Cargando…
Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis
BACKGROUND: Diabetic cardiomyopathy (DCM) is a serious cardiac dysfunction induced by changes in the structure and contractility of the myocardium that are initiated in part by alterations in energy substrates. The underlying mechanisms of DCM are still under controversial. The observation of lipids...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520292/ https://www.ncbi.nlm.nih.gov/pubmed/28736579 http://dx.doi.org/10.1186/s13098-017-0249-6 |
_version_ | 1783251788243140608 |
---|---|
author | Dong, Shifen Zhang, Rong Liang, Yaoyue Shi, Jiachen Li, Jiajia Shang, Fei Mao, Xuezhou Sun, Jianning |
author_facet | Dong, Shifen Zhang, Rong Liang, Yaoyue Shi, Jiachen Li, Jiajia Shang, Fei Mao, Xuezhou Sun, Jianning |
author_sort | Dong, Shifen |
collection | PubMed |
description | BACKGROUND: Diabetic cardiomyopathy (DCM) is a serious cardiac dysfunction induced by changes in the structure and contractility of the myocardium that are initiated in part by alterations in energy substrates. The underlying mechanisms of DCM are still under controversial. The observation of lipids, especially lipidomics profiling, can provide an insight into the know the biomarkers of DCM. The aim of our research was to detect changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy. METHODS: Diabetic cardiomyopathy was induced by feeding a high-sucrose/fat diet (HSFD) for 28 weeks and streptozotocin (30 mg/kg, intraperitoneally). The ultra-high-performance liquid chromatography (UPLC) coupled to quadruple time-of flight (QTOF) mass spectrometer was used to acquire and analyze the lipidomics profiling of myocardial tissue. Meanwhile, parameters of cardiac function were collected using cardiac catheterization, and the cardiac index was calculated, and fasting blood glucose and lipid levels were measured by an ultraviolet spectrophotometric method. RESULTS: We detected 3023 positive ion peaks and 300 negative ion peaks. Levels of phosphatidylcholine (PC) (22:6/18:2), PC (22:6/18:1), PC (20:4/16:1), PC (16:1/18:3), phosphatidylethanolamine (PE) (20:4/18:2), and PE (20:4/16:0) were down-regulated, and PC (20:2/18:2), PC (18:0/16:0), and PC (20:4/18:0) were up-regulated in DCM model rats, when compared with control rats. Cardiac functions signed as values of left ventricular systolic pressure, maximal uprising velocity of left ventricular pressure and maximal decreasing velocity of left ventricular pressure were injured by 21–44%, and the cardiac index was increased by 25%, and fasting blood glucose and lipids were increased by 34–368%. Meanwhile, the cardiac lipid-related biomarkers have significant correlation with changes of cardiac function and cardiac index. CONCLUSIONS: UPLC/Q-TOF/MS analysis data suggested changes of some potential lipid biomarkers in the development of cardiac dysfunction and hypertrophy of diabetic cardiomyopathy, which may serve as potential important targets for clinical diagnosis and therapeutic intervention of DCM in the future. |
format | Online Article Text |
id | pubmed-5520292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55202922017-07-21 Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis Dong, Shifen Zhang, Rong Liang, Yaoyue Shi, Jiachen Li, Jiajia Shang, Fei Mao, Xuezhou Sun, Jianning Diabetol Metab Syndr Research BACKGROUND: Diabetic cardiomyopathy (DCM) is a serious cardiac dysfunction induced by changes in the structure and contractility of the myocardium that are initiated in part by alterations in energy substrates. The underlying mechanisms of DCM are still under controversial. The observation of lipids, especially lipidomics profiling, can provide an insight into the know the biomarkers of DCM. The aim of our research was to detect changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy. METHODS: Diabetic cardiomyopathy was induced by feeding a high-sucrose/fat diet (HSFD) for 28 weeks and streptozotocin (30 mg/kg, intraperitoneally). The ultra-high-performance liquid chromatography (UPLC) coupled to quadruple time-of flight (QTOF) mass spectrometer was used to acquire and analyze the lipidomics profiling of myocardial tissue. Meanwhile, parameters of cardiac function were collected using cardiac catheterization, and the cardiac index was calculated, and fasting blood glucose and lipid levels were measured by an ultraviolet spectrophotometric method. RESULTS: We detected 3023 positive ion peaks and 300 negative ion peaks. Levels of phosphatidylcholine (PC) (22:6/18:2), PC (22:6/18:1), PC (20:4/16:1), PC (16:1/18:3), phosphatidylethanolamine (PE) (20:4/18:2), and PE (20:4/16:0) were down-regulated, and PC (20:2/18:2), PC (18:0/16:0), and PC (20:4/18:0) were up-regulated in DCM model rats, when compared with control rats. Cardiac functions signed as values of left ventricular systolic pressure, maximal uprising velocity of left ventricular pressure and maximal decreasing velocity of left ventricular pressure were injured by 21–44%, and the cardiac index was increased by 25%, and fasting blood glucose and lipids were increased by 34–368%. Meanwhile, the cardiac lipid-related biomarkers have significant correlation with changes of cardiac function and cardiac index. CONCLUSIONS: UPLC/Q-TOF/MS analysis data suggested changes of some potential lipid biomarkers in the development of cardiac dysfunction and hypertrophy of diabetic cardiomyopathy, which may serve as potential important targets for clinical diagnosis and therapeutic intervention of DCM in the future. BioMed Central 2017-07-20 /pmc/articles/PMC5520292/ /pubmed/28736579 http://dx.doi.org/10.1186/s13098-017-0249-6 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Dong, Shifen Zhang, Rong Liang, Yaoyue Shi, Jiachen Li, Jiajia Shang, Fei Mao, Xuezhou Sun, Jianning Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title | Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title_full | Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title_fullStr | Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title_full_unstemmed | Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title_short | Changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using UPLC/Q-TOF/MS analysis |
title_sort | changes of myocardial lipidomics profiling in a rat model of diabetic cardiomyopathy using uplc/q-tof/ms analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520292/ https://www.ncbi.nlm.nih.gov/pubmed/28736579 http://dx.doi.org/10.1186/s13098-017-0249-6 |
work_keys_str_mv | AT dongshifen changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT zhangrong changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT liangyaoyue changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT shijiachen changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT lijiajia changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT shangfei changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT maoxuezhou changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis AT sunjianning changesofmyocardiallipidomicsprofilinginaratmodelofdiabeticcardiomyopathyusinguplcqtofmsanalysis |