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神经原性高血压、血脑屏障与靶向纳米疗法的潜在作用。

Neurogenic Hypertension, the Blood-Brain Barrier, and the Potential Role of Targeted Nanotherapeutics.

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, College of Health Professions, North Dakota State University, Fargo, ND 58105, USA.

出版信息

Int J Mol Sci. 2023 Jan 22;24(3):2213. doi: 10.3390/ijms24032213.

Abstract

Hypertension is a major health concern globally. Elevated blood pressure, initiated and maintained by the brain, is defined as neurogenic hypertension (NH), which accounts for nearly half of all hypertension cases. A significant increase in angiotensin II-mediated sympathetic nervous system activity within the brain is known to be the key driving force behind NH. Blood pressure control in NH has been demonstrated through intracerebrovascular injection of agents that reduce the sympathetic influence on cardiac functions. However, traditional antihypertensive agents lack effective brain permeation, making NH management extremely challenging. Therefore, developing strategies that allow brain-targeted delivery of antihypertensives at the therapeutic level is crucial. Targeting nanotherapeutics have become popular in delivering therapeutics to hard-to-reach regions of the body, including the brain. Despite the frequent use of nanotherapeutics in other pathological conditions such as cancer, their use in hypertension has received very little attention. This review discusses the underlying pathophysiology and current management strategies for NH, as well as the potential role of targeted therapeutics in improving current treatment strategies.

摘要

高血压是全球主要的健康关注点。由大脑引发和维持的血压升高被定义为神经性高血压(NH),占所有高血压病例的近一半。已知大脑中血管紧张素 II 介导的交感神经系统活动的显著增加是 NH 的关键驱动力。通过向脑血管内注射可减少交感神经对心脏功能影响的药物,已经证明可以控制 NH 中的血压。然而,传统的降压药物缺乏有效的脑部渗透,使得 NH 的管理极具挑战性。因此,开发允许将降压药在治疗水平上靶向递送至大脑的策略至关重要。纳米疗法已成为将治疗药物递送至包括大脑在内的难以到达的身体区域的热门方法。尽管纳米疗法在癌症等其他病理条件下经常使用,但它们在高血压中的应用却很少受到关注。本文综述了 NH 的潜在病理生理学和当前管理策略,以及靶向治疗在改善当前治疗策略方面的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f676/9916775/e8007f8ac77c/ijms-24-02213-g001.jpg

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