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脂质体虾青素在血管内皮细胞中的摄取及其抗炎作用的拉曼和荧光成像追踪。

Uptake and anti-inflammatory effects of liposomal astaxanthin on endothelial cells tracked by Raman and fluorescence imaging.

机构信息

Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University, 14 Bobrzynskiego Str., 30-348, Krakow, Poland.

Faculty of Chemistry, Jagiellonian University, 2 Gronostajowa Str., 30-387, Krakow, Poland.

出版信息

Mikrochim Acta. 2023 Jul 27;190(8):332. doi: 10.1007/s00604-023-05888-8.

Abstract

Astaxanthin (AXT) is a lipophilic antioxidant and anti-inflammatory natural pigment whose cellular uptake and bioavailability could be improved via liposomal encapsulation. Endothelial cells (EC) line the lumen of all blood vessels and are tasked with multiple roles toward maintaining cardiovascular homeostasis. Endothelial dysfunction is linked to the development of many diseases and is closely interconnected with oxidative stress and vascular inflammation. The uptake of free and liposomal AXT into EC was investigated using Raman and fluorescence microscopies. AXT was either encapsulated in neutral or cationic liposomes. Enhanced uptake and anti-inflammatory effects of liposomal AXT were observed. The anti-inflammatory effects of liposomal AXT were especially prominent in reducing EC lipid unsaturation, lowering numbers of lipid droplets (LDs), and decreasing intercellular adhesion molecule 1 (ICAM-1) overexpression, which is considered a well-known marker for endothelial inflammation. These findings highlight the benefits of AXT liposomal encapsulation on EC and the applicability of Raman imaging to investigate such effects.

摘要

虾青素 (AXT) 是一种亲脂性抗氧化剂和抗炎天然色素,通过脂质体包封可以提高其细胞摄取和生物利用度。内皮细胞 (EC) 排列在所有血管的管腔中,负责维持心血管稳态的多种功能。内皮功能障碍与许多疾病的发展有关,与氧化应激和血管炎症密切相关。使用拉曼和荧光显微镜研究了游离和脂质体 AXT 在内皮细胞中的摄取。AXT 分别被包裹在中性或阳离子脂质体中。观察到脂质体 AXT 的摄取增加和抗炎作用增强。脂质体 AXT 的抗炎作用尤为明显,可降低 EC 脂质不饱和度、减少脂滴 (LD) 的数量,并降低细胞间黏附分子 1 (ICAM-1) 的过度表达,ICAM-1 被认为是内皮炎症的一个众所周知的标志物。这些发现强调了 AXT 脂质体包封对 EC 的益处,以及拉曼成像在研究此类作用中的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2842/10374751/fc72a6b0b8aa/604_2023_5888_Fig1_HTML.jpg

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