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Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite

Naja atra bite is one of the most common severe snakebites in emergency departments. Unfortunately, the pathophysiological changes caused by Naja atra bite are unclear due to the lack of good animal models. In this study, an animal model of Naja atra bite in Guangxi Bama miniature pigs was establish...

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Autores principales: He, Dongling, Hu, Shaocong, Huang, Zhi, Mo, Caifeng, Cheng, Xiaoyang, Song, Pengshu, Li, Yalan, Song, Tianlin, Guan, Zhezhe, Zhou, Yi, Zhang, Xuerong, Liao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461852/
https://www.ncbi.nlm.nih.gov/pubmed/37639406
http://dx.doi.org/10.1371/journal.pntd.0011507
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author He, Dongling
Hu, Shaocong
Huang, Zhi
Mo, Caifeng
Cheng, Xiaoyang
Song, Pengshu
Li, Yalan
Song, Tianlin
Guan, Zhezhe
Zhou, Yi
Zhang, Xuerong
Liao, Ming
author_facet He, Dongling
Hu, Shaocong
Huang, Zhi
Mo, Caifeng
Cheng, Xiaoyang
Song, Pengshu
Li, Yalan
Song, Tianlin
Guan, Zhezhe
Zhou, Yi
Zhang, Xuerong
Liao, Ming
author_sort He, Dongling
collection PubMed
description Naja atra bite is one of the most common severe snakebites in emergency departments. Unfortunately, the pathophysiological changes caused by Naja atra bite are unclear due to the lack of good animal models. In this study, an animal model of Naja atra bite in Guangxi Bama miniature pigs was established by intramuscular injection at 2 mg/kg of Naja atra venom, and serum metabolites were systematically analyzed using untargeted metabolomic and targeted metabolomic approaches. Untargeted metabolomic analysis revealed that 5045 chromatographic peaks were obtained in ESI+ and 3871 chromatographic peaks were obtained in ESI-. Screening in ESI+ modes and ESI- modes identified 22 and 36 differential metabolites compared to controls. The presence of 8 core metabolites of glutamine, arginine, proline, leucine, phenylalanine, inosine, thymidine and hippuric acid in the process of Naja atra bite was verified by targeted metabolomics significant difference (P<0.05). At the same time, during the verification process of the serum clinical samples with Naja atra bite, we found that the contents of three metabolites of proline, phenylalanine and inosine in the serum of the patients were significantly different from those of the normal human serum (P<0.05). By conducting functional analysis of core and metabolic pathway analysis, we revealed a potential correlation between changes in key metabolites after the Naja atra bite and the resulting pathophysiological alterations, and our research aims to establish a theoretical foundation for the prompt diagnosis and treatment of Naja atra bite.
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spelling pubmed-104618522023-08-29 Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite He, Dongling Hu, Shaocong Huang, Zhi Mo, Caifeng Cheng, Xiaoyang Song, Pengshu Li, Yalan Song, Tianlin Guan, Zhezhe Zhou, Yi Zhang, Xuerong Liao, Ming PLoS Negl Trop Dis Research Article Naja atra bite is one of the most common severe snakebites in emergency departments. Unfortunately, the pathophysiological changes caused by Naja atra bite are unclear due to the lack of good animal models. In this study, an animal model of Naja atra bite in Guangxi Bama miniature pigs was established by intramuscular injection at 2 mg/kg of Naja atra venom, and serum metabolites were systematically analyzed using untargeted metabolomic and targeted metabolomic approaches. Untargeted metabolomic analysis revealed that 5045 chromatographic peaks were obtained in ESI+ and 3871 chromatographic peaks were obtained in ESI-. Screening in ESI+ modes and ESI- modes identified 22 and 36 differential metabolites compared to controls. The presence of 8 core metabolites of glutamine, arginine, proline, leucine, phenylalanine, inosine, thymidine and hippuric acid in the process of Naja atra bite was verified by targeted metabolomics significant difference (P<0.05). At the same time, during the verification process of the serum clinical samples with Naja atra bite, we found that the contents of three metabolites of proline, phenylalanine and inosine in the serum of the patients were significantly different from those of the normal human serum (P<0.05). By conducting functional analysis of core and metabolic pathway analysis, we revealed a potential correlation between changes in key metabolites after the Naja atra bite and the resulting pathophysiological alterations, and our research aims to establish a theoretical foundation for the prompt diagnosis and treatment of Naja atra bite. Public Library of Science 2023-08-28 /pmc/articles/PMC10461852/ /pubmed/37639406 http://dx.doi.org/10.1371/journal.pntd.0011507 Text en © 2023 He et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
He, Dongling
Hu, Shaocong
Huang, Zhi
Mo, Caifeng
Cheng, Xiaoyang
Song, Pengshu
Li, Yalan
Song, Tianlin
Guan, Zhezhe
Zhou, Yi
Zhang, Xuerong
Liao, Ming
Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title_full Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title_fullStr Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title_full_unstemmed Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title_short Metabolomics analyses of serum metabolites perturbations associated with Naja atra bite
title_sort metabolomics analyses of serum metabolites perturbations associated with naja atra bite
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461852/
https://www.ncbi.nlm.nih.gov/pubmed/37639406
http://dx.doi.org/10.1371/journal.pntd.0011507
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