Literature DB >> 2509571

Amphotericin B: a novel class of antiscrapie drugs.

M Pocchiari1, P Casaccia, A Ladogana.   

Abstract

Amphotericin B (AmB) has been able to lengthen the incubation period of intracerebrally (ic) scrapie-injected hamsters to 45 d. This article reports a linear relationship between AmB doses and the duration of the incubation periods of ic-treated animals compared with controls, a greater effect of AmB treatment administered 2 w before or the same day of ic scrapie incubation, and the ineffectiveness of mepartricin, an AmB analogue, in prolonging the incubation period of ic scrapie-injected hamsters. The beneficial effect of AmB appears due to a delay in the replication of the scrapie agent in the brain of infected hamsters. Moreover, AmB suppresses scrapie replication in the spleen of treated animals. Three hypotheses may explain these results: (1) AmB alters a hypothetical scrapie receptor, preventing the entry of the agent into central nervous system (CNS) target cells; (2) AmB interferes with mechanisms involved in scrapie replication; (3) AmB prevents the formation and accumulation of a scrapie-specific amyloid protein responsible for the disease. Whatever the mechanism of action, AmB is the only currently available drug to modify experimental CNS scrapie infection, so AmB is proposed as a novel class of antiscrapie drugs.

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Year:  1989        PMID: 2509571     DOI: 10.1093/infdis/160.5.795

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  13 in total

1.  Opposite effects of dextran sulfate 500, the polyene antibiotic MS-8209, and Congo red on accumulation of the protease-resistant isoform of PrP in the spleens of mice inoculated intraperitoneally with the scrapie agent.

Authors:  V Beringue; K T Adjou; F Lamoury; T Maignien; J P Deslys; R Race; D Dormont
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

2.  Levels of infectivity in the blood throughout the incubation period of hamsters peripherally injected with scrapie.

Authors:  P Casaccia; A Ladogana; Y G Xi; M Pocchiari
Journal:  Arch Virol       Date:  1989       Impact factor: 2.574

3.  Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals.

Authors:  R Demaimay; K T Adjou; V Beringue; S Demart; C I Lasmézas; J P Deslys; M Seman; D Dormont
Journal:  J Virol       Date:  1997-12       Impact factor: 5.103

4.  MS-8209, a new amphotericin B derivative, provides enhanced efficacy in delaying hamster scrapie.

Authors:  K T Adjou; R Demaimay; C Lasmezas; J P Deslys; M Seman; D Dormont
Journal:  Antimicrob Agents Chemother       Date:  1995-12       Impact factor: 5.191

5.  Congo red prolongs the incubation period in scrapie-infected hamsters.

Authors:  L Ingrosso; A Ladogana; M Pocchiari
Journal:  J Virol       Date:  1995-01       Impact factor: 5.103

6.  Measurement of the concentration of amphotericin B in brain tissue of scrapie-infected hamsters with a simple and sensitive method.

Authors:  P Casaccia; A Ladogana; Y G Xi; L Ingrosso; M Pocchiari; M C Silvestrini; A Cittadini
Journal:  Antimicrob Agents Chemother       Date:  1991-07       Impact factor: 5.191

Review 7.  Experimental drug treatment of scrapie: a pathogenetic basis for rationale therapeutics.

Authors:  M Pocchiari; M Salvatore; A Ladogana; L Ingrosso; Y G Xi; M Cibati; C Masullo
Journal:  Eur J Epidemiol       Date:  1991-09       Impact factor: 8.082

8.  Amphotericin B delays both scrapie agent replication and PrP-res accumulation early in infection.

Authors:  D McKenzie; J Kaczkowski; R Marsh; J Aiken
Journal:  J Virol       Date:  1994-11       Impact factor: 5.103

9.  Effects of the polyene antibiotic derivative MS-8209 on the astrocyte lysosomal system of scrapie-infected hamsters.

Authors:  Vladimir B Grigoriev; Karim T Adjou; Nicole Salès; Steve Simoneau; Jean-Philippe Deslys; Michel Seman; Dominique Dormont; Jean-Guy Fournier
Journal:  J Mol Neurosci       Date:  2002-06       Impact factor: 3.444

Review 10.  Recent advances in prion chemotherapeutics.

Authors:  Valerie L Sim; Byron Caughey
Journal:  Infect Disord Drug Targets       Date:  2009-02
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