Old and new natural products as the source of modern antithrombotic drugs
Research article published in Planta medica (1991)
Abstract
Natural compounds have been the first historical source of antithrombotic compounds (heparin, vitamin K antagonists, streptokinase, urokinase); molecules extracted from plants or animals still provide some of the most original and promising approaches for the discovery of new drugs in this class. In this review, we will briefly describe three examples of current research trends that could lead to the development of new antithrombotic drugs of natural origin. Flavonoids have been shown to be inhibitors of cyclic nucleotide phosphodiesterase; this enzymatic activity is one of the main mechanisms of inhibition of aggregation of blood platelets by flavonoids. Some of these compounds could represent templates for the development of new inhibitors of platelet activation. Garlic ( ALLIUM SATIVUM) has been shown to inhibit platelet aggregation IN VIVO and IN VITRO; a number of active principles has now been identified and their mechanisms of action are currently being explored. An ancient remedy, the medicinal leech ( HIRUDO MEDICINALIS), has been found to contain several potent anticoagulant proteins. Among them, hirudin, a polypeptide of 65 amino acids, has been identified as one of the most potent inhibitors of thrombin. The production of sufficient amounts of hirudin through molecular biology techniques has now allowed the performance of clinical trials. These three examples show that careful consideration of biochemical, ethnopharmacological, or toxicological properties of natural products can still constitute a valuable basis for the development of new drugs.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Peer-reviewed research on therapeutic compound development relevant to leech-derived anticoagulants and antithrombotic agents. Indexed in PubMed and verified against the NCBI record.
Por qué esto importa para la hirudoterapia
Esta revisión examina productos naturales como fuentes de fármacos antitrombóticos, cubriendo flavonoides inhibidores de la plaqueta, ajo (*Allium sativum*) y la sanguijuela medicinal (*Hirudo medicinalis*), y destaca la hirudina, un polipéptido de sanguijuela de 65 aminoácidos identificado como uno de los inhibidores de trombina más potentes conocidos, señalando que para entonces la producción recombinante había permitido ensayos clínicos. Se sitúa en el centro de la narrativa de descubrimiento de fármacos del secretoma de la ASH, documentando cómo un anticoagulante clásico de sanguijuela pasó de ser un remedio antiguo a una molécula definida y un modelo para terapéuticas modernas dirigidas a la trombina. Nota: esta es una revisión narrativa de 1991 que resume el estado de la investigación en ese momento en lugar de informar sobre resultados de nuevos ensayos, por lo que es mejor citarla para el marco histórico y mecanicista del significado del descubrimiento de fármacos de la hirudina, y no como evidencia clínica actual.
Citación
Old and new natural products as the source of modern antithrombotic drugs.
Beretz A et al. · Planta medica, 1991
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 28, 2026 · Última actualización del sitio: June 18, 2026