Current Issues in Molecular Biology (Jun 2024)

Network Pharmacology Analysis, Molecular Docking Integrated Experimental Verification Reveal the Mechanism of <i>Gynostemma pentaphyllum</i> in the Treatment of Type II Diabetes by Regulating the IRS1/PI3K/Akt Signaling Pathway

  • Songqin Yang,
  • Mao Zhao,
  • Mingxing Lu,
  • Yuhan Feng,
  • Xia Zhang,
  • Daoping Wang,
  • Wenwen Jiang

DOI
https://doi.org/10.3390/cimb46060333
Journal volume & issue
Vol. 46, no. 6
pp. 5561 – 5581

Abstract

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Gynostemma pentaphyllum (Thunb.) Makino (GP), a plant with homology of medicine and food, as a traditional Chinese medicine, possesses promising biological activities in the prevention and treatment of type 2 diabetes mellitus (T2DM). However, the material basis and the mechanism of action of GP in the treatment of T2DM have not been fully elucidated. This study aimed to clarify the active components, potential targets and signaling pathways of GP in treating T2DM. The chemical ingredients of GP were collected by combining UPLC-HRMS analysis and literature research. Network pharmacology revealed that GP had 32 components and 326 potential targets in treating T2DM. The results showed that GP affected T2DM by mediating the insulin resistance signaling pathway, PI3K/Akt signaling pathway and FoxO1 signaling pathway, which had a close relationship with T2DM. Molecular docking results showed that STAT3, PIK3CA, AKT1, EGFR, VEGFA and INSR had high affinity with the active compounds of GP. In vitro, GP extracts obviously increased the glucose uptake and glucose consumption in IR-HepG2 cells. GP extracts increased the levels of PI3K, p-AKT, p-GSK3β and p-FoxO1 and decreased the expression of p-IRS1, p-GS, PEPCK and G6Pase, which indicated that GP could promote glycogen synthesis and inhibit gluconeogenesis by regulating the IRS1/PI3K/Akt signaling pathway. The results demonstrated that GP could improve insulin resistance by promoting glucose uptake and glycogen synthesis and inhibiting gluconeogenesis through regulating the IRS1/PI3K/Akt signaling pathway, which might be a potential alternative therapy for T2DM.

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