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运用独立作用和浓度相加的概念来区分双壳贝类鳃中不同类型ABC外排泵的活性。

Teasing apart activities of different types of ABC efflux pumps in bivalve gills using the concepts of independent action and concentration addition.

作者信息

Luckenbach Till, Altenburger Rolf, Epel David

机构信息

UFZ - Helmholtz Centre for Environmental Research, Permoserstr. 15, Leipzig, Germany.

出版信息

Mar Environ Res. 2008 Jul;66(1):75-6. doi: 10.1016/j.marenvres.2008.02.027. Epub 2008 Feb 26.

DOI:10.1016/j.marenvres.2008.02.027
PMID:18396325
Abstract

Fluorescent dyes and inhibitor compounds are commonly used to detect activity of multixenobiotic resistance (MXR) efflux pumps in marine invertebrates. We here address the question whether compounds acting as specific inhibitors of certain mammalian transporters can be used in dye efflux assays to distinguish different transporter activities in gill tissue from a marine mussel. We quantified effects of PSC833, a specific inhibitor of mammalian P-gp (P-glycoprotein, ABCB1), and MK571, which blocks MRP (Multidrug resistance associated protein, ABCC) type transporters, on calcein-am efflux in gill tissue of Mytilus californianus. Calcein-am acts as a substrate of both P-gp and MRP. Effects of single compounds and mixtures were determined and combined effect models predicting independent action (IA) and concentration addition (CA) of the chemicals were applied. Effect values predicted by IA showed better correspondence with the experimentally obtained data. This indicates that the inhibitor compounds target different mechanisms of calcein-am efflux and points to P-gp and MRP activities in mussel gills. Our approach could be a simple way for identifying the efflux transporter types targeted by chemosensitizers, including environmentally relevant compounds, in native tissues from marine invertebrates.

摘要

荧光染料和抑制剂化合物通常用于检测海洋无脊椎动物中多药耐药(MXR)外排泵的活性。我们在此探讨充当某些哺乳动物转运蛋白特异性抑制剂的化合物是否可用于染料外排试验,以区分海洋贻贝鳃组织中的不同转运蛋白活性。我们量化了哺乳动物P-糖蛋白(P-gp,ABCB1)的特异性抑制剂PSC833和阻断多药耐药相关蛋白(MRP,ABCC)型转运蛋白的MK571对加州贻贝鳃组织中钙黄绿素-AM外排的影响。钙黄绿素-AM既是P-gp的底物,也是MRP的底物。测定了单一化合物和混合物的影响,并应用了预测化学物质独立作用(IA)和浓度相加(CA)的联合效应模型。IA预测的效应值与实验获得的数据显示出更好的对应关系。这表明抑制剂化合物靶向钙黄绿素-AM外排的不同机制,并表明贻贝鳃中存在P-gp和MRP活性。我们的方法可能是一种简单的方法,用于识别包括环境相关化合物在内的化学增敏剂在海洋无脊椎动物天然组织中靶向的外排转运蛋白类型。

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