Comparative Metabolomics Analysis of Cervicitis in Human Patients and a Phenol Mucilage-Induced Rat Model Using Liquid Chromatography Tandem Mass Spectrometry

Cervicitis is an exceedingly common gynecological disorder that puts women at high risk of sexually transmitted infections and induces a series of reproductive system diseases. This condition also has a significant impact on quality of life and is commonly misdiagnosed in clinical practice due to it...

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Published in:Frontiers in pharmacology Vol. 9; p. 282
Main Authors: Zhang, Xiaoyong, Li, Junmao, Xie, Bin, Wu, Bei, Lei, Shuangxia, Yao, Yun, He, Mingzhen, Ouyang, Hui, Feng, Yulin, Xu, Wen, Yang, Shilin
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 04-04-2018
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Summary:Cervicitis is an exceedingly common gynecological disorder that puts women at high risk of sexually transmitted infections and induces a series of reproductive system diseases. This condition also has a significant impact on quality of life and is commonly misdiagnosed in clinical practice due to its complicated pathogenesis. In the present study, we performed non-targeted plasma metabolomics analysis of cervicitis in both plasma samples obtained from human patients and plasma samples from a phenol mucilage induced rat model of cervicitis, using ultra-performance liquid chromatography coupled to quadrupole time-of-flight tandem mass spectrometry. In addition to differences in histopathology, we identified differences in the metabolic profile between the cervicitis and control groups using unsupervised principal component analysis and orthogonal projections to latent structures discriminant analysis. These results demonstrated changes in plasma metabolites, with 27 and 22 potential endogenous markers identified in rat and human samples, respectively. The metabolic pathway analysis showed that linoleic acid, arachidonic acid, ether lipid, and glycerophospholipid metabolism are key metabolic pathways involved in cervicitis. This study showed the rat model was successfully created and applied to understand the pathogenesis of cervicitis.
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Reviewed by: Helena Idborg, Karolinska Institute (KI), Sweden; Georgios Paschos, University of Pennsylvania, United States
Edited by: Emanuela Ricciotti, University of Pennsylvania, United States
These authors have contributed equally to this work.
This article was submitted to Inflammation Pharmacology, a section of the journal Frontiers in Pharmacology
ISSN:1663-9812
1663-9812
DOI:10.3389/fphar.2018.00282