ReviewFrontiers in pharmacology2025
Targeting type H vessels with bioactive metabolites from traditional Chinese botanical drugs: a therapeutic strategy for skeletal disorders.
Review in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- A mild photothermal-mediated neuroimmunomodulatory composite hydrogel reverses the inflammatory osteoclast precursor phenotype to promote osteoporotic bone defect healing.Bioactive materials · 2026Article
- Review
- Breaking the immune "cold niche" in bone metastasis: core mechanisms of the multidimensional interwoven regulatory network and precision breakthrough strategies.Molecular cancer · 2026Review
- Single-cell RNA sequencing analysis reveals the evolution and regulatory features of specialized endothelial cell subsets in non-traumatic osteonecrosis of the femoral head.Biology direct · 2026Article
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Authors and funding
7 authors.
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Abstract
Type H vessels are a specialized subtype of bone capillaries, first identified in 2014, characterized by high co-expression of CD31 and Endomucin. These vessels play a key regulatory role in bone development, repair, and remodeling through angiogenesis-osteogenesis coupling, which is essential for maintaining skeletal homeostasis. Type H vessels are abundant in the bones of young individuals but gradually decline with age, and their dysregulation is closely associated with skeletal disorders, including osteoporosis, osteoarthritis, bone defects, fractures, and osteonecrosis of the femoral head. Previous studies have identified the molecular mechanisms underlying the regulation of type H vessels, and recent investigations have examined pharmacological strategies to modulate these pathways. Among these, bioactive metabolites derived from traditional Chinese botanical drugs have attracted attention for their ability to regulate type H vessel formation and improve skeletal health. This review summarizes the molecular mechanisms by which these bioactive metabolites target type H vessels, highlighting their therapeutic potential in skeletal disorders and suggesting that modulation of type H vessel formation represents a promising strategy for intervention. Future studies are needed to further clarify the mechanisms of action of these metabolites and to assess their safety and clinical efficacy for translation into human therapy.
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