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. 2019 Feb 28;8(3):204. doi: 10.3390/cells8030204

Table 1.

Summarized effects and mechanisms of ginsenoside Rb1 on different targets related to diabetes mellitus in animal and in vitro studies.

Model Type Inducer Animal/Cell Effects Mechanisms Ref.
DM In vitro AdipoR1 sense siRNA C2C12 myotubes ↑Basal AdipoR levels
↑GLUT4 translocations
↑Translocations of GLUT4;
Adiponectin signaling pathway
[61]
T2DM; Obesity In vivo HFD Obese mouse ↓Body weight gain
↓Fat accumulation
↑Glucose tolerance
Modulate inflammation
↑Central leptin sensitivity
↓Pro-inflammatory cytokines
[62]
T2DM In vivo db/db C57;
db/db mice
↑Insulin sensitivity
↓Adipocyte lipolysis
↓Levels of free fatty acids
↑Hepatic fat accumulation
↓Liver weight, hepatic triglyceride
↓TNF-α
↑Perilipin
↑Insulin sensitivity
↑Level of adiponectin
[64]
T2DM;
Obesity
In vivo HFD Rat ↓Food intake
↓Body weight gain
↓Body fat content
↑Energy expenditure
↑c-Fos
↓NPY
↓PI3k/Akt signaling pathway
[71]
Obesity In vivo KK-Ay C57
KK-Ay mice
↓Body weight gain
↓FBG and food consumption
↑Insulin/leptin sensitivities
↓Insulin resistance index
[73]
T2DM; Obesity In vitro Differentiation inducer 3T3-L1 cells ↑Glucose uptake
↑Lipid accumulation
↑Proliferation of 3T3-L1 preadipocytes
↑ap2, GLUT4
↑Adipogenesis
↑PPARγ2 and C/EBPα
[74]
T2DM; Obesity In vitro Differentiation inducer 3T3-L1 cells; C2C12 myotubes ↑PI3K activity
↑Glucose uptake
↑IRS1 and PKB phosphorylation
Activating insulin signaling pathway [75]
T2DM; Obesity In vivo db/db db/db mice ↑GLUT1 and GLUT4
↑Akt Phosphorylation
↓HOMA-IR and FBG and FINS
↑Glucose metabolism
↑Insulin sensitizing activity
[78]
T2DM In vivo HFD C57BL/C mice ↑Glucose tolerance
↓11β-HSD1 levels
↑Fasting blood glucose
↓11β-HSD1
↑Insulin sensitivity
[79]
DM In vitro HG;
Cytokine
Rin-m5F ↓iNOS expression and NO
↓Pancreatic β-cell apoptosis
↓Caspase-3
↓Apoptosis-related genes
[84]
T2DM In vivo; In vitro HFD;
STZ
Male SD rats;
NCI-H716 cells
↑GLP-1 secretion
↑ATP:ADP ratio
↑GLP-1
↑Proglucagon
[86]

C/EBPα, recombinant human CCAAT/enhancer binding protein alpha; DM, diabetes mellitus; DC, diabetic cardiomyopathy; DN, diabetic nephropathy; FBG, fasting blood glucose; FINS, fasting insulin; HOMA-IR, homeostasis model assessment-insulin resistance; HG, high glucose; HFD, high-fat diet; GLUT, glucose transporter; HOCl, hypochlorous acid; GLP-1, glucagon-like peptide-1; IL-6 and/or IL-1β, pro-inflammatory cytokines; IRS1, insulin receptor substrate-1; iNOS, inducible nitric oxide synthase; MAPK, mitogen activated protein kinase; MI/R, myocardial ischemia/reperfusion; NO, nitric oxide; PPARγ, peroxisome proliferator-activated receptor γ; PKB/Akt, protein kinase B; PI3K, phosphatidylinositol 3-kinase; Rin-m5F, Rattus pancreatic β-cell line; RF stands for references; STZ, streptozotocin; SD, Sprague–Dawley rat; T2DM, type 2 diabetes; TNF-α, tumor necrosis factor-α; 11β-HSD1, 11β-Hydroxysteroid dehydrogenase type I.