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Anti-fatigue effect of Wujia Shengmai Yin in mice and its mechanism
Jianan HAN,Zhuorui LIU,Peiyong ZENG,Shuang JIANG,Hongyu LI
PDF(729 KB)
PDF(729 KB)
Anti-fatigue effect of Wujia Shengmai Yin in mice and its mechanism
Objective To discuss the anti-fatigue effect of Wujia Shengmai Yin,and to clarify its mechanism. Methods Thirty-six male ICR mice were randomly devided into control group (equivalent volume of distilled water), Shengmai Yin group (500 mg·kg?1 of Shengmai Yin), and Wujia Shengmai Yin group (600 mg·kg?1 of Wujia Shengmai Yin). The body weights of the mice in various groups were detected every 7 d, and the mental states were observed. The rotating rod test and exhaustive swimming test were used to detect the duration on the rod and the swimming time to exhaustion of the mice in various groups, respectively;the levels of urea nitrogen (BUN) and lactate (LA), and the activities of lactate dehydrogenase (LDH) in serum, the levels of liver glycogen (LG), muscle glycogen (MG), and malondialdehyde (MDA), and activities of glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) in muscle tissue of the mice in various groups were detected by kits; the expression levels of glucose metabolism-related proteins in liver tissue of the mice in various groups were detected by Western blotting method. Results Compared with before experiment, the body weights after experiment of the mice in various groups showed a increasing trend but the differences were not statistically significant (P>0.05). The rotating rod test results showed that compared with control group, the duration on the rod of the mice in Wujia Shengmai Yin group was significantly increased (P<0.01). The exhaustive swimming test results showed that compared with control group, the swimming time to exhaustion of the mice in Shengmai Yin group and Wujia Shengmai Yin group was significantly increased (P<0.01). Compared with control group, the levels of BUN in serum of the mice in Shengmai Yin group and Wujia Shengmai Yin group were significantly decreased (P<0.01), and the activities of LDH were significantly increased (P<0.01); the level of LA of the mice in Wujia Shengmai Yin group was significantly decreased(P<0.01). Compared with Shengmai Yin group,the levels of BUN and LA in the serum and LDH activity of the mice in Wujia Shengmai Yin group were significantly decreased (P<0.01). Compared with control group, the levels of LG in liver tissue and the levels of MG in muscle tissue of the mice in Shengmai Yin group and Wujia Shengmai Yin group were significantly increased (P<0.01); compared with Shengmai Yin group, the level of LG in liver tissue and the level of MG in muscle tissue of the mice in Wujia Shengmai Yin group were increased (P<0.01). Compared with control group, the activities of GSH-Px and SOD in muscle tissue of the mice in Shengmai Yin group and Wujia Shengmai Yin group were significantly increased, and the levels of MDA in Shengmai Yin group and Wujia Shengmai Yin group was significantly decreased (P<0.01); compared with Shengmai Yin group, the activities of GSH-Px and SOD in muscle tissue of the mice in Wujia Shengmai Yin group were significantly increased and the level of MDA was decreased (P<0.01). The Western blotting results showed that compared with control group, the expression levels of phosphorylated phosphoinositide 3-kinase (p-PI3K), phosphorylated protein kinase B (p-AKT), phosphorylated glycogen synthase kinase 3 beta (p-GSK3β), and glycogen synthase (GS) proteins in liver tissue of the mice in Shengmai Yin group and Wujia Shengmai Yin group were significantly increased (P<0.05 or P<0.01); compared with Shengmai Yin group, the expression levels of p-PI3K, p-AKT, p-GSK3β, and GS proteins in liver tissue of the mice in Wujia Shengmai Yin group were significantly increased(P<0.01). Conclusion Wujia Shengmai Yin enhances the anti-fatigue effect by activating the phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/glycogen synthase kinase 3 beta (GSK3β) signaling pathways, and improves the body’s antioxidant capacity, and increases the glycogen synthesis.
Wujia Shengmai Yin / Oxidative stress / Anti-fatigue / Glycometabolism / Urea nitrogen / Lactate
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| 1 | 郑哲君, 李晓莉, 王 朔. 抗疲劳功能食品的研究进展[J]. 食品科技, 2006, 31(2): 4-7. |
| 2 | WANG N L, LIOU Y L, LIN M T, et al. Chinese herbal medicine, Shengmai San, is effective for improving circulatory shock and oxidative damage in the brain during heatstroke[J]. J Pharmacol Sci, 2005, 97(2): 253-265. |
| 3 | ZHANG K, ZHANG J Y, WANG X R, et al. Cardioprotection of Sheng Mai Yin a classic formula on adriamycin induced myocardial injury in Wistar rats[J]. Phytomedicine, 2018, 38: 1-11. |
| 4 | HUANG L Z, HUANG B K, LIANG J, et al. Antifatigue activity of the liposoluble fraction from Acanthopanax senticosus[J]. Phytother Res, 2011, 25(6): 940-943. |
| 5 | HUANG L Z, HUANG B K, YE Q, et al. Bioactivity-guided fractionation for anti-fatigue property of Acanthopanax senticosus[J]. J Ethnopharmacol, 2011, 133(1): 213-219. |
| 6 | 国家药典委员会. 中华人民共和国药典-二部: 2020年版[M]. 北京: 中国医药科技出版社, 2020: 853. |
| 7 | LEE B H, KIM J, LEE R M, et al. Gintonin enhances performance of mice in rotarod test: involvement of lysophosphatidic acid receptors and catecholamine release[J]. Neurosci Lett, 2016, 612: 256-260. |
| 8 | NI W H, GAO T T, WANG H L, et al. Anti-fatigue activity of polysaccharides from the fruits of four Tibetan Plateau indigenous medicinal plants[J]. J Ethnopharmacol, 2013, 150(2): 529-535. |
| 9 | HUANG L Z, ZHAO H F, HUANG B K, et al. Acanthopanax senticosus: review of botany, chemistry and pharmacology[J]. Pharmazie, 2011, 66(2): 83-97. |
| 10 | 汪 洪, 方 昊, 冯 纬, 等. 生晒参-甘草-桂花提取物对 Balb/C 小鼠运动疲劳抗性的影响[J]. 食品工业科技, 2023, 44(5): 356-362. |
| 11 | LAURENT D, SCHNEIDER K E, PRUSACZYK W K, et al. Effects of caffeine on muscle glycogen utilization and the neuroendocrine axis during exercise[J]. J Clin Endocrinol Metab, 2000, 85(6): 2170-2175. |
| 12 | XIN C, ZHAO M Y, WANG J H, et al. Hawthorn polyphenols, D-chiro-inositol, and epigallocatechin gallate exert a synergistic hypoglycemic effect[J]. J Food Biochem, 2021, 45(7): e13771. |
| 13 | QU Y S, JI H W, SONG W K, et al. The anti-fatigue effect of the Auxis thazard oligopeptide via modulation of the AMPK/PGC-1α pathway in mice[J]. Food Funct, 2022, 13(3): 1641-1650. |
| 14 | DING D X, WANG Y, YAN W, et al. MYCT1 alters the glycogen shunt by regulating selective translation of RACK1-mediated enzymes[J]. iScience, 2022, 25(3): 103955. |
| 15 | CUI X R, SAWASHITA J, DAI J, et al. Exercise suppresses mouse systemic AApoAⅡ amyloidosis through enhancement of the p38 MAPK signaling pathway[J]. Dis Models Mech, 2022, 15(3): 1-16. |
| 16 | LI D J, LI Y H, YUAN H B, et al. The novel exercise-induced hormone irisin protects against neuronal injury via activation of the Akt and ERK1/2 signaling pathways and contributes to the neuroprotection of physical exercise in cerebral ischemia[J]. Metabolism, 2017, 68: 31-42. |
| 17 | LIU X H, LIU T, YANG K L, et al. Antifatigue effect of asiaticoside in mice by attenuating oxidative stress[J]. Discov Med, 2023, 35(176): 275-282. |
| 18 | LU X D, CHEN J Q, HUANG L Y, et al. The anti-fatigue effect of glycoprotein from hairtail fish (Trichiurus lepturus) on BALB/c mice[J]. Foods, 2023, 12(6): 1245. |
| 19 | DURONIO V. The life of a cell: apoptosis regulation by the PI3K/PKB pathway[J]. Biochem J, 2008, 415(3): 333-344. |
| 20 | FRANKE T F, KAPLAN D R, CANTLEY L C. PI3K: downstream AKTion blocks apoptosis[J]. Cell, 1997, 88(4): 435-437. |
| 21 | ENGELMAN J A, CHEN L, TAN X H, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers[J]. Nat Med, 2008, 14(12): 1351-1356. |
| 22 | REN Z L, ZHONG H, SONG C C, et al. Insulin promotes mitochondrial respiration and survival through PI3K/AKT/GSK3 pathway in human embryonic stem cells[J]. Stem Cell Reports, 2020, 15(6): 1362-1376. |
| 23 | LYU S Y, WANG H R, MA T J. Optimization of supercritical fluid CO2 extraction from yellow horn seed and its anti-fatigue and antioxidant activity[J]. Molecules, 2023, 28(12): 4853. |
| 24 | SUN W D, ZU S L, SHAO G F, et al. Long non-coding DANCR targets miR-185-5p to upregulate LIM and SH3 protein 1 promoting prostate cancer via the FAK/PI3K/AKT/GSK3β/snail pathway[J]. J Gene Med, 2021, 23(7): e3344. |
| 25 | YADAV U C, NAURA A S, AGUILERA-AGUIRRE L, et al. Aldose reductase inhibition prevents allergic airway remodeling through PI3K/AKT/GSK3β pathway in mice[J]. PLoS One, 2013, 8(2): e57442. |
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