PROTECTIVE EFFECT OF CARRAGEENAN AGAINST MURINE CYTOMEGALOVIRUS-INFECTION IN MICE

Citation
R. Hamasuna et al., PROTECTIVE EFFECT OF CARRAGEENAN AGAINST MURINE CYTOMEGALOVIRUS-INFECTION IN MICE, Antiviral chemistry & chemotherapy, 4(6), 1993, pp. 353-360
Citations number
41
Categorie Soggetti
Biology,"Pharmacology & Pharmacy
ISSN journal
09563202
Volume
4
Issue
6
Year of publication
1993
Pages
353 - 360
Database
ISI
SICI code
0956-3202(1993)4:6<353:PEOCAM>2.0.ZU;2-5
Abstract
The protective effect of iota-carrageenan (CAR) was evaluated against murine cytomegalovirus (MCMV) infection in mice. Female ICR mice were challenged intraperitoneally (i.p.) with 3 LD50 of salivary gland-pass aged MCMV. More than 0.5 mg of CAR showed a protective effect on mice only when CAR was administered i.p. and then MCMV was inoculated i.p. The protective effect of CAR was evidenced by an increase in plaque-fo rming unit per LD50 and a decrease in the titre of infectious viruses in the target organs. Neither a virucidal nor a virustatic effect on M CMV was evidenced for CAR. The protective effect of CAR seemed to be h ost-mediated. Pretreatment of mice with CAR augmented natural killer ( NK) activity of the spleen cells without elevating the serum interfero n level. However, administration of anti-asialo GM1 antibody did not n ullify the inhibitory effect of CAR on virus replication in the target organs. MCMV infection induced leukopenia including neutropenia and l ymphopenia in saline-treated mice. Pre-treatment with CAR protected mi ce from those signs, except for slight lymphopenia. Administration of cyclophosphamide induced severe leukopenia including neutropenia and l ymphopenia even in CAR-treated mice. Under such conditions, the protec tive effect of CAR against MCMV infection was abrogated by cyclophosph amide. Thus, the protective effect of CAR seems to be non-NK-mediated.