Effect of Shengmai San on Insulin Resistance, Tumor Necrosis Factor-Alpha and Oxidative Stress in Rats Fed on a High-Fat Diet

被引:0
作者
Yao, Hsien-Tsung [1 ]
Chiang, Meng-Tsan [2 ]
Lii, Chong-Kuei [1 ]
Chang, Yi-Wei [3 ]
Hsieh, Su-Huei [4 ]
Lin, Jia-Hsuan [1 ]
Chou, Ruey-Hwang [5 ,6 ]
Yeh, Teng-Kuang [4 ]
机构
[1] China Med Univ, Dept Nutr, Taichung 404, Taiwan
[2] Natl Taiwan Ocean Univ, Dept Food Sci, Chilung 202, Taiwan
[3] SunTen Phytotech Co, Taipei 235, Taiwan
[4] Natl Hlth Res Inst, Div Biotechnol & Pharmaceut Res, Zhunan Town 350, Miaoli, Taiwan
[5] China Med Univ Hosp, Ctr Mol Med, Taichung 404, Taiwan
[6] Asia Univ, Dept Biotechnol, Taichung 413, Taiwan
关键词
shengmai san; insulin resistance; high-fat diet; TNF-alpha; rats; MAI-SAN; FRUCTUS-SCHISANDRAE; AQUEOUS EXTRACT; HEART-FAILURE; IN-VIVO; LIVER; DISEASE; GLUCOSE; DYSFUNCTION; THERAPY;
D O I
暂无
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Shengmai San (SMS) is a well-known traditional Chinese medicine formula prescribed for patients with coronary heart disease (CHD). Insulin resistance is the most likely explanation for the development and progression of this disease. To investigate the effect of SMS on high-fat diet-induced insulin resistance, inflammatory cytokine production and oxidative stress, male Wistar rats were fed with low-fat control diet, high-fat diet and high-fat diet supplemented with 4% SMS for eight weeks. An oral glucose tolerance test was conducted in the seventh week. Rats fed the SMS diet had significantly lower plasma fructosamine concentration (p < 0.05) and tended to have lower (p < 0.1) AUC values of plasma glucose and insulin concentrations after glucose challenge, compared to those fed the high-fat diet. Moreover, SMS reduced TNF-alpha and lipid peroxidation levels in the liver and heart. However, SMS had no effect on fasting plasma concentrations of glucose, insulin, triglyceride, non-esterified fatty acids, total cholesterol, HDL-cholesterol and insulin resistance index (homeostasis model assessment; HOMA) in rats. Our results show that SMS may have little or no significant effect on reducing insulin resistance, but display anti-oxidative and anti-inflammatory properties.
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页码:40 / 48
页数:9
相关论文
共 41 条
  • [1] Synergistic role of inflammation and insulin resistance as coronary artery disease risk factors in African Americans and Caucasians
    Anuurad, Erdembileg
    Tracy, Russell P.
    Pearson, Thomas A.
    Kim, Kyoungmi
    Berglund, Lars
    [J]. ATHEROSCLEROSIS, 2009, 205 (01) : 290 - 295
  • [2] Anti-tumour necrosis factor-α therapy in heart failure:: Future directions
    Balakumar, Pitchai
    Singh, Manjeet
    [J]. BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2006, 99 (06) : 391 - 397
  • [3] Berk Bradford C, 2007, Trans Am Clin Climatol Assoc, V118, P209
  • [4] CARLSON E, 1979, CLIN CHIM ACTA, V79, P575
  • [5] Exposure to static magnetic field of pregnant rats induces hepatic GSH elevation but not oxidative DNA damage in liver and kidney
    Chater, Sihem
    Abdelmelek, Hafedh
    Douki, Thierry
    Garrel, Cathrine
    Favier, Alain
    Sakly, Mohsen
    Ben Rhouma, Khemais
    [J]. ARCHIVES OF MEDICAL RESEARCH, 2006, 37 (08) : 941 - 946
  • [6] Review: Drug therapy in Chinese traditional medicine
    Cheng, JT
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 2000, 40 (05) : 445 - 450
  • [7] Probiotics Reduce the Inflammatory Response Induced by a High-Fat Diet in the Liver of Young Rats
    Esposito, Emanuela
    Iacono, Anna
    Bianco, Giuseppe
    Autore, Giuseppina
    Cuzzocrea, Salvatore
    Vajro, Pietro
    Canani, Roberto Berni
    Calignano, Antonio
    Raso, Giuseppina Mattace
    Meli, Rosaria
    [J]. JOURNAL OF NUTRITION, 2009, 139 (05) : 905 - 911
  • [8] High-fat diets promote insulin resistance through cytokine gene expression in growing female rats
    Flanagan, Anne M.
    Brown, Jackie L.
    Santiago, Consuelo A.
    Aad, Pauline Y.
    Spicer, Leon J.
    Spicer, Maria T.
    [J]. JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2008, 19 (08) : 505 - 513
  • [9] FOLCH J, 1957, J BIOL CHEM, V226, P497
  • [10] FUNGWE TV, 1993, J LIPID RES, V34, P933