首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Attenuation of maitotoxin-induced cytotoxicity in rat aortic smooth muscle cells by inhibitors of Nau+/Cau2u+ exchange, and calpain activation
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Attenuation of maitotoxin-induced cytotoxicity in rat aortic smooth muscle cells by inhibitors of Nau+/Cau2u+ exchange, and calpain activation

机译:Nau + / Cau2u +交换和钙蛋白酶激活的抑制剂可减轻大鼠主动脉平滑肌细胞中人毒素对细胞毒性的影响

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摘要

The highly potent marine toxin maitotoxin (MTX) evoked an increase in cytosolic Cau2u+ levels in fura-2 loaded rat aortic smooth muscle cells, which was dependent on extracellular Cau2u+. This increase was almost fully inhibited by KB-R7943, a potent selective inhibitor of the reverse mode of the Nau+/Cau2u+ exchanger (NCX). Cell viability was assessed using ethidium bromide uptake and the alamarBlue cytotoxicity assay. In both assays MTX-induced toxicity was attenuated by KB-R7943, as well as by MDL 28170, a membrane permeable calpain inhibitor. Maitotoxin-evoked contractions of rat aortic strip preparations in vitro, which persist following washout of the toxin, were relaxed by subsequent addition of KB-R7943 or MDL 28170, either in the presence of, or following washout of MTX. These results suggest that MTX targets the Nau+/Cau2u+ exchanger and causes it to operate in reverse mode (Nau+ efflux/Cau2u+ influx), thus leading to calpain activation, NCX cleavage, secondary Cau2u+ overload and cell death.
机译:强效海洋毒素麦芽毒素(MTX)引起呋喃2加载的大鼠主动脉平滑肌细胞中胞质Cau2u +含量增加,这取决于细胞外Cau2u +。 KB-R7943是Nau + / Cau2u +交换子(NCX)反向模式的有效选择性抑制剂,几乎完全抑制了这种增加。使用溴化乙锭摄取和alamarBlue细胞毒性测定法评估细胞活力。在两种试验中,KB-R7943以及膜渗透性钙蛋白酶抑制剂MDL 28170均减弱了MTX诱导的毒性。在存在或清除MTX的情况下,通过随后添加KB-R7943或MDL 28170可以放松大鼠毒素在冲刷后持续存在的体外由人毒素引起的大鼠主动脉条制剂的收缩。这些结果表明,MTX靶向Nau + / Cau2u +交换子并使其以反向模式运行(Nau +外排/ Cau2u +流入),从而导致钙蛋白酶激活,NCX裂解,继发性Cau2u +超负荷和细胞死亡。

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