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首次发现小白菊内酯具有抑制 NPC1L1 的降胆固醇活性。

First Discovery of Cholesterol-Lowering Activity of Parthenolide as NPC1L1 Inhibitor.

机构信息

Cancer Institute, The Affiliated Hospital of Qingdao University, School of Basic Medicine of Qingdao University, Qingdao 266071, China.

Qingdao Cancer Institute, Qingdao 266071, China.

出版信息

Molecules. 2022 Sep 23;27(19):6270. doi: 10.3390/molecules27196270.

Abstract

Elevated cholesterol significantly increases the risk of developing atherosclerosis and coronary heart disease. The key to treating hypercholesterolemia is lowering plasma cholesterol levels. There have been no studies on the cholesterol-lowering potential of parthenolide (PTL), a naturally occurring small molecule from Tanacetum parthenium. Here, we first put forth PTL's cholesterol-lowering ability to inhibit cellular uptake of cholesterol in a dose-dependent manner. Its performance was on par with the positive control drug, ezetimibe. Niemann-Pick C1 Like-1 (NPC1L1) has been identified as a potential therapeutic target for hypercholesterolemia. The interaction of PTL with NPC1L1 could be explained by the results of molecular docking and filipin staining further reinforces this hypothesis. Furthermore, PTL reduced the expression of NPC1L1 in HepG2 cells in a concentration-dependent manner, which suggests that PTL functions as a potential NPC1L1 inhibitor with therapeutic potential for hypercholesterolemia.

摘要

胆固醇升高显著增加了动脉粥样硬化和冠心病的发病风险。治疗高胆固醇血症的关键是降低血浆胆固醇水平。目前还没有研究过倍半萜内酯(PTL)的降胆固醇潜力,PTL 是一种来自菊科植物春黄菊的天然存在的小分子。在这里,我们首次提出 PTL 能够通过抑制细胞摄取胆固醇来降低胆固醇,其效果与阳性对照药物依折麦布相当。Niemann-Pick C1 Like-1(NPC1L1)已被确定为高胆固醇血症的潜在治疗靶点。分子对接和 filipin 染色的结果进一步解释了 PTL 与 NPC1L1 的相互作用。此外,PTL 以浓度依赖的方式降低了 HepG2 细胞中 NPC1L1 的表达,这表明 PTL 作为一种潜在的 NPC1L1 抑制剂,具有治疗高胆固醇血症的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c14f/9572688/2b571da098af/molecules-27-06270-g001.jpg

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