Effects of Amomum cadamomum Linne Extract on TNF-α-induced Inflammation and Insulin Resistance in 3T3-L1 Adipocytes

Kyung‑Hwa Kang, Choon-Ho Song
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引用次数: 1

Abstract

Amomum cadamomum Linne (ACL) has long been utilized against the inhibited qi movement related diseases such as dyspepsia, acute gastroenteritis, vomiting and diarrhea in Korean medicine. We speculated that ACL could improve the metabolic disorders such as obesity and type 2 diabetes through removing the phlegm-dampness and promoting the qi movement or stagnation. This study was designed to investigate effects and molecular mechanisms of ACL extract on the improvement of adipocyte dysfunction induced by TNF-α in 3T3-L1 adipocytes. Potential roles of ACL extract in the lipogenesis, inhibition of inflammatory cytokines and insulin resistance, were investigated in this study. Also, we examined the adipose genes and signaling molecules related to insulin resistance and glucose uptake to elucidate its mechanism. Our data demonstrated that TNF-α significantly incresed the release of lipid droplets and the production of MCP-1 and IL-6 from adipocytes. In gene expression, TNF-α reduced the expression of aP2, PPARγ, C/EBPα, GLUT4, and IRS-1 related to lipogenesis and insulin sesitivity, while TNF-α increased the expression of MCP-1 related to inflammation. In addition, TNF-α down-regulated the PPARγ and IRS-1 protein and up-regulated the IRS-1 Ser307 phosphorylation. These alterations induced by TNF-α were prevented by the treatment of ACL extract. Thus, our results indicate that ACL extract can be used to prevent from the TNF-α-induced adipocyte dysfunction through insulin and PPARγ pathways.
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砂仁提取物对TNF-α-诱导的3T3-L1脂肪细胞炎症和胰岛素抵抗的影响
早在韩国医学中,砂仁就被用于治疗消化不良、急性胃肠炎、呕吐、腹泻等气运抑制相关疾病。我们推测ACL可以通过化痰湿、通气滞来改善肥胖、2型糖尿病等代谢性疾病。本研究旨在探讨ACL提取物对TNF-α诱导的3T3-L1脂肪细胞功能障碍的改善作用及其分子机制。本研究探讨了ACL提取物在脂肪生成、抑制炎症细胞因子和胰岛素抵抗中的潜在作用。此外,我们还研究了与胰岛素抵抗和葡萄糖摄取相关的脂肪基因和信号分子,以阐明其机制。我们的数据表明,TNF-α显著增加脂肪细胞的脂滴释放和MCP-1和IL-6的产生。在基因表达方面,TNF-α降低了与脂肪生成和胰岛素敏感性相关的aP2、PPARγ、C/EBPα、GLUT4和IRS-1的表达,而TNF-α增加了与炎症相关的MCP-1的表达。此外,TNF-α下调PPARγ和IRS-1蛋白,上调IRS-1 Ser307磷酸化。ACL提取物可阻止TNF-α诱导的这些改变。因此,我们的研究结果表明,ACL提取物可以通过胰岛素和PPARγ途径预防TNF-α-诱导的脂肪细胞功能障碍。
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