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中国精品科技期刊2020
范土贵,陈建平,高加龙,等. 姜黄素超分子包合物对乙醇诱导LO2细胞损伤的保护作用[J]. 华体会体育,2021,42(18):366−371. doi: 10.13386/j.issn1002-0306.2020120083.
引用本文: 范土贵,陈建平,高加龙,等. 姜黄素超分子包合物对乙醇诱导LO2细胞损伤的保护作用[J]. 华体会体育,2021,42(18):366−371. doi: 10.13386/j.issn1002-0306.2020120083.
FAN Tugui, CHEN Jianping, GAO Jialong, et al. Protective Effect of Curcumin/Cyclodextrin Polymer Inclusion Complex on LO2 Cells Damaged by Ethanol[J]. Science and Technology of Food Industry, 2021, 42(18): 366−371. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020120083.
Citation: FAN Tugui, CHEN Jianping, GAO Jialong, et al. Protective Effect of Curcumin/Cyclodextrin Polymer Inclusion Complex on LO2 Cells Damaged by Ethanol[J]. Science and Technology of Food Industry, 2021, 42(18): 366−371. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020120083.

姜黄素超分子包合物对乙醇诱导LO2细胞损伤的保护作用

Protective Effect of Curcumin/Cyclodextrin Polymer Inclusion Complex on LO2 Cells Damaged by Ethanol

  • 摘要: 本文考察了姜黄素超分子包合物(Curcumin/Cyclodextrin polymer inclusion complex, CUR/CDP)对乙醇诱导LO2细胞损伤的保护作用。采用MTT法建立乙醇诱导LO2细胞损伤的模型,通过谷氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)、乳酸脱氢酶(LDH)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-PX)、丙二醛(MDA)和活性氧(ROS)等试剂盒考察了CUR/CDP对乙醇诱导LO2细胞损伤的保护效果。结果表明,经CUR/CDP(80 μg/mL)处理后,LO2细胞的存活率从54.75%±8.97%(模型对照组)提高到85.27%±2.64%,且细胞培养液中ALT、AST和LDH活力分别从(26.47±0.90)、(41.02±4.41)、(63.77±4.95)U/L(模型对照组)降低到(16.17±0.42)、(22.62±0.79)、(32.25±1.69)U/L(P<0.01),LO2细胞内GSH-PX、SOD活力分别从(21.82±1.34)、(8.45±1.11)U/mg prot(模型对照组)升高到(36.70±0.56)、(16.47±1.27)U/mg prot,LO2细胞内MDA和ROS含量分别从(1.19±0.15)nmol/mg prot、(198.02%±11.76%)(模型对照组)降低到(0.72±0.05)nmol/mg prot、(110.87%±10.22%)(P<0.01)。综上所述,CUR/CDP通过提高LO2细胞相关抗氧化酶的活力和降低细胞内ROS含量来改善乙醇诱导LO2细胞的损伤。

     

    Abstract: This study investigated the protective effect of curcumin/cyclodextrin polymer inclusion complex(CUR/CDP) on LO2 cells damaged by ethanol. The MTT method was used to establish a model of LO2 cells damaged by ethanol. Glutamate alanine aminotransferase(ALT), aspartate aminotransferase(AST), lactate dehydrogenase(LDH), superoxide dismutase(SOD), glutathione peroxidase(GSH-PX), malondialdehyde(MDA) and reactive oxygen species(ROS) kits were used to investigate the protective effect of CUR/CDP on LO2 cells damaged by ethanol. The results showed that after CUR/CDP (80 μg/mL) treatment, the cell activity of LO2 cells increased from (54.75%±8.97%) (model group) to 85.27%±2.64%, and the activities of ALT, AST, and LDH in the LO2 cell culture medium decreased from (26.47±0.90), (41.02±4.41), (63.77±4.95) U/L (model group) to (16.17±0.42), (22.62±0.79), (32.25±1.69) U/L (P<0.01), respectively; the activities of GSH-PX and SOD in LO2 cells increased from (21.82±1.34), (8.45±1.11) U/mg prot (model group) to (36.70±0.56), (16.47±1.27) U/mg prot; the content of MDA and ROS in LO2 cells decreased from (1.19±0.15) nmol/mg prot, (198.02%±11.76%) (model group) to (0.72±0.05) nmol/mg prot, (110.87%±10.22%) (P<0.01), respectively. In conclusion, CUR/CDP could improve the damage of LO2 cells induced by ethanol by increasing the activity of antioxidant enzymes and reducing the content of ROS.

     

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