Trinity College Dublin, Smurfit Institute of Genetics, Dublin 2, Ireland.
Biochim Biophys Acta Biomembr. 2020 Sep 1;1862(9):183298. doi: 10.1016/j.bbamem.2020.183298. Epub 2020 Apr 27.
The blood-brain barrier (BBB) is the one of the most robust physical barriers in the body, comprised of tight junction (TJ) proteins in brain microvascular endothelial cells. The need for drugs to treat central nervous systems diseases is ever increasing, however the presence of the BBB significantly hampers the uptake of drugs into the brain. To overcome or circumvent the barrier, many kinds of techniques are being developed. Modulating the paracellular route by disruption of the TJ complex has been proposed as a potential drug delivery system to treat brain diseases, however, it has several limitations and is still in a developmental stage. However, recent significant advance in medical equipment /tools such as targeted ultra-sound technologies may resolve these limitations. In this review, we introduce recent advances in site- or molecular size-selective BBB disruption/modulation technologies and we include details on pharmacological inhibitory molecules against intercellular TJ proteins to modulate the BBB.
血脑屏障(BBB)是人体中最强大的物理屏障之一,由脑微血管内皮细胞中的紧密连接(TJ)蛋白组成。治疗中枢神经系统疾病的药物需求不断增加,然而,BBB 的存在极大地阻碍了药物进入大脑。为了克服或绕过这一障碍,正在开发许多种技术。通过破坏 TJ 复合物来调节细胞旁途径已被提议作为治疗脑部疾病的潜在药物递送系统,但它存在一些局限性,仍处于发展阶段。然而,最近医疗设备/工具的显著进步,如靶向超声技术,可能会解决这些限制。在这篇综述中,我们介绍了最近在基于部位或分子大小选择性 BBB 破坏/调节技术方面的进展,并详细介绍了针对细胞间 TJ 蛋白的药理学抑制分子来调节 BBB。