Literature DB >> 22260899

Neospora caninum: in vivo and in vitro treatment with artemisone.

Monica L Mazuz1, Richard Haynes, Varda Shkap, Leah Fish, Ricardo Wollkomirsky, Benjamin Leibovich, Thea Molad, Igor Savitsky, Jacob Golenser.   

Abstract

Neosporosis caused by Neospora caninum has global economic, clinical, and epidemiological impacts, mainly in the cattle industry. Currently, there is no useful drug for treatment of neosporosis. This publication is the first to describe the significant benefits that artemisone has on Neospora infections both in vitro and in vivo. Artemisone is a new semi-synthetic 10-alkylamino artemisinin that is superior to other artemisinin derivatives in terms of its significantly higher antimalarial activity, its tolerance in vivo, lack of detectable neurotoxic potential, improved in vivo pharmacokinetics and metabolic stability. Low micromolar concentrations of artemisone inhibited in vitro Neospora development. Prophylactic and post-infection treatment profoundly reduced the number of infected cells and parasites per cell. In the in vivo gerbil model, a non-toxic dose prevented typical cerebral symptoms, in most animals. There were no signs of clinical symptoms and brain PCR was negative. Most treated gerbils produced high specific antibody titer and were protected against a challenge. Overall, artemisone could be considered as a future drug for neosporosis.
Copyright © 2011 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22260899     DOI: 10.1016/j.vetpar.2011.12.020

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  7 in total

Review 1.  Artemisinin and its derivatives in treating protozoan infections beyond malaria.

Authors:  Cecilia Shi Ni Loo; Nelson Siu Kei Lam; Deying Yu; Xin-Zhuan Su; Fangli Lu
Journal:  Pharmacol Res       Date:  2016-11-17       Impact factor: 7.658

2.  Treatment of murine cerebral malaria by artemisone in combination with conventional antimalarial drugs: antiplasmodial effects and immune responses.

Authors:  W Armand Guiguemde; Nicholas H Hunt; Jintao Guo; Annael Marciano; Richard K Haynes; Julie Clark; R Kiplin Guy; Jacob Golenser
Journal:  Antimicrob Agents Chemother       Date:  2014-06-09       Impact factor: 5.191

3.  Buparvaquone is active against Neospora caninum in vitro and in experimentally infected mice.

Authors:  Joachim Müller; Adriana Aguado-Martinez; Vera Manser; Vreni Balmer; Pablo Winzer; Dominic Ritler; Isabel Hostettler; David Arranz-Solís; Luis Ortega-Mora; Andrew Hemphill
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2015-02-13       Impact factor: 4.077

4.  Neospora caninum calcium-dependent protein kinase 1 is an effective drug target for neosporosis therapy.

Authors:  Kayode K Ojo; Molly C Reid; Latha Kallur Siddaramaiah; Joachim Müller; Pablo Winzer; Zhongsheng Zhang; Katelyn R Keyloun; Rama Subba Rao Vidadala; Ethan A Merritt; Wim G J Hol; Dustin J Maly; Erkang Fan; Wesley C Van Voorhis; Andrew Hemphill
Journal:  PLoS One       Date:  2014-03-28       Impact factor: 3.240

5.  A quantitative reverse-transcriptase PCR assay for the assessment of drug activities against intracellular Theileria annulata schizonts.

Authors:  Isabel Hostettler; Joachim Müller; Chad E Stephens; Richard Haynes; Andrew Hemphill
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2014-09-19       Impact factor: 4.077

6.  Inhibitory action of phenothiazinium dyes against Neospora caninum.

Authors:  Luiz Miguel Pereira; Caroline Martins Mota; Luciana Baroni; Cássia Mariana Bronzon da Costa; Jade Cabestre Venancio Brochi; Mark Wainwright; Tiago Wilson Patriarca Mineo; Gilberto Úbida Leite Braga; Ana Patrícia Yatsuda
Journal:  Sci Rep       Date:  2020-05-04       Impact factor: 4.379

7.  Repurposing of antiparasitic drugs: the hydroxy-naphthoquinone buparvaquone inhibits vertical transmission in the pregnant neosporosis mouse model.

Authors:  Joachim Müller; Adriana Aguado-Martínez; Vera Manser; Ho Ning Wong; Richard K Haynes; Andrew Hemphill
Journal:  Vet Res       Date:  2016-02-17       Impact factor: 3.683

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.