Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.
Department of Food and Drug, University of Parma, Parma, Italy.
Can J Cardiol. 2019 Oct;35(10):1400-1408. doi: 10.1016/j.cjca.2019.05.033. Epub 2019 May 30.
Among strategies to reduce the remaining risk of cardiovascular disease, interest has focused on using infusions of synthetic high-density lipoprotein (sHDL).
New Zealand rabbits underwent a perivascular injury at both carotids and were randomly allocated into 2 protocols: (1) a single-dose study, where rabbits were treated with a single infusion of sHDL containing a trimeric form of human apoA-I (TN-sHDL, 200 mg/kg) or with Placebo; (2) a multiple-dose study, where 4 groups of rabbits were treated 5 times with Placebo or TN-sHDL at different doses (8, 40, 100 mg/kg). Plaque changes were analysed in vivo by intravascular ultrasound. Blood was drawn from rabbits for biochemical analyses and cholesterol efflux capacity evaluation.
In both protocols, atheroma volume in the Placebo groups increased between the first and the second intravascular ultrasound evaluation. A stabilization or a slight regression was instead observed vs baseline in the TN-sHDL-treated groups (P < 0.005 vs Placebo after infusion). TN-sHDL treatment caused a sharp rise of plasma-free cholesterol levels and a significant increase of total cholesterol efflux capacity. Histologic analysis of carotid plaques showed a reduced macrophage accumulation in TN-sHDL-treated rabbits compared with Placebo (P < 0.05).
Our results demonstrate that acute and subacute treatments with TN-sHDL are effective in stabilizing atherosclerotic plaques in a rabbit model. This effect appears to be related to a reduced intraplaque accumulation of inflammatory cells. Besides recent failures in proving its efficacy, sHDL treatment remains a fascinating therapeutic option for the reduction of cardiovascular risk.
在降低心血管疾病剩余风险的策略中,人们对使用合成高密度脂蛋白(sHDL)输注的兴趣日益浓厚。
新西兰兔双侧颈动脉周围血管损伤后,随机分为 2 个方案:(1)单次剂量研究,兔单次输注含三聚体形式人载脂蛋白 A-I 的 sHDL(TN-sHDL,200mg/kg)或安慰剂;(2)多次剂量研究,4 组兔分别用安慰剂或不同剂量(8、40、100mg/kg)的 TN-sHDL 治疗 5 次。采用血管内超声在体内分析斑块变化。从兔采血进行生化分析和胆固醇外排能力评估。
在这两个方案中,安慰剂组的动脉粥样硬化体积在第 1 次和第 2 次血管内超声评估之间增加。与安慰剂相比,TN-sHDL 治疗组的动脉粥样硬化体积则稳定或略有消退(输注后与安慰剂相比 P<0.005)。TN-sHDL 治疗导致血浆游离胆固醇水平急剧升高,胆固醇总外排能力显著增加。颈动脉斑块的组织学分析显示,与安慰剂相比,TN-sHDL 治疗组的巨噬细胞积累减少(P<0.05)。
我们的研究结果表明,TN-sHDL 的急性和亚急性治疗可有效稳定兔动脉粥样硬化斑块。这种作用可能与斑块内炎症细胞积累减少有关。除了最近在证明其疗效方面的失败外,sHDL 治疗仍然是降低心血管风险的一种很有吸引力的治疗选择。