Abstract |
The effects of route and starting time of administration on FK-565 inhibition of splenomegaly by Friend leukemia virus (FLV) were studied in mice, and the concomitant effect of FK-565 in allowing reduction of zidovudine dosage was estimated. FK-565 inhibited splenomegaly in intravenous and oral doses of 0.01 to 1 mg/kg, but time of initial dosing had little effect on this inhibition. When 0.01 or 1 mg/kg of FK-565 was given intravenously with intraperitoneal doses of 0.63, 2.5, 10 and 40m g/kg of zidovudine, the inhibition rate of splenomegaly at all doses was markedly and dose-dependently higher than when either drug was given alone, and the concomitant use of FK-565 with zidovudine enabled a 16-fold reduction of the dose of zidovudine. The survival rate and survival time after infection with massive amounts of FLV were higher when FK-565 1 mg/kg and zidovudine 20 mg/kg were given in combination than when either drug was given alone. Inhibition of FLV splenomegaly was reflected in the prolonged survival time of the infected mice.
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Authors | Y Yokota, Y Wakai, Y Watanabe, Y Mine |
Journal | The Journal of antibiotics
(J Antibiot (Tokyo))
Vol. 41
Issue 10
Pg. 1479-87
(Oct 1988)
ISSN: 0021-8820 [Print] England |
PMID | 3192497
(Publication Type: Journal Article)
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Chemical References |
- Oligopeptides
- Zidovudine
- heptanoyl-gamma-D-glutamyl-L-meso-diaminopimelyl-D-alanine
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Topics |
- Animals
- Cell Survival
(drug effects)
- Dose-Response Relationship, Drug
- Drug Therapy, Combination
- Friend murine leukemia virus
(drug effects)
- Leukemia, Experimental
(drug therapy)
- Male
- Mice
- Mice, Inbred C3H
- Oligopeptides
(administration & dosage, pharmacology)
- Virus Replication
(drug effects)
- Zidovudine
(administration & dosage, pharmacology)
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