• Chinese Core Journal
  • Chinese Science Citation Database (CSCD) Source journal
  • Journal of Citation Report of Chinese S&T Journals (Core Edition)
ZHANG Ziqi, WU Min, LAN Hainan, et al. Astaxanthin alleviates lipopolysaccharide-induced acute liver injury of mice[J]. Journal of South China Agricultural University, 2019, 40(1): 40-45. DOI: 10.7671/j.issn.1001-411X.201805004
Citation: ZHANG Ziqi, WU Min, LAN Hainan, et al. Astaxanthin alleviates lipopolysaccharide-induced acute liver injury of mice[J]. Journal of South China Agricultural University, 2019, 40(1): 40-45. DOI: 10.7671/j.issn.1001-411X.201805004

Astaxanthin alleviates lipopolysaccharide-induced acute liver injury of mice

More Information
  • Received Date: May 05, 2018
  • Available Online: May 17, 2023
  • Objective 

    To investigate the effect of astaxanthin (AST) treatment on acute liver injury induced by lipopolysaccharide (LPS) in mouse.

    Method 

    Forty healthy male ICR mice were randomly allocated into four groups including control group(CK), AST group, LPS group and AST preprotection group (AST+LPS group). Body weight and liver index of mice were recorded. Myeloperoxidase (MPO) level in serum was measured by ELISA. Malondialdehyde (MDA) content and the activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-px) and catalase(CAT) were measured by biochemical methods. The relative mRNA expression levels of antioxidant enzymes including SOD, GSH-Px, CAT and glutamate cysteine ligase catalytic subunit (GCLC) were measured by fluorescence quantitative PCR. HE staining was used to observe the histopathological changes.

    Result 

    The initial weight of mice in each group was 18 g. The final weight was 9−11 g higher than the initial weight, and there was no significant difference among groups(P>0.05). Compared with LPS group, the liver index (0.054), serum MPO level (10.20 ng·mL–1), and MDA content (2.83 μmol·g–1) in liver tissue were significantly reduced in AST+LPS group (P<0.05). Astaxanthin increased the activities of SOD(512.14 U·mg–1), GSH-Px(848.91 U·mg–1) and CAT (61.53 U·mg–1) as well as the relative mRNA expression levels of tested antioxidases. In addition, the damage degree of liver in AST+LPS group was low, and hepatocyte structure was perfectly aligned.

    Conclusion 

    Astaxanthin treatment can protect the morphology of hepatocyte, increase antioxidant level and the mRNA expression of antioxidase in liver, and thereby relive liver oxidative stress and alleviate LPS-induced acute liver injury in mice.

  • [1]
    LI S, TAN H Y, WANG N, et al. The role of oxidative stress and antioxidants in liver diseases[J]. Int J Mol Sci, 2015, 16(11): 26087-26124.
    [2]
    冉茂良, 高环, 尹杰. 氧化应激与DNA损伤[J]. 动物营养学报, 2013, 25(10): 2238-2245. doi: 10.3969/j.issn.1006-267x.2013.10.007
    [3]
    SINGAL A K, JAMPANA S C, WEINMAN S A. Antioxidants as therapeutic agents for liver disease[J]. LiverInt, 2011, 31(10): 1432-1448.
    [4]
    DEY A, LAKSHMANAN J. The role of antioxidants and other agents in alleviating hyperglycemia mediated oxidative stress and injury in liver[J]. Food Funct, 2013, 4(8): 1148-1184.
    [5]
    ESREFOGLU M. Oxidative stress and benefits of antioxidant agents in acute and chronic hepatitis[J]. Hepat Mon, 2012, 12(3): 160-167. doi: 10.5812/hepatmon
    [6]
    FASSETT R G, COOMBES J S. Astaxanthin: A potential therapeutic agent in cardiovascular disease[J]. Mar Drugs, 2011, 9(3): 447-465. doi: 10.3390/md9030447
    [7]
    PARK J S, CHYUN J H, KIM Y K, et al. Astaxanthin decreased oxidative stress and inflammation and enhanced immune response in humans[J]. Nutr Metab, 2010, 7: 18. doi: 10.1186/1743-7075-7-18.
    [8]
    STEWART J S, LIGNELLÅ, PETTERSSON A, et al. Safety assessment of astaxanthin-rich microalgae biomass: Acute and subchronic toxicity studies in rats[J]. Food Chem Toxicol, 2008, 46(9): 3030-3036.
    [9]
    RAO A R, BASKARAN V, SARADA R, et al. In vivo bioavailability and antioxidant activity of carotenoids from microalgal biomass: A repeated dose study[J]. Food Res Int, 2013, 54(1): 711-717. doi: 10.1016/j.foodres.2013.07.067
    [10]
    ADEREM A, ULEVITCH R J. Toll-like receptors in the induction of the innate immune response[J]. Nature, 2000, 406(6797): 782-787. doi: 10.1038/35021228
    [11]
    REUTER S, GUPTA S C, CHATURVEDI M M, et al. Oxidative stress, inflammation, and cancer: How are they linked?[J]. Free Radical Bio Med, 2010, 49(11): 1603-1616. doi: 10.1016/j.freeradbiomed.2010.09.006
    [12]
    KANCZKOWSKI W, CHATZIGEORGIOU A, SAMUS M, et al. Characterization of the LPS-induced inflammation of the adrenal gland in mice[J]. Mol Cell Endocrinol, 2013, 371(1/2): 228-235.
    [13]
    LOVE D, BARRETT T, HAWKINS C. Role of the myeloperoxidase oxidant hypothiocyanous acid (HOSCN) in the adaption of cells to oxidative stress during inflammation[J]. Free Radical Bio Med, 2017, 108: S30. doi: 10.1016/j.freeradbiomed.2017.04.123.
    [14]
    FRIJHOFF J, WINYARD P G, ZARKOVIC N, et al. Clinical relevance of biomarkers of oxidative stress[J]. Antioxid Redox Signal, 2015, 23(14): 1144-1170. doi: 10.1089/ars.2015.6317
    [15]
    MCCORD J M. The evolution of free radicals and oxidative stress[J]. Am J Med, 2000, 108(8): 652-659. doi: 10.1016/S0002-9343(00)00412-5
    [16]
    KLAASSEN C D, REISMAN S A. Nrf2 the rescue: Effects of the antioxidative/electrophilic response on the liver[J]. Toxicol Appl Pharmacol, 2010, 244(1): 57-65.
    [17]
    高婷, 王子旭, 陈祝茗. ROS介导的氧化应激与自噬[J]. 中国畜牧兽医, 2018, 45(3): 656-662.
    [18]
    CICHOŻ-LACH H, MICHALAK A. Oxidative stress as a crucial factor in liver diseases[J]. World J Gastroenterol, 2014, 20(25): 8082-8091. doi: 10.3748/wjg.v20.i25.8082
    [19]
    DALTON T P, DIETER M Z, YANG Y, et al. Knockout of the mouse glutamate cysteine ligase catalytic subunit (Gclc) gene: Embryonic lethal when homozygous, and proposed model for moderate glutathione deficiency when heterozygous[J]. Biochem Biophys Res Commun, 2000, 279(2): 324-329. doi: 10.1006/bbrc.2000.3930
    [20]
    URSO M L, CLARKSON P M. Oxidative stress, exercise, and antioxidant supplementation[J]. Toxicology, 2003, 189(1/2): 41-54.
    [21]
    ZHOU L, GAO M, XIAO Z, et al. Protective effect of astaxanthin against multiple organ injury in a rat model of sepsis[J]. J Surg Res, 2015, 195(2): 559-567. doi: 10.1016/j.jss.2015.02.026
  • Cited by

    Periodical cited type(8)

    1. 彭俊杰,汪泓,王宇,肖玖军,李可相,邢丹. 基于GA-PLS-SPA的辣椒叶片叶绿素含量高光谱估测. 江苏农业科学. 2024(07): 184-192 .
    2. 田婷,张青,徐雯. 光谱技术在作物养分监测中的应用研究进展. 江苏农业科学. 2024(14): 31-39 .
    3. 魏萱,蒋一凡,蔡玥乐,周子滨,赵艳茹,邹金平,叶大鹏. 农业无人机高光谱成像遥感研究现状和进展. 中国农业信息. 2024(04): 27-46 .
    4. 何爽,张森,田家,卢霞. 结合多模态数据的滨海湿地碱蓬叶面积指数无人机高光谱反演. 遥感学报. 2023(06): 1441-1453 .
    5. 马子媛,李海莲,蔺望东. 基于PCA-IPSO-RBF神经网络的沥青路面破损状况预测. 大连理工大学学报. 2022(02): 197-205 .
    6. 彭晓伟,张爱军,杨晓楠,王楠,赵丽. 谷子叶绿素含量高光谱特征分析及其反演模型构建. 干旱地区农业研究. 2022(02): 69-77 .
    7. 杨光远,韩磊,邓少鹏,刘强,王闻. 卷烟滤棒中三醋酸甘油酯含量的现场快速检测研究. 分析测试学报. 2022(05): 792-796 .
    8. 江凯伦,安吉庆,赵雨薇,罗俊盈,曹英丽. 采用RNCA-PSO-ELM的水稻叶绿素光谱特征分析与反演. 农业工程学报. 2022(08): 178-186 .

    Other cited types(15)

Catalog

    Article views (1369) PDF downloads (1124) Cited by(23)

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return