2019
DOI: 10.1016/j.ejphar.2019.04.005
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Baicalein improves glucose metabolism in insulin resistant HepG2 cells

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Cited by 69 publications
(44 citation statements)
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“…In addition, kaempferol also can reduce myocardial ischemia-reperfusion injury/MAPK-induced oxidative stress and inflammation by reducing AGE-RAGE, thereby improving myocardial injury in diabetic rats [ 23 ]. Yang discovered that baicalein (10 −6 and 10 −5 mol/L) may promote glucose uptake and glycolysis through the InsR/IRS-1/PI3K/AKT pathway and inhibit gluconeogenesis in liver cells, thus have strong anti-IR hepatocyte activity [ 24 ]. Therefore, the above active components indicate the effectiveness and diversity of chemical ingredients in HLJDD for treating T2DM.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, kaempferol also can reduce myocardial ischemia-reperfusion injury/MAPK-induced oxidative stress and inflammation by reducing AGE-RAGE, thereby improving myocardial injury in diabetic rats [ 23 ]. Yang discovered that baicalein (10 −6 and 10 −5 mol/L) may promote glucose uptake and glycolysis through the InsR/IRS-1/PI3K/AKT pathway and inhibit gluconeogenesis in liver cells, thus have strong anti-IR hepatocyte activity [ 24 ]. Therefore, the above active components indicate the effectiveness and diversity of chemical ingredients in HLJDD for treating T2DM.…”
Section: Discussionmentioning
confidence: 99%
“…The baicalein mechanism of action could upregulate AMPK signaling pathways, which can attenuate insulin resistance and inhibit inflammation [187]. The treatment of baicalein in HepG2 cells (0.001 umol/L and 0.01 umol/L) enhanced glucose uptake and glycolysis and suppressed [188]. In addition, baicalein prevents oxidative stress and inflammation in diabetic cardiomyopathy rats through the regulation of PI3K/AKT signaling [189].…”
Section: Anti-diabetic Effects Of Selected Flavonoidsmentioning
confidence: 99%
“…It had been reported that GQD could significantly decrease fasting blood glucose, glycosylated serum protein, glycosylated hemoglobin, and fasting serum insulin and promote myocardial glycolysis in diabetic rats [ 9 , 10 ]. Isoflavonoids (3′-hydroxy puerarin, puerarin, daidzin, daidzein, genistin, and genistein), flavonoids (baicalin, baicalein, wogonoside, wogonin, liquiritin, and liquiritigenin), alkaloids (berberine, jatrorrhizine, palmatine, and coptisine), and glycyrrhetic acid have been identified within the preparation [ 11 – 13 ], and these components are correlated to the antidiabetic, antioxidant, and immunoregulative effects [ 14 17 ]. Notably, the administration of GQD has also yielded a potential hypoglycemic effect associated with multitarget therapy.…”
Section: Introductionmentioning
confidence: 99%