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肠肌间神经元中的钙摄取和蛋白质磷酸化,与血管活性肠肽和乙酰胆碱的释放一样,是频率依赖性的。

Calcium uptake and protein phosphorylation in myenteric neurons, like the release of vasoactive intestinal polypeptide and acetylcholine, are frequency dependent.

作者信息

Agoston D V, Lisziewicz J

机构信息

Abteilung Neurocheemie, Max-Planck-Institut für biophysikalische Chemie, Göttingen, F.R.G.

出版信息

J Neurochem. 1989 May;52(5):1637-40. doi: 10.1111/j.1471-4159.1989.tb09219.x.

Abstract

The mechanism of the electrical-to-chemical decoding involved in the preferential release of the transmitters acetylcholine and vasoactive intestinal polypeptide (VIP) by electrical field stimulation at low (5 Hz) and high (50 Hz) frequencies was studied in superfused myenteric neurons. The stimulation-induced uptake of 45Ca2+ accompanying high frequency stimulation was markedly reduced by 10 microM nifedipine, a specific blocker of L-type voltage-sensitive Ca2+ channels (VSCCs), as was also the preferential high-frequency release of VIP. By contrast, the 45Ca2+ uptake during low-frequency stimulation was somewhat lower per pulse, and neither this uptake nor the preferential release of acetylcholine occurring at this frequency was significantly reduced by nifedipine. These findings suggest that the release of acetylcholine and VIP involve different VSCCs. The pattern of in vitro protein thiophosphorylation in tissue extracts of differentially stimulated myenteric neurons involved polypeptides of 205, 173, 86, 73, 57, 54, 46, 32, 28, and 24 kDa and was also markedly stimulus and nifedipine dependent. This suggests that different phosphoproteins are involved during the frequency-dependent activation of the different Ca2+ channels and exocytotic mechanisms.

摘要

在灌流的肌间神经元中,研究了在低(5赫兹)和高(50赫兹)频率下通过电场刺激优先释放递质乙酰胆碱和血管活性肠肽(VIP)所涉及的电 - 化学解码机制。10微摩尔硝苯地平(一种L型电压敏感性钙通道(VSCCs)的特异性阻滞剂)可显著降低高频刺激时伴随的刺激诱导的45Ca2+摄取,VIP的优先高频释放也会降低。相比之下,低频刺激期间每个脉冲的45Ca2+摄取略低,硝苯地平对该摄取以及此频率下发生的乙酰胆碱优先释放均无显著降低作用。这些发现表明,乙酰胆碱和VIP的释放涉及不同的VSCCs。不同刺激频率的肌间神经元组织提取物中的体外蛋白质硫代磷酸化模式涉及205、173、86、73、57、54、46、32、28和24千道尔顿的多肽,并且也明显依赖于刺激和硝苯地平。这表明在不同钙通道和胞吐机制的频率依赖性激活过程中涉及不同的磷蛋白。

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