한국해양대학교

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광나무(Ligustrum japonicum)로부터 생리활성 성분의 탐색

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dc.contributor.author 백승오 -
dc.date.accessioned 2017-02-22T05:51:00Z -
dc.date.available 2017-02-22T05:51:00Z -
dc.date.issued 2015 -
dc.date.submitted 57071-01-11 -
dc.identifier.uri http://kmou.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002174626 ko_KR
dc.identifier.uri http://repository.kmou.ac.kr/handle/2014.oak/8687 -
dc.description.abstract Ligustrum japonicum is distributed along the feet of the mountains adjacent to the coasts of Korea, China and Japan. L. japonicum is commonly used as an herbal medicine to strengthen the function of the heart and the liver as well as to treat a ringing in the ears, dizziness and eye pain. Samples of L. japonicum were purchased from ‘Chungmyungyakcho,’ the pharmaceutical company specializing in herbal medicine. Dried samples were extracted twice: with methylene chloride and with methanol (MeOH), respectively. The combined crude extracts were evaporated in vacuo, and then the residue was partitioned between water and methylene chloride. The aqueous layer was re-partitioned between H2Oandn-butanol (n-BUOH), and then the organic layer (i.e. between 85% aqueous methanol (85% aq. MeOH) and n-hexane). The crude extract and its solvent-partitioned fractions were evaluated for their antioxidant and antiproliferative effects. In the DPPH radical assay system, only the n-BuOH fraction showed a significant radical scavenging effect. In the peroxynitrite assay system, the 85% aq.MeOH and the n-BuOH fractions showed a strong scavenging effect on both authentic peroxynitrite and peroxynitrite induced from SIN-1. In a cellular system using 2',7'-dichlorofluorescin diacetate (DCF-DA) as the fluorescence probe in HT-1080 cells, all tested samples remarkably decreased the level of intracellular reactive oxygen species (ROS) at the concentration of 100 μg/ml. Among them, the 85% aq.MeOH fraction revealed the strongest scavenging effect. In the cytotoxicity bioassay system using the MTT reduction method, on the other hand, the crude extract showed a weak cytotoxic effect on all human cancer cells. For the solvent-partitioned fractions, however, the 85% aq.MeOH fraction showed a potent inhibitory effect on the growth of all human cancer cells ( HT-1080, AGS, HT-29, and MCF-7). The n-BuOH fraction exhibited a good inhibition effect on the growth of AGS cells at the concentration of 100 μg/ml. Six known compounds were isolated from L. japonicum: Oleanolic acid (1), Maslinic acid (2), Ursolic acid (3), Tyrosol (4), Ligustruoside (5), and 8-(E)-Nuezhenide (6). These six compounds were also evaluated for their antioxidant and antiproliferative effects. In the antioxidant bioassay, compound 6 not only showed a potent scavenging effect on peroxinitrites but also remarkably decreased the level of intracellular reactive oxygen species (ROS) in HT 1080 cells. In the cytotoxicity test, compound 3 of all tested compounds exhibited the strongest inhibitory effect on growth of HT-1080, AGS, HT-29, and MCF-7 cells. Therefore, these results suggest that L. japonicum may be useful as a potential biomaterial, as a natural antioxidant to alleviate oxygen-induced damage as well as a chemopreventive agent for cancer. -
dc.description.tableofcontents List of schemes ⅰ List of tables ⅱ List of figures ⅲ List of abbreviations ⅵ Abstract 1 1. 서론 4 2. 재료 및 방법 6 2-1. 재료 6 2-2. 시약 6 (1) 추출, 분획 및 분리 6 (2) 활성 6 (3) 기기 7 (4) 세포배양 8 2-3. 추출 및 분리 9 (1) 광나무(L. japonicum)의 추출 및 분획 9 (2) 광나무(L. japonicum)의 활성 성분 분리 11 (3) 광나무(L. japonicum)에서 분리된 화합물들의 1H NMR 14 2-4. 항산화 활성 실험 19 (1) DPPH radical 소거 활성 측정 19 (2) Peroxynitrite 소거 활성 측정 22 (3) 세포 독성 측정 25 (4) 세포내 활성 산소종(ROS) 측정 27 (5) GSH 함량 측정 29 (6) Genomic DNA 추출 및 Genomic DNA의 산화 생성물 측정 31 2-5. 암세포 증식 억제 실험 32 (1) MTT assay를 이용한 세포 생존율 측정 32 2-6. 항염증 활성 실험 33 (1) NO 생성 억제 효과 33 2-7. 통계처리 33 3. 결과 및 고찰 35 3-1. 광나무(L. japonicum)로부터 분리한 물질의 구조 결정 35 3-2. 광나무(L. japonicum)의 In vitro 항산화 활성 38 (1) DPPH radical 소거 활성 38 (2) Peroxynitrite 소거 활성 40 3-3. 광나무(L. japonicum)의 세포 수준에서의 항산화 활성 43 (1) HT-1080 세포에 대한 조추출물과 용매분획물의 독성 효과 43 (2) Raw 264.7 세포에 대한 조추출물과 용매분획물의 독성 효과 45 (3) 세포내 활성 산소종(ROS) 소거 활성 47 (4) 세포내 Glutathione (GSH) 함량 측정 51 (5) Genomic DNA의 산화 생성물 측정 53 3-4. 광나무(L. japonicum)의 인체 유래 암세포에 대한 세포증식 억제 효과 55 (1) HT-1080 세포 증식 억제 효과 55 (2) AGS 세포 증식 억제 효과 55 (3) HT-29 세포 증식 억제 효과 57 (4) MCF-7 세포 증식 억제 효과 57 3-5. 광나무(L. japonicum)의 NO 생성 억제 효과 59 3-6. 광나무에서 분리된 화합물들의 In vitro 항산화 활성 61 (1) DPPH radical 소거 활성 61 (2) Peroxynitrite 소거 활성 63 3-7. 광나무에서 분리된 화합물들의 세포내 항산화 활성 66 (1) HT-1080 세포생존율 측정 66 (2) 세포내 활성 산소종(ROS) 소거 활성 68 (3) 세포내 Glutathione (GSH) 함량 측정 72 (4) Genomic DNA의 산화 생성물 측정 74 3-8. compounds의 인체 유래 암세포에 대한 세포 증식 억제 효과 76 (1) HT-1080 세포 증식 억제 효과 76 (2) AGS 세포 증식 억제 효과 76 (3) HT-29 세포 증식 억제 효과 78 (4) MCF-7 세포 증식 억제 효과 78 4. 요약 및 결론 80 5. 참고문헌 83 부록 90 -
dc.language kor -
dc.publisher 한국해양대학교 대학원 -
dc.title 광나무(Ligustrum japonicum)로부터 생리활성 성분의 탐색 -
dc.title.alternative An exploratory study on bioactive constituents from the halophyte Ligustrum japonicum -
dc.type Thesis -
dc.date.awarded 2015-08 -
dc.contributor.alternativeName SEUNGOH BAEK -
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해양생명환경학과 > Thesis
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