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首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Stimulatory effect of taurine on calcium ion uptake in rod outer segments of the rat retina is independent of taurine uptake.
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Stimulatory effect of taurine on calcium ion uptake in rod outer segments of the rat retina is independent of taurine uptake.

机译:牛磺酸对大鼠视网膜杆外节段钙离子摄取的刺激作用与牛磺酸摄取无关。

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摘要

Taurine stimulates ATP-dependent Ca(2+) uptake in the rat rod outer segments (ROS). This stimulation has been linked to the function of the cyclic nucleotide-gated cation channel, implying an important physiologic role for taurine in visual signal transduction. Calmodulin (CaM) has been reported to affect taurine transport in the choroid plexus and also to inhibit the cyclic nucleotide-gated channel; thus, the effects of the competitive CaM inhibitors trifluoperazine (TFP) and N-(8-aminooctyl)-5-iodonaphthalene-1-sulfonamide (J-8) were studied on Ca(2+) and taurine uptake in the rat ROS. Pretreatment of the ROS preparation with TFP and J-8 for 5 min before measurement of Ca(2+)-uptake activity produced inhibition of the effects of taurine on ATP-dependent Ca(2+) uptake. Both TFP and J-8 also were effective in inhibiting high-affinity taurine uptake. In both uptake systems, inhibition by TFP was noncompetitive. These data initially suggested that the stimulatory effects of taurine on ATP-dependent Ca(2+) uptake are dependent on taurine uptake. However, competitive inhibition of taurine uptake by guanidinoethane sulfonate did not produce any effect on the stimulatory effects of taurine. Previous studies have proposed that taurine binds directly to the plasma membrane, and our study demonstrated that TFP inhibits taurine binding to the ROS. In addition, our study demonstrated that taurine uptake is unaffected by varying the concentration of Ca(2+) and that the effects of TFP are independent of Ca(2+), suggesting that TFP acts through a CaM-independent mechanism.
机译:牛磺酸刺激大鼠杆外部部分(ROS)中ATP依赖的Ca(2+)吸收。这种刺激作用与环状核苷酸门控阳离子通道的功能有关,这暗示了牛磺酸在视觉信号转导中的重要生理作用。据报道钙调蛋白(CaM)会影响牛磺酸在脉络丛中的转运,并抑制环核苷酸门控通道。因此,研究了竞争性CaM抑制剂三氟哌嗪(TFP)和N-(8-氨基辛基)-5-碘萘-1-磺酰胺(J-8)对大鼠ROS中Ca(2+)和牛磺酸摄取的影响。在测量Ca(2+)吸收活性之前,用TFP和J-8对ROS制剂进行5分钟的预处理可抑制牛磺酸对ATP依赖性Ca(2+)吸收的影响。 TFP和J-8均可有效抑制高亲和性牛磺酸的摄取。在两种吸收系统中,TFP抑制都是非竞争性的。这些数据最初表明,牛磺酸对ATP依赖的Ca(2+)的刺激作用取决于牛磺酸的摄取。但是,胍基乙烷磺酸盐竞争性抑制牛磺酸摄取对牛磺酸的刺激作用没有任何作用。先前的研究提出牛磺酸直接与质膜结合,我们的研究表明TFP抑制牛磺酸与ROS结合。此外,我们的研究表明,牛磺酸摄取不受改变Ca(2+)的浓度的影响,并且TFP的作用独立于Ca(2+),表明TFP通过CaM独立机制起作用。

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