基础研究

肠道菌群对高脂饮食诱导肥胖小鼠糖脂代谢紊乱的免疫调节作用

  • 毕馨文 ,
  • 崔远捷 ,
  • 陆秋娴 ,
  • 崔佳 ,
  • 卜凡 ,
  • 何方 ,
  • 杨华 ,
  • 李鸣
展开
  • 1.四川大学华西公共卫生学院/四川大学华西第四医院 (成都 610041 )
    2.宜宾市第二人民医院/四川大学华西医院宜宾医院 (四川 宜宾 644000 )
    3.四川省医学科学院,四川省人民医院(电子科技大学附属医院) (成都 610072 )

收稿日期: 2023-11-24

  网络出版日期: 2024-06-13

基金资助

国家自然科学基金面上项目(82073550)

Immunomodulatory effects of intestinal flora on glucose and lipid metabolism disorders in high⁃fat diet induced obese mice

  • Xinwen BI ,
  • Yuanjie CUI ,
  • Qiuxian LU ,
  • Jia CUI ,
  • Fan BU ,
  • Fang HE ,
  • Hua YANG ,
  • Ming. LI
Expand
  • *.West China School of Public Health and West China Fourth Hospital,Sichuan University,Chengdu 610041,China

Received date: 2023-11-24

  Online published: 2024-06-13

摘要

目的 探讨混合抗生素作用于小鼠肠道菌群从而影响机体免疫调节,探索肠道菌群在肥胖发生发展中的作用,为肥胖防治提供新思路与途径。 方法 72只10周龄C57BL/6雄性小鼠随机分为空白对照(Ctrl)组、高脂喂养(HF)组、抗生素(ABX)组和联合(COMB)组(n = 18)。前2周(灌胃干预周)Ctrl组和HF组采用生理盐水灌胃,ABX组和COMB组采用混合抗生素灌胃,灌胃体积均为0.2 mL/(只·d);后8周(饲料喂养周)Ctrl组和ABX组采用普通饲料喂养,HF组和COMB组采用高脂饲料喂养。每周测量小鼠体质量,灌胃干预周前后、饲料喂养第4、8周测量小鼠空腹血糖;实验结束时进行口服糖耐量实验;测定脏器系数,镜下观察白色和棕色脂肪组织细胞形态,测定血清游离脂肪酸、高密度脂蛋白、低密度脂蛋白、甘油三酯、总胆固醇含量,ELISA法检测血清TNF-α、IL-10、IL-4、IL-13、IL-33、MCP-1含量;小鼠粪便进行二代测序。 结果 高脂饮食引起小鼠体质量增加,血清总胆固醇、低密度脂蛋白、IL-13、IL-33、TNF-α、MCP-1含量增加,糖耐量和脏器系数降低(P < 0.05)。饲喂第1周至实验结束,COMB组体质量低于HF组(P < 0.05)。COMB组较HF组糖耐量、血清总胆固醇、低密度脂蛋白、IL-13、IL-33、TNF-α、MCP-1含量降低(P < 0.05)。HF组白色脂肪组织可见微血管充血出血,脂肪细胞不完整且极度膨胀,细胞质极度压缩;COMB组白色脂肪组织未见充血出血,脂肪细胞较完整。ABX组肠道菌群α多样性低于Ctrl组(P < 0.05);ABX和HF组分别与Ctrl和COMB组微生物群落组成较为相近。 结论 高脂饮食诱导小鼠肥胖、糖脂代谢紊乱和机体炎症,短期混合抗生素使用能够调节小鼠肠道菌群,介导相关抗炎因子表达增加,上调宿主免疫,改善小鼠糖脂代谢。

本文引用格式

毕馨文 , 崔远捷 , 陆秋娴 , 崔佳 , 卜凡 , 何方 , 杨华 , 李鸣 . 肠道菌群对高脂饮食诱导肥胖小鼠糖脂代谢紊乱的免疫调节作用[J]. 实用医学杂志, 2024 , 40(11) : 1505 -1512 . DOI: 10.3969/j.issn.1006-5725.2024.11.007

Abstract

Objective To explore the effect of mixed antibiotics on the intestinal flora of mice to affect the immune regulation of the body, explore the role of intestinal flora in the development of obesity, and provide new ideas and ways for the prevention and treatment of obesity. Methods Seventy-two 10-week-old male C57BL/6 mice were randomly divided into blank control (Ctrl) group, high-fat diet (HF) group, antibiotic (ABX) group, and combined (COMB) group (n = 18). At the first 2 weeks (lavage intervention weeks), Ctrl and HF group were given normal saline gavage; ABX and COMB group were given mixed antibiotics gavage, and the gavage volume was 0.2 mL/ animal/day. For the following 8 weeks (feeding weeks), Ctrl and ABX group were fed with ordinary diet, HF and COMB group were fed with high-fat diet. Body weight was measured weekly, and fasting blood glucose was measured before and after gavage, and at the 4th and 8th week of feeding. Oral glucose tolerance test was performed at the end of the experiment. The organ coefficient was measured and the cell morphology of white and brown adipose tissue was observed. Serum was collected for the determination of free fatty acid, high-density lipoprotein, low-density lipoprotein, triglyceride, and total cholesterol. Serum TNF-α, IL-10, IL-4, IL-13, IL-33 and MCP-1 was detected by ELISA. The stool of mice was collected for second generation sequencing. Results High-fat diet increased body weight, serum total cholesterol, low-density lipoprotein, IL-13, IL-33, TNF-α, MCP-1 content, and decreased glucose tolerance and organ coefficient in mice (P < 0.05). From the first feeding week to the end of the experiment, body weight in COMB group was significantly lower than that in HF group(P < 0.05). The level of glucose tolerance, serum total cholesterol, low density lipoprotein, IL-13, IL-33, TNF-α and MCP-1 in COMB group was lower than those in HF group (P < 0.05). The α diversity of intestinal flora in ABX group was lower than that in Ctrl group (P < 0.05). Congestion and bleeding in WAT were obvious in HF group, but not in COMB group. The microbial community composition of ABX and HF group was similar to that of Ctrl and COMB group, respectively. Conclusion High-fat diet induces obesity, disorder of glucose and lipid metabolism and inflammation in mice. Short-term mixed antibiotic use can regulate the intestinal flora of mice, mediate increased expression of related anti-inflammatory factors, up-regulate host immunity, and improve glucose and lipid metabolism in mice.

参考文献

1 PICHé M E, TCHERNOF A, DESPRéS J P. Obesity phenotypes,diabetes,and cardiovascular diseases[J]. Circ Res,2020,126(11):1477-1500. doi:10.1161/circresaha.120.316101
2 DIAF M, BENCHIKH H, BENNOUR I,et al. The relationship between body mass index, blood pressure, and atherosclerosis risk factors in type 1 and 2 diabetic patients from northwestern Algeria[J]. Endocr Regul,2022,56(3):190-200. doi:10.2478/enr-2022-0020
3 LI G, XIE C, LU S,et al.Intermittent fasting promotes white adipose browning and decreases obesity by shaping the gut microbiota[J]. Cell Metab,2017,26(4):671-685. doi:10.1016/j.cmet.2017.08.019
4 CHEVALIER C,STOJANOVI?O, COLIN D J,et al. Gut microbiota orchestrates energy homeostasis during cold[J].Cell,2015,163(6):1360-1374. doi:10.1016/j.cell.2015.11.004
5 GOU W, LING C W, HE Y,et al. Interpretable machine learning framework reveals robust gut microbiome features associated with type 2 diabetes[J]. Diabetes Care,2021,44(2):358-366. doi:10.2337/dc20-1536
6 STANFORD K I, MIDDELBEEK R J, TOWNSEND K L,et al.Brown adipose tissue regulates glucose homeostasis and insulin sensitivity[J]. J Clin Invest,2013,123(1):215-223. doi:10.1172/jci62308
7 BETZ M J, ENERBACK S. Targeting thermogenesis in brown fat and muscle to treat obesity and metabolic disease[J]. Nat Rev Endocrinol,2018,14:77-87. doi:10.1038/nrendo.2017.132
8 MORENO-NAVARRETE J M, FERNANDEZ-REA J M. The gut microbiota modulates both browning of white adipose tissue and the activity of brown adipose tissue[J]. Rev Endocr Metab disord,2019,20(4):387-397. doi:10.1007/s11154-019-09523-x
9 张雪晴,吴斌. 间歇性禁食对肥胖个体代谢与免疫的影响及作用机制研究进展[J]. 实用医学杂志,2021,37(2):272-276. doi:10.3969/j.issn.1006-5725.2021.02.028
10 LE CHATELIER E, NIELSEN T, QIN J,et al. Richness of human gut microbiome correlates with metabolic markers[J]. Nature,2013;500(7464):541-546.
11 ZHANG X, JIN C, LIU H,et al. Polysaccharide extract from Rosa laevigata fruit attenuates inflammatory obesity by targeting redox balance and gut interface in high-fat diet-fed rats[J]. Food Science and Human Wellness,2023,12(2): 442-453. doi:10.1016/j.fshw.2022.07.046
12 KAWANO Y, EDWARDS M, HUANG Y,et al. Microbiota imbalance induced by dietary sugar disrupts immune-mediated protection from metabolic syndrome[J]. Cell, 2022,185(19):3501-3519.e20. doi:10.1016/j.cell.2022.08.005
13 WAN Y, WANG F, YUAN J,et al. Effects of dietary fat on gut microbiota and faecal metabolites, and their relationship with cardiometabolic risk factors: a 6-month randomised controlled-feeding trial[J]. Gut, 2019,68(8):1417-1429. doi:10.1136/gutjnl-2018-317609
14 SO S Y, WU Q, LEUNG K S,et al. Yeast beta-glucan reduces obesity-associated Bilophila abundance and modulates bile acid metabolism in healthy and high-fat diet mouse models[J]. Am J Physiol Gastrointest Liver Physiol, 2021,321(6):G639-G655. doi:10.1152/ajpgi.00226.2021
15 LUO S, ZHANG H, JIANG X,et al. Antibiotics ad ministration alleviates the high fat diet-induced obesity through altering the lipid metabolism in young mice[J]. Lipids, 2023;58(1):19-32. doi:10.1002/lipd.12361
16 MURUGESAN S, NIRMALKAR K, HOYOVADILLO C,et al. Gut microbiome Production of short-chain fatty acids and obesity in children[J]. Eur J Clin Microbiol Infect Dis, 2018,37(4):621. doi:10.1007/s10096-017-3143-0
17 ASHRAFIAN F, KESHAVARZ AZIZI RAFTAR S, LARI A,et al.Extracellular vesicles and pasteurized cells derived from Akkermansia muciniphila protect against high-fat induced obesity in mice[J]. Microb Cell Fact, 2021,20(1):219. doi:10.1186/s12934-021-01709-w
18 OUYANG J, LIN J, ISNARD S,et al. The Bacterium Akkermansia muciniphila: A Sentinel for Gut Permeability and Its Relevance to HIV-Related Inflammation[J]. Front Immunol, 2020,11:645. doi:10.3389/fimmu.2020.00645
19 GU Z, PEI W, SHEN Y,et al.Akkermansia muciniphila and its outer protein Amuc_1100 regulates tryptophan metabolism in colitis[J]. Food Funct, 2021,12(20):10184-10195. doi:10.1039/d1fo02172a
20 SHI Z, LEI H, CHEN G,et al. Impaired intestinal Akkermansia muciniphila and aryl hydrocarbon receptor ligands contribute to nonalcoholic fatty liver disease in mice[J]. mSystems, 2021,6(1):e00985-20. doi:10.1128/msystems.00985-20
21 VILLARROYA F, CEREIJO R, VILLARROYA J,et al. Toward an Understanding of How Immune Cells Control Brown and Beige Adipobiology[J]. Cell Metab, 2018,27(5):954-961. doi:10.1016/j.cmet.2018.04.006
22 SUáREZ-ZAMORANO N, FABBIANO S, CHEVALIER C,et al.Microbiota depletion Promotes browning of white adipose tissue and reduces obesity[J]. Nat Med, 2015,21(12):1497-1501. doi:10.1038/nm.3994
23 NGUYEN K D, QIU Y, CUI X,et al. Alternatively activated macrophages Produce catechola mines to sustain adaptive thermogenesis[J]. Nature, 2011,480(7375):104-108. doi:10.1038/nature10653
24 RAO R R, LONG J Z, WHITE J P,et al. Meteorin-like is a hormone that regulates immune-adipose interactions to increase beige fat thermogenesis[J]. Cell, 2014,157(6):1279-1291. doi:10.1016/j.cell.2014.03.065
25 FABBIANO S, SUAREZ-ZAMORANO N, RIGO D,et al. Caloric Restriction Leads to Browning of White Adipose Tissue through Type 2 Immune Signaling[J]. Cell Metab, 2016,24(3),434-446. doi:10.1016/j.cmet.2016.07.023
26 GARCIA M C, PAZOS P, LIMA L,et al. Regulation of energy expenditure and brown/beige thermogenic activity by interleukins: New roles for old actors[J]. Int J Mol Sci, 2018,19(9):2569. doi:10.3390/ijms19092569
27 商佳琪,郭宇帆,张梦洁,等. 抗生素处理对高脂饲料诱导肥胖SD大鼠肠道菌群与血清炎性因子的影响[J]. 营养学报, 2021,43(5):498-503. doi:10.3969/j.issn.0512-7955.2021.05.014
28 KWON H, LAURENT S, TANG Y,et al. Adipocyte-Specific IKKbeta Signaling Suppresses Adipose Tissue Inflammation through an IL-13-Dependent Paracrine Feedback Pathway[J]. Cell Rep,2014,9(5):1574-1583. doi:10.1016/j.celrep.2014.10.068
29 CAYROL C, GIRARD J P. Interleukin-33(IL-33): A nuclear cytokine from the IL-1 family[J]. Immunol Rev, 2018,281(1):154-168. doi:10.1111/imr.12619
30 TAKENAGA K, AKIMOTO M, KOSHIKAWA N,et al. Cancer cell-derived interleukin-33 decoy receptor sST2 enhances orthotopic tumor growth in a murine pancreatic cancer model[J]. PLoS One, 2020,15(4):e0232230. doi:10.1371/journal.pone.0232230
31 ZEYDA M, WERNLY B, DEMYANETS S,et al. Severe obesity increases adipose tissue expression of interleukin-33 and its receptor ST2, both Predo minantly detectable in endothelial cells of human adipose tissue[J]. Int J Obes (Lond), 2013,37(5):658-665. doi:10.1038/ijo.2012.118
32 KAI Y, GAO J, LIU H,et al. Effects of IL-33 on 3T3-L1 cells and obese mice models induced by a high-fat diet[J]. Int Immunopharmacol, 2021,101(Pt A):108209. doi:10.1016/j.intimp.2021.108209
33 TANG H, LIU N, FENG X,et al. Circulating levels of IL-33 are elevated by obesity and positively correlated with metabolic disorders in Chinese adults[J]. J Transl Med, 2021,19(1):52. doi:10.1186/s12967-021-02711-x
34 SYARIF, RASYID H, AMAN M,et al. High-fat diet increases the level of circulating Monocyte Chemoattractant Protein-1 in Wistar rats, independent of obesity[J]. Ann Med Surg (Lond), 2021,65:102266. doi:10.1016/j.amsu.2021.102266
35 AHMED B, SULTANA R, GREENE M W. Adipose tissue and insulin resistance in obese[J]. Biomed Pharmacother, 2021,137:111315. doi:10.1016/j.biopha.2021.111315
文章导航

/