2017 Fiscal Year Final Research Report
Search for the target molecule of the licorice component inhibiting NLRP3 inflammasome and development into drug discovery research
Project/Area Number |
15K07960
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biological pharmacy
|
Research Institution | Toyama Prefectural Institute. for Pharmaceutical Research. |
Principal Investigator |
HONDA Hiroe 富山県薬事研究所, 主任研究員 (10463134)
|
Co-Investigator(Renkei-kenkyūsha) |
NAGAI Yoshinori 富山大学, 大学院医学薬学研究部(医学), 客員教授 (30431761)
|
Project Period (FY) |
2015-04-01 – 2018-03-31
|
Keywords | NLRP3 / IL-1β / 糖尿病 / イソリクイリチゲニン |
Outline of Final Research Achievements |
Isoliquiritigenin(ILG) , one of the licorice components, suppressed visceral adipose tissue inflammation and fibrosis in high-fat diet (HFD)-fed model mice of type 2 diabetes. As a result of in-vitro analysis, ILG suppressed the expression of fibrosis-related genes induced by Mincle and TLR4 in macrophages. We also demonstrated that the administration of ILG to db/db mice improves insulin resistance and glucose tolerance test. In db/db mice, ILG did not suppress the chronic inflammation of visceral adipose tissue unlike HFD-fed mice, and improved the pancreatic damage state. In addition, we identified several candidate target proteins of ILG inhibiting the NLRP3 inflammasome activation by the DARTS method.
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Free Research Field |
免疫学
|