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藤黄果通过增强钙/钙调蛋白依赖性蛋白激酶 II/腺苷酸活化蛋白激酶/葡萄糖转运蛋白 4 介导的骨骼肌葡萄糖摄取来改善高脂肪饮食诱导的葡萄糖失衡。

Garcinia Cambogia Improves High-Fat Diet-Induced Glucose Imbalance by Enhancing Calcium/CaMKII/AMPK/GLUT4-Mediated Glucose Uptake in Skeletal Muscle.

机构信息

Department of Pharmacology, College of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.

出版信息

Mol Nutr Food Res. 2022 May;66(10):e2100669. doi: 10.1002/mnfr.202100669. Epub 2022 Mar 6.

Abstract

SCOPE

Garcinia cambogia (G. cambogia) is known to have antiobesity effects. In this study, the therapeutic effects of G. cambogia on glucose homeostasis in obesity-induced diabetes are explored and the underlying mechanisms are investigated.

METHODS AND RESULTS

C2C12 myotubes are treated with G. cambogia; glucose uptake, intracellular Ca levels, and related alterations in signaling pathways are examined. High-fat diet (HFD)-fed mice are administered G. cambogia for 8 weeks; oral glucose tolerance is evaluated, and the regulation of identified targets of signaling pathways in quadriceps skeletal muscle are examined in vivo. G. cambogia increases glucose uptake in C2C12 myotubes and induces the upregulation of AMPK, ACC, and p38 MAPK phosphorylation. Notably, G. cambogia markedly elevates both intracellular Ca levels, activating CaMKII, a Ca -sensing protein, and TBC1D4-mediated GLUT4 translocation, to facilitate glucose uptake. Furthermore, high-glucose-induced inhibition of glucose uptake and signal transduction is reverted by G. cambogia. In an HFD-induced diabetes mouse model, G. cambogia administration results in significant blood glucose-lowering effects, which are attributed to the regulation of targets that have been identified in vitro, in quadricep skeletal muscle.

CONCLUSION

These findings provide new insights into the mechanism by which G. cambogia regulates glucose homeostasis in obesity-induced diabetes.

摘要

范围

藤黄果(G. cambogia)具有抗肥胖作用。本研究探讨了藤黄果在肥胖型糖尿病中对葡萄糖稳态的治疗作用,并研究了其潜在机制。

方法和结果

用藤黄果处理 C2C12 肌管;检查葡萄糖摄取、细胞内 Ca 水平以及相关信号通路的改变。用高脂肪饮食(HFD)喂养的小鼠给予藤黄果 8 周;评估口服葡萄糖耐量,并在体内检查四头肌骨骼肌中鉴定的信号通路靶标的调节。藤黄果增加 C2C12 肌管中的葡萄糖摄取,并诱导 AMPK、ACC 和 p38 MAPK 磷酸化的上调。值得注意的是,藤黄果显着提高细胞内 Ca 水平,激活 CaMKII(一种 Ca 感应蛋白)和 TBC1D4 介导的 GLUT4 易位,以促进葡萄糖摄取。此外,高葡萄糖诱导的葡萄糖摄取和信号转导抑制被藤黄果逆转。在 HFD 诱导的糖尿病小鼠模型中,藤黄果的给药导致显著的降血糖作用,这归因于在体外和四头肌骨骼肌中鉴定的靶标的调节。

结论

这些发现为藤黄果调节肥胖型糖尿病中葡萄糖稳态的机制提供了新的见解。

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