation Inhibitors / Platelet Glycoprotein GPIIb-IIIa Complex / Fibrinolytic Agents Type of study: Guideline Limits: Animals Language: En Year: 1997 Type: Article