Cargando…

Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats

BACKGROUND: The brain development of preterm infants is easily affected by various adverse extrauterine factors and complications, resulting in abnormal neurological and cognitive development. Recent studies have found that there is a significant correlation between intestinal microbial changes and...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Xiang, Xue, Zhengyang, Qian, Yu, Wei, Shanjie, Qiao, Yu, Zhang, Wen, Lu, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437323/
https://www.ncbi.nlm.nih.gov/pubmed/36061856
http://dx.doi.org/10.3389/fcimb.2022.945851
_version_ 1784781578222698496
author Lu, Xiang
Xue, Zhengyang
Qian, Yu
Wei, Shanjie
Qiao, Yu
Zhang, Wen
Lu, Hongyan
author_facet Lu, Xiang
Xue, Zhengyang
Qian, Yu
Wei, Shanjie
Qiao, Yu
Zhang, Wen
Lu, Hongyan
author_sort Lu, Xiang
collection PubMed
description BACKGROUND: The brain development of preterm infants is easily affected by various adverse extrauterine factors and complications, resulting in abnormal neurological and cognitive development. Recent studies have found that there is a significant correlation between intestinal microbial changes and cognitive behavior. Nevertheless, the correlation between the cognitive impairment and abnormal changes of intestinal microflora in the preterm newborn has been rarely elucidated. AIM: To analyze the differences of fecal intestinal flora, short chain fatty acids (SCFAs) and microbiota-gut-brain axis (MGBA)-related serum factors between preterm birth with and without cognitive impairment. METHODS: Healthy female rats (body weight 410 ± 40 g) of 16-17 days of gestation were selected for the establishment of preterm cognitive impairment model and screened by Morris water maze navigation experiments. The pathological change of rat hippocampus was confirmed by HE staining. The abundance of fecal intestinal microflora was determined by 16sRNA sequencing, while the contents of fecal SCFAs were examined by gas chromatography. RESULTS: Compared with the control group, the cognitive impairment group had decreased abundance and diversity of intestinal microflora and increased abundance of Proteobacteria at the level of phylum. While the abundances of Alistipes, Bacteroides, Prevotella, and Lactobacillus decreased significantly at the level of order, family, and genus, the abundances of Staphylococcaceae, Enterococci, Psychrobacter, and Oligella increased significantly. Moreover, the levels of total SCFAs and acetic acid in the disease group were significantly lower. The fecal abundance of acetic acid was positively correlated with that of Lactobacillaceae or Peptostreptococcaceae, and negatively correlated with that of Aerococcaceae, and Alcaligenaceae in disease rats. Furthermore, cognitive impairment caused significantly decreased levels of 5-HT, GABA, and BDNF, and increased levels of GR, CRH, IL-6, and TNF-α in rat blood. CONCLUSION: Alterations in intestinal microflora structure and the abundances of SCFAs contributed substantially to the cognitive impairment in preterm rats, which was associated with significant changes in MGBA-related soluble factors.
format Online
Article
Text
id pubmed-9437323
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94373232022-09-03 Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats Lu, Xiang Xue, Zhengyang Qian, Yu Wei, Shanjie Qiao, Yu Zhang, Wen Lu, Hongyan Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND: The brain development of preterm infants is easily affected by various adverse extrauterine factors and complications, resulting in abnormal neurological and cognitive development. Recent studies have found that there is a significant correlation between intestinal microbial changes and cognitive behavior. Nevertheless, the correlation between the cognitive impairment and abnormal changes of intestinal microflora in the preterm newborn has been rarely elucidated. AIM: To analyze the differences of fecal intestinal flora, short chain fatty acids (SCFAs) and microbiota-gut-brain axis (MGBA)-related serum factors between preterm birth with and without cognitive impairment. METHODS: Healthy female rats (body weight 410 ± 40 g) of 16-17 days of gestation were selected for the establishment of preterm cognitive impairment model and screened by Morris water maze navigation experiments. The pathological change of rat hippocampus was confirmed by HE staining. The abundance of fecal intestinal microflora was determined by 16sRNA sequencing, while the contents of fecal SCFAs were examined by gas chromatography. RESULTS: Compared with the control group, the cognitive impairment group had decreased abundance and diversity of intestinal microflora and increased abundance of Proteobacteria at the level of phylum. While the abundances of Alistipes, Bacteroides, Prevotella, and Lactobacillus decreased significantly at the level of order, family, and genus, the abundances of Staphylococcaceae, Enterococci, Psychrobacter, and Oligella increased significantly. Moreover, the levels of total SCFAs and acetic acid in the disease group were significantly lower. The fecal abundance of acetic acid was positively correlated with that of Lactobacillaceae or Peptostreptococcaceae, and negatively correlated with that of Aerococcaceae, and Alcaligenaceae in disease rats. Furthermore, cognitive impairment caused significantly decreased levels of 5-HT, GABA, and BDNF, and increased levels of GR, CRH, IL-6, and TNF-α in rat blood. CONCLUSION: Alterations in intestinal microflora structure and the abundances of SCFAs contributed substantially to the cognitive impairment in preterm rats, which was associated with significant changes in MGBA-related soluble factors. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437323/ /pubmed/36061856 http://dx.doi.org/10.3389/fcimb.2022.945851 Text en Copyright © 2022 Lu, Xue, Qian, Wei, Qiao, Zhang and Lu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Lu, Xiang
Xue, Zhengyang
Qian, Yu
Wei, Shanjie
Qiao, Yu
Zhang, Wen
Lu, Hongyan
Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title_full Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title_fullStr Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title_full_unstemmed Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title_short Changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
title_sort changes in intestinal microflora and its metabolites underlie the cognitive impairment in preterm rats
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437323/
https://www.ncbi.nlm.nih.gov/pubmed/36061856
http://dx.doi.org/10.3389/fcimb.2022.945851
work_keys_str_mv AT luxiang changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT xuezhengyang changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT qianyu changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT weishanjie changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT qiaoyu changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT zhangwen changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats
AT luhongyan changesinintestinalmicrofloraanditsmetabolitesunderliethecognitiveimpairmentinpretermrats