A New Therapeutic Approach Using a Schizophyllan-based Drug Delivery System for Inflammatory Bowel Disease
Project/Area Number |
25460963
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Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Gastroenterology
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Research Institution | Kurume University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
MOCHIZUKI Shinichi 北九州市立大学, 国際環境工学部, 講師 (10520702)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | 炎症性腸疾患 / ドラッグデリバリーシステム / アンチセンス / シゾフィラン |
Outline of Final Research Achievements |
Antisense technologies for the inhibition of gene expression provide an effective strategy in inflammatory bowel disease (IBD). We have developed a delivery system for antisense using schizophyllan (SPG), a polysaccharide that belongs to the β- glucan family. This system has several advantages enabling the effective suppression of targeted RNA or DNA: SPG complex is stable and effectively taken up into macrophages through Dectin-1. TNF-alpha mainly produced by macrophages has been shown to have a pathogenetic role in IBD. The effect of antisense TNF-alpha/SPG complex to intestinal macrophages of DSS colitis was shown the increase of uptake into macrophages and the suppression of TNF-alpha. The rectal administration of antisense TNF-alpha/SPG complex effectively suppressed TNF-alpha production and significantly ameliorated intestinal inflammation. Our result demonstrated the usefulness of local administered antisense/SPG as new therapeutic approach in IBD.
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Report
(4 results)
Research Products
(3 results)