The effect of oral treatment with 6-O-butanoyl castanospermine (MDL 28,574) in the murine zosteriform model of HSV-1 infection.

Abstract:

:Oral treatment of mice, cutaneously infected with herpes simplex virus type 1 (HSV-1) (strain SC16), with the alpha-glucosidase 1 inhibitor 6-O-butanoyl castanospermine (MDL 28,574) produced a significant delay in lesion development and reduced the amount of virus recovered from the brain. Virus load in the brains of mice, whose treatment started 2 days prior to infection, was reduced approximately 100-fold when compared to untreated controls. Treatment initiated at the time of infection, while less effective than pre-treatment, nevertheless reduced virus recovery from the brain by 10-fold. Consistent with its antiviral activity, orally administered MDL 28,574 was rapidly incorporated by brain tissue and mice fed with compound over extended periods maintained relatively high levels of drug at this site.

journal_name

Glycobiology

journal_title

Glycobiology

authors

Bridges CG,Ahmed SP,Kang MS,Nash RJ,Porter EA,Tyms AS

doi

10.1093/glycob/5.2.249

subject

Has Abstract

pub_date

1995-03-01 00:00:00

pages

249-53

issue

2

eissn

0959-6658

issn

1460-2423

journal_volume

5

pub_type

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