Literature DB >> 29431198

Metabolomic analysis for the protective effects of mangiferin on sepsis-induced lung injury in mice.

Yilin Wang1, Yang Liu1, Qiqi Cao1, Xuan Shi2, Hongtao Lu3, Songyan Gao4, Rui Yang5.   

Abstract

This study aimed to investigate the efficacy of mangiferin, including its known antioxidant and anti-inflammatory effects on sepsis-induced lung injury induced by a classical cecal ligation and puncture (CLP) models in mouse using a metabolomics approach. A total of 24 mice were randomly divided into four groups: the sham group was given saline before sham operation. The CLP group received the CLP operation only. HMF and LMF groups were given mangiferin treatment of high dose and low dose of mangiferin, respectively, before the CLP operation. One week after treatment, the mice were sacrificed and their lungs were collected for metabolomics analysis. We developed ultra-performance liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry to perform lung metabolic profiling analysis. With the methods of principal component analysis and partial least squares discriminant analysis, 58 potential metabolites associated with amino acid metabolism, purine metabolism, lipid metabolism and energy regulation were observed to be increased or reduced in HMF and LMF groups compared with the CLP group. Conclusively, our results suggest that mangiferin plays a protective role in the moderation of sepsis-induced lung injury through reducing oxidative stress, regulating lipid metabolism and energy biosynthesis.
Copyright © 2018 John Wiley & Sons, Ltd.

Entities:  

Keywords:  UHPLC-Q-TOF/MS; lung injury; mangiferin; metabolomics

Mesh:

Substances:

Year:  2018        PMID: 29431198     DOI: 10.1002/bmc.4208

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  3 in total

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Authors:  Amro Ilaiwy; Gabriella A M Ten Have; James R Bain; Michael J Muehlbauer; Sara K O'Neal; Jessica M Berthiaume; Traci L Parry; Nicolaas E Deutz; Monte S Willis
Journal:  Am J Pathol       Date:  2019-09       Impact factor: 4.307

2.  CBP Bromodomain Inhibition Rescues Mice From Lethal Sepsis Through Blocking HMGB1-Mediated Inflammatory Responses.

Authors:  Xiaowen Bi; Baolin Jiang; Jinyi Zhou; Xirui Fan; Xintong Yan; Juanjuan Liang; Lan Luo; Zhimin Yin
Journal:  Front Immunol       Date:  2021-02-02       Impact factor: 7.561

3.  Liang-Ge decoction ameliorates acute lung injury in septic model rats through reducing inflammatory response, oxidative stress, apoptosis, and modulating host metabolism.

Authors:  Wenju He; Qiang Xi; Huantian Cui; Pingping Zhang; Rui Huang; Taihuan Wang; Dongqiang Wang
Journal:  Front Pharmacol       Date:  2022-09-16       Impact factor: 5.988

  3 in total

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