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二氢吡啶改变去极化诱导的钙摄取进入小脑颗粒细胞原代培养物中的情况。

Dihydropyridines change the uptake of calcium induced by depolarization into primary cultures of cerebellar granule cells.

作者信息

Carboni E, Wojcik W J, Costa E

出版信息

Neuropharmacology. 1985 Nov;24(11):1123-6. doi: 10.1016/0028-3908(85)90202-3.

DOI:10.1016/0028-3908(85)90202-3
PMID:2417155
Abstract

The uptake of calcium (Ca++) into cerebellar granule cells in primary culture was increased by depolarizing the cells with either 60 mM KC1 or veratridine. Nitrendipine, at concentrations of 100 nM or greater, antagonized approximately 40 percent of the depolarization induced Ca++ uptake. The half maximal concentration of nitrendipine was 7nM. Furthermore, another dihydropyridine derivative, BAY K 8644 enhanced the uptake of Ca++ and in the presence of nitrendipine, this facilitation of Ca++ uptake was reduced. Thus, these data indicate the existence of voltage dependent Ca++ channels which are sensitive to dihydropyridines in primary cultures of cerebellar granule cells.

摘要

用60 mM氯化钾或藜芦碱使原代培养的小脑颗粒细胞去极化,可增加细胞对钙离子(Ca++)的摄取。硝苯地平浓度在100 nM及以上时,可拮抗约40%的去极化诱导的Ca++摄取。硝苯地平的半数最大浓度为7 nM。此外,另一种二氢吡啶衍生物BAY K 8644可增强Ca++的摄取,而在硝苯地平存在的情况下,这种对Ca++摄取的促进作用会减弱。因此,这些数据表明在小脑颗粒细胞的原代培养物中存在对二氢吡啶敏感的电压依赖性Ca++通道。

相似文献

1
Dihydropyridines change the uptake of calcium induced by depolarization into primary cultures of cerebellar granule cells.二氢吡啶改变去极化诱导的钙摄取进入小脑颗粒细胞原代培养物中的情况。
Neuropharmacology. 1985 Nov;24(11):1123-6. doi: 10.1016/0028-3908(85)90202-3.
2
Dihydropyridine binding sites regulate calcium influx through specific voltage-sensitive calcium channels in cerebellar granule cells.二氢吡啶结合位点通过小脑颗粒细胞中特定的电压敏感性钙通道调节钙内流。
J Neurochem. 1988 Apr;50(4):1279-86. doi: 10.1111/j.1471-4159.1988.tb10605.x.
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Dihydropyridine sensitive calcium channels in a smooth muscle cell line.一种平滑肌细胞系中的二氢吡啶敏感性钙通道。
Biochem Biophys Res Commun. 1985 Feb 28;127(1):71-9. doi: 10.1016/s0006-291x(85)80127-3.
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Interaction of steroidal alkaloid toxins with calcium channels in neuronal cell lines.甾体生物碱毒素与神经元细胞系中钙通道的相互作用。
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Stimulation of calcium uptake in PC12 cells by the dihydropyridine agonist BAY K 8644.二氢吡啶激动剂BAY K 8644对PC12细胞钙摄取的刺激作用。
J Neurochem. 1985 Sep;45(3):990-3. doi: 10.1111/j.1471-4159.1985.tb04095.x.
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Stimulus-coupled taurine efflux from cerebellar neuronal cultures: on the roles of Ca++ and Na+.小脑神经元培养物中刺激偶联的牛磺酸外流:关于Ca++和Na+的作用
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Calcium channel activation: a different type of drug action.钙通道激活:一种不同类型的药物作用。
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Potassium depolarization elevates cytosolic free calcium concentration in rat anterior pituitary cells through 1,4-dihydropyridine-sensitive, omega-conotoxin-insensitive calcium channels.钾离子去极化通过对1,4-二氢吡啶敏感、对ω-芋螺毒素不敏感的钙通道提高大鼠垂体前叶细胞胞质游离钙浓度。
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Am J Physiol. 1986 Jan;250(1 Pt 1):C95-102. doi: 10.1152/ajpcell.1986.250.1.C95.

引用本文的文献

1
Glutamate receptor activation in cultured cerebellar granule cells increases cytosolic free Ca2+ by mobilization of cellular Ca2+ and activation of Ca2+ influx.培养的小脑颗粒细胞中谷氨酸受体的激活通过动员细胞内钙离子和激活钙离子内流来增加胞质游离钙离子浓度。
Exp Brain Res. 1989;76(2):281-91. doi: 10.1007/BF00247888.
2
Dihydropyridine inhibition of neuronal calcium current and substance P release.二氢吡啶对神经元钙电流和P物质释放的抑制作用。
Pflugers Arch. 1987 Aug;409(4-5):361-6. doi: 10.1007/BF00583789.
3
Dihydropyridines alter adenosine sensitivity in the rat hippocampal slice.
二氢吡啶改变大鼠海马切片中的腺苷敏感性。
Br J Pharmacol. 1990 Sep;101(1):97-102. doi: 10.1111/j.1476-5381.1990.tb12096.x.