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Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry

BACKGROUND: In the pathological study of necrozoospermia—a form of sperm mortality—the underlying metabolic mechanism remains unclear. Thus, the aim of this study was to characterize metabolic alterations in the seminal plasma of necrozoospermic patients and to provide insights into the etiology of...

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Autores principales: Deng, Tianqin, Li, Xuemei, Yao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406541/
https://www.ncbi.nlm.nih.gov/pubmed/37554525
http://dx.doi.org/10.21037/tau-23-14
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author Deng, Tianqin
Li, Xuemei
Yao, Bing
author_facet Deng, Tianqin
Li, Xuemei
Yao, Bing
author_sort Deng, Tianqin
collection PubMed
description BACKGROUND: In the pathological study of necrozoospermia—a form of sperm mortality—the underlying metabolic mechanism remains unclear. Thus, the aim of this study was to characterize metabolic alterations in the seminal plasma of necrozoospermic patients and to provide insights into the etiology of the disease. METHODS: Seminal plasma samples were collected from patients diagnosed with necrozoospermia (n=28) as well as normozoospermia (n=37). The samples were analyzed using nontargeted metabolomics based on liquid chromatography-mass spectrometry (LC-MS). The raw data were subjected to multivariate analysis to identify metabolites correlated with necrozoospermia. Differential metabolites were subjected to pathway analysis using MetaboAnalyst. RESULTS: The results of the metabolomic analysis showed that there were 194 differential metabolites between the two groups; 129 metabolites were upregulated and 65 metabolites were downregulated. Among the differential metabolites, the top ten differential metabolites were choline, benzaldehyde, pyrazinamide, 5-aminoimidazole-4-carboxamide, and dihydrothymine. The following differential metabolite pathways were identified, and the top five metabolite pathways were arachidonic acid metabolism, steroid hormone biosynthesis, alanine aspartate and glutamate metabolism, bile secretion, and prostate cancer. CONCLUSIONS: The elevation of choline and 2-hydroxyglutarate levels in seminal plasma was an important finding, and the results also indicate that abnormalities in arachidonic acid metabolism and glutamate metabolism were an underlying pathological mechanism of necrozoospermia.
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spelling pubmed-104065412023-08-08 Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry Deng, Tianqin Li, Xuemei Yao, Bing Transl Androl Urol Original Article BACKGROUND: In the pathological study of necrozoospermia—a form of sperm mortality—the underlying metabolic mechanism remains unclear. Thus, the aim of this study was to characterize metabolic alterations in the seminal plasma of necrozoospermic patients and to provide insights into the etiology of the disease. METHODS: Seminal plasma samples were collected from patients diagnosed with necrozoospermia (n=28) as well as normozoospermia (n=37). The samples were analyzed using nontargeted metabolomics based on liquid chromatography-mass spectrometry (LC-MS). The raw data were subjected to multivariate analysis to identify metabolites correlated with necrozoospermia. Differential metabolites were subjected to pathway analysis using MetaboAnalyst. RESULTS: The results of the metabolomic analysis showed that there were 194 differential metabolites between the two groups; 129 metabolites were upregulated and 65 metabolites were downregulated. Among the differential metabolites, the top ten differential metabolites were choline, benzaldehyde, pyrazinamide, 5-aminoimidazole-4-carboxamide, and dihydrothymine. The following differential metabolite pathways were identified, and the top five metabolite pathways were arachidonic acid metabolism, steroid hormone biosynthesis, alanine aspartate and glutamate metabolism, bile secretion, and prostate cancer. CONCLUSIONS: The elevation of choline and 2-hydroxyglutarate levels in seminal plasma was an important finding, and the results also indicate that abnormalities in arachidonic acid metabolism and glutamate metabolism were an underlying pathological mechanism of necrozoospermia. AME Publishing Company 2023-07-28 2023-07-31 /pmc/articles/PMC10406541/ /pubmed/37554525 http://dx.doi.org/10.21037/tau-23-14 Text en 2023 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Deng, Tianqin
Li, Xuemei
Yao, Bing
Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title_full Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title_fullStr Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title_full_unstemmed Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title_short Metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
title_sort metabonomic analysis of seminal plasma in necrozoospermia patients based on liquid chromatography-mass spectrometry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406541/
https://www.ncbi.nlm.nih.gov/pubmed/37554525
http://dx.doi.org/10.21037/tau-23-14
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