培养的神经胶质细胞在电场刺激下释放嘌呤:可能的离子机制

Caciagli F., Ciccarelli R., Di Iorio P., Ballerini P., Tacconelli L.
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引用次数: 46

摘要

分离的神经胶质细胞原代培养物在静息和电场刺激时释放了大量的嘌呤。通过HPLC对3h -腺苷(3H-Ado)衍生的标记化合物(用于预载培养物)进行鉴定,发现核苷酸和核苷在过清液中的比例相等(分别为43.86%和56.14%)。大量的未标记嘌呤通常由核苷酸化合物构成(91.10%)也被释放并在过清液中检测到。在所有的实验条件下,它们的诱发释放结果不依赖于频率。由于:o-发现释放的标记化合物与刺激频率相关的线性增加;在5×10-5M双嘧达莫处理的培养物中没有检测标记嘌呤;-任何标记核苷酸的显著存在,在1×10-5M 2′-脱氧可甲酸素和1×10-4M 1-(-5-异喹啉胰岛素酰基)-2-甲基哌嗪(H7)同时处理的培养物中未发现肌苷和次xantine(在这些实验条件下,3H-Ado的量增加了一倍以上);标记的化合物被认为是胶质嘌呤率的示踪剂,其释放与电诱发动作电位有关。从神经胶质细胞流出的嘌呤不依赖于钠,事实上TTX (5×10-7M)不影响它们的基础或电诱发释放。1×10-4M维拉帕米诱导的基底和诱发释放抑制也证明了显著的钙依赖性。TEA (1×10-2M)是一种通过钙介导的特定通道的钾外排的特异性抑制剂,它强烈地减少了诱发的嘌呤流出,当与钙拮抗剂同时使用时,它的任何加性效应都无法检测到。这些发现表明,培养的神经胶质细胞的频率依赖性嘌呤释放与离子机制有关,其中钙和钾主要参与其中。
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Cultures of glial cells release purines under field electrical stimulation: The possible ionic mechanisms

Dissociated primary cultures of glial cells released a remarkable amount of purines, at rest and during field electrical stimulation.

The HPLC identification of labelled compounds derived from 3H-Adenosine (3H-Ado) (employed to preload the cultures) indicated that nucleotides and nucleosides were represented in the superfusate in equivalent proportions (43.86% and 56.14% respectively). Very much higher amounts of unlabelled purines prevalently constituted by nucleotides compounds (91.10%) were also released and detectable in the superfusate. In all the experimental conditions their evoked release did not result frequency-dependent.

Since:o

  1. -

    a linear increase related to the stimulation frequencies was found for the released labelled compounds;

  2. -

    no labelled purines were assayed in 5×10-5M Dipyridamole-treated cultures;

  3. -

    any significant presence of labelled nucleotides, inosine and hypoxantine was not found in cultures simultaneously treated with 1×10-5M 2′-deoxycoformycin and 1×10-4M 1-(-5-isoquinolinsulfonyl)-2-methylpiperizine (H7) (3H-Ado amounts resulted more than doubled in these experimental conditions);

labelled compounds have been assumed as tracers of a glial purine rate whose release can be connetted to electrically-evoked action potentials.

Purine outflow from glial cells is not sodium dependent, in fact TTX (5×10-7M) did not affect their basal or electrically-evoked release. A remarkable calcium-dependence was also evidentiated by the 1×10-4M Verapamil-induced inhibition of basal and evoked release. TEA (1×10-2M), a specific inhibitor of potassium efflux throughout calcium-mediated specific channels, strongly reduced the evoked purine outflow and any additive effect of its was not detectable when administered simultaneously to the calcium antagonist.

These findings indicate that the frequency-dependent purine release from cultured glial cells is linked to ionic mechanisms, which calcium and potassium are mainly involved in.

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