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基于整合方法评价制川乌与姜黄对阿霉素诱导的大鼠慢性心力衰竭的治疗作用。

Therapeutic effects of Aconiti Lateralis Radix Praeparata combined with Zingiberis Rhizoma on doxorubicin-induced chronic heart failure in rats based on an integrated approach.

机构信息

College of Pharmacy, Provincial and State Key Laboratory Breeding Base of System Research, Development and Utilization of Chinese Herbal Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Department of Pharmacy, Fifth Medical Center, General Hospital of Chinese PLA, Beijing, China.

出版信息

J Pharm Pharmacol. 2020 Feb;72(2):279-293. doi: 10.1111/jphp.13191. Epub 2019 Nov 19.

DOI:10.1111/jphp.13191
PMID:31743450
Abstract

OBJECTIVES

This study was aimed to explore the mechanism of Aconiti Lateralis Radix Praeparata (ALRP) and Zingiberis Rhizoma (ZR) on doxorubicin (DOX)-induced chronic heart failure (CHF) in rats by integrated approaches.

METHODS

Effects of ALRP and ZR on cardiac function, serum biochemical indicators and histopathology in rats were analysed. Moreover, UHPLC-Q-TOF/MS was performed to identify the potential metabolites affecting the pathological process of CHF. Metabolomics and network pharmacology analyses were conducted to illustrate the possible pathways and network in CHF treatment. The predicted gene expression levels in heart tissue were verified and assessed by RT-PCR.

KEY FINDINGS

ALRP-ZR demonstrated remarkable promotion of hemodynamic indices and alleviated histological damage of heart tissue. Metabolomics analyses showed that the therapeutic effect of ALRP and ZR is mainly associated with the regulation of eight metabolites and ten pathways, which may be responsible for the therapeutic efficacy of ALRP-ZR. Moreover, the results of RT-PCR showed that ALRP-ZR could substantially increase the expression level of energy metabolism-related genes, including PPARδ, PPARγ, Lpl, Scd, Fasn and Pla2g2e.

CONCLUSIONS

The results highlighted the role of ALRP-ZR in the treatment of CHF by influencing the metabolites related to energy metabolism pathway via metabolomics and network pharmacology analyses.

摘要

目的

本研究旨在采用整合方法探讨制川乌和姜黄对多柔比星(DOX)致大鼠慢性心力衰竭(CHF)的作用机制。

方法

分析制川乌和姜黄对大鼠心功能、血清生化指标和组织病理学的影响。此外,采用 UHPLC-Q-TOF/MS 鉴定影响 CHF 病理过程的潜在代谢物。通过代谢组学和网络药理学分析阐明 CHF 治疗的可能途径和网络。通过 RT-PCR 验证和评估心脏组织中预测的基因表达水平。

主要发现

制川乌和姜黄显示出显著促进血流动力学指标的作用,并减轻了心脏组织的组织学损伤。代谢组学分析表明,制川乌和姜黄的治疗效果主要与 8 种代谢物和 10 条途径的调节有关,这可能是制川乌和姜黄治疗效果的原因。此外,RT-PCR 结果表明,制川乌和姜黄可以显著增加与能量代谢途径相关的基因的表达水平,包括 PPARδ、PPARγ、Lpl、Scd、Fasn 和 Pla2g2e。

结论

通过代谢组学和网络药理学分析,结果强调了制川乌和姜黄通过影响与能量代谢途径相关的代谢物在 CHF 治疗中的作用。

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