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研究实验性缺血性中风后血脑屏障药物摄取的方法:体外和体内方法。

Methods to Study Drug Uptake at the Blood-Brain Barrier Following Experimental Ischemic Stroke: In Vitro and In Vivo Approaches.

机构信息

Department of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.

出版信息

Methods Mol Biol. 2023;2616:403-418. doi: 10.1007/978-1-0716-2926-0_28.

DOI:10.1007/978-1-0716-2926-0_28
PMID:36715949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10804953/
Abstract

Drug permeability across the blood-brain barrier (BBB) is an important concept in the development of therapeutic strategies to treat neurological diseases such as ischemic stroke. These mechanisms can be evaluated in detail using cultured brain microvascular endothelial cells or intact animals subjected to experimental stroke. Here, we describe state-of-the-art approaches to study BBB transport of therapeutics using our in vitro and in vivo approaches. These methodologies allow for precise determination of transporter kinetic properties for currently marketed therapeutics or for new chemical entities that are under development as stroke drugs.

摘要

血脑屏障(BBB)的药物渗透性是开发治疗缺血性中风等神经疾病治疗策略的一个重要概念。可以使用培养的脑微血管内皮细胞或接受实验性中风的完整动物详细评估这些机制。在这里,我们描述了使用我们的体外和体内方法研究治疗药物 BBB 转运的最新方法。这些方法学允许精确确定目前市售治疗药物或正在开发为中风药物的新化学实体的转运体动力学特性。

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1
Methods to Study Drug Uptake at the Blood-Brain Barrier Following Experimental Ischemic Stroke: In Vitro and In Vivo Approaches.研究实验性缺血性中风后血脑屏障药物摄取的方法:体外和体内方法。
Methods Mol Biol. 2023;2616:403-418. doi: 10.1007/978-1-0716-2926-0_28.
2
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本文引用的文献

1
Blood-Brain Barrier Transporters: Opportunities for Therapeutic Development in Ischemic Stroke.血脑屏障转运体:在缺血性脑卒中治疗开发中的机遇。
Int J Mol Sci. 2022 Feb 8;23(3):1898. doi: 10.3390/ijms23031898.
2
Transport Properties of Statins by Organic Anion Transporting Polypeptide 1A2 and Regulation by Transforming Growth Factor- Signaling in Human Endothelial Cells.他汀类药物通过有机阴离子转运多肽 1A2 的转运特性及转化生长因子-β 信号通路对人内皮细胞的调节作用。
J Pharmacol Exp Ther. 2021 Feb;376(2):148-160. doi: 10.1124/jpet.120.000267. Epub 2020 Nov 9.
3
Transporter-Mediated Delivery of Small Molecule Drugs to the Brain: A Critical Mechanism That Can Advance Therapeutic Development for Ischemic Stroke.转运体介导的小分子药物脑内递送:一种可推动缺血性脑卒中治疗进展的关键机制
Pharmaceutics. 2020 Feb 14;12(2):154. doi: 10.3390/pharmaceutics12020154.
4
Functional Expression of Organic Anion Transporting Polypeptide 1a4 Is Regulated by Transforming Growth Factor-/Activin Receptor-like Kinase 1 Signaling at the Blood-Brain Barrier.功能性表达有机阴离子转运多肽 1a4 受血脑屏障转化生长因子-/激活素受体样激酶 1 信号的调节。
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5
Sex-specific differences in organic anion transporting polypeptide 1a4 (Oatp1a4) functional expression at the blood-brain barrier in Sprague-Dawley rats.在 Sprague-Dawley 大鼠血脑屏障中有机阴离子转运多肽 1a4(Oatp1a4)功能表达的性别特异性差异。
Fluids Barriers CNS. 2018 Sep 13;15(1):25. doi: 10.1186/s12987-018-0110-9.
6
A new era for stroke therapy: Integrating neurovascular protection with optimal reperfusion.卒中治疗新时代:神经血管保护与最佳再灌注相结合。
J Cereb Blood Flow Metab. 2018 Dec;38(12):2073-2091. doi: 10.1177/0271678X18798162. Epub 2018 Sep 7.
7
Blood-brain barrier dysfunction in ischemic stroke: targeting tight junctions and transporters for vascular protection.缺血性脑卒中的血脑屏障功能障碍:针对紧密连接和转运体的血管保护作用。
Am J Physiol Cell Physiol. 2018 Sep 1;315(3):C343-C356. doi: 10.1152/ajpcell.00095.2018. Epub 2018 Jun 27.
8
Bone morphogenetic protein-9 increases the functional expression of organic anion transporting polypeptide 1a4 at the blood-brain barrier via the activin receptor-like kinase-1 receptor.骨形态发生蛋白-9通过激活素受体样激酶-1受体增加血脑屏障处有机阴离子转运多肽1a4的功能表达。
J Cereb Blood Flow Metab. 2017 Jul;37(7):2340-2345. doi: 10.1177/0271678X17702916. Epub 2017 Apr 7.
9
Astrocyte-Derived Pentraxin 3 Supports Blood-Brain Barrier Integrity Under Acute Phase of Stroke.星形胶质细胞衍生的五聚体蛋白3在中风急性期维持血脑屏障的完整性。
Stroke. 2016 Apr;47(4):1094-100. doi: 10.1161/STROKEAHA.115.012133. Epub 2016 Mar 10.
10
Hypoxia/reoxygenation stress signals an increase in organic anion transporting polypeptide 1a4 (Oatp1a4) at the blood-brain barrier: relevance to CNS drug delivery.缺氧/复氧应激信号会增加血脑屏障中的有机阴离子转运多肽 1a4(Oatp1a4):与中枢神经系统药物递送相关。
J Cereb Blood Flow Metab. 2014 Apr;34(4):699-707. doi: 10.1038/jcbfm.2014.4. Epub 2014 Jan 29.