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日用化学工业(中英文) ›› 2026, Vol. 56 ›› Issue (7): 910-918.doi: 10.3969/j.issn.2097-2806.2026.07.009

• 基础研究 • 上一篇    下一篇

四酶分步法制备蛹虫草多肽及其通过Nrf2通路缓解UVB氧化损伤的研究

潘蕾1,*(),何美玲1,刘冉2,吕景娣3   

  1. 1 濮阳医学高等专科学校河南 濮阳 457000
    2 清丰县妇幼保健院河南 濮阳 457399
    3 河南中医药大学河南 郑州 450046
  • 收稿日期:2026-01-21 修回日期:2026-06-26 出版日期:2026-07-22 发布日期:2026-08-06
  • 基金资助:
    2025年度河南省高校人文社会科学研究一般项目(2025-ZZJH-128)

Sequential four-enzyme hydrolysis of Cordyceps militaris polypeptides: Antioxidant protection via Nrf2/Keap1 pathway in UVB-Irradiated HaCaT cells

Lei Pan1,*(),Meiling He1,Ran Liu2,Jingdi Lv3   

  1. 1 Puyang Medical College, Puyang, Henan 457000, China
    2 Qingfeng County Maternal and Child Health Hospital, Puyang, Henan 457399, China
    3 Henan University of Chinese Medicine, Zhengzhou, Henan 450046, China
  • Received:2026-01-21 Revised:2026-06-26 Online:2026-07-22 Published:2026-08-06
  • Contact: *E-mail: cjw_83@126.com.

摘要:

为了优化基于酶解法的蛹虫草多肽(CMP)制备方法,并进一步揭示蛹虫草多肽的抗氧化活性和机制。本研究以蛹虫草提取虫草素后的剩余物为原料,采用碱提酸沉法提取蛹虫草蛋白,优化了蛹虫草多肽的复合酶解工艺。检测了不同质量浓度蛹虫草多肽及粗蛋白(0.1,0.2,0.5,1.0,2.0,4.0 mg/mL)对DPPH、ABTS和·OH自由基的清除率。另外,将HaCaT细胞分别用0.5,1.0,2.0 mg/mL蛹虫草多肽预处理24 h,然后再用UVB照射24 h后,采用CCK-8法检测细胞活力。DCFH-DA荧光探针法测定细胞内活性氧(ROS)水平。按试剂盒说明书分别检测细胞内SOD、CAT、GSH-Px活性以及MDA含量。采用Western blot测定细胞内Nrf2/Keap1通路活性。结果显示,蜗牛酶+胃蛋白酶+木瓜蛋白酶+碱性蛋白酶复合酶解的蛹虫草多肽指数为84.25%±6.15%,为最佳酶组合。蛹虫草多肽对DPPH、ABTS和·OH自由基的IC50依次为1.67,3.02和1.49 mg/mL。与M组比较,CMP-L/M/H组和VC组的相对细胞活力升高,ROS相对荧光强度降低,SOD、CAT和GSH-Px活性升高,MDA含量降低,Nrf2(细胞核)蛋白水平升高,Keap1蛋白水平降低,且有剂量依赖性(P<0.05)。本研究优化的四酶分步酶解工艺可高效制备蛹虫草多肽,该多肽通过直接清除自由基及激活Nrf2/Keap1通路增强细胞内源性抗氧化能力,从而缓解UVB诱导的HaCaT细胞氧化损伤。

关键词: 蛹虫草, 多肽, 酶解法, 抗氧化活性, Nrf2/Keap1通路

Abstract:

This study aimed to optimize the enzymatic preparation of Cordyceps militaris polypeptides and to elucidate their antioxidant activities and underlying mechanisms. The residual biomass of Cordyceps militaris after cordycepin extraction was ustilized as the raw materials. Cordyceps militaris protein was extracted via alkali extraction-acid precipitation method, followed by the optimization of a multi-enzyme hydrolysis process to produce Cordyceps militaris polypeptides. The scavenging capacities of Cordyceps militaris polypeptides and crude protein against DPPH, ABTS, and ·OH free radicals were determined at different mass concentrations(0.1, 0.2, 0.5, 1.0, 2.0, 4.0 mg/mL). In addition, HaCaT cells were pretreated with 0.5, 1.0, and 2.0 mg/mL of Cordyceps militaris polypeptides for 24 h, followed by UVB irradiation. At 24 h post-UVB irradiation, cell viability was assessed by the CCK-8 assay; intracellular reactive oxygen species(ROS)levels were measured using the DCFH-DA fluorescent probe method; and the activities of SOD, CAT, and GSH-Px, as well as the cellular content of MDA were detected according to the kit instructions. The activity of the intracellular Nrf2/Keap1 pathway was determined by Western blot. The results show that the degree of hydrolysis of Cordyceps militaris hydrolyzed by the sequential combination of snail enzyme + pepsin + papain + alkaline protease is 84.25%±6.15%, which is identified as the optimal enzyme combination. The IC50 values of Cordyceps militaris polypeptides for DPPH, ABTS, and ·OH free radicals are 1.67, 3.02 and 1.49 mg/mL, respectively. Compared with the model group(M), pretreatment with low-, medium-, and high-dose Cordyceps militaris polypeptide groups(CMP-L/M/H)and the vitamin C(VC)group significantly increase relative cell viability, decrease relative ROS fluorescence intensity, enhance the activities of SOD, CAT, and GSH-Px, and reduce MDA content, while upregulating nuclear Nrf2 protein levels and downregulating Keap1 protein levels in a dose-dependent manner(P<0.05). In conclusion, the optimized four-enzyme sequential hydrolysis process developed in this study can efficiently produce Cordyceps militaris polypeptides, which can alleviate UVB-induced oxidative damage in HaCaT cells by directly scavenging free radicals and activating the Nrf2/Keap1 pathway to enhance endogenous antioxidant defenses.

Key words: Cordyceps militaris, polypeptides, enzymatic hydrolysis, antioxidant activity, Nrf2/Keap1 pathway

中图分类号: 

  • TQ658