EFFECTS OF PORTULACA OLERACEA L. POLYSACCHARIDES ON INTESTINAL FLORA STRUCTURE IN AGED RATS

HUANG Xiao-liu, LUO Hui, LONG Shu-jin, JIANG Hui, ZHANG Xing, YAN Hong-yu, HUNAG Yu-shan

Acta Nutrimenta Sinica ›› 2024, Vol. 46 ›› Issue (3) : 276-282.

Acta Nutrimenta Sinica ›› 2024, Vol. 46 ›› Issue (3) : 276-282.
ORIGINAL ARTICLES

EFFECTS OF PORTULACA OLERACEA L. POLYSACCHARIDES ON INTESTINAL FLORA STRUCTURE IN AGED RATS

  • HUANG Xiao-liu1, LUO Hui1, LONG Shu-jin1, JIANG Hui1, ZHANG Xing1, YAN Hong-yu2, HUNAG Yu-shan3
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Abstract

Objective To investigate the effects of Portulaca oleracea polysaccharides (POP) on intestinal flora structure in aged rats. Methods Twenty elderly SD rats (21 months of age) were randomly divided into two groups with ten rats in each group. Control group (Con) rats were fed a normal diet, and intervention group (POP) rats were fed a diet supplemented with 1.0% POPs. All rats were fed for 15 consecutive weeks. At the end of the experiment, high-throughput sequencing technology (16S rRNA) was used to analyze the composition of intestinal flora. Results The results showed that there were 6087 identical operational taxonomic units (OTUs) in the two groups. Con group had 1025 characteristic OTUs, and POP group had 1131 characteristic OTUs. The intestinal flora of the two groups had similar alpha-diversity, but beta-diversity was significantly different between two groups. After ingestion of Portulaca oleracea polysaccharides, the relative abundances of Fusobacteria, Lactobacillus, Ruminiclostridium_9, Intestiniamonas, Faecalibacium, Desulfovibrio, [Bacteroides]_pectinophilus_group and Ruminiclostridium in the intestinal flora of aged rats decreased significantly, while the relative abundances of Parabacteroides, Ruminococcaceae_UCG-005 and Marvinbryantia increased significantly. The ingestion of Portulaca oleracea polysaccharides up-regulated the expression of genes related to cellular processes, metabolism and organismal systems, and down-regulated the expression of genes related to environmental information processing, human disease and genetic information processing in aged rats. Conclusion POP influences the structure of intestinal microflora in aged rats, and the Ruminococcaceae_UCG.005 and Parabacteroides are the main biomarkers.

Key words

Portulaca oleracea L. polysaccharides / intestinal flora / aged rat

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HUANG Xiao-liu, LUO Hui, LONG Shu-jin, JIANG Hui, ZHANG Xing, YAN Hong-yu, HUNAG Yu-shan. EFFECTS OF PORTULACA OLERACEA L. POLYSACCHARIDES ON INTESTINAL FLORA STRUCTURE IN AGED RATS[J]. Acta Nutrimenta Sinica. 2024, 46(3): 276-282

References

[1] Li J, Jia H, Cai X, et al. Meta HITC: An integrated catalog of reference genes in the human gut microbiome[J]. Nat Biotechnol, 2014, 32: 834–841.
[2] 顾燕云,钟焕姿,李俊桦.肠道菌群与代谢疾病[J]. 自然杂志, 2019, 41:431–438.
[3] Mariat D, Firmesse O, Levenez F, et al. The Firmicutes/Bacteroidetes ratio of the human microbiota changes with age[J]. BMC Microbiol, 2009, 9:123.
[4] 冯美江. 肠道微生物与老年相关疾病[J]. 实用老年医学, 2018, 32:401–402.
[5] 周起, 孙亮, 齐海梅, 等. 肠道菌群与老龄健康的研究进展[J]. 中华老年医学杂志, 2018, 37:1428–1432.
[6] Beam A, Clinger E, Hao L.Effect of diet and dietary components on the composition of the gut microbiota[J].Nutrients, 2021,13:2795.
[7] 齐容. 车前子粗多糖胶囊对老年高血压患者肠道微生态环境的影响[D]. 兰州:甘肃中医药大学, 2017.
[8] 吴荣昆, 黄小流, 刘美金, 等. 井冈山马齿苋多糖的体外抗氧化作用及总糖含量测定[J]. 井冈山大学学报(自然科学版), 2016, 37: 102–106.
[9] 梁彦, 吕艳荣. 马齿苋多糖的抗衰老作用[J]. 江苏农业科学, 2014, 42: 270–272.
[10] 陶贵斌, 何慧楠, 李雪惠, 等. 马齿苋多糖体外免疫调节活性研究[J]. 食品研究与开发, 2017, 38: 176–179.
[11] 牛广财, 李世燕, 朱丹, 等. 马齿苋多糖POPⅡ和POPⅢ的抗肿瘤及提高免疫力作用[J]. 食品科学, 2017, 38: 201–205.
[12] 杨阳. 马齿苋多糖改善溃疡性结肠炎小鼠的作用及相关机制研究[D].大庆:黑龙江八一农垦大学,2022.
[13] Fu Q, Zhou SY, Yu MT, et al. Portulaca oleracea polysaccharides modulate intestinal microflora in aged rats in vitro[J]. Front Microbiol, 2022, 13:841397.
[14] 胡新俊, 李春香, 王广, 等. 马齿苋多糖对肠道微生态失调小鼠的调整作用研究[J]. 中国微生态学杂志, 2010, 22:781–783.
[15] 克里斯, 郭建状, 冯澜, 等. 马齿苋多糖对衰老小鼠肠道微生态调节作用的研究[J]. 中国微生态学杂志, 2012, 24:233–235.
[16] Forno E, Onderdonk AB, Mccracken J, et al. Diversity of the gut microbiota and eczema in early life[J]. Clin Mol Allergy, 2008, 6:11.
[17] 孙亦阳, 顾超广, 华小庆, 等. 幼年大鼠和老年大鼠肠道菌群结构及多样性分析[J]. 浙江理工大学学报, 2021, 45:76–83.
[18] 向沁雪, 田瑞, 吴波, 等. 改性豆渣对高脂血症大鼠生理和肠道菌群的影响[J].食品科学,2022,43:180–186.
[19] Ley RE, Turnbaugh PJ, Klein S, et al. Microbial ecology: human gut microbes associated with obesity[J]. Nature 2006,444:1022–1023.
[20] Fu Q, Huang H, Ding AW, et al. Portulaca oleracea polysaccharides reduce serum lipid levels in aging rats by modulating intestinal microbiota and metabolites[J].Front Nutr, 2022, 9:965653.
[21] Fu J, Xu K, Ni X, et al. Habitual dietary fiber intake, fecal microbiota, and hemoglobin A1C level in Chinese patients with type 2 diabetes[J]. Nutrients, 2022, 14:1003.
[22] Li Q, Wu WJ, Chen HJ, et al. In vitro fecal fermentation characteristics of bamboo shoot (Phyllostachys edulis) polysaccharide[J]. Food Chem X, 2021, 11:100129.
[23] Zeng H, Larson KJ, Cheng WH, et al. Advanced liver steatosis accompanies an increase in hepatic inflammation, colonic, secondary bile acids and lactobacillaceae/lachnospiraceae bacteria in C57bl/6 mice fed a high-fat diet[J]. J Nutr Biochem, 2020, 78:108336.
[24] Million M, Maraninchi M, Henry M, et al. Obesity-associated gut microbiota is enriched in lactobacillus reuteri and depleted in bifidobacterium animalis and methanobrevibacter smithii[J]. Int J Obesity, 2012,36:817–825.
[25] Wang K, Liao MF, Zhou N, et al. Parabacteroides distasonis alleviates obesity and metabolic dysfunc-tions via production of succinate and secondary bile acids[J].Cell Rep, 2019, 26:222–235.e5.
[26] Liao RR, Xie XH, Lv YH, et al. Ages of weaning influence the gut microbiota diversity and function in Chongming white goats[J]. Appl Microbiol Biotechnol,2021,105:3649–3658.
[27] Zhao L, Zhang Q, Ma WN, et al. A combination of quercetin and resveratrol reduces obesity in high–fat diet-fed rats by modulation of gut microbiota[J]. Food Funct, 2017, 8:4644–4656.
[28] Vojinovic D, Radjabzadeh D, Kurilshikov A, et al. Relationship between gut microbiota and circulating metabolites in population-based cohorts[J].Nat Commun, 2019, 10:5813.
[29] 随子房. 芦笋汁改善记忆和调节肠道菌群的研究[D]. 无锡:江南大学,2017.
[30] Song XF, Zhong L, Lyu N, et al. Inulin can alleviate metabolism disorders in ob/ob mice by partially restoring leptin-related pathways mediated by gut microbiota[J]. Genomics Proteomics Bioinformatics, 2019,17:64–75.
[31] Qin S, He ZL, Wu YJ, et al. Instant dark tea alleviates hyperlipidaemia in high-fat diet-fed rat: from molecular evidence to redox balance and beyond[J]. Front Nutr,2022,9:819980.
[32] Qi JQ, You T, Li J, et al. Circulating trimethylamine N-oxide and the risk of cardiovascular diseases: a systematic review and meta-analysis of 11 prospective cohort studies[J]. J Cell Mol Med, 2018, 22:185–194.
[33] Yin J, Liao SX, He Y, et al. Dysbiosis of gut microbiota with reduced trimethylamine-N-oxide level in patients with large-artery atherosclerotic stroke or transient ischemic attack[J]. J Am Heart Assoc,2015, 4:e002699.
[34] Verstreken I, Laleman W, Wauters G, et al. Desulfovibrio desulfuricans bacteremia in an immunocompromised host with a liver graft and ulcerative colitis[J].J Clin Microbiol,2012, 50:199–201.
[35] Yan XY, Chen XS, Tian XL, et al. Co-exposure to inorganic arsenic and fluoride prominently disrupts gut microbiota equilibrium and induces adverse cardiova-scular effects in offspring rats[J].Sci Total Environ, 2021,767:144924.
[36] Filippis FD, Pasolli E, Ercolini D, et al. Newly explored faecalibacterium diversity is connected to age, lifestyle, geography, and disease[J]. Curr Biol, 2020,30:4932–4943.
[37] 黄小流, 许东风, 罗辉, 等. 马齿苋多糖对断奶大鼠血清氨基酸代谢谱及肠道菌群影响[J]. 营养学报, 2022, 44:276–283.
[38] 余莉, 李红, 王思平. 基于高通量测序技术研究老年人肠道菌群结构变化[J].胃肠病学, 2019, 24:517–523.

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