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Published on: October 13, 2023
Iridoid Glycoside Cornuside Alleviates the Symptom of Gestational Diabetes Mellitus by Suppressing Inflammation and
Xiaorong Cui1, Yani Yu1, Jia Yu1
1Department of Gynecology, Zibo Central Hospital, Zibo, China.
Objective:
Gestational diabetes mellitus (GDM) is a frequently occurring complication during pregnancy and has adverse effects on both mother and offspring. β-Cell dysfunction and inflammation play important roles in GDM pathogenesis. Cornuside (CNS) is an iridoid glycoside that exhibits anti-inflammation activities. In the present study, we explored the effects of CNS on β-cell and GDM.
Design:
MIN6 β-cell line cells were treated with varying concentrations of CNS. The content and secretion of insulin were measured.
Methods:
The expression of Pdx1, Rac1, Piezo, and NeuroD1 and cell proliferation in CNS-treated MIN6 cells were detected. CNS was administered to GDM mice, and the symptoms of GDM, expression of IL-6 and TNF-α, and activation of NF-κB in GDM mice were measured.
Results:
CNS promoted cell proliferation of MIN6 cells, enhanced insulin content and secretion, and expression of Pdx1, Rac1, Piezo, and NeuroD1 in MIN6 cells. CNS alleviated symptoms of GDM mice and decreased serum levels of IL-6 and TNF-α in GDM mice. CNS suppressed the expression of IL-6 and TNF-α, as well as the activation of NF-κB in the placenta of GDM mice.
Conclusion:
CNS ameliorates GDM symptoms by suppressing inflammation and enhancing β-cell functions.
Insights
Cornuside (CNS) improves gestational diabetes mellitus (GDM) by boosting pancreatic beta-cell function and reducing inflammation. This natural compound enhances insulin secretion and alleviates GDM symptoms in mice.
Area of Science:
- Pharmacology
- Endocrinology
- Reproductive Biology
Background:
- Gestational diabetes mellitus (GDM) is a common pregnancy complication with significant risks.
- Pancreatic beta-cell dysfunction and inflammation are key factors in GDM development.
- Cornuside (CNS), an iridoid glycoside, possesses known anti-inflammatory properties.
Purpose of the Study:
- To investigate the therapeutic effects of Cornuside (CNS) on pancreatic beta-cells and GDM.
- To elucidate the underlying mechanisms of CNS action in GDM pathogenesis.
Main Methods:
- MIN6 beta-cell line treated with varying CNS concentrations to assess insulin production and secretion.
- Analysis of key gene expression (Pdx1, Rac1, Piezo, NeuroD1) and cell proliferation in treated MIN6 cells.
- Administration of CNS to a mouse model of GDM to evaluate GDM symptom amelioration, inflammatory marker levels (IL-6, TNF-α), and NF-κB activation.
Main Results:
- CNS significantly promoted MIN6 cell proliferation and enhanced insulin content and secretion.
- CNS treatment upregulated the expression of Pdx1, Rac1, Piezo, and NeuroD1 in beta-cells.
- CNS administration alleviated GDM symptoms in mice, reducing serum IL-6 and TNF-α levels and suppressing placental NF-κB activation.
Conclusions:
- Cornuside (CNS) demonstrates therapeutic potential for GDM by improving beta-cell function.
- CNS ameliorates GDM by mitigating inflammation and enhancing pancreatic beta-cell activity.
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