EntomoPharm R&D, Medicon Village, Lund, Sweden.
J Pharmacol Exp Ther. 2013 Aug;346(2):211-8. doi: 10.1124/jpet.113.205476. Epub 2013 May 13.
The aim of the present study was to develop a blood-brain barrier (BBB) permeability model that is applicable in the drug discovery phase. The BBB ensures proper neural function, but it restricts many drugs from entering the brain, and this complicates the development of new drugs against central nervous system diseases. Many in vitro models have been developed to predict BBB permeability, but the permeability characteristics of the human BBB are notoriously complex and hard to predict. Consequently, one single suitable BBB permeability screening model, which is generally applicable in the early drug discovery phase, does not yet exist. A new refined ex vivo insect-based BBB screening model that uses an intact, viable whole brain under controlled in vitro-like exposure conditions is presented. This model uses intact brains from desert locusts, which are placed in a well containing the compound solubilized in an insect buffer. After a limited time, the brain is removed and the compound concentration in the brain is measured by conventional liquid chromatography-mass spectrometry. The data presented here include 25 known drugs, and the data show that the ex vivo insect model can be used to measure the brain uptake over the hemolymph-brain barrier of drugs and that the brain uptake shows linear correlation with in situ perfusion data obtained in vertebrates. Moreover, this study shows that the insect ex vivo model is able to identify P-glycoprotein (Pgp) substrates, and the model allows differentiation between low-permeability compounds and compounds that are Pgp substrates.
本研究旨在开发一种适用于药物发现阶段的血脑屏障(BBB)通透性模型。BBB 确保了适当的神经功能,但它限制了许多药物进入大脑,这使得治疗中枢神经系统疾病的新药的开发变得复杂。已经开发出许多体外模型来预测 BBB 通透性,但人 BBB 的通透性特征非常复杂,难以预测。因此,目前还不存在一个适用于药物发现早期阶段的单一合适的 BBB 通透性筛选模型。本文提出了一种新的改良的基于昆虫的体外 BBB 筛选模型,该模型在受控的体外样暴露条件下使用完整的、存活的全脑。该模型使用来自沙漠蝗的完整大脑,将其置于含有溶解在昆虫缓冲液中的化合物的小瓶中。在有限的时间后,取出大脑并通过常规液相色谱-质谱法测量大脑中的化合物浓度。本文提供的 25 种已知药物的数据表明,该体外昆虫模型可用于测量药物穿过血脑屏障的脑内摄取量,并且脑内摄取量与在脊椎动物中获得的原位灌流数据呈线性相关。此外,本研究表明,昆虫体外模型能够识别 P-糖蛋白(Pgp)底物,并且该模型允许区分低通透性化合物和 Pgp 底物化合物。