Effects of Exogenous Hydrogen Sulfide on Diabetic Metabolic Disorders in db/db Mice Are Associated With Gut Bacterial and Fungal Microbiota

被引:6
|
作者
Liu, Jian [1 ]
Zhao, Wei [1 ]
Gao, Zi-Wei [1 ]
Liu, Ning [2 ]
Zhang, Wei-Hua [2 ]
Ling, Hong [1 ,3 ,4 ,5 ]
机构
[1] Harbin Med Univ, Dept Microbiol, Harbin, Peoples R China
[2] Harbin Med Univ, Dept Pathophysiol, Harbin, Peoples R China
[3] Harbin Med Univ, Wu Lien Teh Inst, Harbin, Peoples R China
[4] Heilongjiang Prov Key Lab Infect & Immun, Harbin, Peoples R China
[5] Key Lab Pathogen Biol, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
exogenous H2S; type; 2; diabetes; db; db mice; metabolic disorders; gut microbiota; GLUCOSE; OBESITY; PROTECTS; H2S; EXPRESSION; IMPROVE; PATHWAY; INJURY; DIET;
D O I
10.3389/fcimb.2022.801331
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effects of hydrogen sulfide (H2S) on diabetic metabolic disorders are still controversial, and the mechanisms underlying these effects remain largely unknown. This study was conducted to investigate the potential relationship between the gut microbiota and the improvement of diabetic metabolic disorders by exogenous H2S in obese db/db mice. The db/db mice were treated with sodium hydrosulfide (NaHS) (80 mu mol/kg), or vehicle for 16 weeks, respectively. We measured the serum H2S, obesity parameters, glucose homeostasis, and triglyceride. The sequencing of bacterial 16S rRNA gene and fungal internal transcribed spacer (ITS) in the cecal contents of NaHS-treated mice was performed to evaluate the gut microbial communities. We found that supplying exogenous H2S for 16 weeks significantly inhibited the increase of serum triglyceride, blood glucose, and insulin levels and altered specifically the gut bacterial microbiota structure in db/db mice. The relative abundance of some bacterial genera was correlated with the H2S or blood glucose level. Indeed, exogenous H2S increased Firmicutes and decreased Bacteroidetes at the phylum level along with changes of abundance of multifarious genera. Among them, Unclassified_Enterobacteriaceae, Prevotella, and Lactobacillus decreased and Unclassified_Ruminococcaceae, Oscillospira, Ruminococcus, Sutterella, and Desulfovibrio increased. For fungi, exogenous H2S decreased the abundance of Candida and Aspergillus. Here we demonstrated that, in diabetes, microbial dysbiosis may not be just limited to bacteria due to the inter-linked metabolic interactions among bacteria and fungi in the gut. The beneficial effects of exogenous H2S on diabetic metabolic disorders are likely associated with the alterations of specific microbiota.
引用
收藏
页数:13
相关论文
共 50 条
  • [41] Protective effects of Huang-Lian-Jie-Du Decoction on diabetic nephropathy through regulating AGEs/RAGE/Akt/Nrf2 pathway and metabolic profiling in db/db mice
    Tang Dan
    He Wen-Jiao
    Zhang Zhi-Tong
    Shi Jing-Jing
    Wang Xue
    Gu Wen-Ting
    Chen Zhi-Quan
    Xu You-Hua
    Chen Yun-Bo
    Wang Shu-Mei
    PHYTOMEDICINE, 2022, 95
  • [42] ALTERED METABOLIC INCORPORATION OF FUCOSE AND LEUCINE INTO PNS MYELIN OF 25-WEEK-OLD DIABETIC (C57BL/KS(DB/DB)) MICE - EFFECTS OF UNTREATED DIABETES ON NERVE METABOLISM
    CHEZ, MG
    PETERSON, RG
    NEUROCHEMICAL RESEARCH, 1983, 8 (04) : 465 - 472
  • [43] ALTERED METABOLIC INCORPORATION OF FUCOSE AND LEUCINE INTO PNS MYELIN OF 25-WEEK-OLD DIABETIC (C57 BL KS(DB DB)) MICE - EFFECTS OF UNTREATED DIABETES ON NERVE METABOLISM
    CHEZ, MG
    PETERSON, RG
    CLINICAL RESEARCH, 1983, 31 (04): : A810 - A810
  • [44] The differential modulatory effects of Eurotium cristatum on the gut microbiota of obese dogs and mice are associated with improvements in metabolic disturbances
    Lu, Xiaojie
    Jing, Yue
    Li, Yanyi
    Zhang, Naisheng
    Zhang, Wenlong
    Cao, Yongguo
    FOOD & FUNCTION, 2021, 12 (24) : 12812 - 12825
  • [45] SGLT2 inhibitor-empagliflozin treatment ameliorates diabetic retinopathy manifestations and exerts protective effects associated with augmenting branched chain amino acids catabolism and transportation in db/db mice
    Gong, Qiaoyun
    Zhang, Rulin
    Wei, Fang
    Fang, Junwei
    Zhang, Jingfa
    Sun, Jun
    Sun, Qian
    Wang, Haiyan
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 152
  • [46] Ginsenoside Rb1 protects against diabetes-associated metabolic disorders in Kkay mice by reshaping gut microbiota and fecal metabolic profiles
    Zhou, Rongrong
    He, Dan
    Zhang, Haichao
    Xie, Jing
    Zhang, Shuihan
    Tian, Xuefei
    Zeng, Hongliang
    Qin, Yuhui
    Huang, Luqi
    JOURNAL OF ETHNOPHARMACOLOGY, 2023, 303
  • [47] Gut microbiota and short chain fatty acids partially mediate the beneficial effects of inulin on metabolic disorders in obese ob/ob mice
    Guo, Jing
    Zhang, Mengyuan
    Wang, He
    Li, Na
    Lu, Zongliang
    Li, Long
    Hui, Suocheng
    Xu, Hongxia
    JOURNAL OF FOOD BIOCHEMISTRY, 2022, 46 (05)
  • [48] Positive metabolic effects of selected probiotic bacteria on diet-induced obesity in mice are associated with improvement of dysbiotic gut microbiota
    Soundharrajan, Ilavenil
    Kuppusamy, Palaniselvam
    Srisesharam, Srigopalram
    Lee, Jeong Chae
    Sivanesan, Ravikumar
    Kim, Dahye
    Choi, Ki Choon
    FASEB JOURNAL, 2020, 34 (09): : 12289 - 12307
  • [49] Beneficial metabolic effects of selected probiotics on diet-induced obesity and insulin resistance in mice are associated with improvement of dysbiotic gut microbiota
    Alard, Jeanne
    Lehrter, Veronique
    Rhimi, Moez
    Mangin, Irene
    Peucelle, Veronique
    Abraham, Anne-Laure
    Mariadassou, Mahendra
    Maguin, Emmanuelle
    Waligora-Dupriet, Anne-Judith
    Pot, Bruno
    Wolowczuk, Isabelle
    Grangette, Corinne
    ENVIRONMENTAL MICROBIOLOGY, 2016, 18 (05) : 1484 - 1497
  • [50] The dual peroxisome proliferator-activated receptor alpha/delta agonist GFT505 exerts anti-diabetic effects in db/db mice without peroxisome proliferator-activated receptor gamma-associated adverse cardiac effects
    Hanf, Remy
    Millatt, Lesley J.
    Cariou, Bertrand
    Noel, Benoit
    Rigou, Geraldine
    Delataille, Philippe
    Daix, Valerie
    Hum, Dean W.
    Staels, Bart
    DIABETES & VASCULAR DISEASE RESEARCH, 2014, 11 (06): : 440 - 447