Lipid- and gut microbiota-modulating effects of graphene oxide nanoparticles in high-fat diet-induced hyperlipidemic mice

被引:20
|
作者
Li, Juan [1 ]
Yang, Shengmei [1 ]
Yu, Jiaqi [3 ,4 ]
Cui, Rongli [1 ]
Liu, Ru [1 ]
Lei, Runhong [1 ]
Chang, Yanan [1 ]
Geng, Huan [1 ]
Qin, Yanxia [1 ]
Gu, Weihong [1 ]
Xia, Shibo [1 ]
Chen, Kui [1 ]
Kong, Jianglong [1 ]
Chen, Guogang [2 ]
Wu, Chongming [3 ,4 ]
Xing, Gengmei [1 ]
机构
[1] Chinese Acad Sci, Inst High Energy Phys, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100049, Peoples R China
[2] Shihezi Univ, Coll Food Sci, Shihezi 832000, Peoples R China
[3] Chinese Acad Med Sci, Inst Med Plant Dev, Pharmacol & Toxicol Res Ctr, Beijing 100193, Peoples R China
[4] Peking Union Med Coll, Beijing 100193, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
ANTIMICROBIAL ACTIVITY; EFFICIENT REMOVAL; NANOCOMPOSITE; MEMBRANES; POLYMER; NANOSHEETS; NANOTUBES; TOXICITY; IMPACT; ACID;
D O I
10.1039/c8ra06058d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene oxide (GO) suspensions can act as a good dispersant and drug delivery system for effective dispersion and drug sustained release. In this study, we investigated the impact of GO on blood/liver lipids and gut microbiota structure in high-fat diet (HFD)-induced hyperlipidemic mice. Oral administration of GO for 28 days remarkably decreased the lipid levels in blood and liver. GO did not decrease the total number of gut bacteria but increased the relative abundance of short-chain fatty acid (SCFA)-producing bacteria such as Clostridium clusters IV and Allobaculum spp. GO also enhanced the copying of bacterial butyryl coenzyme A transferase (BcoA), a key butyrate-producing gene. Although further pharmacological studies are still needed, these results provided an interesting hint that GO may exert beneficial effects on the host's metabolism via selective modulation of SCFA-producing gut microbes.
引用
收藏
页码:31366 / 31371
页数:6
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