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首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Lithium chloride inhibits thrombin-induced intracellular calcium mobilization in C6 rat glioma cells.
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Lithium chloride inhibits thrombin-induced intracellular calcium mobilization in C6 rat glioma cells.

机译:氯化锂抑制凝血酶诱导的C6大鼠神经胶质瘤细胞中的细胞内钙动员。

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In this study, the authors have demonstrated the effect of lithium, a typical mood stabilizer, on thrombin-evoked Ca2+ mobilization in C6 cells to elucidate the action mechanisms of the drug. Thrombin-induced Ca2 mobilization was reduced 24 hr after 1 or 10 mM lithium chloride (LiCl) pretreatment. The Ca2+ rise was reduced in a time-dependent manner, and the significant inhibition was observed 9 hr pretreatment with 10 mM LiCl. On the other hand, pretreatment of the cells with 10 mM LiCl for 24 hr did not alter the amount of Galphaq/11 significantly. Pretreatment with 10 mM LiCl for 24 hr failed to reduce the 5-HT-induced Ca2+ mobilization or to affect the desensitization of the 5-HT signal. Finally, thrombin-elicited Ca2+ rise was markedly inhibited in the presence of 0.05 U/ml plasmin, however, the Ca2+ rise was not further attenuated in the presence of plasmin in C6 cells pretreated with LiCl for 24 hr. These results indicate that pretreatment with LiCl attenuated thrombin-evoked intracellular Ca2+ mobilization in plasmin sensitive manner in C6 rat glioma cells. Thus, it is important to investigate the effect of lithium on thrombin-induced cellular responses to clarify the action mechanism of lithium in relation to some abnormality in thrombin-evoked Ca2+ rise observed in bipolar disorders.
机译:在这项研究中,作者证明了锂(一种典型的情绪稳定剂)对C6细胞中凝血酶诱发的Ca2 +动员的作用,以阐明该药物的作用机理。在1或10 mM氯化锂(LiCl)预处理后24小时,凝血酶诱导的Ca2动员减少。 Ca 2+上升以时间依赖性方式减少,并且在用10 mM LiCl预处理9小时后观察到明显的抑制作用。另一方面,用10 mM LiCl预处理细胞24小时不会显着改变Galphaq / 11的量。用10 mM LiCl预处理24小时无法降低5-HT诱导的Ca2 +动员或影响5-HT信号的脱敏。最后,在0.05U / ml纤溶酶的存在下,凝血酶引起的Ca 2+的升高被显着抑制,但是在纤溶酶的存在下,在用LiCl预处理24小时的C6细胞中,Ca 2+的升高并没有进一步减弱。这些结果表明,在C6大鼠神经胶质瘤细胞中,用LiCl预处理以纤溶酶敏感的方式减弱了凝血酶诱发的细胞内Ca2 +的迁移。因此,重要的是研究锂对凝血酶诱导的细胞反应的影响,以阐明锂与双相障碍中凝血酶引起的Ca2 +升高的某些异常有关的作用机制。

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