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Thymol-evoked Ca~(2+) mobilization and ion currents in pituitary GH_3 cells

机译:垂体GH_3细胞中百里酚诱发的Ca〜(2+)动员和离子流

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In this study, an attempt was made to elucidate the effects of thymol, a monocyclic phenolic compound, on Ca~(2+) mobilization and ion currents in pituitary GH_3 cells with the aid of fura-2 fluorimetry and the whole-cell voltage-clamp technique. Thymol increased intracellular Ca ~(2+) concentrations ([Ca~(2+)]_i) in GH_3 cells loaded with Ca~(2+)-sensitive dye fura-2. Removing extracellular Ca~(2+) reduced the thymol-induced [Ca~(2+)]_i rise. In Ca~(2+)-free solution, thymol-evoked [Ca~(2+)]_i rise was unchanged by depleting the Ca~(2+) store with thapsigargin (1 μM), while the thapsigargin-induced [Ca~(2+)]_i rise was reduced by pretreatment with thymol. These results imply that the Ca ~(2+) stores depleted by thymol comprise thapsigargin-sensitive and thapsigargin-insensitive pools. In addition, after depletion of the internal Ca~(2+) store with 100 μM thymol in Ca~(2+)-free solution, a subsequent application of Ca~(2+) greatly induced a [Ca ~(2+)]_i increase. The results indicate that, similar to thapsigargin, 100 μM thymol may activate the capacitative calcium entry (CCE) channel. However, thymol (100 μM) had a slight depressant action in L-type calcium current (I_(CaL)). The stimulatory actions of thymol on Ca ~(2+) signaling may partly be responsible for the underlying cellular mechanisms through which it affects neuroendocrine functions.
机译:在这项研究中,我们尝试借助fura-2荧光测定法和全细胞电压分析技术来阐明百里香酚(单环酚类化合物)对垂体GH_3细胞Ca〜(2+)动员和离子电流的影响。钳技术。在装有Ca〜(2+)敏感染料fura-2的GH_3细胞中,百里香酚增加了细胞内Ca〜(2+)的浓度([Ca〜(2 +)] _ i)。去除细胞外Ca〜(2+)降低了百里酚诱导的[Ca〜(2 +)] _ i升高。在不含Ca〜(2+)的溶液中,通过用thapsigargin(1μM)耗尽Ca〜(2+)储存,百里香酚诱发的[Ca〜(2 +)] _ i升高没有改变,而thapsigargin诱导的[Ca百里酚预处理可减少〜(2 +)] _ i升高。这些结果表明,百里酚耗尽的Ca〜(2+)库包括对毒胡萝卜素敏感和对毒胡萝卜素不敏感的库。此外,在不含Ca〜(2+)的溶液中用100μM百里香酚耗尽内部Ca〜(2+)的存储后,随后的Ca〜(2+)的应用大大诱导了[Ca〜(2+) ] _i增加。结果表明,与毒胡萝卜素相似,100μM百里酚可激活钙离子通道(CCE)通道。然而,百里酚(100μM)在L型钙电流(I_(CaL))中具有轻微的抑制作用。百里香酚对Ca〜(2+)信号的刺激作用可能部分负责其影响神经内分泌功能的潜在细胞机制。

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