人参
免疫印迹
炎症
内分泌学
化学
脂肪组织
下调和上调
安普克
药理学
脂质代谢
内科学
脂肪生成
医学
生物化学
酶
蛋白激酶A
替代医学
病理
基因
作者
Xueyue Tai,Jiating Li,Jingjing Song,Bao Zhong,Fenglin Li
标识
DOI:10.29219/fnr.v69.12230
摘要
Administration of high-dose fermented ginseng powder (2.385 mg/g) resulted in a reduction in body weight and an improvement in blood biochemical parameters in high-fat diet (HFD)-fed mice. Significant reductions in lipid droplet size were observed in both liver and epididymal adipose tissues. Western blot analysis showed increased protein levels of PPAR-α, PPAR-γ, and PGC-1 in the HFD + low-dose lyophilized fermented ginseng powder (HDL), HFD + medium-dose lyophilized fermented ginseng powder (HDM), and HFD + high-dose lyophilized fermented ginseng powder (HDH) groups compared to the HD group. Furthermore, the phosphorylation of AMPK (P-AMPK) and ACC (P-ACC) was significantly elevated. Conversely, western blot analysis demonstrated a decrease in the expression of inflammatory cytokines IL-1, IL-6, and TNF-α in the CG, HDL, HDM, and HDH groups compared to the HD group. Gene expression analysis revealed a downregulation of lipid anabolism-related genes, including SREBP-1c and FAS, along with an upregulation of PPAR-γ and ACOX-1 mRNA levels. Additionally, the expression of inflammation-related genes such as IL-1, IL-6, and TNF-α was reduced. High-dose freeze-dried fermented ginseng powder (2.385 mg/g) significantly influenced lipid metabolism and inflammatory responses, highlighting its potential as a therapeutic agent for the management of dyslipidemia.
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