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脑肿胀与梗死灶大小:一项引发问题的综述

Brain Swelling versus Infarct Size: A Problematizing Review.

作者信息

Simard J Marc, Wilhelmy Bradley, Tsymbalyuk Natalya, Shim Bosung, Stokum Jesse A, Evans Madison, Gaur Anandita, Tosun Cigdem, Keledjian Kaspar, Ciryam Prajwal, Serra Riccardo, Gerzanich Volodymyr

机构信息

Department of Neurosurgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Brain Sci. 2024 Feb 28;14(3):229. doi: 10.3390/brainsci14030229.

Abstract

In human stroke, brain swelling is an important predictor of neurological outcome and mortality, yet treatments to reduce or prevent brain swelling are extremely limited, due in part to an inadequate understanding of mechanisms. In preclinical studies on cerebroprotection in animal models of stroke, historically, the focus has been on reducing infarct size, and in most studies, a reduction in infarct size has been associated with a corresponding reduction in brain swelling. Unfortunately, such findings on brain swelling have little translational value for treating brain swelling in patients with stroke. This is because, in humans, brain swelling usually becomes evident, either symptomatically or radiologically, days after the infarct size has stabilized, requiring that the prevention or treatment of brain swelling target mechanism(s) that are independent of a reduction in infarct size. In this problematizing review, we highlight the often-neglected concept that brain edema and brain swelling are not simply secondary, correlative phenomena of stroke but distinct pathological entities with unique molecular and cellular mechanisms that are worthy of direct targeting. We outline the advances in approaches for the study of brain swelling that are independent of a reduction in infarct size. Although straightforward, the approaches reviewed in this study have important translational relevance for identifying novel treatment targets for post-ischemic brain swelling.

摘要

在人类中风中,脑肿胀是神经功能预后和死亡率的重要预测指标,但减少或预防脑肿胀的治疗方法极为有限,部分原因是对其机制了解不足。在中风动物模型的脑保护临床前研究中,从历史上看,重点一直是缩小梗死灶大小,并且在大多数研究中,梗死灶大小的缩小与脑肿胀的相应减轻相关。不幸的是,这些关于脑肿胀的发现对治疗中风患者的脑肿胀几乎没有转化价值。这是因为在人类中,脑肿胀通常在梗死灶大小稳定数天后才会在症状上或影像学上变得明显,这就要求预防或治疗脑肿胀的靶点机制应独立于梗死灶大小的缩小。在这篇提出问题的综述中,我们强调一个常被忽视的概念,即脑水肿和脑肿胀并非简单地是中风的继发性、相关现象,而是具有独特分子和细胞机制的不同病理实体,值得直接作为靶点。我们概述了独立于梗死灶大小缩小的脑肿胀研究方法的进展。尽管简单,但本研究中综述的方法对于确定缺血后脑肿胀的新治疗靶点具有重要的转化意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee9/10968884/bbdc45063812/brainsci-14-00229-g001.jpg

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