首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Effect of diphenyl diselenide, diphenyl ditelluride and ebselen on cerebral Na(+), K(+)-ATPase activity in rats.
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Effect of diphenyl diselenide, diphenyl ditelluride and ebselen on cerebral Na(+), K(+)-ATPase activity in rats.

机译:二苯二硒化物,二苯二碲化物和依布硒啉对大鼠脑Na(+),K(+)-ATPase活性的影响。

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摘要

In the present study, we investigated the in vitro effect of diphenyl ditelluride, diphenyl diselenide and ebselen on Na(+), K(+)-ATPase activity of rat brain. The results demonstrated that all compounds significantly inhibited (in the muM range) Na(+), K(+)-ATPase activity. Diphenyl ditelluride, at low concentrations, provoked an increase in Na(+), K(+)-ATPase activity. Dithiothreitol (DTT), at 3mM, protected the inhibition caused by diphenyl ditelluride, diphenyl diselenide and ebselen in Na(+), K(+)-ATPase activity. Post-incubation of diphenyl diselenide-treated homogenate with DTT completely recovered enzyme activity. DTT was able to recover the enzyme inhibition induced by 20muM of diphenyl ditelluride, but was partially able to recover inhibition induced by high concentrations of organotellurium compound. Conversely, DTT did not recover ebselen-induced Na(+), K(+)-ATPase inhibition. The mechanism of inhibition by diphenyl diselenide, diphenyl ditelluride and ebselen in Na(+), K(+)-ATPase activityrevealed: decreased maximal velocity and K(m). Cerebral Na(+), K(+)-ATPase is a potential molecular target for the toxic effect of organochalcogens and the inhibition may occur through a change in the crucial thiol groups of this enzyme.
机译:在本研究中,我们调查了二苯基二碲化物,二苯基二硒化物和依布硒啉对大鼠脑Na(+),K(+)-ATPase活性的体外作用。结果表明,所有化合物均显着抑制(在muM范围内)Na(+),K(+)-ATPase活性。低浓度的二苯基二碲化物引起Na(+),K(+)-ATPase活性的增加。二硫苏糖醇(DTT)在3mM时可保护二苯基二碲化物,二苯基二硒化物和依布硒啉对Na(+),K(+)-ATPase活性的抑制作用。用DTT孵育二苯二硒化物处理的匀浆后可完全恢复酶活性。 DTT能够恢复20μM二苯基二碲化物诱导的酶抑制作用,但部分能够恢复高浓度有机碲化合物诱导的酶抑制作用。相反,DTT不能恢复依布硒仑诱导的Na(+),K(+)-ATPase抑制作用。揭示了二苯基二硒化物,二苯基二碲化物和依布硒啉在Na(+),K(+)-ATPase活性中的抑制机制:降低了最大速度和K(m)。脑Na(+),K(+)-ATPase是有机硫属元素的毒性作用的潜在分子靶标,其抑制作用可能是通过改变该酶的关键硫醇基团来实现的。

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