Intense light as anticoagulant therapy in humans
Yoshimasa Oyama1, Sydney Shuff1, Pavel Davizon-Castillo2
1Department of Anesthesiology, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, United States of America.
Intense light therapy boosts Period 2 (PER2) protein, inhibiting platelet aggregation and reducing clotting. This suggests light therapy as a novel treatment for preventing or treating blood clots.
Area of Science:
- Cardiovascular Biology
- Hematology
- Chronobiology
Background:
- Blood coagulation is critical in myocardial ischemia and reperfusion (IR) injury.
- Conflicting data exist regarding the role of Period 2 (PER2) in IR injury and clotting.
- Platelet-specific PER2 function in coagulation and IR injury requires clarification.
Purpose of the Study:
- To investigate the role of platelet-specific PER2 in blood coagulation.
- To determine the impact of platelet-specific PER2 on myocardial IR injury.
- To assess the translational potential of intense light therapy in modulating coagulation.
Main Methods:
- Generated mice with tissue-specific deletion of Per2 in megakaryocytes (Per2loxP/loxP-PF4-CRE).
- Assessed platelet aggregation and clotting times in knockout and control mice.
- Evaluated myocardial infarct size and plasma troponin levels.
- Conducted translational studies using intense light therapy in healthy human subjects to assess effects on coagulation.
Main Results:
- Platelets from Per2loxP/loxP-PF4-CRE mice exhibited significantly faster clotting.
- Per2-deficient mice showed increased infarct sizes and plasma troponin levels.
- Intense light therapy repressed procoagulant pathways and reduced clot rate in human plasma samples.
Conclusions:
- Platelet-specific PER2 deficiency accelerates blood clotting.
- Intense light-induced PER2 inhibits platelet aggregation.
- Intense light therapy shows promise as a novel clinical approach for managing clotting disorders.
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