Killing of Schistosoma japonicum in the administration of NOS inhibitors and its mechanism
| Project/Area Number |
14570227
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
寄生虫学(含医用動物学)
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| Research Institution | KURUME UNIVERSITY |
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Principal Investigator |
HIRATA Mizuki KURUME UNIVERSITY, PARASITOLOGY, Associate Professor, 医学部, 助教授 (70080629)
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| Co-Investigator(Kenkyū-buntansha) |
HIRATA Kazuho KYUSHU UNIVERSITY, ANATOMY AND CELL BIOLOGY, 医学部, 講師 (00037425)
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| Project Period (FY) |
2002 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 2003: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2002: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | Schistosoma japonicum / protection / nitric oxide / L-NAME / D-NAME / NOS阻害剤 / NO / 殺滅 |
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| Research Abstract |
The effect of nitric oxydase synthase inhibitors in Schistosoma japonicum-infected mice was studied. It was surprisingly found that oral administration of NOS inhibitors, L-NAME and its inactive enantiomer D-NAME, had significant decreasing effects on the worm burden when mice were scarified at 6 week of infection and that D-NAME was more effective than L-NAME in C57BL/6 mice in comprison. In detailed study of D-NAME administration schedules, significant effects were shown when 50-100mg/ml concentration were given, whereas higher concentrations, 200 or 400mg/ml, had no apparent effects. The time of administration examined between 3 to 42 day of infection indicated that the protective effects were apparent when the inhibitor was given during 14-24 day of infection for consecutive 6 days. In the use of several cytokine deficient mice, the effect of the enantiomers interestingly differed with each strain. D-NAME was effective in IFN-g KO mice, while in IL-4 and IL-13KO mice L-NAME showed the effect. Measurement of serum NO levels showed that there was increase in NO in D-NAME-administered C57BL/6, while decreased NO was seen in the administration of L-NAME. In IL-13 KO mice there was exactly reverse relationship, showing increase in NO with L-NAME. Cytokine analysis of splenic cells in protective mice showed a tendency of decrease in IL-10 level, while there was no significant changes in IFN-g level. These observations strongly suggests NO plays a protective role in S.japonicum infection. In whole, our present study indicates several interesting aspects of NOS inhibitors in defensive mechanism of infectious disease.
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Report
(3 results)
Research Products
(14 results)
