Rutin, a Flavonoid and Principal Component of Saussurea Involucrata, Attenuates Physical Fatigue in a Forced Swimming Mouse Model

被引:78
作者
Su, Kang-Yi [2 ,3 ]
Yu, Chao Yuan [1 ]
Chen, Yue-Wen [1 ]
Huang, Yi-Tsau [4 ]
Chen, Chun-Ting [1 ]
Wu, Hsueh-Fu [1 ]
Chen, Yi-Lin Sophia [1 ]
机构
[1] Natl Ilan Univ, Dept Biotechnol & Anim Sci, Ilan City 260, Taiwan
[2] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei 100, Taiwan
[4] Natl Res Inst Chinese Med, Minist Hlth & Welf, Taipei, Taiwan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2014年 / 11卷 / 05期
关键词
rutin; S; involucrate; physical fatigue; ANTIOXIDANT ACTIVITY; MITOCHONDRIAL BIOGENESIS; ENDOTHELIAL-CELLS; INDUCED APOPTOSIS; EXERCISE; RATS; PGC-1-ALPHA; HOMEOSTASIS; INHIBITION; STRESS;
D O I
10.7150/ijms.8220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study investigated the antifatigue effects of rutin, a flavonoid extracted from the ethyl acetate extract of S. involucrata. Mice were subjected to a weight-loaded forced swim test (WFST) on alternate days for 3 wk. Rutin was administered orally to the mice for 7 days in dosages of 15, 30, and 60 mg/kg body weight, and several biomarkers of physical fatigue were evaluated: swimming time, change in body weight, lipid peroxidation, lactic acid (LA), glycogen, and the activities of the antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx). On Day 7, the rutin-treated mice had a 3-fold longer exhaustive swimming time than the control mice, as well as significantly reduced blood LA concentrations. The 15, 30, and 60 mg/kg body weight rutin-supplemented groups displayed 11.2%, 22.5%, and 37.7% reduced malondialdehyde (MDA) concentrations, respectively, in brain and muscle tissues compared with the control exercised group. Our results indicated that the administration of rutin protected the mice against the depletion of SOD and GPx activities significantly. Following 7 days of rutin treatment, we sacrificed the mice and analyzed their soleus muscle and brain for peroxisome proliferator-activated receptor-a coactivator (PGC-1 alpha) and sirtuin 1 (SIRT1) mRNA expression. We observed that rutin treatment increased PGC-1 alpha and SIRT1 mRNA and protein expression. The changes in these markers of mitochondrial biogenesis were associated with increased maximal endurance capacity. The application of 2D gel electrophoresis to analyze the rutin-responsive protein profiles in the WFST mouse brain further revealed the upregulation of the CBI cannabinoid receptor-interacting protein 1, myelin basic protein, Rho GDP dissociation inhibitor (GDI) alpha, and TPI, indicating that rutin might inhibit anxiety through the upregulation of the expression of anxiety-associated proteins. Western blot analysis of MAPK expression further confirmed the antianxiety effects of rutin. Our study results thus indicate that rutin treatment ameliorates the various impairments associated with physical fatigue.
引用
收藏
页码:528 / 537
页数:10
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