金亚敏,胡丹丹,王立甜,殷怀留,杨祥璇,刘华戎,黄业伟.天然化合物抑制前蛋白转化酶枯草溶菌素9的作用机制研究进展[J].食品安全质量检测学报,2024,15(5):147-156 |
天然化合物抑制前蛋白转化酶枯草溶菌素9的作用机制研究进展 |
Research progress on the mechanism of natural compounds inhibitingproprotein convertase subtilisin/kexin type 9 |
投稿时间:2023-12-05 修订日期:2024-03-07 |
DOI: |
中文关键词: 动脉粥样硬化 天然化合物 前蛋白转化酶枯草溶菌素9 LDL-C |
英文关键词:atherosclerosis natural compounds proprotein convertase subtilisin/kexin type 9 low density
lipoprotein-cholesterol |
基金项目:云南省科技人才支撑计划(YNWR-QNBJ-2018-083)、云南省基础研究计划(202301BD070001-029)、云南开放大学科研团队-植物活性成分发掘与利用项目 |
作者 | 单位 |
金亚敏 | 1. 云南开放大学开放教育学院,2. 云南农业大学,普洱茶学教育部重点实验室, 3. 云南农业大学食品科学技术学院 |
胡丹丹 | 2. 云南农业大学,普洱茶学教育部重点实验室,4. 云南农业大学理学院 |
王立甜 | 2. 云南农业大学,普洱茶学教育部重点实验室, 3. 云南农业大学食品科学技术学院 |
殷怀留 | 2. 云南农业大学,普洱茶学教育部重点实验室, 3. 云南农业大学食品科学技术学院 |
杨祥璇 | 2. 云南农业大学,普洱茶学教育部重点实验室, 3. 云南农业大学食品科学技术学院 |
刘华戎 | 1. 云南开放大学开放教育学院 |
黄业伟 | 2. 云南农业大学,普洱茶学教育部重点实验室,4. 云南农业大学理学院 |
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Author | Institution |
JIN Ya-Min | 1.Open Education College of Yunnan Open University,Yunnan Open University,2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University,3.College of Food Science and Technology, Yunnan Agricultural University |
HU Dan-Dan | 2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University4.College of Science, Yunnan Agricultural University |
WANG Li-Tian | 2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University,3.College of Food Science and Technology, Yunnan Agricultural University |
YIN Huai-Liu | 2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University,3.College of Food Science and Technology, Yunnan Agricultural University |
YANG Xiang-Xuan | 2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University,3.College of Food Science and Technology, Yunnan Agricultural University |
LIU Hua-Rong | 1.Open Education College of Yunnan Open University,Yunnan Open University |
HUANG Ye-Wei | 2. Key Laboratory of Pu’er Tea Science of Ministry of Education,Yunnan Agricultural University4.College of Science, Yunnan Agricultural University |
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中文摘要: |
动脉粥样硬化(atherosclerosis,AS)是一种复杂的慢性进行性动脉疾病,被视为全球死亡的重要原因。高水平的血浆低密度脂蛋白胆固醇(low density lipoprotein-cholesterol,LDL-C)是动脉粥样硬化发生和发展的关键危险因素。血浆中循环的前蛋白转化酶枯草溶菌素9(proprotein convertase subtilisin/kexin type 9,PCSK9)是一种肝细胞合成的丝氨酸蛋白酶,是低密度脂蛋白受体(low density lipoprotein receptor,LDLR)的关键调节因子,在控制血浆LDL-C水平方面发挥着关键作用,它通过与肝脏低密度脂蛋白受体结合, 形成PCSK9-LDLR复合物导致LDLR在溶酶体中降解,并减少肝细胞膜表面的LDLR的数量,进而导致血浆LDL-C水平升高。目前临床常用他汀类降脂药物,如阿托伐他汀调节LDL-C水平,延缓动脉粥样硬化,但药物起效慢,单一应用难以达到理想的效果,且会在不同程度上产生不良影响。因此PCSK9是一种新的降低胆固醇的治疗靶点。在本综述中,我们旨在阐明了调控PCSK9的途径及改善AS的天然物化合物的研究现状和潜在的治疗意义。 |
英文摘要: |
Atherosclerosis (AS) is a complex chronic progressive arterial disease, which is regarded as an important cause of death worldwide. High levels of plasma low density lipoprotein-cholesterol (LDL-C) are key risk factors for the occurrence and development of atherosclerosis. Proprotein convertase subtilisin/kexin type 9 (PCSK9) circulating in plasma is a serine protease synthesized by liver cells, which is a key regulator of low density lipoprotein receptor (LDLR) and plays a crucial role in controlling plasma LDL-C levels. It binds to liver LDLR to form the PCSK9 LDLR complex, which leads to degradation of LDLR in lysosomes, and reduce the amount of LDLR on the surface of liver cell membrane, which in turn leads to elevated plasma LDL-C levels. At present, statin based lipid-lowering drugs are commonly used in clinical practice, such as atorvastatin, which regulates LDL-C levels and delays AS, but the drug takes effect slowly, and single use is difficult to achieve the desired effect, and can have adverse effects to varying degrees. Therefore, PCSK9 is a new therapeutic target for lowering cholesterol. This review aims to elucidated the research status and potential therapeutic significance of natural compounds that regulate PCSK9 and improve AS, in order to provide reference for the prevention and treatment of AS. |
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