Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells
碩士 === 嘉南藥理大學 === 保健營養系 === 106 === Piper methysticum (PM) in Taiwan, China and Japan, etc. PM is popularly used as traditional medicines and health foods for antioxidant, anti-inflammatory and anti-cancer effects. In this study, our aims were (i) to examine the anti-diabetic and anti-inflammatory e...
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ndltd-TW-106CNUP02170092019-11-16T05:27:06Z http://ndltd.ncl.edu.tw/handle/5dt5q5 Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells 以小鼠骨骼肌(C2C12)細胞模式探討Flavokawain A之抗糖尿病及抗發炎相關之分子機轉 SU, YI-JYUN 蘇依君 碩士 嘉南藥理大學 保健營養系 106 Piper methysticum (PM) in Taiwan, China and Japan, etc. PM is popularly used as traditional medicines and health foods for antioxidant, anti-inflammatory and anti-cancer effects. In this study, our aims were (i) to examine the anti-diabetic and anti-inflammatory effects of a PM bioactive compound, flavokawain A (FKA) in palmitate (PA)-induced murine C2C12 skeletal muscle cells, and (ii) examine the effect of FKA on insulin, Akt/PI3K, MAPKs and GLUT-4 molecular mechanism (s) in PA-induced cells. As 10 to 30 μM FKA significantly up-regulated the glucose absorption and increased the cell growth. 30 μM FKA significantly up-regulated the glucose up-take, down-regulated ROS formation, as well as decreased the expression of NFκB in PA-induced cells. Results showed that only PA-treated cells, cell viability reduced to 81.80%, but FKA protected the cells to 100%. Co-treatment of cells with PA plus 30 μM FKA significantly up-regulated GLUT-4, down-regulated the activation of JNK, p38 and ERK proteins as well as inhibited the formation of ROS and decreased the levels of NFκB. WU, SHU-JUNG 吳淑靜 2018 學位論文 ; thesis 65 zh-TW |
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碩士 === 嘉南藥理大學 === 保健營養系 === 106 === Piper methysticum (PM) in Taiwan, China and Japan, etc. PM is popularly used as traditional medicines and health foods for antioxidant, anti-inflammatory and anti-cancer effects. In this study, our aims were (i) to examine the anti-diabetic and anti-inflammatory effects of a PM bioactive compound, flavokawain A (FKA) in palmitate (PA)-induced murine C2C12 skeletal muscle cells, and (ii) examine the effect of FKA on insulin, Akt/PI3K, MAPKs and GLUT-4 molecular mechanism (s) in PA-induced cells. As 10 to 30 μM FKA significantly up-regulated the glucose absorption and increased the cell growth. 30 μM FKA significantly up-regulated the glucose up-take, down-regulated ROS formation, as well as decreased the expression of NFκB in PA-induced cells. Results showed that only PA-treated cells, cell viability reduced to 81.80%, but FKA protected the cells to 100%. Co-treatment of cells with PA plus 30 μM FKA significantly up-regulated GLUT-4, down-regulated the activation of JNK, p38 and ERK proteins as well as inhibited the formation of ROS and decreased the levels of NFκB.
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WU, SHU-JUNG |
author_facet |
WU, SHU-JUNG SU, YI-JYUN 蘇依君 |
author |
SU, YI-JYUN 蘇依君 |
spellingShingle |
SU, YI-JYUN 蘇依君 Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
author_sort |
SU, YI-JYUN |
title |
Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
title_short |
Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
title_full |
Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
title_fullStr |
Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
title_full_unstemmed |
Anti-diabetic and Anti-inflammatory Effects of Flavokawain A and Its Related Molecular Mechanism (s) in Murine Skeletal C2C12 Cells |
title_sort |
anti-diabetic and anti-inflammatory effects of flavokawain a and its related molecular mechanism (s) in murine skeletal c2c12 cells |
publishDate |
2018 |
url |
http://ndltd.ncl.edu.tw/handle/5dt5q5 |
work_keys_str_mv |
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