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Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis

BACKGROUND: To provide a basis for the diagnosis and treatment of acalculous biliary pancreatitis, this study investigated the impact of serum metabolites on the pancreatic transcriptome in acute acalculous cholecystitis (AAC). METHODS: Fourteen rabbits were randomly divided into two groups (a norma...

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Autores principales: Sun, Yuanyuan, Wang, Qiang, Hao, Chenjun, Xue, Dongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674085/
https://www.ncbi.nlm.nih.gov/pubmed/34925503
http://dx.doi.org/10.1155/2021/2368571
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author Sun, Yuanyuan
Wang, Qiang
Hao, Chenjun
Xue, Dongbo
author_facet Sun, Yuanyuan
Wang, Qiang
Hao, Chenjun
Xue, Dongbo
author_sort Sun, Yuanyuan
collection PubMed
description BACKGROUND: To provide a basis for the diagnosis and treatment of acalculous biliary pancreatitis, this study investigated the impact of serum metabolites on the pancreatic transcriptome in acute acalculous cholecystitis (AAC). METHODS: Fourteen rabbits were randomly divided into two groups (a normal control group of 7 rabbits and an AAC group of 7 rabbits), blood was collected from the 14 rabbits, and metabolomic analysis was performed through (1)H NMR. Two pancreatic tissue chips of the AAC group and the normal control group were prepared and sequenced. We utilized the limma package of R software, the DAVID database, the STRING database, Cytoscape software, and the CFinder analysis tool to perform differential expression gene analysis, gene function enrichment analysis, protein interaction network (PPI) construction, and network module mining, and we performed gene enrichment analysis in each module. RESULTS: Serum metabolism analysis showed that in AAC, the metabolism of sugar, lipids, and protein, that is, the three major nutrients, was affected to varying degrees, and levels of serum trimethylamine N-oxide (TMAO) increased. Bioinformatic methods were utilized to identify a total of 183 differentially expressed genes and 3 key genes. Enrichment analysis showed that differentially expressed genes were significantly enriched in cation transport, the inflammatory response, the NF-κB pathway, and the cancer signaling pathway. CONCLUSION: Metabolomic analysis and functional analysis of 3 key genes demonstrated that abnormal serum metabolites affected the pancreatic transcriptome and induced a sensitive state of inflammation in the pancreas. These metabolites may represent important targets for future research on the pathogenesis, clinical diagnosis, and treatment of noncalculous biliary pancreatitis.
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spelling pubmed-86740852021-12-16 Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis Sun, Yuanyuan Wang, Qiang Hao, Chenjun Xue, Dongbo Gastroenterol Res Pract Research Article BACKGROUND: To provide a basis for the diagnosis and treatment of acalculous biliary pancreatitis, this study investigated the impact of serum metabolites on the pancreatic transcriptome in acute acalculous cholecystitis (AAC). METHODS: Fourteen rabbits were randomly divided into two groups (a normal control group of 7 rabbits and an AAC group of 7 rabbits), blood was collected from the 14 rabbits, and metabolomic analysis was performed through (1)H NMR. Two pancreatic tissue chips of the AAC group and the normal control group were prepared and sequenced. We utilized the limma package of R software, the DAVID database, the STRING database, Cytoscape software, and the CFinder analysis tool to perform differential expression gene analysis, gene function enrichment analysis, protein interaction network (PPI) construction, and network module mining, and we performed gene enrichment analysis in each module. RESULTS: Serum metabolism analysis showed that in AAC, the metabolism of sugar, lipids, and protein, that is, the three major nutrients, was affected to varying degrees, and levels of serum trimethylamine N-oxide (TMAO) increased. Bioinformatic methods were utilized to identify a total of 183 differentially expressed genes and 3 key genes. Enrichment analysis showed that differentially expressed genes were significantly enriched in cation transport, the inflammatory response, the NF-κB pathway, and the cancer signaling pathway. CONCLUSION: Metabolomic analysis and functional analysis of 3 key genes demonstrated that abnormal serum metabolites affected the pancreatic transcriptome and induced a sensitive state of inflammation in the pancreas. These metabolites may represent important targets for future research on the pathogenesis, clinical diagnosis, and treatment of noncalculous biliary pancreatitis. Hindawi 2021-12-08 /pmc/articles/PMC8674085/ /pubmed/34925503 http://dx.doi.org/10.1155/2021/2368571 Text en Copyright © 2021 Yuanyuan Sun et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sun, Yuanyuan
Wang, Qiang
Hao, Chenjun
Xue, Dongbo
Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title_full Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title_fullStr Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title_full_unstemmed Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title_short Effects of Serum Metabolites on the Pancreatic Transcriptome in Acute Acalculous Cholecystitis
title_sort effects of serum metabolites on the pancreatic transcriptome in acute acalculous cholecystitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674085/
https://www.ncbi.nlm.nih.gov/pubmed/34925503
http://dx.doi.org/10.1155/2021/2368571
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