Vascular Risks, Aging, and Late-Onset Dementia: Overlapping Etiologies Point to 'Scavenger Receptor'-Mediated Therapeutics

J. D’Arrigo
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引用次数: 0

Abstract

Early changes in systemic vascular stiffness and endothelial function can contribute to altered cerebrovascular hemodynamics and impaired cognitive function; additionally, these vascular changes point to potential targets for prevention and treatment strategies in people with mild cognitive impairment. Although the pathogenic mechanisms underlying these vascular changes are heterogeneous and complex, one common feature is the development of cerebral blood flow (CBF) dysregulation, resulting in chronic cerebral hypoperfusion (CCH) and subsequently an insufficient blood supply to the brain. However, the incorporation of drugs, or other bioactive molecules, into specifically a "high density lipoprotein-like" ("HDL-like") lipid nanocarrier can result in the production of a multitasking "combination therapeutic" – capable of targeting cell-surface scavenger receptors (mainly SR-BI). Such targeting behavior of this proposed (biomimetic-nanocarrier) therapeutic vehicle can facilitate the nanocarrier's enhanced endocytosis into various target cells which, in turn, increases the likelihood that this multitasking "combination therapeutic" provides some enhanced efficacy at different stages of dementia.
血管风险、衰老和迟发性痴呆:重叠病因指向“清除率受体”介导的治疗
早期系统性血管僵硬和内皮功能的改变可导致脑血管血流动力学改变和认知功能受损;此外,这些血管变化指出了轻度认知障碍患者预防和治疗策略的潜在目标。尽管这些血管变化的致病机制是不同的和复杂的,但一个共同的特征是脑血流量(CBF)失调的发展,导致慢性脑灌注不足(CCH)和随后的脑血供不足。然而,将药物或其他生物活性分子掺入“高密度脂蛋白样”(“hdl样”)脂质纳米载体中可以产生多任务“联合治疗”——能够靶向细胞表面清道夫受体(主要是SR-BI)。这种提出的(仿生-纳米载体)治疗载体的靶向行为可以促进纳米载体对各种靶细胞的增强内吞作用,这反过来又增加了这种多任务“联合治疗”在不同阶段痴呆提供一些增强疗效的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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