AI Article Synopsis

  • Cardiovascular diseases are major global health issues, often linked to conditions like diabetes and obesity that lead to abnormal blood clotting.
  • The FeCl3-induced carotid injury model is an effective method to study how thrombosis develops after vascular damage, allowing researchers to observe clot formation in controlled conditions.
  • This model can help investigate the underlying mechanisms of thrombosis, the behavior of platelets, and the effectiveness of medications designed to prevent excessive clotting.

Article Abstract

Cardiovascular diseases are a leading cause of mortality and morbidity worldwide. Aberrant thrombosis is a common feature of systemic conditions like diabetes and obesity, and chronic inflammatory diseases like atherosclerosis, cancer, and autoimmune diseases. Upon vascular injury, usually the coagulation system, platelets, and endothelium act in an orchestrated manner to prevent bleeding by forming a clot at the site of the injury. Abnormalities in this process lead to either excessive bleeding or uncontrolled thrombosis/insufficient antithrombotic activity, which translates into vessel occlusion and its sequelae. The FeCl3-induced carotid injury model is a valuable tool in probing how thrombosis initiates and progresses in vivo. This model involves endothelial damage/denudation and subsequent clot formation at the injured site. It provides a highly sensitive, quantitative assay to monitor vascular damage and clot formation in response to different degrees of vascular damage. Once optimized, this standard technique can be used to study the molecular mechanisms underlying thrombosis, as well as the ultrastructural changes in platelets in a growing thrombus. This assay is also useful to study the efficacy of antithrombotic and antiplatelet agents. This article explains how to initiate and monitor FeCl3-induced arterial thrombosis and how to collect samples for analysis by electron microscopy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11042049PMC
http://dx.doi.org/10.3791/64985DOI Listing

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