FTZ通过AMPK/ACC/SREBP信号通路缓解糖尿病肾病的脂质沉积。

IF 3.1 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Jie Tao, Xiao-Yu Zhang, Hai-Bo Tan, Min-Yi Huang, Yi-Qi Yang, Jiao Guo
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引用次数: 0

摘要

复方贞珠调脂胶囊(FTZ)是一种具有近10年临床应用历史的专利中药制剂,用于治疗高血糖、高脂血症及其他糖脂代谢疾病。已有研究表明,自由贸易区可改善糖尿病肾病(DKD)。然而,FTZ在减少DKD患者肾脏脂质积累中的作用和机制尚不清楚。腺苷5′-单磷酸活化蛋白激酶(AMPK)是能量稳态的关键调节因子,其磷酸化可抑制乙酰辅酶a羧化酶(ACC)信号,从而减少脂肪酸合成,并通过肉碱棕榈酰基转移酶-1 (CPT-1)促进脂肪酸氧化。甾醇调节元件结合蛋白1 (SREBP-1)是一种通过脂肪酸合成调节脂质代谢的转录因子。本研究通过体外和体内实验研究了FTZ的抗脂质堆积作用及其机制。采用链脲佐菌素(40 mg/kg/d, ig,连续5 d)联合高脂饲料(HFD)诱导C57BL/6J小鼠DKD模型,然后分别给予FTZ(1、2 g/kg/d, ig)或氯沙坦(30 mg/kg/d, ig)治疗12周。用高糖(HG, 30 mM)联合棕榈酸(PA, 250µM)诱导HK-2细胞损伤,然后用FTZ(25、50或100µg/ml)或Compound C(一种AMPK抑制剂,10µM)处理24 h。结果表明,FTZ降低了DKD小鼠的血脂,改善了肾功能。此外,与对照组相比,DKD小鼠和细胞的脂质沉积明显增加。然而,FTZ减轻脂质积累的作用被化合物c逆转。此外,FTZ增加了p-AMPK、p-ACC和CPT-1蛋白的表达,同时降低了SREBP-1。这些结果表明,FTZ通过调节AMPK/ACC/SREBP通路,抑制新生脂肪生成,有效地防止DKD中的脂质积累,为DKD提供了一种新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FTZ alleviates lipid deposition in diabetic kidney disease by AMPK/ACC/SREBP signaling pathway.

Fufang Zhenzhu Tiaozhi capsule (FTZ) is a patented traditional Chinese medicine preparation that has been used clinically for nearly 10 years to treat hyperglycemia, hyperlipidemia, and other glucolipid metabolic diseases. Previous studies have shown that FTZ can improve diabetic kidney disease (DKD). However, the role and mechanism of FTZ in reducing renal lipid accumulation in DKD remain unclear. Phosphorylation of Adenosine 5'-Monophosphate-Activated Protein Kinase (AMPK), a key regulator of energy homeostasis, inhibits Acetyl-CoA Carboxylase (ACC) signaling, thereby reducing fatty acid synthesis and promoting fatty acid oxidation via carnitine palmitoyltransferase-1 (CPT-1). Sterol regulatory element-binding protein 1 (SREBP-1), a transcription factor, regulates lipid metabolism through fatty acid synthesis. This study investigated the anti-lipid accumulation effect and mechanism of FTZ in vitro and in vivo. Streptozotocin (40 mg/kg/d, i.p. for 5 days, consecutively) combined with a high-fat diet (HFD) were used to induce a DKD model in C57BL/6J mice, followed by FTZ (1, 2 g/kg/d, i.g.) or Losartan (30 mg/kg/d, i.g.) treatments for 12 weeks. High glucose (HG, 30 mM) combined with palmitic-acid (PA, 250 µM) were used to induce HK-2 cells injury, followed by FTZ (25, 50, or 100 µg/ml) or Compound C (an AMPK inhibitor, 10 µM) treatments for 24 h. Results showed that FTZ reduced blood lipids and improved renal function in DKD mice. In addition, compared with the control group, DKD mice and cells exhibited significantly increased lipid deposition. However, the effect of FTZ in alleviating lipid accumulation was reversed by Compound C. Furthermore, FTZ increased p-AMPK, p-ACC and CPT-1 protein expression while decreasing SREBP-1. These results indicate that FTZ effectively protects against lipid accumulation in DKD by regulating the AMPK/ACC/SREBP pathway, inhibiting de novo lipogenesis, providing a novel therapeutic strategy for DKD.

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来源期刊
Acta Diabetologica
Acta Diabetologica 医学-内分泌学与代谢
CiteScore
7.30
自引率
2.60%
发文量
180
审稿时长
2 months
期刊介绍: Acta Diabetologica is a journal that publishes reports of experimental and clinical research on diabetes mellitus and related metabolic diseases. Original contributions on biochemical, physiological, pathophysiological and clinical aspects of research on diabetes and metabolic diseases are welcome. Reports are published in the form of original articles, short communications and letters to the editor. Invited reviews and editorials are also published. A Methodology forum, which publishes contributions on methodological aspects of diabetes in vivo and in vitro, is also available. The Editor-in-chief will be pleased to consider articles describing new techniques (e.g., new transplantation methods, metabolic models), of innovative importance in the field of diabetes/metabolism. Finally, workshop reports are also welcome in Acta Diabetologica.
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