Liver and urine metabolomics reveal the protective effect of Gandou decoction in copper-laden Hepatolenticular degeneration model rats.
Animals
Biomarkers
/ analysis
Chromatography, High Pressure Liquid
Disease Models, Animal
Drugs, Chinese Herbal
/ chemistry
Hepatolenticular Degeneration
/ metabolism
Liver
/ drug effects
Male
Mass Spectrometry
Metabolome
/ drug effects
Metabolomics
Protective Agents
/ chemistry
Rats
Rats, Wistar
Reproducibility of Results
Gandou decoction
Hepatolenticular degeneration
Metabolic pathways
Metabolomics
UPLC-Q-TOF-MS
Wilson's disease
Journal
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
ISSN: 1873-376X
Titre abrégé: J Chromatogr B Analyt Technol Biomed Life Sci
Pays: Netherlands
ID NLM: 101139554
Informations de publication
Date de publication:
01 Aug 2021
01 Aug 2021
Historique:
received:
09
02
2021
revised:
11
05
2021
accepted:
16
06
2021
pubmed:
11
7
2021
medline:
11
11
2021
entrez:
10
7
2021
Statut:
ppublish
Résumé
Hepatolenticular degeneration (HLD) is an inherited disorder associated with human copper metabolism. Gandou decoction (GDD), a traditional Chinese medicinal formula, has been used as a therapeutic agent for the treatment of HLD in China for decades. Recent pharmacological evaluation in our laboratory has demonstrated that GDD exerts positive and beneficial effects on HLD model rats. However, its underlying therapeutic mechanisms are not yet well understood. To explore the potential therapeutic effects of GDD against HLD, liver and urine metabolomics approach combined with histopathological examination were performed to reveal the underlying mechanisms. Changes in metabolic profiles were estimated by ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) coupled with multivariate statistical analyses. The results indicated that GDD could significantly improve liver pathological variations. Moreover, 19 and 11 significantly altered metabolites were found in the liver and urine between the normal and model groups, respectively. After GDD treatment, the levels of all these disordered metabolites showed different degrees of improvement compared with the model group, including lysoPC(18:2), lysoPE(20:2/0:0), PC(18:1/14:1), alpha-linolenic acid, sphinganine, taurochenodesoxycholic acid, tetracosahexaenoic acid, 13-OxoODE, and 13-L-hydroperoxyl inoleic acid. Metabolic pathway enrichment suggested that lipid and oxidative stress metabolism were the two main pathways that participated in copper-laden rat models with GDD administration. This work indicates that GDD could achieve a therapeutic effect on HLD by ameliorating the associated metabolic disturbances.
Identifiants
pubmed: 34246170
pii: S1570-0232(21)00325-1
doi: 10.1016/j.jchromb.2021.122844
pii:
doi:
Substances chimiques
Biomarkers
0
Drugs, Chinese Herbal
0
Protective Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
122844Informations de copyright
Copyright © 2021. Published by Elsevier B.V.