Sociedad Americana de Hirudoterapia

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

Animal model study published in Brain Research (2026)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Preclinical (animal)Desarrollo de fármacosFarmacología salivalLiu 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

Resumen

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.

Por qué esto importa para la hirudoterapia

Este estudio investigó un péptido de sanguijuela procedente de Whitmania pigra en un modelo de rata de lesión por isquemia/reperfusión cerebral mediante oclusión de la arteria cerebral media seguida de reperfusión. El péptido de sanguijuela redujo significativamente el volumen del infarto, mejoró las puntuaciones neurológicas, incrementó la perfusión cerebral y moduló parámetros relacionados con la trombina, la coagulación y factores fibrinolíticos, mostrando la dosis baja una eficacia comparable o superior a la dosis alta y sin toxicidad ni hemólisis significativas. Esto es directamente relevante para el ámbito de la ASH: el resumen describe explícitamente péptidos derivados de sanguijuela de Whitmania pigra con efectos antitrombóticos y neuroprotectores en el ictus. El estudio está limitado por su diseño preclínico (en rata).

Citación

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

Liu R et al. · Brain Research, 2026

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.