Literature DB >> 6144043

Trypanocidal action of neuroleptic phenothiazines in Trypanosoma brucei.

T Seebeck, P Gehr.   

Abstract

This paper reports the effects of a series of phenothiazine derivatives on trypanosomes in vitro. Our results demonstrate that trypanosomes are very sensitive to some of these compounds at micromolar concentrations. Electron microscopic analysis of drug-treated cells shows that the pellicular layer of microtubules is selectively disintegrated by phenothiazine treatment, while the flagellar axoneme is entirely resistant to the drug. These observations suggest that phenothiazines might constitute a promising candidate group for the development of new trypanocidal drugs. Furthermore, they indicate that the mechanism of drug action is mediated through a specific interaction of phenothiazines with the pellicular, but not with the flagellar, microtubules.

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Year:  1983        PMID: 6144043     DOI: 10.1016/0166-6851(83)90097-x

Source DB:  PubMed          Journal:  Mol Biochem Parasitol        ISSN: 0166-6851            Impact factor:   1.759


  14 in total

1.  Rationally designed selective inhibitors of trypanothione reductase. Phenothiazines and related tricyclics as lead structures.

Authors:  T J Benson; J H McKie; J Garforth; A Borges; A H Fairlamb; K T Douglas
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

2.  Two related subpellicular cytoskeleton-associated proteins in Trypanosoma brucei stabilize microtubules.

Authors:  Cécile Vedrenne; Christiane Giroud; Derrick R Robinson; Sébastien Besteiro; Christophe Bosc; Frédéric Bringaud; Théo Baltz
Journal:  Mol Biol Cell       Date:  2002-03       Impact factor: 4.138

3.  A 60-kDa cytoskeletal protein from Trypanosoma brucei brucei can interact with membranes and with microtubules.

Authors:  T Seebeck; V Küng; T Wyler; M Müller
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

4.  Image-based high-throughput drug screening targeting the intracellular stage of Trypanosoma cruzi, the agent of Chagas' disease.

Authors:  Juan C Engel; Kenny K H Ang; Steven Chen; Michelle R Arkin; James H McKerrow; Patricia S Doyle
Journal:  Antimicrob Agents Chemother       Date:  2010-06-14       Impact factor: 5.191

5.  Calcium and calmodulin antagonists inhibit human malaria parasites (Plasmodium falciparum): implications for drug design.

Authors:  L W Scheibel; P M Colombani; A D Hess; M Aikawa; C T Atkinson; W K Milhous
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

6.  Calcium entry in Trypanosoma brucei is regulated by phospholipase A2 and arachidonic acid.

Authors:  J Eintracht; R Maathai; A Mellors; L Ruben
Journal:  Biochem J       Date:  1998-12-15       Impact factor: 3.857

7.  Effect of calmodulin inhibitors on viability and mitochondrial potential of Plasmodium falciparum in culture.

Authors:  T G Geary; A A Divo; J B Jensen
Journal:  Antimicrob Agents Chemother       Date:  1986-11       Impact factor: 5.191

8.  Feeder layer-free in vitro assay for screening antitrypanosomal compounds against Trypanosoma brucei brucei and T. b. evansi.

Authors:  R Kaminsky; E Zweygarth
Journal:  Antimicrob Agents Chemother       Date:  1989-06       Impact factor: 5.191

9.  A MAP6-related protein is present in protozoa and is involved in flagellum motility.

Authors:  Denis Dacheux; Nicolas Landrein; Magali Thonnus; Guillaume Gilbert; Annelise Sahin; Harald Wodrich; Derrick R Robinson; Mélanie Bonhivers
Journal:  PLoS One       Date:  2012-02-15       Impact factor: 3.240

10.  A novel microtubule-binding motif identified in a high molecular weight microtubule-associated protein from Trypanosoma brucei.

Authors:  A Hemphill; M Affolter; T Seebeck
Journal:  J Cell Biol       Date:  1992-04       Impact factor: 10.539

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