Bergaptol Ameliorates Insulin Sensitivity in Gestational Diabetes Mellitus by Inhibiting the Inflammatory Pathway in Streptozotocin-Induced Diabetic Rats
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
40126146
PubMed Central
PMC11995933
DOI
10.33549/physiolres.935474
PII: 935474
Knihovny.cz E-resources
- MeSH
- Diabetes Mellitus, Experimental * drug therapy metabolism chemically induced MeSH
- Diabetes, Gestational * drug therapy metabolism chemically induced blood MeSH
- Insulin Resistance * physiology MeSH
- Blood Glucose drug effects metabolism MeSH
- Rats MeSH
- Inflammation Mediators * antagonists & inhibitors metabolism MeSH
- Oxidative Stress drug effects MeSH
- Rats, Wistar MeSH
- Signal Transduction drug effects MeSH
- Molecular Docking Simulation MeSH
- Streptozocin MeSH
- Pregnancy MeSH
- Inflammation metabolism drug therapy MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Blood Glucose MeSH
- Inflammation Mediators * MeSH
- Streptozocin MeSH
Investigation determines the beneficial effect of bergaptol against gestational diabetes (GD). Gestational diabetes was induced in female rats and treated them with bergaptol 20 and 40 mg/kg for eighteen days. Effect of bergaptol was assessed on blood glucose and insulin level in GD rat. Inflammatory mediators and oxidative stress parameters were also assessed in GD rats. Moreover, mRNA expression of INSR, NF-kappaB, Akt and GSK-3beta were assessed in the GD rats by qRT-PCR method. In silico network pharmacology study was performed, along with gene ontology and egg pathway to assessed the targets of bergaptol, molecular docking study was also performed for the confirmation of possible pathway involved in the management of GD. Blood glucose and insulin level was significantly reduces in the blood bergaptol treated group than GD group of rats. Treatment with bergaptol ameliorates the altered level of mediators of inflammation and oxidative stress parameters in GD rats. There was significant reduction in the mRNA expression of NF-kappaB and GSK-3beta and increase in expression of INSR and Akt in the tissue homogenate of bergaptol treated GD rats. Docking study shows effective binding strength of bergaptol individually with INSR, NF-kappaB, Akt and GSK-3beta-protein targets. In conclusion, data of investigation suggest that bergaptol improves the sensitivity of insulin receptor in GD, as it reduces parameters of oxidative stress and inflammatory mediators by regulating INSR/NF-kappaB/Akt/GSK-3beta pathway. Key words Gestational diabetes, Bergaptol, Insulin resistance, Inflammation, Oxidative stress.
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