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Uncovering the key pharmacodynamic material basis and possible molecular mechanism of Xiaoke formulation improve insulin resistant through a comprehensive investigation

Bibliographic Data

ID14743157
AuthorsWenjuan Ma (0000-0001-8637-0800, Shenyang Pharmaceutical University), Jianglan Long (Beijing Friendship Hospital), Linjie Dong (Shenyang Pharmaceutical University), Jian Zhang (0000-0001-7681-8747, Chengdu University of Traditional Chinese Medicine), Aiting Wang (0000-0003-2723-888X, Beijing Friendship Hospital), Yu Zhang (0000-0002-0059-270X, Beijing Friendship Hospital, corresponding author), Dan Yan (0000-0003-1219-9646, Beijing Friendship Hospital, corresponding author)
Year2024
Volume323
Pages117752
Publication date2024-04-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueJournal of Ethnopharmacology (JOURNAL)
Journal identifiersISSN: 0378-8741 • E-ISSN: 1872-7573
PublisherElsevier BV (PUBLISHER)
DOI10.1016/j.jep.2024.117752
PMID38216099
OpenAlexW4390806134
LanguageEN
Citations received1
References cited33

The key pharmacodynamic material basis of XKF, such as berberine and its metabolites (berberrubine and demethyleneberberine), chlorogenic acid and its metabolites (3-O-feruloylquinic acid and 5-O-feruloylquinic acid), calycosin and swertiamarin influence the glucose metabolism disorder of IR-HepG2 cells by regulating the PI3K/AKT signalling pathway, leading to an improvement in IR

Berberine · Bioinformatics · Biology · Insulin · Insulin receptor · Insulin resistance · Metabolome · Metabolomics · Pharmacodynamics · Pharmacokinetics · PI3K/AKT/mTOR pathway · Protein kinase B · Signal transduction · Berberine and alkaloids research · Chemistry · Chromatography in Natural Products · Traditional Chinese Medicine Analysis · Biochemistry · Endocrinology · Pharmacology

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Unique citing works1
Citations per year0,5
Citation span2024 - 2024 (1)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 1

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