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Updated: Jan 7, 2026

Ferric Chloride-induced Murine Thrombosis Models
Published on: September 5, 2016
Xanthium strumarium L. Exhibits Potent Antiplatelet and Antithrombotic Effects by Modulating MAPK and PI3K/AKT
Abdul Wahab Akram1, Ga Hee Lee2, Su-Min Baek1
1Department of Veterinary Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Republic of Korea.
Insights
Xanthium strumarium extract shows potent antiplatelet and antithrombotic effects by inhibiting platelet aggregation and thrombosis. This natural compound improves blood flow and survival, offering a promising avenue for cardiovascular disease treatment.
Area of Science:
- Pharmacology
- Cardiovascular Research
- Natural Product Chemistry
Background:
- Cardiovascular diseases (CVDs) are a leading cause of death globally, largely due to platelet hyperactivation and thrombosis.
- Current antiplatelet therapies face limitations, necessitating the search for safer and more effective alternatives.
- Xanthium strumarium (X. strumarium) possesses known anti-inflammatory and antioxidant properties, but its antiplatelet and antithrombotic potential was unexplored.
Purpose of the Study:
- To comprehensively evaluate the antiplatelet and antithrombotic effects of X. strumarium.
- To investigate the underlying mechanisms of X. strumarium's action on platelet function.
- To assess the efficacy of X. strumarium in preventing thrombosis in vivo.
Main Methods:
- GC-MS analysis to identify bioactive compounds in X. strumarium extract.
- In vitro assays including light transmission aggregometry, SEM, ATP/calcium mobilization, αIIbβ3 binding, clot retraction, and Western blotting.
- In vivo ferric chloride-induced murine thrombus model to assess antithrombotic activity.
Main Results:
- X. strumarium significantly inhibited platelet aggregation induced by various agonists (collagen, ADP, U46619, thrombin).
- The extract preserved platelet morphology, inhibited granule secretion, and modulated key signaling pathways (MAPK, PI3K/Akt, αIIbβ3).
- In vivo studies showed improved blood flow, increased survival rates, and prevention of arterial occlusion.
Conclusions:
- X. strumarium exhibits significant antiplatelet and antithrombotic properties.
- The plant extract effectively inhibits platelet activation and thrombus formation through multiple mechanisms.
- X. strumarium represents a promising natural therapeutic agent for managing cardiovascular diseases associated with thrombosis.
Abstract:
Background: Cardiovascular diseases, driven by platelet hyperactivation and thrombosis, remain the leading global cause of death. Excessive platelet activation contributes to atherosclerosis and thrombo-inflammatory disorders, underscoring the urgent need for safer and more effective antiplatelet agents. Objectives:Xanthium strumarium L. (X. strumarium) has been reported to exhibit a wide range of pharmacological effects, including anti-inflammatory and antioxidant activities. However, its antiplatelet and antithrombotic effects remain unexplored. Therefore, the present study aimed to comprehensively evaluate the antiplatelet and antithrombotic effects of X. strumarium through integrated in vitro and in vivo experiments. Methods: The principal bioactive compounds present in the X. strumarium extract were identified through GC-MS analysis. In vitro antiplatelet effects were evaluated via light transmission aggregometry, scanning electron microscopy (SEM), ATP and calcium mobilization assays, αIIbβ3 binding assay, clot retraction assay, and Western blotting. In vivo ferric chloride-induced (FeCl3) murine thrombus model was established to evaluate thrombogenesis. Results: Our results demonstrated that X. strumarium at 25, 50, or 100 μg/mL significantly inhibited collagen, ADP, U46619, and thrombin-induced platelet aggregation. SEM revealed that X. strumarium pretreatment markedly preserved the resting platelet morphology and inhibited collagen-induced activation and shape changes. Further, the granule secretion, integrin-αIIbβ3 signaling, and the MAPK and PI3K/Akt pathways were also concentration-dependently inhibited. The in vivo blood flow rate and mice survival were improved, and H&E staining further revealed a concentration-dependent prevention of arterial occlusion following X. strumarium treatment. Conclusions: Collectively, X. strumarium demonstrated potent antiplatelet and antithrombotic effects, improving blood flow and survival while preventing arterial occlusion.
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