Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis
Giardia duodenalis is a significant protozoan that affects humans and animals. An estimated 280 million G. duodenalis diarrheal cases are recorded annually. Pharmacological therapy is crucial for controlling giardiasis. Metronidazole is the first-line therapy for treating giardiasis. Several metroni...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Article |
Published: |
2023
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/82203 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
id |
th-mahidol.82203 |
---|---|
record_format |
dspace |
spelling |
th-mahidol.822032023-05-19T14:53:49Z Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis Popruk S. Mahidol University Pharmacology, Toxicology and Pharmaceutics Giardia duodenalis is a significant protozoan that affects humans and animals. An estimated 280 million G. duodenalis diarrheal cases are recorded annually. Pharmacological therapy is crucial for controlling giardiasis. Metronidazole is the first-line therapy for treating giardiasis. Several metronidazole targets have been proposed. However, the downstream signaling pathways of these targets with respect to their antigiardial action are unclear. In addition, several giardiasis cases have demonstrated treatment failures and drug resistance. Therefore, the development of novel drugs is an urgent need. In this study, we performed a mass spectrometry-based metabolomics study to understand the systemic effects of metronidazole in G. duodenalis. A thorough analysis of metronidazole processes helps identify potential molecular pathways essential for parasite survival. The results demonstrated 350 altered metabolites after exposure to metronidazole. Squamosinin A and N-(2-hydroxyethyl)hexacosanamide were the most up-regulated and down-regulated metabolites, respectively. Proteasome and glycerophospholipid metabolisms demonstrated significant differential pathways. Comparing glycerophospholipid metabolisms of G. duodenalis and humans, the parasite glycerophosphodiester phosphodiesterase was distinct from humans. This protein is considered a potential drug target for treating giardiasis. This study improved our understanding of the effects of metronidazole and identified new potential therapeutic targets for future drug development. 2023-05-19T07:53:49Z 2023-05-19T07:53:49Z 2023-03-01 Article Pharmaceuticals Vol.16 No.3 (2023) 10.3390/ph16030408 14248247 2-s2.0-85151682465 https://repository.li.mahidol.ac.th/handle/123456789/82203 SCOPUS |
institution |
Mahidol University |
building |
Mahidol University Library |
continent |
Asia |
country |
Thailand Thailand |
content_provider |
Mahidol University Library |
collection |
Mahidol University Institutional Repository |
topic |
Pharmacology, Toxicology and Pharmaceutics |
spellingShingle |
Pharmacology, Toxicology and Pharmaceutics Popruk S. Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
description |
Giardia duodenalis is a significant protozoan that affects humans and animals. An estimated 280 million G. duodenalis diarrheal cases are recorded annually. Pharmacological therapy is crucial for controlling giardiasis. Metronidazole is the first-line therapy for treating giardiasis. Several metronidazole targets have been proposed. However, the downstream signaling pathways of these targets with respect to their antigiardial action are unclear. In addition, several giardiasis cases have demonstrated treatment failures and drug resistance. Therefore, the development of novel drugs is an urgent need. In this study, we performed a mass spectrometry-based metabolomics study to understand the systemic effects of metronidazole in G. duodenalis. A thorough analysis of metronidazole processes helps identify potential molecular pathways essential for parasite survival. The results demonstrated 350 altered metabolites after exposure to metronidazole. Squamosinin A and N-(2-hydroxyethyl)hexacosanamide were the most up-regulated and down-regulated metabolites, respectively. Proteasome and glycerophospholipid metabolisms demonstrated significant differential pathways. Comparing glycerophospholipid metabolisms of G. duodenalis and humans, the parasite glycerophosphodiester phosphodiesterase was distinct from humans. This protein is considered a potential drug target for treating giardiasis. This study improved our understanding of the effects of metronidazole and identified new potential therapeutic targets for future drug development. |
author2 |
Mahidol University |
author_facet |
Mahidol University Popruk S. |
format |
Article |
author |
Popruk S. |
author_sort |
Popruk S. |
title |
Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
title_short |
Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
title_full |
Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
title_fullStr |
Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
title_full_unstemmed |
Mass Spectrometry-Based Metabolomics Revealed Effects of Metronidazole on Giardia duodenalis |
title_sort |
mass spectrometry-based metabolomics revealed effects of metronidazole on giardia duodenalis |
publishDate |
2023 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/82203 |
_version_ |
1781414665600892928 |