Американское общество гирудотерапии

The great diversity: monomeric and oligomeric hirudins, hirudin-like factors and decorsins in the Asian medicinal leeches Hirudo nipponia and Hirudo tianjinensis

Basic science / preclinical published in Parasitol Res (2026)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Preclinical (animal)Геномика и протеомикаФармакология секрета слюнных желёзРазработка лекарственных препаратовKalatehjari P et al. · Parasitology research, 2026

Abstract

Medicinal leeches express a broad variety of anticoagulants and other bioactive factors that are involved in the blood feeding process. For most of the anticoagulants, several genes exist that may encode isoforms of the respective proteins, including hirudins and decorsins. Decorsins negatively affect platelet aggregation, whereas hirudins are potent thrombin inhibitors. Both factors belong to the hirudin superfamily that also includes the group of hirudin-like factors, and all hematophagous leeches analyzed so far contain several gene copies that encode representatives of at least two of the three groups of these factors. Members of the hirudin superfamily may contain only one central globular domain, but others may contain two or more copies. Here we describe the molecular identification and partial functional characterization of a broad variety of putative mono-, bi and multimeric hirudins, decorsins and hirudin-like factors in two Asian medicinal leech species, namely Hirudo nipponia and H. tianjinensis. Some of the monomeric hirudins and decorsins have already been described before, but they represent only a small part of the overall diversity. For the first time, putative monomeric and one oligomeric decorsins of H. tianjinensis were expressed as recombinant proteins, functionally characterized and successfully verified as platelet aggregation inhibitors. In addition we have conducted phylogenetic analyses based on genomic and mitochondrial markers and found convincing evidence that H. nipponia and H. tianjinensis together with members of the genus Whitmania form a monophyletic clade that is clearly distinct from clades that are formed either by European members of the genus Hirudo or by members of the genus Hirudinaria.

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

Publication typeJournal Article
Indexed MeSH termsAnimalsHirudinsLeechesPhylogenyPlatelet AggregationAmino Acid Sequence

Резюме

Identification and partial functional characterization of mono-, bi-, and multimeric hirudins, decorsins, and hirudin-like factors in two Asian medicinal leeches (Hirudo nipponia and H. tianjinensis). Phylogenetic analysis clarifies Asian Hirudo / Whitmania clade structure relative to European Hirudo and Hirudinaria.

Почему это важно для гирудотерапии

This study molecularly identified and partially functionally characterized a broad diversity of monomeric, bimeric, and multimeric hirudins, decorsins, and hirudin-like factors in the Asian medicinal leeches Hirudo nipponia and Hirudo tianjinensis. Novel monomeric and one oligomeric decorsin from H. tianjinensis were recombinantly expressed and confirmed as platelet aggregation inhibitors, and phylogenetic analyses placed these species alongside Whitmania in a clade distinct from European Hirudo species. This is directly relevant to ASH's domain, as it deepens understanding of the anticoagulant and antiplatelet arsenal in medicinal leech saliva. However, the functional characterization is partial and limited to recombinant expression of select factors; no clinical or whole-organism hirudotherapy data are presented.

Цитирование

The great diversity: monomeric and oligomeric hirudins, hirudin-like factors and decorsins in the Asian medicinal leeches Hirudo nipponia and Hirudo tianjinensis.

Kalatehjari P et al. · Parasitology research, 2026

Связанный клинический контекст

Добавлено в библиотеку ASH: May 27, 2026 · Последнее обновление сайта: June 18, 2026

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