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中国精品科技期刊2020
南婷婷, 许东霞, 王余宸铭, 杨丽, 史璐, 郑义. 蝉花孢子粉多糖的酶辅助提取及其对酒精性肝损伤小鼠的保护作用[J]. 食品工业科技, 2021, 42(2): 295-301,309. DOI: 10.13386/j.issn1002-0306.2020010123
引用本文: 南婷婷, 许东霞, 王余宸铭, 杨丽, 史璐, 郑义. 蝉花孢子粉多糖的酶辅助提取及其对酒精性肝损伤小鼠的保护作用[J]. 食品工业科技, 2021, 42(2): 295-301,309. DOI: 10.13386/j.issn1002-0306.2020010123
NAN Tingting, XU Dongxia, WANG Yuchenming, YANG Li, SHI Lu, ZHENG Yi. Enzyme-assisted Extraction of Polysaccharides from Cordyceps cicadae Spores and Its Hepatoprotective Effect against Alcohol-induced Liver Injury in Mice[J]. Science and Technology of Food Industry, 2021, 42(2): 295-301,309. DOI: 10.13386/j.issn1002-0306.2020010123
Citation: NAN Tingting, XU Dongxia, WANG Yuchenming, YANG Li, SHI Lu, ZHENG Yi. Enzyme-assisted Extraction of Polysaccharides from Cordyceps cicadae Spores and Its Hepatoprotective Effect against Alcohol-induced Liver Injury in Mice[J]. Science and Technology of Food Industry, 2021, 42(2): 295-301,309. DOI: 10.13386/j.issn1002-0306.2020010123

蝉花孢子粉多糖的酶辅助提取及其对酒精性肝损伤小鼠的保护作用

Enzyme-assisted Extraction of Polysaccharides from Cordyceps cicadae Spores and Its Hepatoprotective Effect against Alcohol-induced Liver Injury in Mice

  • 摘要: 采用响应面法优化纤维素酶辅助提取蝉花孢子粉多糖的工艺参数,并以急性酒精性肝损伤小鼠为模型,评价蝉花孢子粉多糖的保肝作用。小鼠随机分为正常组、模型组、阳性对照组(150 mg/kg水飞蓟宾)和蝉花孢子粉多糖低、中、高剂量组(50、100和200 mg/kg),各组预防给药20 d,第21 d灌胃50%乙醇(12 mL/kg),每隔12 h一次,连续3次,测定小鼠血清中谷丙转氨酶(ALT)和天冬氨酸氨基转移酶(AST)活性,肝组织中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)活性和丙二醛(MDA)含量。结果表明,酶辅助提取蝉花孢子粉多糖的最佳工艺条件为液料比35 mL/g,纤维素酶用量0.64%、酶解时间80 min、酶解pH6.0、酶解温度50℃,在此条件下蝉花孢子粉多糖得率为7.46%±0.12%(n=3)。蝉花孢子粉多糖能显著(P<0.05)降低酒精性肝损伤小鼠的血清丙氨酸氨基转移酶和天冬氨酸氨基转移酶水平,提高小鼠肝脏超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性,降低丙二醛含量(P<0.05)。蝉花孢子粉多糖可通过抗氧化活性发挥其对酒精性肝损伤小鼠的保护作用。

     

    Abstract: Enzyme-assisted extraction of polysaccharides from Cordyceps cicadae(CCSP)spores was optimized by response surface methodology. Hepatoprotective effects of CCSP were evaluated by alcohol-induced liver injury model mice. The mice were randomly divided into six groups,including normal group,model group,positive group(silibinin,150 mg/kg)and CCSP groups(50,100 and 200 mg/kg). All the groups of mice were intragastrically administered for 20 days. At the 21st day,all the groups except the normal were intragastrically administered with 12 mL/kg of 50% alcohol every twelve hours for three times. Activities of serum ALT and AST and levels of liver SOD,CAT,GSH-Px and MDA were estimated by reagent kits. The results showed that the optimal enzyme-assisted extraction parameters were indicated as below:Ratio of water to raw material 35 mL/g,cellulase amount 0.64%,enzymolysis pH6.0,enzymolysis time 80 min and enzymolysis temperature 50 ℃. Under this condition,the yield of CCSP was 7.46%±0.12%(n=3). Pre-treatment with CCSP effectively increased the liver index and spleen index in alcohol-treated mice. The elevated serum alanine aminotransferase and aspartate aminotransferase activities of mice after alcohol exposure were inhibited by CCSP administration. Furthermore,pre-treatment with CCSP could efficiently boost the superoxidase dismutase,catalase,and glutathione peroxidase activities,and observably constrain the malondialdehyde level(P<0.05). The findings suggestted that CCSP would be useful for alleviating the alcohol-induced hepatotoxicity via its antioxidant potential.

     

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