Gut Microbiota and Metabolome Changes in Three Pulmonary Hypertension Rat Models

被引:8
|
作者
Luo, Lingjie [1 ,2 ]
Yin, Haoyang [1 ]
Gou, Deming [1 ]
机构
[1] Shenzhen Univ, Coll Life Sci & Oceanog, Vasc Dis Res Ctr, Shenzhen Key Lab Microbial Genet Engn, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Hlth Sci Ctr, Sch Pharmaceut Sci, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
pulmonary hypertension (PH); gut microbiota; biomarker; metabolites; INTESTINAL MICROBIOTA; FAILURE;
D O I
10.3390/microorganisms11020472
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dysbiosis of the gut microbiota and metabolites is found in both pulmonary hypertension patients and pulmonary hypertension rodent models. However, the exact changes in gut microbiota during the development of pulmonary hypertension is unclear. The function of the gut microbiota is also ambiguous. Here, this study showed that the gut microbiota was disrupted in rats with hypoxia (Hyp)-, hypoxia/Sugen5416 (HySu)-, and monocrotaline (MCT)-induced pulmonary hypertension. The gut microbiota is dynamically changed during the development of Hyp-, HySu-, and MCT-induced rat pulmonary hypertension. The variation in the alpha diversity of the gut microbiota in Hyp-induced pulmonary hypertension rats was similar to that in rats with MCT-induced pulmonary hypertension and different from that in rats with HySu-induced pulmonary hypertension. In addition, six plasma biomarkers, His, Ala, Ser, ADMA, 2-hydroxybutyric acid, and cystathionine, were identified in Hyp-induced pulmonary hypertension rats. Furthermore, a disease-associated network connecting Streptococcus with Hyp-induced pulmonary hypertension-associated metabolites was described here, including trimethylamine N-oxide, Asp, Asn, Lys, His, Ser, Pro, and Ile.
引用
收藏
页数:16
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