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Microbiota Analysis Using Two-step PCR and Next-generation 16S rRNA Gene Sequencing
Published on: October 15, 2019
The Role and Mechanism of Gut Microbiota in Pulmonary Arterial Hypertension
Yi-Hang Chen1,2,3, Wen Yuan2, Liu-Kun Meng4
1Heart Center and Beijing Key Laboratory of Hypertension, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
Abstract:
Pulmonary arterial hypertension (PAH) is a malignant pulmonary vascular disease characterized by increased pulmonary vascular resistance, pulmonary vasoconstriction, and right ventricular hypertrophy. Recent developments in genomics and metabolomics have gradually revealed the roles of the gut microbiota (GM) and its metabolites in cardiovascular diseases. Accumulating evidence reveals that the GM plays important roles in the occurrence and development of PAH. Gut microbiota dysbiosis directly increases the gut permeability, thereby facilitating pathological bacterial translocation and allowing translocation of bacterial products such as lipopolysaccharides from the gut into circulation. This process aggravates pulmonary perivascular inflammation and exacerbates PAH development through the endothelial-mesenchymal transition. Additionally, a shift in the composition of PAH also affects the gut metabolites. Changes in gut metabolites, such as decreased short-chain fatty acids, increased trimethylamine N-oxide, and elevated serotonin, contribute to pulmonary perivascular inflammation and pulmonary vascular remodeling by activating several signaling pathways. Studies of the intestinal microbiota in treating pulmonary hypertension have strengthened linkages between the GM and PAH. Probiotic therapy and fecal microbiota transplantation may supplement existing PAH treatments. In this article, we provide new insight for diagnosing, preventing and treating PAH by adding to the current knowledge of the intestinal flora mechanisms and its metabolites efficacy involved in PAH.
Insights
Gut microbiota dysbiosis contributes to pulmonary arterial hypertension (PAH) by increasing gut permeability and altering metabolites. Therapies targeting the gut microbiome may offer new strategies for treating PAH.
Area of Science:
- Cardiovascular Research
- Microbiome Science
- Pulmonary Hypertension
Background:
- Pulmonary arterial hypertension (PAH) is a severe vascular disease impacting the lungs and heart.
- The gut microbiota (GM) and its metabolites are increasingly recognized for their role in cardiovascular conditions.
- Evidence links GM alterations to the development and progression of PAH.
Purpose of the Study:
- To explore the intricate relationship between gut microbiota, its metabolites, and pulmonary arterial hypertension.
- To elucidate the mechanisms by which GM dysbiosis influences PAH pathogenesis.
- To highlight the potential of microbiome-targeted therapies for PAH treatment.
Main Methods:
- Review of current literature on gut microbiota, metabolites, and PAH.
- Analysis of molecular mechanisms linking gut dysbiosis to pulmonary vascular inflammation and remodeling.
- Examination of emerging therapeutic strategies involving probiotics and fecal microbiota transplantation.
Main Results:
- Gut microbiota dysbiosis increases intestinal permeability, leading to bacterial translocation and inflammation.
- Altered gut metabolites (e.g., reduced SCFAs, increased TMAO, elevated serotonin) promote pulmonary vascular changes.
- GM alterations contribute to endothelial-mesenchymal transition and exacerbate PAH.
Conclusions:
- The gut microbiota and its metabolites are significant factors in PAH development and progression.
- Targeting the gut microbiome presents a promising avenue for novel diagnostic, preventive, and therapeutic approaches to PAH.
- Further research into microbiome-based interventions could revolutionize PAH management.
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