LU Meitong, SUN Jingmeng, FANG Chenchen, ZHANG Weiyu. Safety Evaluation of Jingshen Tablet and Its Anti-acute Alcoholic Liver Injury[J]. Science and Technology of Food Industry, 2021, 42(6): 325-331,336. DOI: 10.13386/j.issn1002-0306.2020040286
Citation: LU Meitong, SUN Jingmeng, FANG Chenchen, ZHANG Weiyu. Safety Evaluation of Jingshen Tablet and Its Anti-acute Alcoholic Liver Injury[J]. Science and Technology of Food Industry, 2021, 42(6): 325-331,336. DOI: 10.13386/j.issn1002-0306.2020040286

Safety Evaluation of Jingshen Tablet and Its Anti-acute Alcoholic Liver Injury

More Information
  • Received Date: April 25, 2020
  • Available Online: March 15, 2021
  • Objective: This article evaluates the safety of Jingshen Tablets and studies its auxiliary protective function on acute alcoholic liver injury. Methods: Through the acute toxicity test in mice, the micronucleus test in mouse bone marrow polychromatic erythrocytes, the sperm deformity test in mice, the Ames test and the 30-day feeding test in rats, the safety and toxicological evaluation of Jingshen tablets were carried out.60 mice were randomly divided into 5 groups. The control group of the blank group was given sterile water, and the model control group and each dose group were given 50% ethanol to establish an alcoholic liver injury model. After successful model building, the Jingshen tablets were administered orally and administered at 5, 10, and 30 times(0.40, 0.80, 2.40 g·kg-1) of the recommended human dose(4.8 g/60 kg·BW), and the scene was recorded and observed. The effect of ginseng tablets on the contents of malondialdehyde(MDA), reduced glutathione(GSH) and triglyceride(TG) in mouse liver tissue.Results: The maximum dose in the acute oral test in mice was all greater than 15 g/(kg·BW), and the acute toxicity was classified as non-toxic, the micronucleus rate of bone marrow polychromatic erythrocytes and the incidence of sperm abnormalities in each dose group of mice were no significant difference(P>0.05), compared with those in the solvent control group. In the Ames test, the number of reverted colonies in each dose group did not exceed the number of reverted colonies in the solvent control group and the untreated control group by more than 2 times, indicating that Jingshen tablets have no mutagenic effect, There was no significant difference in organ index, biochemical and blood indexes between rats fed for 30 days and solvent control group(P>0.05), compared with model control group, 2.40 g·(kg·BW) -1 group could significantly reduce liver tissue the content of malondialdehyde and triglyceride in the medium(P<0.05). The pathological results showed that all dose groups of Jingshen tablets could alleviate steatosis and inflammatory infiltration in liver cells. Conclusion: Jingshen tablets have the effect of anti-acute alcoholic liver injury, and are safe and non-toxic within the scope of the dose.
  • [1]
    陈绍红,钟赣生,刘明,等.枳榧具子解酒作用的药用部位记载[J].科技导报,2013,31(Z2):107-111.
    [2]
    李志满,邵紫君,李珊珊,等.人参枳椇子提取物对小鼠酒精性肝损伤的保护作用[J].食品工业科技,2019,40(14):302-306

    ,313.
    [3]
    陈春晓,朱肖鸿.酒精性肝炎大鼠模型建立及枳椇子的干预作用[J].浙江中西医结合杂志,2007,17(5):285-287.
    [4]
    余选良,朱肖鸿,冯舒婷.枳椇子治疗酒精性肝病现状[J].浙江中西医结合杂志,2017,27(4):342-344.
    [5]
    叶倩男,徐列明,平键.红景天苷保肝作用及相关机制的研究进展[J].上海中医药大学学报,2020,34(1):83-87

    ,100.
    [6]
    Xu N,Huang F,Jian C,et al. Neuroprotective effect of salidroside against central nervous system inflammation-induced cognitive deficits:A pivotal role of sirtuin 1-dePendent Nrf-2/HO-1/NF-KB Pathway[J]. Phytother Res,2019,33(5):1438-1447.
    [7]
    Xu J,Li Y. Effects of salidroside on exhaustive exercise-induced oxidative stress in rats[J]. Mol Med ReP,2012,6(5):1195-1198.
    [8]
    陈娅,蔡静,李勇,等.海参胶原低聚肽对抗结核药物性肝损伤改善效果[J].中国食物与营养,2018,24(5):68-72.
    [9]
    Orman E S,Odena G,Bataller R. Alcoholic liver disease:Pathogenesis,management,and novel targets for therapy[J]. Journal of Gastroenterology and Hepatology,2013,28(1):77-84.
    [10]
    孙晓梅,阎姝,田书霞. 中药治疗肝损伤的研究进展[J]. 中药材,2016,39(11):2661-2664.
    [11]
    史保银,刘新宇,邸琳,等. 葛根护肝片组方配伍及其辅助护肝功能研究[J].食品工业科技,2020,41(10):299-305.
    [12]
    瞿文生,尹继业,高月求,等.天然多糖对化学性肝损伤的干预和治疗效果评价研究进展[J].国际药学研究杂志,2018,45(12):885-898.
    [13]
    Leung T M,Nieto N. CYP2E1 and oxidant stress in alcoholic and nonalcoholic fatty liver disease[J]. Journal of Hepatology,2013,58:395-398.
    [14]
    耿文学,丁宏翼,易云苏.枳椇子提取物对实验性大鼠肝纤维化的防治作用[J].中药材,2008,31(10):1550-1552.
    [15]
    李钇垚,蹇瑜璇,窦纯,等. 红景天苷对呋喃所致小鼠肝损伤的保护作用研究[J].农产品加工,2019(15):53-57,60.
    [16]
    王丹,丁琳,董平,等. 海参皂苷对脂肪肝大鼠胆固醇代谢的调节作用[J].营养学报,2016,38(1):67-70.
    [17]
    赵麟萱,高卓林,金向群,等.保肝软胶囊对化学性肝损伤的辅助保护作用[J].特产研究,2019,41(2):62-65.
    [18]
    李谚语,刘丽,范颖,等.保肝汤对小鼠四氯化碳致慢性化学性肝损伤的保护作用[J].天津中医药,2018,35(12):935-938.
    [19]
    Fubini B. Surface reactivity in the Pathogenic response to particulates[J].Environ Health Perspect,1997,105(15):1013-1120.
    [20]
    赵春红,张力,姜淑卿,等. 4种常见残留农药联合作用对小鼠遗传毒性研究[J].职业与健康,2018,34(20):2774-2781.
    [21]
    曾惠芬,戴卫波,欧焕娇.素馨护肝方对ANIT诱导的大鼠胆汁淤积肝损伤的保护作用[J].海南医学,2019,30(13):1633-1638.
    [22]
    Yao P,Nussler A,Liu L,et al. Quercetin protects human hepatocytes from ethanol-derived oxidative stress by inducing heme oxygenase-1 via the MAPK/Nrf2 Pathways[J]. Journal of HePatology,2007,47(2):253-261.
    [23]
    向晓燕,余忠姝,张敏,等.吴茱萸碱复合纳米粒对小鼠急性肝损伤的保护作用[J/OL].中国医院药学杂志:1-5[2020-05-29

    ].http://kns.cnki.net/kcms/detail/42.1204.R.20200508.0905.014.html.
    [24]
    王楠,杜双奎,冯宪超,等.枳椇乳酸菌发酵饮料对小鼠酒精肝损伤的保护作用[J].现代食品科技,2016,32(8):28-33

    ,41.
    [25]
    刘泽鑫,刘畅,钱和.芦荟多糖联合低聚果糖缓解小鼠酒精性肝损伤[J].现代食品科技,2019,35(5):68-74

    ,295.

Catalog

    Article Metrics

    Article views (234) PDF downloads (24) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return