Colchicine Pharmacokinetics and Mechanism of Action

Author:

Angelidis Christos1,Kotsialou Zoi1,Kossyvakis Charalampos2,Vrettou Agathi-Rosa1,Zacharoulis Achilleas1,Kolokathis Fotios1,Kekeris Vasilios2,Giannopoulos Georgios2

Affiliation:

1. 2nd Department of Cardiology, Medical School, Attikon Hospital, National and Kapodistrian University of Athens, Athens, Greece

2. Department of Cardiology, "G. Gennimatas" General Hospital of Athens, Athens, Greece

Abstract

Colchicine is a tricyclic, lipid-soluble alkaloid derived from the plant of the Lily family Colchicum autumnale, sometimes called the “autumn crocus”. It is predominantly metabolized in the gastrointestinal tract. Two proteins, P-glycoprotein (P-gp) and CYP3A4 seem to play a pivotal role, governing its pharmacokinetic. The commonest side effects are gastrointestinal (nausea, vomiting and particularly dose-related-diarrhea) occurring in 5-10% of patients. Colchicine exerts its unique action mainly through inhibition of microtubule polymerization. Microtubule polymerization affects a variety of cellular processes including maintenance of shape, signaling, division, migration, and cellular transport. Colchicine interferes with several inflammatory pathways including adhesion and recruitment of neutrophils, superoxide production, inflammasome activation, the RhoA/Rho effector kinase (ROCK) pathway and the tumor necrosis factor alpha (TNF-α) -induced nuclear factor κΒ (NF-κΒ) pathway attenuating the inflammatory response. This concise paper attempts to give a brief review of its pharmacokinetic properties and its main mechanisms of action.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology

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