Why calpain inhibitors are interesting leading compounds to search for new therapeutic options to treat leishmaniasis?

Parasitology. 2017 Feb;144(2):117-123. doi: 10.1017/S003118201600189X. Epub 2016 Nov 21.

Abstract

Leishmaniasis is a neglected disease, which needs improvements in drug development, mainly due to the toxicity, parasite resistance and low compliance of patients to treatment. Therefore, the development of new chemotherapeutic compounds is an urgent need. This opinion article will briefly highlight the feasible use of calpain inhibitors as leading compounds to search for new therapeutic options to treat leishmaniasis. The milestone of this approach is to take advantage on the myriad of inhibitors developed against calpains, some of which are in advanced clinical trials. The deregulated activity of these enzymes is associated with several pathologies, such as strokes, diabetes and Parkinson's disease, to name a few. In Leishmania, calpain upregulation has been associated to drug resistance and virulence. Whereas the difficulties in developing new drugs for neglected diseases are more economical than biotechnological, repurposing approach with compounds already approved for clinical use by the regulatory agencies can be an interesting shortcut to a successful chemotherapeutic treatment for leishmaniasis.

Keywords: Calpain inhibitors; MDL28170; leishmaniasis; repurpose approach.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiprotozoal Agents / chemistry
  • Antiprotozoal Agents / pharmacology*
  • Calpain / antagonists & inhibitors*
  • Calpain / metabolism*
  • Humans
  • Leishmania / drug effects
  • Leishmania / metabolism*
  • Leishmaniasis / drug therapy*
  • Neglected Diseases / drug therapy

Substances

  • Antiprotozoal Agents
  • Calpain