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dc.contributor.advisor Yu, Seong Woon -
dc.contributor.author Cho, Hyo Jin -
dc.date.accessioned 2017-05-10T08:51:27Z -
dc.date.available 2015-01-12T00:00:00Z -
dc.date.issued 2015 -
dc.identifier.uri http://dgist.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000001923092 en_US
dc.identifier.uri http://hdl.handle.net/20.500.11750/1399 -
dc.description.abstract Microglia are the resident macrophages in the central nervous system. Under normal conditions, microglia cells contribute to brain development and maintenance of tissue homeostasis. However, chronic microglial activation can cause tissue damage and eventually lead to neurodegenerative diseases and neuronal death. In terms of phenotype,activated microglia can be divided into two different types: M1 state and M2 state. The first is classical activation, M1 state, which is typified by the production of inflammatory cytokines and reactive oxygen species (ROS). In contrast with pro-inflammatory M1 cells, alternative activation, M2 state has an anti-inflammatory phenotype promoting wound repair and debris clearance.Recently, the effects of flavonoids on a variety of inflammatory processes and immune functions have been reported.
Flavonoids, which are plant pigments, are anti-oxidants that possess anti-inflammatory properties and may modulate signaling pathways.
This study aims to investigate the anti-inflammatory effect of flavonoids and their role on the NF-kB pathway in BV2 microglial cells. Flavonoids treatment suppress production of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), nitric oxide (NO) and interleukin-6 (IL-6) in lipopolysaccharide (LPS)-stimulated BV2 cells.
Flavonoids treatment also attenuated activation of nuclear factor-kappaB (NF-κB) transcriptional activity. Furthermore,flavonoids suppress mRNA expressions related with pro-inflammatory M1 state. These observations suggest that flavonoids may contribute as an anti-inflammatory agent and provide evidence about its role in the prevention of neurodegenerative diseases associated with inflammation. ⓒ 2015 DGIST
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dc.description.tableofcontents I. INTRODUCTION 1--
1. 1. Introduction 1--
II. Methods and Materials 3--
2. 1. Chemicals and reagents 3--
2. 2. Cell culture 3--
2. 3. Cell viability 3--
2. 4.Nitrite assay 4--
2. 5.ELISA 4--
2. 6. NF-kB luciferase reporter assay 4--
2. 7. RT-PCR 5--
2. 8. Statistical analyses 5--
III. Results 7--
3. 1. Flavonoids reduce NO production in LPS-stimulated BV2 microglia 7--
3. 2. Flavonoids number 1, 53, 61 do not affect cell viability in LPS-stimulated BV2 microglia 7--
3. 3. Flavonoids suppress production of inflammatory cytokines in LPS-stimulated BV2 microglia 13--
3. 4. Flavonoids blocks NF- ĸB activity in LPS-stimulated BV2 microglia 15--
3. 5. Flavonoids affect production of mRNA levels in M1, M2 state 17--
IV. Discussion 22--
V. References 24
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dc.format.extent 28 -
dc.language eng -
dc.publisher DGIST -
dc.subject flavonoid -
dc.subject neuroinflammation -
dc.subject microglia -
dc.subject NF-κB -
dc.subject 신경염증 -
dc.subject 미세아교세포 -
dc.title Flavonoids have modulatory effects on neuroinflammation in microglia -
dc.title.alternative 미세아교세포에서 flavonoid 의 신경염증 억제 효과 -
dc.type Thesis -
dc.identifier.doi 10.22677/thesis.1923092 -
dc.description.alternativeAbstract 미세아교세포 (microglia)는 뇌와 척수를 포함하는 중추신경계(Central Nervous System; CNS)에서 주요하게 면역 기능을 수행하는 세포이다. 일반적인 상태에서 신경염증은 항상성을 유지하고 조직을 보호하는 기능을 한다. 하지만 오랜 시간 동안 외부에서 또는 내부의 자극이나 스트레스를 받게 되면 미세아교세포를 과도하게 활성화시켜 신경독성을 가진 물질을 배출하거나 조직에 손상을 주게 된다. 나아가 퇴행성 뇌질환을 유발하게 된다. 따라서 신경염증을 조절하는 메커니즘에 대한 연구는 퇴행성 뇌질환의 치료제 개발에 기여할 수 있다.
Flavonoid 는 식물의 색소로 알려져 있으며 최근 염증을 억제하는 기능을 가진다는 연구가 있다.
이 연구에서는 flavonoids 가 미세아교세포 BV2 세포에서 뇌신경염증을 억제하는 기능을 하는지 알아보고자 하였다. Flavonoid 를 lipopolysaccharide (LPS) 처리한 BV2 세포에 전처리 하였을 때 대표적인 신경염증 사이토카인 (cytokine)인 TNF-α 와 NO, IL-6 가 현저히 억제되는 효과를 관찰하였다.또한, MAP kinase 단백질과 NF-ĸB 의 활성화 역시 억제되는 결과를 나타내었다.정량 중합효소 연쇄반응 (Quantitative PCR) 분석 결과 염증 효과를 가지는 M1 연관 유전자의 발현이 감소되는 것을 관찰하였다.
이 연구에서는 Flavonoid 가 뇌신경염증을 억제하는 메커니즘을 밝힘으로서 안전한 항염증 치료제를 비롯, 더 나아가 퇴행성 뇌질환의 치료제제로의 발전 가능성을 제시하고 있다. ⓒ 2015 DGIST
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dc.description.degree Master -
dc.contributor.department Brain Science -
dc.contributor.coadvisor Choi, Hong Soo -
dc.date.awarded 2015. 2 -
dc.publisher.location Daegu -
dc.description.database dCollection -
dc.date.accepted 2015-01-12 -
dc.contributor.alternativeDepartment 대학원 뇌과학전공 -
dc.contributor.affiliatedAuthor Cho, Hyo Jin -
dc.contributor.affiliatedAuthor Yu, Seong Woon -
dc.contributor.affiliatedAuthor Choi, Hong Soo -
dc.contributor.alternativeName 조효진 -
dc.contributor.alternativeName 유성운 -
dc.contributor.alternativeName 최홍수 -
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