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钙离子在突触前α受体介导的对大鼠大脑皮质突触体[3H]去甲肾上腺素释放的抑制作用中的角色。

On the role of calcium ions in the presynaptic alpha-receptor mediated inhibition of [3H]noradrenaline release from rat brain cortex synaptosomes.

作者信息

De Langen C D, Mulder A H

出版信息

Brain Res. 1980 Mar 10;185(2):399-408. doi: 10.1016/0006-8993(80)91077-x.

Abstract

Rat brain cortex synaptosomes, previously labeled by incubation with [3H]noradrenaline ([3H]NA) were continuously superfused with Krebs-Ringer media. Release of [3H]NA was induced by superfusion with medium containing either 15 mM K+, 20 microM veratrine or 1 microM of the calcium-ionophore A 23187 and was strongly dependent on the concentration of Ca2+ in the medium. Noradrenaline (1 microM, in the presence of the uptake inhibitor desipramine) inhibited K+-induced [3H]NA release by activation of presynaptic alpha-receptors. When the Ca2+-concentration in the medium was reduced, or the Mg2+-concentration increased, [3H]NA release appeared to be more susceptible to alpha-receptor mediated inhibition. Noradrenaline (1 microM) inhibited [3H]NA release induced by 15 mM K+, in the presence of 0.075 Ca2+ and 10 mM Mg2+, by 86%. Veratrine-induced release was also inhibited by alpha-receptor activation. However, [3H]NA release induced by the calcium-ionophore was not affected by alpha-receptor agonists. These results strongly support the view that alpha-receptor activation results in a decrease of the availability of Ca2+ for stimulus-secretion coupling processes. Presumably this is effected by an inhibition of voltage-sensitive calcium channels in the neuronal membrane associated with neurotransmitter release.

摘要

先前通过与[3H]去甲肾上腺素([3H]NA)孵育进行标记的大鼠脑皮质突触体,用Krebs-Ringer培养基持续灌流。用含有15 mM K+、20 μM藜芦碱或1 μM钙离子载体A 23187的培养基灌流可诱导[3H]NA的释放,且其强烈依赖于培养基中Ca2+的浓度。去甲肾上腺素(1 μM,在摄取抑制剂地昔帕明存在的情况下)通过激活突触前α受体抑制K+诱导的[3H]NA释放。当培养基中的Ca2+浓度降低或Mg2+浓度升高时,[3H]NA释放似乎对α受体介导的抑制更敏感。在存在0.075 Ca2+和10 mM Mg2+的情况下,去甲肾上腺素(1 μM)抑制15 mM K+诱导的[3H]NA释放达86%。藜芦碱诱导的释放也受到α受体激活的抑制。然而,钙离子载体诱导的[3H]NA释放不受α受体激动剂的影响。这些结果有力地支持了这样一种观点,即α受体激活导致用于刺激-分泌偶联过程的Ca2+可用性降低。据推测,这是通过抑制与神经递质释放相关的神经元膜中的电压敏感性钙通道来实现的。

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