Antioxidants· 2026Q1· Review
Emerging Role, Molecular Mechanisms, and Therapeutic Potential of 2-O, 3-O Desulfated Heparin (ODSH) Across Inflammatory and Vascular Diseases
- 0citations
- Q1SCImago
- 2026year
Short summary
2-O, 3-O desulfated heparin (ODSH), a modified heparin derivative, shows therapeutic potential in inflammatory and vascular diseases by reducing anticoagulant activity while retaining affinity for inflammatory mediators.
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Key points
- ODSH is a heparin derivative with low anticoagulant activity but retains affinity for inflammatory mediators.
- It modulates HMGB1-RAGE/TLR4 signaling, neutrophil elastase, PF4-dependent platelet activation, and selectin-mediated adhesion.
- ODSH reduces cytokine release, improves endothelial barrier stability, and attenuates inflammation-coagulation crosstalk.
- Preclinical studies show benefits in acute lung injury, cystic fibrosis, ischemia-reperfusion injury, traumatic brain injury, thrombocytopenia, and metastatic cancer.
- Pilot clinical observations suggest favorable biological effects in acute myeloid leukemia and septic peritonitis.
AI-generated from the title and abstract; the full text is not read.
Abstract
Glycosaminoglycans (GAGs) are structurally diverse polysaccharides that regulate inflammation, coagulation, and cellular homeostasis through highly specific sulfation patterns and interactions with cationic proteins. Among GAG derivatives, 2-O, 3-O desulfated heparin (ODSH) is a chemically modified heparin derivative characterized by markedly reduced anticoagulant activity yet preserved affinity for key inflammatory mediators. This review summarizes current knowledge on ODSH structure–function relationships, molecular mechanisms, and therapeutic applications across inflammatory, vascular, and immune-mediated diseases. ODSH modulates several convergent pathogenic processes, including HMGB1-RAGE/TLR4 signaling, neutrophil elastase-mediated tissue injury, PF4-dependent platelet activation, selectin-mediated adhesion, and thrombin-induced endothelial permeability. These actions arise from both direct molecular interactions and indirect sequestration of extracellular mediators, collectively associated with reduced cytokine release, enhanced endothelial barrier stability, and attenuation of inflammation–coagulation crosstalk. Preclinical studies report protective effects in acute lung injury, cystic fibrosis, ischemia–reperfusion injury, traumatic brain injury, thrombocytopenia, and metastatic cancer. Some pilot clinical observations in acute myeloid leukemia and septic peritonitis have reported favorable biological effects. Despite multimodal activity, limitations include incomplete pharmacokinetic characterization, limited comparative studies with other desulfated heparins, and the need for dose–response and safety evaluation in human trials. Overall, available evidence suggests that ODSH may have therapeutic relevance in diseases characterized by excessive inflammation, endothelial dysfunction, and dysregulated host responses. This review integrates current evidence to guide future mechanistic and translational investigation into ODSH and related low-anticoagulant heparin derivatives.
The authors' abstract, as published at the source. Antioxidants, 2026 · DOI ↗
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Field: Cell Biology
Cell BiologyBiochemistry, Genetics and Molecular Biology