研究报告

基于高通量测序分析黄酒对D-半乳糖致衰老小鼠模型肠道微生物菌群的影响

  • 刘蓉 ,
  • 栾春光 ,
  • 王德良 ,
  • 覃思 ,
  • 郝飞克
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  • 1 (湖南农业大学 食品科学技术学院,湖南 长沙,410128)
    2 (中国食品发酵工业研究院有限公司,北京,100015)
    3 (酒类品质与安全国际联合研究中心,北京,100015)
硕士研究生(覃思副教授和郝飞克高级工程师为共同通讯作者,E-mail:qinsiman@hunau.edu.cn,haofeike@outlook.com)。

收稿日期: 2019-09-10

  网络出版日期: 2020-03-13

Effect of Yellow rice wine on intestinal microorganism in D-galactose induced aging mice based on high-throughput sequencing analysis

  • LIU Rong ,
  • LUAN Chunguang ,
  • WANG Deliang ,
  • QIN Si ,
  • HAO Feike
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  • 1 (College of Food Science and Technology, Hunan Agricultural University, Changsha 410128, China)
    2 (China National Research Institute of Food and Fermentation Industries Co., Ltd., Beijing 100015, China)
    3 (International Joint Research Center of Quality and Safety of Alcoholic Beverages, Beijing 100015, China)

Received date: 2019-09-10

  Online published: 2020-03-13

摘要

该文用D-半乳糖(D-galactose,D-gal)颈脊皮下注射建立衰老小鼠模型,评价黄酒对衰老小鼠模型肠道菌群结构的影响。通过设立空白对照、模型组、黄酒组,6周后测定其抗氧化酶活力,同时采用Morris水迷宫对小鼠的认知能力进行测试。收集小鼠粪便,利用IonS5TMXL高通量测序平台对肠道细菌16S rDNA基因进行测序,探索黄酒摄入对衰老小鼠肠道微生物菌群的影响。结果表明,D-gal致衰老小鼠模型的抗氧化相关酶活性明显降低,丙二醛(malondialdehyde,MDA)水平显著增高(P<0.05);黄酒干预后,各剂量组小鼠体内多种抗氧化酶活性升高,MDA含量显著下降(P<0.05);在行为学实验中,适量黄酒干预能够显著提高D-gal致衰老小鼠的认知能力(P<0.05);高通量测序发现黄酒干预显著改善了D-gal致衰老小鼠的肠道菌群结构;进一步分析菌群组成发现,黄酒显著改善了衰老小鼠模型的Firmicutes和Bacteroidetes的相对丰度(P<0.05),显著提升了Bacteroides、Lactobacillus、Bifidobacterium、Lachnospiracea和Butyricicoccus的相对丰度(P<0.05)。适量黄酒摄入可一定程度上改善衰老所致的肠道菌群结构失衡现象,有助于延缓衰老。

本文引用格式

刘蓉 , 栾春光 , 王德良 , 覃思 , 郝飞克 . 基于高通量测序分析黄酒对D-半乳糖致衰老小鼠模型肠道微生物菌群的影响[J]. 食品与发酵工业, 2020 , 46(2) : 32 -39 . DOI: 10.13995/j.cnki.11-1802/ts.022229

Abstract

The objective of the study is to investigate the effects of Yellow rice wine (YRW) on intestinal microbiota in D-galactose (D-gal) induced aging mice model. The aging model were established with D-gal injection. Fifty Kunming mice were randomly and equally divided into control group, aging model group (model), YRW group. After six weeks, the antioxidant enzyme activity and the content of malondialdehyde (MDA) in the liver and brain of mice were determined. Morris water maze (MWM) was used to test the learning and memory ability of mice in each group. High-throughput sequencing of the 16S rDNA gene of the intestinal flora was performed using an IonS5TMXL platform to explore the effects of YRW of intestinal flora in aging mice. The results showed that the antioxidant enzyme was significantly reduced in liver and brain of D-gal induced aging mice, and MDA contents were increased significantly compare to control group (P & lt;0.05). After the intervention with YRW, the activity of antioxidant enzymes and MDA contents were improved compare to model (P & lt;0.05). Meanwhile, MWM test showed that moderate administration of YRW could significantly improve the cognitive impairment in D-gal induced aging mice (P & lt;0.05). Compared with the control, the relative abundance of Firmicutes and Bacteroidetes were changed significantly in the model group. Compared with the model group, the relative abundance of Firmicutes and Bacteroidetes were improved in the YRW group (P & lt;0.05). At genus level, the proportion of Bacteroide in the aging group was decreased significantly, and the proportions of the Bacteroide, Lactobacillus, Lachnospiracea, Butyricicoccus in YRW group were increased significantly. Moderate intake of YRW could improve the intestinal environment disorder in D-gal induced aging mice, thereby delaying the aging process.

参考文献

[1] GOTO M,IWAKI-EGAWAS,WATANABEY.Ageing in werner syndrome[J].Bioscience Trends,2012,6(1):33-37.
[2] CEVENINI E,CARUSO C,CANDORE G,et al.Age-related inflammation:The contribution of different organs, tissues and systems. How to face it for therapeutic approaches [J].Curr Pharm Des,2010,16(6):609-618.
[3] SCHIFFRIN E J,MORLEY J E, DONNET-HUGHES A, et al.The inflammatory status of the elderly:The intestinal contribution[J].Mutation Research/Fundamental & Molecular Mechanisms of Mutagenesis,2010,690(1-2):50-56.
[4] XU L Q,XIE Y L,GUI S H,et al.Polydatin attenuates D-galactose-induced liver and brain damage through its anti-oxidative, anti-inflammatory and anti-apoptotic effects in mice[J].Food Funct,2016,7(11):4 545-4 555.
[5] VONMARTELS J Z H,SADABAD M S,BOURGONJE A R,et al.The role of gut microbiota in health and disease:In vitro modeling of host-microbe interactions at the aerobe-anaerobe interphase of the human gut[J].Anaerobe,2017,44(3):3-12.
[6] CHASSARD C,LACROIX C.Carbohydrates and the human gut microbiota[J].Curr Opin Clin Nutr Metab Care,2013,16(4): 453-460.
[7] VAISERMAN A M,KOLIADA A K,MAROTTA F.Gut microbiota:A player in aging and a target for anti-aging intervention[J].Ageing Research Reviews,2017,35:36-45.
[8] DENG,LI Y, ZHAO J.The gut microbiome of healthy long-living people[J].Aging(Albany NY)2019,11(2):289-290.
[9] BISCHOFF S C.Microbiota and aging[J].Current Opinion in Clinical Nutrition & Metabolic Care,2016,19(1):26-30.
[10] 訾雨歌,徐越,肖瀛,等.原花青素B2对D-半乳糖模型小鼠肠道菌群的影响[J].食品科学, 2019,40(9):146-151.
[11] ZHAO J,TIAN F,YAN S,et al.Lactobacillus plantarum CCFM10 alleviating oxidative stress and restoring the gut microbiota in D-galactose-induced aging mice[J].Food & Function,2018,9(2):917-924.
[12] SALAZAR N,VALD & #xC9;S-VARELA L,GONZ & #xC1;LEZ S,et al.Nutrition and the gut microbiome in the elderly[J].Gut Microbes,2017,8(2):82-97.
[13] 罗铝铿,邹浩元,姚海荣,等.客家黄酒延缓皮肤衰老作用的研究[J].酿酒科技,2017(3):121-123.
[14] ZHAO P,WANG J,ZHAO W,et al.Antifatigue and antiaging effects of Chinese rice wine in mice[J].Food Science & Nutrition,2018,6(8):2 386-2 394.
[15] 张元,白卫东,刘功良.黄酒生物活性成分及其功能研究进展[J].中国酿造,2017,36(7):5-9.
[16] 王家林,张颖,于秦峰.黄酒中生物活性成分的探讨[J].酿酒科技,2011(7):47-50.
[17] 王璟,秦雪,仝令印,等.黄酒对小鼠抗疲劳能力和衰老小鼠免疫器官的影响[J].食品科学,2016,37(21):224-228.
[18] SHIN H Y,PARK S J,SEO S W,et al.Gamibojungikki-tang decreases immobility time on the forced swimming test and increases interferon-γ production from MOLT-4 cells[J].Journal of Ethnopharmacology,2005,102(1):113-119.
[19] ZHAO H,LI J,ZHAO J,et al.Antioxidant effects of compound walnut oil capsule in mice aging model induced by D-galactose[J].Food & Nutrition Research,2018:62.
[20] ZHANG H,LI Y,CUI C,et al.Modulation of gut microbiota by dietary supplementation with tuna oil and algae oil alleviates the effects of D-galactose-induced ageing[J].Applied Microbiology & Biotechnology,2018,102(6):2 791-2 801.
[21] VIGNERON A,VOUSDEN K H.p53,ROS and senescence in the control of aging[J].Aging (Hbany NY),2010,2(8):471-474.
[22] HARRAAN D.Aging:A theory based on free radical and radiation chemistry[J].J Gerontol,1956,11(3):298-300.
[23] FORMAN H J.Redox signaling: An evolution from free radicals to aging[J].Free Radic Biol Med,2016,97:387-407.
[24] CONG X,HENDERSON W A,GRAF J,et al.Early life experience and gut microbiome:The brain-gut-microbiota signaling system[J].Advances in Neonatal Care Official Journal of the National Association of Neonatal Nurses,2015,15(5):314.
[25] SUDO N,CHIDA Y,AIBA Y.Gut feelings:the emerging biology of gut-brain communication[J].Nature Reviews Neuroscience,2011,12(8):453-466.
[26] SUDO N,CHIDA Y,AIBA,et al.Postnatal microbial colonization programs the hypothalamic-pituitary-adrenal system for stress response in mice[J].J Physiol,2010,558(1):263-75.
[27] LANCTO T K L,HERMANN N,MAZZOTTAP M,et al.GABAergic function in Alzheimer's disease: Evidence for dysfunction and potential as a therapeutic target for the treatment of behavioural and psychological symptoms of dementia[J].Canadian Journal of Psychiatry Revue Canadienne De Psychiatrie,2004,49(7):439-453.
[28] MCKERNAN R M,WHITING P J.Which GABA A -receptor subtypes really occur in the brain?[J].Trends in Neurosciences,1996,19(4):139-143.
[29] OHSAWA K,UCHIDA N,OHKI K,et al.Lactobacillus helveticus-fermented milk improves learning and memory in mice[J].Nutritional neuroscience,2015,18(5):232-240.
[30] MESSAOUDI M,LALONDE R,VIOLLE N,et al.Assessment of psychotropic-like properties of a probiotic formulation (Lactobacillus helveticus R0052 and Bifidobacterium longum R0175) in rats and human subjects[J].British Journal of Nutrition,2011,105(5):755-764.
[31] ARUMUGAM M,RAES J,PELLETIER E,et al.Addendum:Enterotypes of the human gut microbiome[J].Nature,2011,473(7 346):174.
[32] MARTIN B,MATTSON M P,MAUDSLEY S.Caloric restriction and intermittent fasting:Two potential diets for successful brain aging[J].Ageing Research Reviews,2006,5(3):332-353.
[33] ZHANG J,GOO Z,XUE Z,et al.A phylo-functional core of gut microbiota in healthy young Chinese cohorts across lifestyles,geography and ethnicities[J].Isme Journal Multidisciplinary Journal of Microbial Ecology,2015,9(9):1 979-1 990.
[34] WANG T,CAI G,QIU Y,et al.Structural segregation of gut microbiota between colorectal cancer patients and healthy volunteers[J].The ISME Journal,2012,6(2):320-329.
[35] DEN BESTEN G,VAN EUNEN N,et al.The role of short-chain fatty acids in the interplay between diet,gut microbiota,and host energy metabolism[J].Journal of Lipid Research,2013,54(9):2 325-2 340.
[36] SALONEN A,LAHTI L,SALOJ & #xC3;RVI J,et al.Impact of diet and individual variation on intestinal microbiota composition and fermentation products in obese men[J].The ISME Journal,2014,8(11):2 218-2 230.
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