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首页> 外文期刊>Cardiovascular drugs and therapy >Pharmacological approaches to modifying HDL: more basic science to understand HDL metabolism is necessary. Editorial to: 'NO-1886 up-regulates Niemann-Pick C1 protein (NPC1) expression through liver X receptor alpha signaling pathway in THP-1 macrophage-derived foam cells' by Xin Ma et al.
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Pharmacological approaches to modifying HDL: more basic science to understand HDL metabolism is necessary. Editorial to: 'NO-1886 up-regulates Niemann-Pick C1 protein (NPC1) expression through liver X receptor alpha signaling pathway in THP-1 macrophage-derived foam cells' by Xin Ma et al.

机译:修改HDL的药理学方法:需要更多基础科学来理解HDL代谢。编辑:“ NO-1886通过THP-1巨噬细胞衍生的泡沫细胞中的肝X受体α信号通路上调Niemann-Pick C1蛋白(NPC1)的表达”,作者:Xin Ma等。

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摘要

While lowering LDL-C has well established benefits, modification of HDL by pharmacological therapy remains an elusive goal in demonstrating conclusive improvements in cardiovascular outcomes. Part of the challenge in developing therapeutic approaches to HDL is that it is unclear whether increasing HDL-C levels or modifying HDL function or increasing reverse cholesterol transport is (are) the mechanism(s) by which HDL protects against cardiovascular disease. In light of the spectacular failure of torcetrapib, a CETP inhibitor (with toxic off-target effects), it is prudent to better understand the means by which cells utilize HDL to efflux excess cholesterol.
机译:虽然降低LDL-C具有公认的益处,但通过药理疗法修饰HDL仍然是实现心血管结局的最终改善方面的一个难以实现的目标。开发HDL治疗方法的部分挑战在于,目前尚不清楚增加HDL-C水平或改变HDL功能或增加胆固醇逆向转运是否是HDL预防心血管疾病的机制。考虑到CETP抑制剂torcetrapib的严重失败(具有脱靶毒性作用),谨慎地更好地了解细胞利用HDL排出过量胆固醇的方法。

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