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高密度脂蛋白:升高的水平是否理想且可实现?

High density lipoprotein: are elevated levels desirable and achievable?

作者信息

Bisgaier C L, Pape M E

机构信息

Department of Vascular and Cardiac Diseases, Parke-Davis Pharmaceutical Research, Division of Warner-Lambert Company, Ann Arbor, MI 48105, USA.

出版信息

Curr Pharm Des. 1998 Feb;4(1):53-70.

Abstract

In this review we focus on addressing two questions concerning high density lipoproteins (HDL). First, are elevated levels of HDL a desirable clinical plasma endpoint and secondly, if so, can strategies be devised that would allow the identification of agents to elevate HDL. To address the first question we briefly review the human epidemiologic and prospective data that identifies HDL as a risk factor for coronary heart disease (CHD). To introduce HDL elevating strategies, we next provide a brief review of the structural and enzymatic features of HDL followed by a discussion on the current thinking of the metabolic origin of the lipoprotein. We then turn to discussions on the key plasma and cell associated proteins involved in the synthesis, catabolism, and remodeling of HDL by analyzing data derived from human mutations, genetically engineered animal models with altered HDL metabolism and in vitro experimental systems. Lastly, we propose approaches to raise HDL that are either based on identification of small organic molecules or more unconventional approaches such as gene therapy or delivery of biologicals into plasma. This last section is based on an evaluation of the putative mechanism of actions of both old and new HDL elevating compounds. Our review concludes with an optimistic view that agents can be identified which may have promise in the treatment of human hypoalphalipoproteinemia and CHD.

摘要

在本综述中,我们着重探讨有关高密度脂蛋白(HDL)的两个问题。其一,HDL水平升高是否是一个理想的临床血浆终点;其二,如果是,能否设计出一些策略来识别可升高HDL的药物。为回答第一个问题,我们简要回顾了将HDL确定为冠心病(CHD)风险因素的人类流行病学和前瞻性数据。为介绍升高HDL的策略,接下来我们简要回顾HDL的结构和酶学特征,随后讨论脂蛋白代谢起源的当前观点。然后,我们通过分析来自人类突变、HDL代谢改变的基因工程动物模型以及体外实验系统的数据,转向讨论参与HDL合成、分解代谢和重塑的关键血浆和细胞相关蛋白。最后,我们提出基于识别小分子的升高HDL的方法,以及更非常规的方法,如基因治疗或向血浆中递送生物制剂。最后这部分基于对新旧HDL升高化合物假定作用机制的评估。我们的综述以乐观的观点结尾,即可以识别出可能在治疗人类低α脂蛋白血症和CHD方面有前景的药物。

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