Literature DB >> 6254453

The experimental chemotherapy of leishmaniasis, IV. The development of a rodent model for visceral infection.

E R Trotter, W Peters, B L Robinson.   

Abstract

A description is given of two methods for investigating the action of drugs against a viscerotropic Leishmania in mice. The parasite employed was isolated from a patient with kala-azar in Ethiopia. It is designated 'L. infantum LV9' and produces a visceral infection in NMRI mice. The biochemical typing characters of the parasite are described. In Method A, infected animals were treated from the 5th or 6th day after infection (D + 5 or D + 6) for five consecutive days. They were sacrificed 24 hours after the completion of drug treatment and an estimate was made of the amastigote load in the liver. A comparison of this with untreated controls gives an index of activity of a test drug, from 0 to 3. Method B is similar except that the ED50 and ED90 are determined by graphic analysis of data from graded drug doses. A comparison is made with sodium stibogluconate used as a positive drug control to yield a 'Pentostam Index'. The course of infection in BALB/c and NMRI mice is compared with that in random-bred Swiss mice in which 'L. infantum LV9' produces an inconsistent infection. An inoculum of 10(7) amastigotes produces a peak parasite intensity between D + 15 and D + 20. The ED50 and ED90 of sodium stibogluconate (Pentostam) (as Sbv) in Method B are 22 x 5 and 46 x 5 mg/kg sc daily x 5. (By Method A the single dose figures are 65 and 280 mg/kg.) For routine use a standard dose level of 120 mg/kg sc daily x 5 of Pentostam (Sbv) is used in Method B. The ED50 and ED90 of meglumine antimoniate (Glucantime) (as Sbv) in Method B are 11 x 6 and 66 x 7 mg/kg sc daily x 5. Data are given for other antimonials in Method A. Pentamidine and diminazene aceturate proved to have a slow action which was more readily demonstrated if the observation period was prolonged. Amphotericin B was moderately active but toxic to the host. The relevance of these models and a comparison of data found in the mouse and hamster are debated.

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Year:  1980        PMID: 6254453     DOI: 10.1080/00034983.1980.11687322

Source DB:  PubMed          Journal:  Ann Trop Med Parasitol        ISSN: 0003-4983


  8 in total

1.  Studies on stibanate unresponsive isolates of Leishmania donovani.

Authors:  Anindita Bhattacharyya; Mandira Mukherjee; Swadesh Duttagupta
Journal:  J Biosci       Date:  2002-09       Impact factor: 1.826

2.  Use of in vitro method to assess different brands of anti-leishmanial drugs.

Authors:  S K Arora; R Sinha; S Sehgal
Journal:  Med Microbiol Immunol       Date:  1991       Impact factor: 3.402

3.  A role for tumor necrosis factor-alpha in remodeling the splenic marginal zone during Leishmania donovani infection.

Authors:  Christian R Engwerda; Manabu Ato; Sara E J Cotterell; Tracey L Mynott; Asiya Tschannerl; Patricia M A Gorak-Stolinska; Paul M Kaye
Journal:  Am J Pathol       Date:  2002-08       Impact factor: 4.307

4.  Activity and mode of action of acridine compounds against Leishmania donovani.

Authors:  C M Mesa-Valle; J Castilla-Calvente; M Sanchez-Moreno; V Moraleda-Lindez; J Barbe; A Osuna
Journal:  Antimicrob Agents Chemother       Date:  1996-03       Impact factor: 5.191

5.  Treatment of experimental visceral leishmaniasis in a T-cell-deficient host: response to amphotericin B and pentamidine.

Authors:  H W Murray; J Hariprashad; R E Fichtl
Journal:  Antimicrob Agents Chemother       Date:  1993-07       Impact factor: 5.191

6.  Studies on visceral Leishmania tropica infection in BALB/c mice. I. Clinical features and cellular changes.

Authors:  J Djoko-Tamnou; C Leclerc; F Modabber; L Chedid
Journal:  Clin Exp Immunol       Date:  1981-12       Impact factor: 4.330

7.  Evaluation of nephroprotective and immunomodulatory activities of antioxidants in combination with cisplatin against murine visceral leishmaniasis.

Authors:  Meenakshi Sharma; Rakesh Sehgal; Sukhbir Kaur
Journal:  PLoS Negl Trop Dis       Date:  2012-05-01

8.  Protein malnutrition impairs the immune response and influences the severity of infection in a hamster model of chronic visceral leishmaniasis.

Authors:  Eugenia Carrillo; Maria Angeles Jimenez; Carmen Sanchez; Joana Cunha; Camila Marinelli Martins; Anaiá da Paixão Sevá; Javier Moreno
Journal:  PLoS One       Date:  2014-02-25       Impact factor: 3.240

  8 in total

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