Su Junqing, Effat Khansa, Ding Mengying, Cai Chunyan, Ren Dingxin, Hu Shuxin, Ye Jianzhou, Gao Shan, Niu Weining, Shang Xiaoya
School of Life Sciences, Northwestern Polytechnical University, Xi'an, Shaanxi 710072, P. R. China.
J Agric Food Chem. 2025 Jun 18;73(24):15027-15045. doi: 10.1021/acs.jafc.5c00178. Epub 2025 Jun 6.
Makino, a plant renowned for its dual medicinal and culinary properties, is rich in high-quality phytochemicals with significant therapeutic potential. Polysaccharides represent one of their key bioactive components. This study investigated the mechanism of polysaccharide from Makino (GPMP) in counteracting high-altitude hypoxic stress. Experiment 1 demonstrated that GPMP significantly enhanced hypoxia tolerance and antifatigue capacity in mice ( < 0.05). Experiment 2 established a simulated 6300 m hypobaric hypoxia model, revealing that GPMP intervention (300 mg/kg) ameliorated oxidative stress damage: MDA levels decreased by 44.53%, SOD and GSH-Px activities restored to 73.91% and 91.87% of normal levels, respectively, anti-inflammatory factors IL-10 and TGF-β increased with a 1.33-fold elevation in Bcl-2/Bax ratio, while pro-inflammatory factors IL-1β and TNF-α decreased by 30.06-32.04%. GPMP concurrently improved intestinal barrier integrity (the V/C ratio increased to 1.74-fold of model control) and modulated gut microbiota, reducing the F/B ratio by 3.25-fold while enriching anti-inflammatory and SCFA-producing genera like and , with total cecal SCFA and butyrate elevated by 62.14% and 50.77%, respectively. Mechanistic studies indicated GPMP activates the "microbiota-SCFA-gut barrier" axis through GPR41 and GPR109A activation/HDAC inhibition, regulating the Nrf2 pathway to mitigate oxidative stress, providing theoretical foundations for developing high-altitude functional foods.
牧野(Makino)是一种以兼具药用和食用特性而闻名的植物,富含具有显著治疗潜力的优质植物化学物质。多糖是其关键的生物活性成分之一。本研究调查了牧野多糖(GPMP)对抗高原缺氧应激的机制。实验1表明,GPMP显著增强了小鼠的耐缺氧能力和抗疲劳能力(<0.05)。实验2建立了模拟6300米低压缺氧模型,结果显示GPMP干预(300毫克/千克)减轻了氧化应激损伤:丙二醛(MDA)水平下降了44.53%,超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)活性分别恢复到正常水平的73.91%和91.87%,抗炎因子白细胞介素-10(IL-10)和转化生长因子-β(TGF-β)增加,Bcl-2/Bax比值升高了1.33倍,而促炎因子白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)下降了30.06 - 32.04%。GPMP同时改善了肠道屏障完整性(绒毛高度与隐窝深度比值(V/C比值)增加到模型对照组的1.74倍)并调节了肠道微生物群,使厚壁菌门与拟杆菌门比值(F/B比值)降低了3.25倍,同时富集了如双歧杆菌属和丁酸弧菌属等抗炎和产生短链脂肪酸的菌属,盲肠总短链脂肪酸和丁酸盐分别升高了62.14%和50.77%。机制研究表明,GPMP通过激活GPR41和GPR109A/抑制组蛋白去乙酰化酶(HDAC)来激活“微生物群-短链脂肪酸-肠道屏障”轴,调节核因子E2相关因子2(Nrf2)途径以减轻氧化应激,为开发高原功能性食品提供了理论基础。