PAI-1 Inhibition in experimental venous thrombosis

BackgroundA novel PAI-1 inhibitor, MDI-2268, has been recently developed. The aim of the study was to evaluate the antithrombotic effects and safety of the MDI-2268 in acute venous thrombosis (VT) in vivo.MethodsC57BL/6 mice, 10-12 weeks old, weighing 20-25g, were used in electrolytic model of VT (EIM). MDI-2268 1.5 mg/kg (Group 1), MDI-2268 3 mg/kg (Group 2), enoxaparin 7.3 mg/kg (Group 3), and MDI-2268 1.5 mg/kg plus enoxaparin 1.8 mg/kg (Group 4) were compared to the controls (sham surgery). Animals were sacrificed on Day 2. Thrombus weight and tail bleeding time were measured.ResultsTW was 6.9 ± 3.3 (<i>p</i> > .05), 5.5 ± 1.6 (<i>p</i> = .016), 3.8 ± 1.3 (<i>p</i> = .032), and 4.8 ± 2.4 mg (<i>p</i> = .016) for groups 1, 2, 3, and 4, respectively, compared to the controls. Bleeding time was not significantly affected by the MDI-2268.ConclusionsMDI-2268 is a novel pro-fibrinolytic agent that demonstrates strong antithrombotic properties without prolongation of bleeding time in this experimental model.

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Publication Details

Journal
Phlebology The Journal of Venous Disease
Published
2026-01-22
DOI
https://doi.org/10.1177/02683555261421027
Citations
1
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
Type
article
Field-Weighted Citation Impact
35.41
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article

PAI-1 Inhibition in experimental venous thrombosis

Joshua P Rainey, Maxim E. Shaydakov, Cory D. Emal, Daniel A. Lawrence et al.
1 citations
Phlebology The Journal of Venous Disease
Blood Coagulation and Thrombosis Mechanisms
35.41
article

PAI-1 Inhibition in experimental venous thrombosis

Joshua P Rainey, Maxim E. Shaydakov, Cory D. Emal, Daniel A. Lawrence, José Díaz
article en
1 citations

Abstract

BackgroundA novel PAI-1 inhibitor, MDI-2268, has been recently developed. The aim of the study was to evaluate the antithrombotic effects and safety of the MDI-2268 in acute venous thrombosis (VT) in vivo.MethodsC57BL/6 mice, 10-12 weeks old, weighing 20-25g, were used in electrolytic model of VT (EIM). MDI-2268 1.5 mg/kg (Group 1), MDI-2268 3 mg/kg (Group 2), enoxaparin 7.3 mg/kg (Group 3), and MDI-2268 1.5 mg/kg plus enoxaparin 1.8 mg/kg (Group 4) were compared to the controls (sham surgery). Animals were sacrificed on Day 2. Thrombus weight and tail bleeding time were measured.ResultsTW was 6.9 ± 3.3 (<i>p</i> > .05), 5.5 ± 1.6 (<i>p</i> = .016), 3.8 ± 1.3 (<i>p</i> = .032), and 4.8 ± 2.4 mg (<i>p</i> = .016) for groups 1, 2, 3, and 4, respectively, compared to the controls. Bleeding time was not significantly affected by the MDI-2268.ConclusionsMDI-2268 is a novel pro-fibrinolytic agent that demonstrates strong antithrombotic properties without prolongation of bleeding time in this experimental model.

Phlebology The Journal of Venous Disease
Johnson & Johnson (United States) (US), Eastern Michigan University (US), University of Michigan (US), University of Utah Hospital (US), WellSpan Health (US)
Openalex Percentile: Top 2%
Blood Coagulation and Thrombosis Mechanisms
35.41
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