Suppr超能文献

SNF472,一种新型抗结晶剂,可抑制人主动脉瓣钙化体外模型中的诱导钙化。

SNF472, a novel anti-crystallization agent, inhibits induced calcification in an in vitro model of human aortic valve calcification.

机构信息

Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.

Sanifit Therapeutics, Palma, Spain; Department of Fundamental Biology and Health Sciences, University of the Balearic Islands, Palma, Spain.

出版信息

Vascul Pharmacol. 2019 Nov-Dec;122-123:106583. doi: 10.1016/j.vph.2019.106583. Epub 2019 Aug 19.

Abstract

The purpose of the present study was to investigate whether SNF472, the hexasodium salt of myo-inositol hexaphosphate (IP6 or phytate): 1. Inhibits induced calcification in cultured aortic valve interstitial cells (VIC) as an in vitro model of aortic valve stenosis and 2. Whether inhibition is different in VIC obtained from healthy and calcified aortic valves. VIC from healthy (n = 5) and calcified (n = 7) human aortic valves were seeded in basic growth medium, osteogenic differentiation medium alone, or in osteogenic medium with SNF472 (3, 10, and 30 μM) and cultivated for 3 weeks. Calcification was quantified spectrophotometrically after Alizarin Red staining. In VIC from calcified valves, a complete inhibition of calcification was observed with SNF472 concentrations of 10 and 30 μM (p < .01), significantly stronger than in VIC from healthy valves. When SNF472 was added to VIC after 1 week in osteogenic medium, 30 and 100 μM SNF472 inhibited the progression of ongoing calcification by 81 and 100% (p < .01), respectively. The same concentrations of SNF472 given after 2 weeks reduced calcification by 35 and 40% respectively (not significant). SNF472 inhibited both the formation and the progression of calcification with the strongest effect in VIC from calcified valves.

摘要

本研究旨在探讨肌醇六磷酸六钠(IP6 或植酸)是否:1. 抑制培养的主动脉瓣膜间质细胞(VIC)中的诱导钙化,作为主动脉瓣狭窄的体外模型;2. 在来自健康和钙化主动脉瓣的 VIC 中,抑制作用是否不同。将来自健康(n=5)和钙化(n=7)人主动脉瓣的 VIC 接种于基础生长培养基、单独成骨分化培养基或含有 SNF472(3、10 和 30μM)的成骨培养基中,并培养 3 周。茜素红染色后分光光度法定量钙化。在钙化瓣膜的 VIC 中,用 10 和 30μM 的 SNF472 观察到完全抑制钙化(p<0.01),明显强于来自健康瓣膜的 VIC。当 SNF472 在成骨培养基中添加 1 周后添加到 VIC 中时,30 和 100μM 的 SNF472 分别抑制了 81%和 100%的进行性钙化(p<0.01)。相同浓度的 SNF472 在 2 周后给药分别减少了 35%和 40%的钙化(无统计学意义)。SNF472 抑制钙化的形成和进展,在钙化瓣膜的 VIC 中作用最强。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验