The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats

碩士 === 臺北市立大學 === 運動科學研究所 === 106 === Purpose: (1) Observe whether insulin could improve diabetes in liver, and oxidative stress or antioxidant capacity level after acute exercise challenges. (2) Observe whether the insulin treatment had equal efficacy in the old rats. Method: There were two experim...

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Main Authors: Lin, Ting-Wen, 林亭妏
Other Authors: Tsai, shiow-Chwen
Format: Others
Language:zh-TW
Published: 2018
Online Access:http://ndltd.ncl.edu.tw/handle/q2b72k
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spelling ndltd-TW-106UT0054210092019-05-16T01:16:57Z http://ndltd.ncl.edu.tw/handle/q2b72k The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats 胰島素改善STZ誘發糖尿病大鼠脂肪肝病變之機制探討 Lin, Ting-Wen 林亭妏 碩士 臺北市立大學 運動科學研究所 106 Purpose: (1) Observe whether insulin could improve diabetes in liver, and oxidative stress or antioxidant capacity level after acute exercise challenges. (2) Observe whether the insulin treatment had equal efficacy in the old rats. Method: There were two experiment in this study. Study one: 18 weeks old rats injected STZ to induce diabetes, insulin treatment, and down heel running at the last of the experiment. Rats were divided to control group (C), diabetes group (S), diabetes plus insulin (SI), control with down heel running (EC), diabetes with down heel running (ES), diabetes plus insulin with down heel running (ESI). Study two: 22 months old rats injected STZ to induce diabetes, and insulin treatment. Rats were divided to control group (OC), diabetes group (OS), diabetes plus insulin (OSI). After one week acclimation, rats were individually injected with sodium citrate (also referred to as STZ carrier) or STZ, and fasting blood glucose was measured with a blood glucose meter. When the blood glucose level was 300 mg/ dL or more, they were injected twice daily saline or insulin (0.25 IU/ml). Feeding a total of 14 days, pentobarbital (40 mg/kg) was anesthetized before injection of STZ and at the end of the feeding period. Testing body composition by DEXA, then sacrifice and take the liver and perirenal fat to assay for the production of TBARS and Glutathione. Hematoxylin and eosin stain will be used to determine liver steatosis and size of perirenal fat cell, and Masson's staining will be used to determine fibrosis. Data were analyzed statistically by two-way ANOVA. Post-hoc were performed one-way ANOVA and Bonferroni multiple tests to differentiate the effect of S and SI group. P<0.05 were considered as significant difference. Independent-sample T test was used to differentiate the effect of young and old/ young and exercise groups. P<0.05 were considered as significant difference. Result: Aging and diabetes would cause weight loss. Diabetes in the elderly would cause a rapid decline in lean mass, insulin treatment would slow down the loss of fat after STZ injection. Histological in liver produced more vacuolation in elderly diabetes. After an acute exercise challenge in young rats, the mechanism of antioxidant capacity of glutathione was upregulated. Both insulin treatment and acute exercise challenge can increase antioxidant capacity and decrease oxidative stress. Conclusion: Insulin treatment was effective in diabetes weight loss, acute exercise challenge contributed to increase antioxidant capacity, also with insulin treatment can decrease oxidative stress. Tsai, shiow-Chwen 蔡秀純 2018 學位論文 ; thesis 68 zh-TW
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language zh-TW
format Others
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description 碩士 === 臺北市立大學 === 運動科學研究所 === 106 === Purpose: (1) Observe whether insulin could improve diabetes in liver, and oxidative stress or antioxidant capacity level after acute exercise challenges. (2) Observe whether the insulin treatment had equal efficacy in the old rats. Method: There were two experiment in this study. Study one: 18 weeks old rats injected STZ to induce diabetes, insulin treatment, and down heel running at the last of the experiment. Rats were divided to control group (C), diabetes group (S), diabetes plus insulin (SI), control with down heel running (EC), diabetes with down heel running (ES), diabetes plus insulin with down heel running (ESI). Study two: 22 months old rats injected STZ to induce diabetes, and insulin treatment. Rats were divided to control group (OC), diabetes group (OS), diabetes plus insulin (OSI). After one week acclimation, rats were individually injected with sodium citrate (also referred to as STZ carrier) or STZ, and fasting blood glucose was measured with a blood glucose meter. When the blood glucose level was 300 mg/ dL or more, they were injected twice daily saline or insulin (0.25 IU/ml). Feeding a total of 14 days, pentobarbital (40 mg/kg) was anesthetized before injection of STZ and at the end of the feeding period. Testing body composition by DEXA, then sacrifice and take the liver and perirenal fat to assay for the production of TBARS and Glutathione. Hematoxylin and eosin stain will be used to determine liver steatosis and size of perirenal fat cell, and Masson's staining will be used to determine fibrosis. Data were analyzed statistically by two-way ANOVA. Post-hoc were performed one-way ANOVA and Bonferroni multiple tests to differentiate the effect of S and SI group. P<0.05 were considered as significant difference. Independent-sample T test was used to differentiate the effect of young and old/ young and exercise groups. P<0.05 were considered as significant difference. Result: Aging and diabetes would cause weight loss. Diabetes in the elderly would cause a rapid decline in lean mass, insulin treatment would slow down the loss of fat after STZ injection. Histological in liver produced more vacuolation in elderly diabetes. After an acute exercise challenge in young rats, the mechanism of antioxidant capacity of glutathione was upregulated. Both insulin treatment and acute exercise challenge can increase antioxidant capacity and decrease oxidative stress. Conclusion: Insulin treatment was effective in diabetes weight loss, acute exercise challenge contributed to increase antioxidant capacity, also with insulin treatment can decrease oxidative stress.
author2 Tsai, shiow-Chwen
author_facet Tsai, shiow-Chwen
Lin, Ting-Wen
林亭妏
author Lin, Ting-Wen
林亭妏
spellingShingle Lin, Ting-Wen
林亭妏
The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
author_sort Lin, Ting-Wen
title The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
title_short The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
title_full The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
title_fullStr The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
title_full_unstemmed The mechanism of insulin-improved fatty liver in STZ-induced diabetes male rats
title_sort mechanism of insulin-improved fatty liver in stz-induced diabetes male rats
publishDate 2018
url http://ndltd.ncl.edu.tw/handle/q2b72k
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