石酸改善棕酸诱导的异常葡萄糖吸收通过PDK4/AMPK/TBC1D1路径在C2C12神经管中
Changfa Zhang1, Shuai Li1, Likang Li1
1Center for Clinical Epidemiology and Methodology (CCEM), Guangdong Second Provincial General Hospital, Guangzhou, China.
Endocrinology, diabetes & metabolism
|April 1, 2024
概括
石酸 (SV) 通过调节PDK4/AMPK/TBC1D1通路,增强肌肉细胞中的葡萄糖吸收. 这种天然甜味剂可以通过改善葡萄糖代谢来帮助预防2型糖尿病 (T2DM).
科学领域:
- 生物化学 生物化学
- 细胞生物学 细胞生物学
- 代谢研究研究 代谢研究
背景情况:
- 石酸 (stevioside,SV) 是一种天然的甜味剂,在饮料中广泛使用.
- 它对肌肉细胞中葡萄糖吸收和pyruvate dehydrogenase kinase isoenzyme 4 (PDK4) 的影响尚不清楚.
- 用棕酸 (PA) 诱导的C2C12神经管来研究SV的机制.
研究的目的:
- 为了研究石化 (SV) 对C2C12骨肌细胞葡萄糖吸收的影响.
- 阐明PDK4在SV介导的葡萄糖代谢中的作用.
- 探索涉及PDK4/AMPK/TBC1D1通路的潜在分子机制.
主要方法:
- 用2-NBDG测量细胞葡萄糖摄取量.
- 通过实时PCR量化Pdk4的基因表达.
- 通过西式斑点分析分析了PDK4,p-AMPK,TBC1D1和GLUT4的蛋白质水平.
主要成果:
- 在PA诱导的C2C12神经管中,SV显著增加了葡萄糖的摄取.
- SV降低了PDK4水平,增加了p-AMPK和TBC1D1水平.
- SV促进了GLUT4转移到细胞膜,并改善了PA诱导的葡萄糖吸收异常.
结论:
- 石酸 (SV) 通过PDK4/AMPK/TBC1D1通路改善C2C12神经管中棕酸诱导的异常葡萄糖吸收.
- 这些发现表明SV的潜力作为一种安全的天然甜味剂,用于管理2型糖尿病 (T2DM).
- 需要进一步的研究,以在更广泛的背景下验证这些结果.
更多相关视频
08:35A Model of Experimental Steatosis In Vitro: Hepatocyte Cell Culture in Lipid Overload-Conditioned Medium
Published on: May 18, 2021
6.3K
08:20Investigating the Protective Effects of Platycodin D on Non-Alcoholic Fatty Liver Disease in a Palmitic Acid-Induced In Vitro Model
Published on: December 2, 2022
1.9K
相关概念视频
cAMP-dependent Protein Kinase Pathways
6.3K
Cyclic Adenosine Monophosphate (cAMP) is an essential second messenger that activates protein kinase A (PKA) and regulates various biological processes. A single epinephrine molecule binds to GPCR and activates several heterotrimeric G proteins, each stimulating multiple adenylyl cyclase, amplifying the signal, and synthesizing large numbers of cAMP molecules. Small changes in cAMP concentration affect PKA activity. The binding of four cAMP molecules induces a conformational change in PKA,...
6.3K
Cell Specific Gene Expression
13.6K
Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...
13.6K
PI3K/mTOR/AKT Signaling Pathway
3.5K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
3.5K
Insulin: The Receptor and Signaling Pathways
1.2K
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but...
1.2K
Insulin Secretory Vesicles
4.9K
Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
4.9K
