Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells
碩士 === 元培科技大學 === 生物技術研究所 === 98 === Δ7-eicosatrienoic acid (Δ7-ETrA; Δ7,11,14-20:3), a are polyunsaturated fatty acid (PUFA), is an elongation product of pinolenic acid (PNA; Δ5,9,12-18:3) originally from pine seed oil (PSO). Earlier studies indicated that PNA and its metabolite Δ7-ETrA significant...
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ndltd-TW-098YUST71080012018-04-28T04:30:45Z http://ndltd.ncl.edu.tw/handle/cfux3m Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells 利用巨噬細胞株RAW264.7研究新合成Δ7-二十碳三烯酸(Δ7,11,14-20:3)的生物活性 Yu-Lung Huang 黃于隴 碩士 元培科技大學 生物技術研究所 98 Δ7-eicosatrienoic acid (Δ7-ETrA; Δ7,11,14-20:3), a are polyunsaturated fatty acid (PUFA), is an elongation product of pinolenic acid (PNA; Δ5,9,12-18:3) originally from pine seed oil (PSO). Earlier studies indicated that PNA and its metabolite Δ7-ETrA significantly incorporated and substituted arachidonic acid (AA) in cellular phospholipids, resulting in the reduction of pro-inflammatory prostaglandin E2 (PGE2) synthesis. However, Δ7-ETrA is not commercial available due to limited sources and high production/purification cost, and no studies have been conducted to explore biological effects and possible metabolism to date. In this study, we chemically synthesized, Δ7-ETrA.Using murine macrophage cells as an inflammation model,we determined if Δ7-ETrA can relieve inflammatory response induced by lipopolysaccharide (LPS) through the modulation of cellular PUFA metabolism, pro-inflammatory mediator synthesis,such as nitric oxide (NO), PGE2 and gene expression of inducible nitric oxide synthase (iNOS) and type II cyclooxygenase (COX-2). Results showed that PNA in PSO could be enriched through the combined techniques of saponification and urea saturation. Then, novel Δ7-ETrA was synthesized and indentified by a series of organic chemical reactions and analysis of gas chromatography (GC)/GC-mas spectrum (GC-MS). The purity of new synthesized Δ7-ETrA was approximate 97% after thin layer chromatography (TLC) separation and the following extraction. Δ7-ETrA significantly reduced concentrations of NO, PGE2 and interleukin-6 (IL-6), but enhanced tumor necrotic fator-α (TNF-α) production. The possible mechanisms involved in the reduction of NO and COX-2 could attribute to the inhibition of iNOS and COX-2 expression. Morevoer, based on results of cellular fatty acid analysis, significant amounts of Δ7-ETrA substituting for AA in the phospholipids might also play an important role. Lu-Te Chuang 莊路德 2010 學位論文 ; thesis 71 zh-TW |
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碩士 === 元培科技大學 === 生物技術研究所 === 98 === Δ7-eicosatrienoic acid (Δ7-ETrA; Δ7,11,14-20:3), a are polyunsaturated fatty acid (PUFA), is an elongation product of pinolenic acid (PNA; Δ5,9,12-18:3) originally from pine seed oil (PSO). Earlier studies indicated that PNA and its metabolite Δ7-ETrA significantly incorporated and substituted arachidonic acid (AA) in cellular phospholipids, resulting in the reduction of pro-inflammatory prostaglandin E2 (PGE2) synthesis. However, Δ7-ETrA is not commercial available due to limited sources and high production/purification cost, and no studies have been conducted to explore biological effects and possible metabolism to date. In this study, we chemically synthesized, Δ7-ETrA.Using murine macrophage cells as an inflammation model,we determined if Δ7-ETrA can relieve inflammatory response induced by lipopolysaccharide (LPS) through the modulation of cellular PUFA metabolism, pro-inflammatory mediator synthesis,such as nitric oxide (NO), PGE2 and gene expression of inducible nitric oxide synthase (iNOS) and type II cyclooxygenase (COX-2).
Results showed that PNA in PSO could be enriched through the combined techniques of saponification and urea saturation. Then, novel Δ7-ETrA was synthesized and indentified by a series of organic chemical reactions and analysis of gas chromatography (GC)/GC-mas spectrum (GC-MS). The purity of new synthesized Δ7-ETrA was approximate 97% after thin layer chromatography (TLC) separation and the following extraction. Δ7-ETrA significantly reduced concentrations of NO, PGE2 and interleukin-6 (IL-6), but enhanced tumor necrotic fator-α (TNF-α) production. The possible mechanisms involved in the reduction of NO and COX-2 could attribute to the inhibition of iNOS and COX-2 expression. Morevoer, based on results of cellular fatty acid analysis, significant amounts of Δ7-ETrA substituting for AA in the phospholipids might also play an important role.
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author2 |
Lu-Te Chuang |
author_facet |
Lu-Te Chuang Yu-Lung Huang 黃于隴 |
author |
Yu-Lung Huang 黃于隴 |
spellingShingle |
Yu-Lung Huang 黃于隴 Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
author_sort |
Yu-Lung Huang |
title |
Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
title_short |
Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
title_full |
Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
title_fullStr |
Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
title_full_unstemmed |
Biological effect of newly synthesized Δ7-eicosatrienoic acid (Δ7,11,14-20:3) on RAW264.7 macrophage cells |
title_sort |
biological effect of newly synthesized δ7-eicosatrienoic acid (δ7,11,14-20:3) on raw264.7 macrophage cells |
publishDate |
2010 |
url |
http://ndltd.ncl.edu.tw/handle/cfux3m |
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