4.5 Review

Are Ca2+ channels targets of praziquantel action?

Journal

INTERNATIONAL JOURNAL FOR PARASITOLOGY
Volume 35, Issue 1, Pages 1-9

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2004.09.004

Keywords

praziquantel; Ca2+ channels; schistosoma

Categories

Funding

  1. NIAID NIH HHS [R01 AI040522, AI 40522] Funding Source: Medline
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI040522] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Praziquantel is the current drug of choice for the control of schistosomiasis. It is highly effective against all species of schistosomes and shows minimal adverse effects. Though introduced for the treatment of schistosomiasis more than 20 years ago, the mode of action of praziquantel remains to be elucidated. This review will focus on advances in defining the molecular target of praziquantel action, with particular emphasis on recent work indicating an important role for voltage-gated calcium channels. (C) 2004 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available