Unknown

Dataset Information

0

Potential biomarkers in mouse myocardium of doxorubicin-induced cardiomyopathy: a metabonomic method and its application.


ABSTRACT: BACKGROUND: Doxorubicin (DOX) is one of the most potent antitumor agents available; however, its clinical use is limited because of the risk of severe cardiotoxicity. Though numerous studies have ascribed DOX cardiomyopathy to specific cellular pathways, the precise mechanism remains obscure. Sini decoction (SND) is a well-known formula of Traditional Chinese Medicine (TCM) and is considered as efficient agents against DOX-induced cardiomyopathy. However, its action mechanisms are not well known due to its complex components. METHODOLOGY/PRINCIPAL FINDINGS: A tissue-targeted metabonomic method using gas chromatography-mass spectrometry was developed to characterize the metabolic profile of DOX-induced cardiomyopathy in mice. With Elastic Net for classification and selection of biomarkers, twenty-four metabolites corresponding to DOX-induced cardiomyopathy were screened out, primarily involving glycolysis, lipid metabolism, citrate cycle, and some amino acids metabolism. With these altered metabolic pathways as possible drug targets, we systematically analyzed the protective effect of TCM SND, which showed that SND administration could provide satisfactory effect on DOX-induced cardiomyopathy through partially regulating the perturbed metabolic pathways. CONCLUSIONS/SIGNIFICANCE: The results of the present study not only gave rise to a systematic view of the development of DOX-induced cardiomyopathy but also provided the theoretical basis to prevent or modify expected damage.

SUBMITTER: Tan G 

PROVIDER: S-EPMC3218026 | BioStudies | 2011-01-01

REPOSITORIES: biostudies

Similar Datasets

2013-01-01 | S-EPMC3567130 | BioStudies
2020-01-01 | S-EPMC7044126 | BioStudies
2015-01-01 | S-EPMC4594178 | BioStudies
2015-01-01 | S-EPMC4418690 | BioStudies
2014-01-01 | S-EPMC3949718 | BioStudies
2014-01-01 | S-EPMC3950656 | BioStudies
1000-01-01 | S-EPMC4837341 | BioStudies
2013-01-01 | S-EPMC3680307 | BioStudies
2016-01-01 | S-EPMC4753490 | BioStudies
1000-01-01 | S-EPMC4768318 | BioStudies