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发酵巴戟天中蒽醌提取及其抗氧化与降血糖活性
引用本文:彭东,罗志锋,陶倩,安苗青,朱思阳,黎攀,杜冰. 发酵巴戟天中蒽醌提取及其抗氧化与降血糖活性[J]. 食品工业科技, 2022, 43(7): 214-223. DOI: 10.13386/j.issn1002-0306.2021080091
作者姓名:彭东  罗志锋  陶倩  安苗青  朱思阳  黎攀  杜冰
作者单位:1.华南农业大学食品学院,广东广州 5106422.无限极(中国)有限公司,广东广州 5106233.花安堂生物科技集团有限公司,广东广州 511500
基金项目:财政部和农业农村部:国家现代农业产业技术体系资助(CARS-21);广东省自然科学基金面上项目(2020A151501268);广东省重点领域研发计划项目(2020B020226008)。
摘    要:目的:优化发酵巴戟天蒽醌的提取工艺,并评价其抗氧化和降血糖活性.方法:以蒽醌提取率为指标,通过响应面法确定最佳提取工艺;测定蒽醌对DPPH自由基、OH自由基和超氧阴离子的清除能力来评价体外抗氧化活性;测定蒽醌对线虫寿命和运动能力的影响来评价体内抗氧化活性;测定蒽醌对α-葡萄糖苷酶和α-淀粉酶的抑制率来评价体外降血糖活性...

关 键 词:巴戟天  蒽醌  提取  抗氧化  降血糖  发酵
收稿时间:2021-08-09

Extraction of Anthraquinone from Fermented Morinda officinalis and Its Antioxidant and Hypoglycemic Activities
PENG Dong,LUO Zhifeng,TAO Qian,AN Miaoqing,ZHU Siyang,LI Pan,DU Bing. Extraction of Anthraquinone from Fermented Morinda officinalis and Its Antioxidant and Hypoglycemic Activities[J]. Science and Technology of Food Industry, 2022, 43(7): 214-223. DOI: 10.13386/j.issn1002-0306.2021080091
Authors:PENG Dong  LUO Zhifeng  TAO Qian  AN Miaoqing  ZHU Siyang  LI Pan  DU Bing
Affiliation:1.College of Food Science, South China Agricultural University, Guangzhou 510642, China2.Infinitus(China) Co., Ltd., Guangzhou 510623, China3.Hua An Tang Biological Technology Group Co., Ltd., Guangzhou 511500, China
Abstract:Objective: Optimization of the extraction process of anthraquinone from fermented Morinda officinalis and investigated its antioxidant and hypoglycemic activities. Methods: Taking the extraction ratio of anthraquinone as the evaluation index, the optimal conditions were obtained by response surface methodology. In vitro, the antioxidant activity was evaluated by determining the scavenging ability of anthraquinone against DPPH free radical, hydroxyl free radical and superoxide anion assays. In vivo, the antioxidant activity was evaluated by measuring the effect of anthraquinone on the life span and motility of Caenorhabditis elegans. The hypoglycemic activity in vitro was evaluated by determining the inhibition rate of anthraquinone against alpha-glucosidase and alpha-amylase. The hypoglycemic activity in vivo was evaluated by measuring the effect of anthraquinone on glucose consumption of IR-HepG2 cells. Results: The optimal conditions were obtained as follows: ethanol concentration, 45%; solid-to-solvent ratio, 1:41 (g/mL); temperature, 65 ℃; and time, 1.60 h. Under these conditions, the extraction ratio of anthraquinone was 90.37%. In the antioxidant assay in vitro, anthraquinone exhibited good scavenging ability against DPPH free radicals, hydroxyl free radicals, and superoxide anions. In the antioxidant assay in vivo, anthraquinone significantly prolonged the life span (P<0.05), and enhanced the motility of Caenorhabditis elegans (P<0.05). The IC50 values of anthraquinone on alpha-amylase and alpha-glucosidase were 0.588 and 0.575 mg/mL, respectively. Glucose consumption of IR-HepG2 cells in the anthraquinone group (1.2 mg/mL) was increased by 47.42% compared with the model group. Conclusion: The anthraquinone from fermented Morinda officinalis exhibited good antioxidant and hypoglycemic activities, facilitating the development of natural therapeutic agents for diabetes treatment.
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