研究简报 SHORT COMMUNICATION

酵母β-葡聚糖对脂多糖诱导的绵羊淋巴细胞氧化应激损伤的保护作用

  • 于春微 ,
  • 李冬芳 ,
  • 刘世雄 ,
  • 郝凌魁 ,
  • 高民 ,
  • 胡红莲 ,
  • 刘大程
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  • 1. 内蒙古农业大学兽医学院, 呼和浩特 010018;
    2. 内蒙古农牧业科学院动物营养与饲料研究所, 呼和浩特 010031
于春微(1987-),女,内蒙古赤峰人,博士研究生,从事兽医微生物学与免疫学研究。E-mail:yuchunweicf@163.com

收稿日期: 2019-12-11

  网络出版日期: 2020-06-16

基金资助

国家自然科学基金项目(31260560);现代农业(奶牛)产业技术体系建设专项(CARS-36)

Protective Effects of β-Glucan from Saccharomyces cerevisiae on Lipopolysaccharide Induced Oxidative Stress Injury in Sheep Lymphocyte

  • YU Chunwei ,
  • LI Dongfang ,
  • LIU Shixiong ,
  • HAO Lingkui ,
  • GAO Min ,
  • HU Honglian ,
  • LIU Dacheng
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  • 1. College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China;
    2. Research Institute of Animal Nutrition and Feed, Inner Mongolia Academy of Animal Sciences, Hohhot 010031, China

Received date: 2019-12-11

  Online published: 2020-06-16

摘要

本试验旨在研究酵母β-葡聚糖对绵羊淋巴细胞抗氧化能力的影响。在建立体外脂多糖(LPS)诱导绵羊淋巴细胞氧化应激模型的基础上,通过在培养液中添加不同浓度[0(对照)、5、10、20、50、100 μg/mL]的酵母β-葡聚糖,运用四甲基偶氮唑盐(MTT)比色法测定酵母β-葡聚糖对细胞活性的影响,用生物化学法测定酵母β-葡聚糖对绵羊淋巴细胞抗氧化指标变化的影响。结果表明:0~20 μg/mL酵母β-葡聚糖作用于淋巴细胞,细胞存活率无显著变化(P>0.05),当使用50 μg/mL酵母β-葡聚糖处理淋巴细胞后,细胞存活率显著降低(P<0.05);在LPS作用于淋巴细胞后,与对照组相比较,丙二醛(MDA)含量极显著增多(P<0.01),超氧化物歧化酶(SOD)和氧化氢酶(CAT)活性显著下降(P<0.05),谷胱甘肽过氧化物酶(GSH-Px)活性极显著下降(P<0.01);添加10 μg/mL酵母β-葡聚糖作用6 h后,与LPS组相比较,淋巴细胞内SOD和CAT活性极显著增强(P<0.01),GSH-Px活性显著增强(P<0.05),MDA和ROS含量极显著降低(P<0.01)。综上,LPS可诱导绵羊淋巴细胞氧化应激,酵母β-葡聚糖可抑制LPS诱导的淋巴细胞氧化损伤,对LPS诱导的绵羊淋巴细胞氧化损伤有良好的保护作用,存在剂量依赖效应。

本文引用格式

于春微 , 李冬芳 , 刘世雄 , 郝凌魁 , 高民 , 胡红莲 , 刘大程 . 酵母β-葡聚糖对脂多糖诱导的绵羊淋巴细胞氧化应激损伤的保护作用[J]. 动物营养学报, 2020 , 32(6) : 2904 -2910 . DOI: 10.3969/j.issn.1006-267x.2020.06.051

Abstract

This experiment was conducted to study the effects of β-glucan from Saccharomyces cerevisiae on the antioxidant capacity of sheep lymphocytes. Based on the establishment of lipopolysaccharide (LPS)-induced oxidative stress in sheep lymphocytes, the effects of β-glucan on cell viability were determined by MTT assay by adding different concentrations [0(control), 5, 10, 20, 50 and 100 μg/mL] of β-glucan to the culture medium. The biochemical method was used to determine the effects of β-glucan on the changes of antioxidant indexes in sheep lymphocytes. The results showed as follows: β-glucan showed no cytotoxicity after being applied to lymphocytes at a concentration of 0 to 20 μg/mL, when the concentration of β-glucan was 50 μg/mL, the cell viability decreased significantly (P<0.05); compared with the control group, the malonaldehyde (MDA) content extremely significantly increased (P<0.01), superoxide dismutase (ROS) and catalase (CAT) activities extremely significantly decreased (P<0.05), and glutathion peroxidase (GSH-Px) activity decreased extremely significantly (P<0.01) in lymphocytes treated by LPS. After adding 10 μg/mL β-glucan for 6 h, compared with the LPS group, the activity of SOD and CAT in lymphocytes extremely significantly increased (P<0.01), the activity of GSH-Px significantly increased (P<0.05), and the contents of MDA and ROS extremely significantly decreased (P<0.01). In conclusions, LPS can induce oxidative stress in sheep lymphocytes. β-glucan can inhibit LPS-induced oxidative injury of lymphocytes and has a good protective effect on LPS-induced oxidative injury of sheep lymphocytes, and there is a dose-dependent effect.

参考文献

[1] ENRÍQUEZ D,HÖTZEL M J,UNGERFELD R.Minimising the stress of weaning of beef calves:a review[J].Acta Veterinaria Scandinavica,2011,53:28.
[2] PANDA A K,CHERIAN G.Role of vitamin E in counteracting oxidative stress in poultry[J].The Journal of Poultry Science,2014,51(2):109-117.
[3] 李永义,段绪东,赵娇,等.茶多酚对氧化应激仔猪生长性能和免疫功能的影响[J].中国畜牧杂志,2011,47(15):53-57.
[4] CELI P,DITRANA A,CLAPS S.Effects of plane of nutrition on oxidative stress in goats during the peripartum period[J].The Veterinary Journal,2010,184(1):95-99.  
[5] TSONI S V,BROWN G D.β-glucans and dectin-1[J].Annals of the New York Academy of Sciences,2008,1143(1):45-60.  
[6] SANDVIK A,WANG Y Y,MORTON H C,et al.Oral and systemic administration of β-glucan protects against lipopolysaccharide-induced shock and organ injury in rats[J].Clinical & Experimental Immunology,2010,148(1):168-177.
[7] WILCZAK J,B?ASZCZYK K,KAMOLA D,et al.The effect of low or high molecular weight oat beta-glucans on the inflammatory and oxidative stress status in the colon of rats with LPS-induced enteritis[J].Food & Function,2015,6(2):590-603.  
[8] DHINGRA D,MICHAEL M,RAJPUT H,et al.Dietary fibre in foods:a review[J].Journal of Food Science and Technology,2012,49(3):255-266.  
[9] HA H C,THIAGALINGAM A,NELKIN B D,et al.Reactive oxygen species are critical for the growth and differentiation of medullary thyroid carcinoma cells[J].Clinical Cancer Research,2000,6(9):3783-3787.
[10] MATÉS J M,PÉREZ-GÓMEZ C,DE CASTRO I N,et al.Antioxidant enzymes and human diseases[J].Clinical Biochemistry,1999,32(8):595-603.  
[11] HALLIWELL B,GUTTERIDGE J M C.The importance of free radicals and catalytic metal ions in human diseases[J].Molecular Aspects of Medicine,1985,8(2):89-193.  
[12] HALLIWELL B.Oxidative stress and cancer:have we moved forward?[J].Biochemical Journal,2007,401(1):1-11.  
[13] ANDERSON M E.Glutathione:an overview of biosynthesis and modulation[J].Chemico-Biological Interactions,1998,111-112:1-14.
[14] GRUSE J,KANITZ e,WEITZEL J M,et al.Quercetin feeding in newborn dairy calves cannot compensate colostrum deprivation:study on metabolic,antioxidative and inflammatory traits[J].PLoS One,2016,11(1):e0146932.
[15] SVENSSON C,LINDER A,OLSSON S O.Mortality in swedish dairy calves and replacement heifers[J].Journal of Dairy Science,2006,89(12):4769-4777.  
[16] WINDEYER M C,LESLIE K E,GODDEN S M,et al.Factors associated with morbidity,mortality,and growth of dairy heifer calves up to 3 months of age[J].Preventive Veterinary Medicine,2014,113(2):231-240.  
[17] BATISTA C F,BLAGITZ M G,BERTAGNON H G,et al.Evolution of phagocytic function in monocytes and neutrophils blood cells of healthy calves[J].Journal of Dairy Science,2015,98(12):8882-8888.  
[18] LIU G M,ZHENG J,CAO W,et al.Effects of spermine on liver barrier function,amino acid transporters,immune status,and apoptosis in piglets[J].RSC Advances,2019,9(20):11054-11062.  
[19] HULBERT L E,BALLOU M A.Innate immune responses and health of individually reared Holstein calves after placement into transition-pens 23 d after weaning[J].Journal of Dairy Research,2012,79(3):333-340.  
[20] BACHA U,NASIR M,IQBAL S,et al.Nutraceutical,anti-inflammatory,and immune modulatory effects of β-glucan isolated from yeast[J].Biomed Research International,2017,2017:8972678.
[21] THANNICKAL V J,FANBURG B L.Reactive oxygen species in cell signaling[J].American Journal of Physiology:Lung Cellular and Molecular Physiology,2000,279(6):L1005-L1028.
[22] MONTEIRO H P,STERN A.Redox modulation of tyrosine phosphorylation-dependent signal transduction pathways[J].Free Radical Biology and Medicine,1996,21(3):323-333.  
[23] FREEMAN B A,CRAPO J D.Biology of disease:free radicals and tissue injury[J].Laboratory Investigation,1982,47(5):412-426.
[24] VALKO M,LEIBFRITZ D,MONCOL J,et al.Free radicals and antioxidants in normal physiological functions and human disease[J].The International Journal of Biochemistry & Cell Biology,2007,39(1):44-84.  
[25] GEGOTEK A,SKRZYDLEWSKA E.Biological effect of protein modifications by lipid peroxidation products[J].Chemistry and Physics of Lipids,2019,221:46-52.
[26] KOMOSINSKA-VASSEV K,OLCZYK K,KUCHARZ E J,et al.Free radical activity and antioxidant defense mechanisms in patients with hyperthyroidism due to Graves' disease during therapy[J].Clinica Chimica Acta,2000,300(1/2):107-117.
[27] JAIN S K.The neonatal erythrocyte and its oxidative susceptibility[J].Seminars in Hematology,1989,26(4):286-300.
[28] BERNABUCCI U,RONCHI B,LACETERA N,et al.Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows[J].Journal of Dairy Science,2005,88(6):2017-2026.  
[29] JAIN S K,MCVIE R.Hyperketonemia can increase lipid peroxidation and lower glutathione levels in human erythrocytes in vitro and in type 1 diabetic patients[J].Diabetes,1999,48(9):1850-1855.  
[30] ZHU M,WU S J.The growth performance and nonspecific immunity of loach Paramisgurnus dabryanus as affected by dietary β-1,3-glucan[J].Fish & Shellfish Immunology,2018,83:368-372.
[31] WANG B,YANG C T,DIAO Q Y,et al.The influence of mulberry leaf flavonoids and Candida tropicalis on antioxidant function and gastrointestinal development of preweaning calves challenged with Escherichia coli O141:K99[J].Journal of Dairy Science,2018,101(7):6098-6108.  
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