Faculty of Biology, Medicine and Health, Cardiovascular Research Group, University of Manchester.
NIHR/Wellcome Trust Clinical Research Facility & Department of Diabetes, Metabolism and Endocrinology, Manchester University NHS Foundation Trust, Manchester, UK.
Curr Opin Lipidol. 2024 Aug 1;35(4):171-178. doi: 10.1097/MOL.0000000000000936. Epub 2024 Jun 18.
To review the discoveries which led to the concept that serum paraoxonase 1 (PON1) is inversely related to atherosclerotic cardiovascular disease (ASCVD) incidence, how this association came to be regarded as causal and how such a role might have evolved.
Animal models suggest a causal link between PON1 present on HDL and atherosclerosis. Serum PON1 activity predicts ASCVD with a similar reliability to HDL cholesterol, but at the extremes of high and low HDL cholesterol, there is discordance with PON1 being potentially more accurate. The paraoxonase gene family has its origins in the earliest life forms. Its greatest hydrolytic activity is towards lactones and organophosphates, both of which can be generated in the natural environment. It is active towards a wide range of substrates and thus its conservation may have resulted from improved survival of species facing a variety of evolutionary challenges.
Protection against ASCVD is likely to be the consequence of some promiscuous activity of PON1, but nonetheless has the potential for exploitation to improve risk prediction and prevention of ASCVD.
回顾导致血清对氧磷酶 1(PON1)与动脉粥样硬化性心血管疾病(ASCVD)发生率呈负相关这一概念的发现,以及这种关联如何被认为是因果关系,以及这种作用可能是如何演变的。
动物模型表明,存在于高密度脂蛋白(HDL)上的 PON1 与动脉粥样硬化之间存在因果关系。血清 PON1 活性预测 ASCVD 的可靠性与 HDL 胆固醇相似,但在 HDL 胆固醇极高和极低的极端情况下,与 PON1 相比,其预测结果可能更准确。对氧磷酶基因家族起源于最早的生命形式。它对内酯和有机磷酸酯的水解活性最大,而这两者都可以在自然环境中产生。它对广泛的底物具有活性,因此其保守性可能是由于面临各种进化挑战的物种的生存能力得到了提高。
对 ASCVD 的保护可能是 PON1 的一些混杂活性的结果,但仍有可能被利用来改善 ASCVD 的风险预测和预防。