College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
College of Basic Medicine, Zhejiang Chinese Medical University, Ningbo, China.
Pharm Biol. 2022 Dec;60(1):579-588. doi: 10.1080/13880209.2022.2042567.
Yunpi Heluo (YPHL) decoction is a Chinese herbal formula with particular advantages for treating type 2 diabetes. Yet, its exact mechanism of action is not fully understood.
To examine the therapeutic effect of YPHL on ectopic lipid deposition (EDL) in Zucker diabetic fatty (ZDF) rats and the underlying mechanism.
The ZDF Rats were randomized into five groups, including model, YPHL (200 mg/kg/d for 10 weeks), SIRT1-overexpression (injected with HBAAV2/9-r-SIRT1-3'-flag-GFP), NC (injected with HBAAV2/9-CMV-GFP as blank control) and control group. Pancreatic β-cells obtained from high-lipid-high-glucose fed rats were treated with YPHL (10 mg/mL) for 48 h. Lipid deposition and autophagosomes were analyzed by transmission electron microscopy. Intracellular HO and ROS concentrations were measured by flow cytometry. SIRT1, FOXO1, LC3 and P62 mRNA and protein levels were analyzed using qRT-PCR and Western blots.
Compared with the model group, blood glucose levels in YPHL and si-SIRT1 groups were reduced by 19.3% and 27.9%, respectively. In high-lipid-high-glucose cells treated with YPHL, lipid droplets were reduced and decrease in apoptosis rate (38.6%), HO (31.2%) and ROS (44.5%) levels were observed. After YPHL intervention or SIRT1 overexpression, LC3 and p62 expression increased. Protein expression of SIRT1 and LC3 in model, si-SIRT1, si-NC and si-SIRT1 + YPHL groups was lower than those in control group, while FoxO1 expression was increased. All of these protein level alterations were reversed in the si-NC + YPHL group.
YPHL reduced EDL by regulating the SIRT1-FoxO1 autophagy pathway in diabetic rats, which could lead to future perspectives for the treatment of diabetes.
云皮河洛(YPHL)汤是一种具有治疗 2 型糖尿病特殊优势的中草药配方。然而,其确切的作用机制尚不完全清楚。
观察 YPHL 对 Zucker 糖尿病肥胖(ZDF)大鼠异位脂质沉积(EDL)的治疗作用及其机制。
将 ZDF 大鼠随机分为 5 组,包括模型组、YPHL 组(200mg/kg/d ,10 周)、SIRT1 过表达组(注射 HBAAV2/9-r-SIRT1-3'-flag-GFP)、NC 组(注射 HBAAV2/9-CMV-GFP 作为空白对照)和对照组。用 YPHL(10mg/mL)处理高脂高糖喂养大鼠的胰岛β细胞 48h。用透射电子显微镜分析脂质沉积和自噬体。用流式细胞术测量细胞内 HO 和 ROS 浓度。用 qRT-PCR 和 Western blot 分析 SIRT1、FOXO1、LC3 和 P62 mRNA 和蛋白水平。
与模型组相比,YPHL 组和 si-SIRT1 组的血糖水平分别降低了 19.3%和 27.9%。在 YPHL 处理的高脂高糖细胞中,脂滴减少,细胞凋亡率(38.6%)、HO(31.2%)和 ROS(44.5%)水平降低。YPHL 干预或 SIRT1 过表达后,LC3 和 p62 的表达增加。与对照组相比,模型组、si-SIRT1 组、si-NC 组和 si-SIRT1+YPHL 组的 SIRT1 和 LC3 蛋白表达降低,FoxO1 表达升高。si-NC+YPHL 组的这些蛋白水平变化均得到逆转。
YPHL 通过调节糖尿病大鼠的 SIRT1-FoxO1 自噬通路减少 EDL,这可能为糖尿病的治疗提供新的思路。