AI Article Synopsis

  • Magnesium lithospermate B (MLB) has shown potential benefits such as antidiabetic, neuroprotective, and antioxidant effects, but further research is needed to understand its impact on insulin sensitivity in the liver.
  • Previous studies indicated that MLB acts as a PPARβ/δ agonist, which may enhance insulin-sensitizing and anti-inflammatory effects in liver tissues.
  • Research using aging and obese animal models revealed that MLB improves glucose tolerance and insulin signaling while reducing stress-related responses, suggesting its potential for treating insulin resistance in these populations.

Article Abstract

Magnesium lithospermate B (MLB) is the biologically active compound of the water-soluble fraction of . Magnesium lithospermate B exhibits various biological functions, including antidiabetic, neuroprotective, and antioxidant effects. However, its beneficial effects on insulin sensitivity and related signaling pathways in the liver need to be elucidated. Our previous study reported that MLB is a PPARβ/δ agonist in fibroblasts. Because insulin-sensitizing and anti-inflammatory effects of PPARβ/δ has been reported in the liver, we investigated whether MLB has a beneficial effect on insulin-, ER stress- and inflammasome-related signaling in the livers of aging and obese animal models. Western blotting and protein-ligand docking simulation showed that MLB activated PPARβ/δ and improved glucose tolerance in the livers of aging and obese animal models. MLB supplementation ameliorated aging or obesity-induced disruption of insulin signaling in the liver. Consistently, aging and obesity-induced increase in the protein levels of a gluconeogenic phosphoenolpyruvate carboxykinase was decreased by MLB. When molecular signaling pathways related to insulin signaling were examined in the liver, MLB supplementation suppressed ER stress- and inflammasome-related signaling molecules induced by aging and obesity. These results suggest that MLB may improve insulin resistance in the liver at least partially by suppressing ER stress and inflammasome formation in aging and obese animal models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225288PMC
http://dx.doi.org/10.3390/molecules23092098DOI Listing

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