American Society of Hirudotherapy

Anticoagulant peptide LR from Whitmania pigra ameliorates cerebral ischemia-reperfusion injury

Animal model study published in Brain Research (2026)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Preclinical (animal)Drug DevelopmentSalivary PharmacologyLiu R et al. · Brain Research, 2026

Abstract

BACKGROUND: Ischemic stroke (IS) is a leading cause of death and disability worldwide. Hypercoagulability and thrombus formation play critical roles in its pathogenesis. Leech-derived peptides, especially those obtained from Whitmania pigra, have demonstrated potential antithrombotic and neuroprotective effects. This study aimed to investigate the therapeutic efficacy and underlying mechanisms of a leech peptide in a rat model of cerebral ischemia/reperfusion injury. METHODS: Adult male Sprague-Dawley rats were subjected to middle cerebral artery occlusion followed by reperfusion to establish the IS model. Rats received low-dose or high-dose leech peptide, edaravone as a positive control, or saline. Behavioral assessments, infarct volume measurement, laser speckle imaging for cerebral perfusion, and histopathology were performed. Hemorheology and coagulation parameters were analyzed. Additionally, thrombin levels and fibrinolytic factors were evaluated using ELISA. Biosafety was assessed through hemolysis and histological evaluation of major organs. RESULTS: Leech peptide significantly reduced infarct volume, improved neurological scores, enhanced cerebral perfusion, and preserved brain tissue structure. It modulated thrombin-related parameters, ameliorated coagulation dysfunction, and modulated fibrinolysis-associated factors, thereby contributing to the restoration of coagulation-fibrinolysis homeostasis. Low-dose treatment showed comparable or superior efficacy to the high dose with better safety. No significant toxicity or hemolysis was observed. CONCLUSIONS: Leech peptide derived from Whitmania pigra exerts neuroprotective effects in cerebral ischemia/reperfusion injury through anticoagulation and thrombolysis. These findings support its potential as a novel candidate for IS therapy. TRIAL REGISTRATION: Not applicable. This study did not involve human participants.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article
Indexed MeSH termsAnimalsRats, Sprague-DawleyMaleReperfusion InjuryRatsLeechesNeuroprotective AgentsAnticoagulantsPeptidesBrain IschemiaDisease Models, AnimalInfarction, Middle Cerebral Artery

Summary

Anticoagulant peptide LR from Whitmania pigra significantly reduced infarct volume, improved neurological scores, enhanced cerebral perfusion, and modulated thrombin-related parameters in a middle cerebral artery occlusion rat model; low dose showed comparable or superior efficacy to high dose with better safety.

Why This Matters for Hirudotherapy

This study investigated a leech peptide from Whitmania pigra in a rat model of cerebral ischemia/reperfusion injury using middle cerebral artery occlusion followed by reperfusion. The leech peptide significantly reduced infarct volume, improved neurological scores, enhanced cerebral perfusion, and modulated thrombin-related parameters, coagulation, and fibrinolytic factors, with the low dose showing comparable or superior efficacy to the high dose and no significant toxicity or hemolysis. This is directly relevant to ASH's domain: the abstract explicitly describes leech-derived peptides from Whitmania pigra with antithrombotic and neuroprotective effects in stroke. The study is limited by its preclinical (rat) design.

Citation

Anticoagulant peptide LR from Whitmania pigra ameliorates cerebral ischemia-reperfusion injury.

Liu R et al. · Brain Research, 2026

Added to ASH library: May 27, 2026 · Site last updated: June 18, 2026

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