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Mechanism of Action of Magnesium Lithospermate B against Aging and Obesity-Induced ER Stress Insulin Resistance and Inflammsome Formation in the Liver

机译:硫氰酸镁B对抗衰老和肥胖引起的内质网应激胰岛素抵抗和肝脏炎症形成的作用机理

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摘要

Magnesium lithospermate B (MLB) is the biologically active compound of the water-soluble fraction of Salvia miltiorrhiza. 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.
机译:紫草酸镁B(MLB)是丹参中水溶性部分的生物活性化合物。紫草酸镁B具有多种生物功能,包括抗糖尿病,神经保护和抗氧化作用。然而,需要阐明其对肝脏中胰岛素敏感性和相关信号通路的有益作用。我们先前的研究报道,MLB是成纤维细胞中的PPARβ/δ激动剂。因为已经在肝脏中报道了PPARβ/δ的胰岛素敏感性和抗炎作用,所以我们调查了MLB是否对衰老和肥胖动物模型的肝脏中的胰岛素,ER应激和炎性体相关信号具有有益作用。 Western印迹和蛋白质-配体对接模拟显示,MLB激活了衰老和肥胖动物模型肝脏的PPARβ/δ,并改善了葡萄糖耐量。 MLB补充改善了肝脏中衰老或肥胖引起的胰岛素信号传导破坏。一致地,MLB降低了衰老和肥胖引起的糖异生性磷酸烯醇丙酮酸羧化激酶的蛋白质水平的增加。当在肝脏中检查与胰岛素信号传导相关的分子信号传导途径时,MLB补充会抑制衰老和肥胖引起的与内质网应激和炎症小体相关的信号传导分子。这些结果表明,MLB可以通过抑制衰老和肥胖动物模型中的ER应激和炎症小体形成来至少部分改善肝脏中的胰岛素抵抗。

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