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근거중심한의약 DB

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Title

Evidence construction of Huangkui capsule against chronic glomerulonephritis: A systematic review and network pharmacology.

Authors

Dai Y, Chen X, Yang H, Yang J, Hu Q, Xiao X, Guo X, Zeng J, Ma X.

Journal

Phytomedicine.

Year

2022

Vol (Issue)

102

Page

154189.

doi

10.1016/j.phymed.2022.154189.

PMID

35617887

Url

http://www.ncbi.nlm.nih.gov/pubmed/35617887

MeSH

Angiotensin Receptor Antagonists
Angiotensin-Converting Enzyme Inhibitors
Animals
Drugs, Chinese Herbal* / pharmacology
Drugs, Chinese Herbal* / therapeutic use
Glomerulonephritis* / drug therapy
Network Pharmacology
Rats
Rats, Sprague-Dawley

Keywords

Angiotensin receptor blocker; Chronic glomerulonephritis; Huangkui capsule; Meta-analysis and network pharmacology

한글 키워드

KMCRIC summary and commentary

없음

Korean Study

N

Abstract

Background: Chronic glomerulonephritis (CGN) is a relatively common primary glomerular disease. Huangkui capsule (HKC) combined with angiotensin receptor blocker (ARB) for CGN is frequently used in clinical practice, however, there is still lack of high-quality evidence-based evidence and network pharmacology to clarify the therapeutic efficacy and pharmacological mechanisms.

Purpose: Integrating evidence-based medicine and network pharmacology to explain the therapeutic efficacy and pharmacological mechanisms of ARB combined with HKC for CGN.

Methods: Studies matching the topic were searched from PubMed, Web of Science, Embase database, the Cochrane Library, Chinese National Knowledge Infrastructure, CBM databases, the VIP medicine information system and the Wanfang database and screened according to inclusion and exclusion criteria. The data of the included studies were meta-analyzed by blood urea nitrogen (BUN), serum creatinine (SCR), 24-h urine protein (24hUP) and effective rate (ER). A meta-analysis of the data from the included studies was performed. Then, based on the network pharmacology, the chemical ingredients in HKC and their targets of action, disease targets, common targets and other relevant information were screened, and the key pathways were relevantly annotated based on bioinformatics technology to explore the potential mechanisms of HKC and ARB for CGN.

Results: The results showed that SCR index (p < 0.05), 24hUP index (p < 0.001) in the group treated with HKC and ARB were significantly lower than those in the control group. BUN index in the group treated with HKC and VAL were significantly lower than those in the control group (p < 0.001). Effective rate index in the group treated with HKC and ARB was significantly higher than those in the control group (p < 0.001). There was no significant difference in BUN treated with IRB, LOS, and TEL (p = 0.181; p = 0.811; p = 0.067). Based on network pharmacology, the results were as follows: The PPI network indicated that STAT3, AKT1, MAPK1, TP53 and JUN were key target proteins. The results of KEGG analysis suggested that the pharmacological mechanisms were mainly associated with AGE-RAGE signaling pathway in diabetic complications.

Conclusion: The combination of ARB and HKC can achieve better therapeutic effects in the treatment of CGN, meanwhile, ARB and HKC have a significant improved effectiveness in the treatment of CGN compared with ARB or HKC alone. In addition, HKC and ARB synergistically treated CGN through a multi-pathway network.

Keywords: Angiotensin receptor blocker; Chronic glomerulonephritis; Huangkui capsule; Meta-analysis and network pharmacology.

Copyright © 2022 Elsevier GmbH. All rights reserved.

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