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中国精品科技期刊2020
袁蜜,敬磊,陈乐乐,等. 原花青素微胶囊酸奶片对D-gal致衰老小鼠的体内抗氧化作用J. 食品工业科技,2026,47(4):1−12. doi: 10.13386/j.issn1002-0306.2024120411.
引用本文: 袁蜜,敬磊,陈乐乐,等. 原花青素微胶囊酸奶片对D-gal致衰老小鼠的体内抗氧化作用J. 食品工业科技,2026,47(4):1−12. doi: 10.13386/j.issn1002-0306.2024120411.
YUAN Mi, JING Lei, CHEN Lele, et al. In Vivo Antioxidant Effects of Proanthocyanidin Microencapsulated Yogurt Tablets in D-galactose-induced Aging MiceJ. Science and Technology of Food Industry, 2026, 47(4): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024120411.
Citation: YUAN Mi, JING Lei, CHEN Lele, et al. In Vivo Antioxidant Effects of Proanthocyanidin Microencapsulated Yogurt Tablets in D-galactose-induced Aging MiceJ. Science and Technology of Food Industry, 2026, 47(4): 1−12. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024120411.

原花青素微胶囊酸奶片对D-gal致衰老小鼠的体内抗氧化作用

In Vivo Antioxidant Effects of Proanthocyanidin Microencapsulated Yogurt Tablets in D-galactose-induced Aging Mice

  • 摘要: 目的:研制具有抗氧化作用的原花青素微胶囊酸奶片,为原花青素产品的开发提供新的途径。方法:通过单因素实验及响应面优化方法,确定原花青素微胶囊酸奶片的最佳配方,对酸奶片的营养成分及货架期进行测定;通过小鼠跳台实验和避暗实验对小鼠的短时记忆能力进行评价;建立D-半乳糖(D-gal)诱导衰老小鼠模型,分为空白组、模型组、阳性组,美拉德反应高、中、低剂量组,未发生美拉德反应组、原花青素组和未含原花青素组,每组10只,干预42 d后,测定小鼠血清、肝脏及脑组织中谷胱甘肽过氧化物酶(GSH-Px)、总超氧化物歧化酶(T-SOD)活性以及丙二醛(MDA)含量;结合对小鼠肝脏和脑组织的细胞形态观察,综合分析原花青素微胶囊酸奶片对D-gal致衰老模型小鼠的影响。结果:原花青素微胶囊酸奶片的配方为:发酵乳粉70.5%、原花青素微胶囊20.0%、麦芽糊精5.1%、乳粉3.8%、二氧化硅添加量0.6%。发生美拉德反应的原花青素微胶囊酸奶片(ME-MRPs-PC)高剂量组(MH:202.5 mg/10 g)能显著延长衰老小鼠潜伏期,并减少错误次数(P<0.05,P<0.01)。在生理指标方面,MH组小鼠血清的GSH-Px(P<0.01)、SOD活性极显著提高(P<0.01),降低MDA含量(P<0.05,P<0.01)。MH组小鼠肝脏组织少部分细胞出现凋亡、空泡,被炎症细胞浸润,大部分的细胞排列紧密有序;脑组织少部分神经细胞出现空泡,胞核固缩深染,大部分的细胞排列紧密有序。结论:原花青素微胶囊酸奶片具有潜在的抗衰老作用,可能通过改善氧化应激状态和维持生理功能来延缓衰老过程。

     

    Abstract: To develop proanthocyanidin microencapsulated yogurt tablets with antioxidant properties, providing a new avenue for the development of proanthocyanidin-based products. Methods: The optimal formulation of the proanthocyanidin microencapsulated yogurt tablets was determined through single-factor experiments and response surface optimization. The nutritional composition and shelf life of the yogurt tablets were assessed. The short-term memory of mice was evaluated using the step-down test and the dark avoidance test. A D-galactose (D-gal)-induced aging mouse model was established, with groups including the control group, model group, positive control group, high, medium, and low Maillard reaction dose groups, the non-Maillard reaction group, the proanthocyanidin group, and the non-proanthocyanidin group, each consisting of 10 mice. After 42 days of intervention, the activities of glutathione peroxidase (GSH-Px) and total superoxide dismutase (T-SOD), as well as the malondialdehyde (MDA) content in the serum, liver, and brain tissues of the mice, were measured. Additionally, cell morphology of liver and brain tissues was observed, and the effects of proanthocyanidin microencapsulated yogurt tablets on the D-gal-induced aging mouse model were comprehensively analyzed. Results: The optimal formulation of the proanthocyanidin microencapsulated yogurt tablets was found to be as follows: 70.5% fermented milk powder, 20.0% proanthocyanidin microcapsules, 5.1% maltodextrin, 3.8% milk powder, and 0.6% silica. The high-dose Maillard reaction group (MH: 202.5 mg/10 g) of proanthocyanidin microencapsulated yogurt tablets (ME-MRPs-PC) significantly prolonged the latency period of aging mice and reduced error frequency (P<0.05, P<0.01). In terms of physiological indices, the MH group extremely significantly increased serum GSH-Px (P<0.01) and SOD activity (P<0.01), while decreasing MDA levels (P<0.05, P<0.01). In the liver tissue of MH group mice, some cells exhibited apoptosis, vacuolation, and were infiltrated by inflammatory cells, while most cells were tightly and orderly arranged. In brain tissue, some neurons showed vacuolation and nuclear pyknosis and hyperchromasia, while the majority of cells were closely and orderly arranged. Conclusion: Proanthocyanidin microencapsulated yogurt tablets have potential anti-aging effects, likely through improving oxidative stress and maintaining physiological functions to delay the aging process.

     

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