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花生四烯酸激活牛肾上腺嗜铬细胞中的阳离子通道。

Arachidonic acid activates cation channels in bovine adrenal chromaffin cells.

作者信息

Mochizuki-Oda N, Negishi M, Mori K, Ito S

机构信息

Department of Cell Biology and Neuroscience, Osaka Bioscience Institute, Japan.

出版信息

J Neurochem. 1993 Nov;61(5):1882-90. doi: 10.1111/j.1471-4159.1993.tb09830.x.

Abstract

Microscopic fluorescence analysis of fura-2-loaded bovine adrenal chromaffin cells demonstrates that approximately 70% of the cells responded to arachidonic acid in increasing the intracellular Ca2+ concentration. Because this increase was markedly less in the absence of external Ca2+, we examined the effect of arachidonic acid on Ca2+ influx electrophysiologically. Bath application of 10 microM arachidonic acid induced a long-lasting inward current when the cell was clamped at -50 mV. Other fatty acids, such as oleic acid, linoleic acid, eicosatrienoic acid, and eicosapentaenoic acid, were all ineffective. The current-voltage relationships suggest that arachidonic acid may activate voltage-insensitive channels. Arachidonic acid (> or = 2 microM) activated a single-channel current in the inside-out patch, even in the presence of inhibitors of cyclooxygenase and lipoxygenase, possibly suggesting that arachidonic acid could activate channels directly. The onset delay of the inward channel current in the outside-out patch configuration (54.2 +/- 63.5 s; mean +/- SD) was significantly shorter than that in the inside-out patch one (197.3 +/- 177.7 s). Washout of arachidonic acid decreased the probability of channel openings in the outside-out patch but not in the inside-out one. These results suggest that arachidonic acid activates channels reversibly from outside of the plasma membrane. The unitary conductance for Ca2+ of arachidonic acid-activated channel was approximately 17 pS. The arachidonic acid-activated channel was permeable to Ba2+, Ca2+, and Na+ but not to Cl-. The opening probability of the arachidonic acid-activated channel did not depend on membrane potential.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对负载fura-2的牛肾上腺嗜铬细胞进行显微荧光分析表明,约70%的细胞对花生四烯酸作出反应,使细胞内钙离子浓度升高。由于在无细胞外钙离子时这种升高明显较小,我们用电生理学方法研究了花生四烯酸对钙离子内流的影响。当细胞钳制在-50 mV时,浴槽中加入10 μM花生四烯酸可诱导出持续的内向电流。其他脂肪酸,如油酸、亚油酸、二十碳三烯酸和二十碳五烯酸均无此作用。电流-电压关系表明花生四烯酸可能激活电压不敏感通道。即使存在环氧化酶和脂氧化酶抑制剂,花生四烯酸(≥2 μM)仍能在膜外翻片内激活单通道电流,这可能表明花生四烯酸可直接激活通道。膜外片构型中内向通道电流的起始延迟(54.2±63.5秒;平均值±标准差)明显短于膜内翻片构型中的起始延迟(197.3±177.7秒)。洗脱花生四烯酸可降低膜外片通道开放的概率,但膜内翻片不受影响。这些结果表明花生四烯酸可从质膜外侧可逆地激活通道。花生四烯酸激活通道对钙离子的单位电导约为17 pS。花生四烯酸激活的通道对钡离子、钙离子和钠离子通透,但对氯离子不通透。花生四烯酸激活通道的开放概率不依赖于膜电位。(摘要截短于250词)

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