食品科学 ›› 2026, Vol. 47 ›› Issue (6): 214-225.doi: 10.7506/spkx1002-6630-20250910-079

• 营养卫生 • 上一篇    

西南手参醇提物通过抗氧化途径延缓秀丽隐杆线虫衰老的机制

陈周雯,任雨敏,唐鲜,聂申明,马丹炜   

  1. (1.四川师范大学生命科学学院,四川 成都 610101;2.九龙县润德中药材科技有限公司,四川 甘孜藏族自治州 626200)
  • 发布日期:2026-04-14
  • 基金资助:
    第四次全国中药资源普查项目(2019PC006);九龙县中藏药资源调查及研究项目(HX20220274)

Mechanism by Which Alcohol Extract from Gymnadenia orchidis Delays Aging in Caenorhabditis elegans via the Antioxidant Pathway

CHEN Zhouwen, REN Yumin, TANG Xian, NIE Shenming, MA Danwei   

  1. (1. College of Life Science, Sichuan Normal University, Chengdu 610101, China; 2. Jiulong County Runde Chinese Herbal Medicine Technology Co., Ltd., Ganzi Tibetan Autonomous Prefecture 626200, China)
  • Published:2026-04-14

摘要: 为了评价西南手参醇提物(alcohol extract from Gymnadenia orchidis,GoAE)的抗衰老活性及其机制,以四川省九龙县产西南手参块茎为材料,研究了不同质量浓度GoAE(0、0.5、1.0、2.0 mg/mL)及其活性成分天麻素(gastrodin,Gas)对N2秀丽隐杆线虫寿命、咽泵频率、摆动能力、体长、体宽和生殖力的影响。以20 μmol/L鱼藤酮(rotenone,RO)构建线粒体氧化损伤线虫模型,应用生理生化技术、荧光显微技术、透射电镜技术和聚合酶链式反应技术研究2.0 mg/mL GoAE干预下氧化损伤线虫抗氧化系统和线粒体数量、形态、膜电位、膜蛋白及其基因表达的变化规律。结果表明:在GoAE和Gas作用下,线虫寿命显著延长,咽泵频率、摆动能力、体长和体宽明显增加(Gas处理组体宽变化不显著),但线虫产卵量变化不大,GoAE的这些效应显著优于Gas;在GoAE干预下,RO诱导产生的过量活性氧和丙二醛含量显著下降,超氧化物歧化酶(superoxide dismutase,SOD)和过氧化氢酶活性显著升高,SOD-3蛋白和热休克蛋白16.2蛋白表达量以及daf-16、sod-1、sod-3、ctl-1和hsp-16.2基因的表达量显著上调。同时,RO诱导的线粒体功能障碍明显改善,线虫体内的线粒体数量增加,线粒体空泡现象减少,膜电位升高,线粒体膜相关基因gas-1、clk-1、isp-1和atp-2表达量以及内、外膜蛋白表达量均升高。线粒体融合基因eat-3、fzo-1和自噬基因unc-51、atg-7、bec-1、Igg-2和vps-34的表达量上调,分裂基因drp-1的表达量下调。上述结果说明,GoAE可通过激活DAF-16/SOD-3抗氧化通路、修复线粒体功能障碍,从而延缓线虫衰老。

关键词: 秀丽隐杆线虫;西南手参醇提物;衰老;抗氧化防御网络;线粒体功能障碍

Abstract: To evaluate the anti-aging activity and mechanism of alcohol extract from Gymnadenia orchidis (GoAE), we prepared GoAE from G. orchidis tubers from Jiulong County, Sichuan Province and investigated the effects of different concentrations of GoAE (0, 0.5, 1.0, and 2.0 mg/mL) and its active component gastrodin (Gas) on the lifespan, pharyngeal pumping rate, locomotion frequency, body size (length and width), and fecundity of Caenorhabditis elegans (strain N2). A nematode model of mitochondrial oxidative damage was established using 20 μmol/L rotenone (RO). Physiological and biochemical techniques, fluorescence microscopy, transmission electron microscopy (TEM), and polymerase chain reaction (PCR) were used to investigate the changes in the antioxidant system, mitochondrial number, morphology, membrane potential, membrane proteins, and related gene expression in oxidatively damaged nematodes following 2.0 mg/mL GoAE intervention. The results showed that GoAE and Gas significantly extended nematode lifespan and markedly increased pharyngeal pumping rate, locomotion frequency, body length, and body width (except for body width in the Gas treatment group), while they minimally affected fecundity; the effects of GoAE were significantly superior to those of Gas. Under GoAE intervention, the excessive levels of reactive oxygen species (ROS) and malondialdehyde (MDA) content induced by RO significantly decreased, superoxide dismutase (SOD) and catalase activities significantly increased, and the expression levels of SOD-3 and heat shock protein (HSP)-16.2, as well as those of the genes daf-16, sod-1, sod-3, ctl-1, and hsp-16.2, were significantly upregulated. Furthermore, RO-induced mitochondrial dysfunction was significantly ameliorated, as evidenced by increased mitochondrial number, decreased mitochondrial vacuolation, increased membrane potential, and upregulated expression levels of mitochondrial membrane-related genes (gas-1, clk-1, isp-1, and atp-2) as well as inner and outer membrane proteins. Additionally, the expression levels of mitochondrial fusion genes (eat-3 and fzo-1) and autophagy genes (unc-51, atg-7, bec-1, lgg-1, and vps-34) were upregulated, while the expression of the fission gene drp-1 was downregulated. These results indicate that the GoAE extract can delay aging in C. elegans by activating the DAF-16/SOD-3 antioxidant pathway and ameliorating mitochondrial dysfunction.

Key words: Caenorhabditis elegans; alcohol extract from Gymnadenia orchidis; aging; antioxidant defense network; mitochondrial dysfunction

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