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钙通道激动剂Bay K 8644对大鼠C细胞系降钙素分泌的影响。

Effect of calcium channel agonist Bay K 8644 on calcitonin secretion from a rat C-cell line.

作者信息

Hishikawa R, Fukase M, Takenaka M, Fujita T

出版信息

Biochem Biophys Res Commun. 1985 Jul 16;130(1):454-9. doi: 10.1016/0006-291x(85)90438-3.

DOI:10.1016/0006-291x(85)90438-3
PMID:2411262
Abstract

Bay K 8644, a novel dihydropyridine, stimulates calcitonin secretion in a dose-dependent manner from a rat medullary thyroid carcinoma cell line, rMTC 6-23, and causes an increase in cytosolic free calcium concentration, as measured by quin-2. These effects are competitively inhibited by nifedipine, and completely abolished in the absence of extracellular calcium. These data suggest that calcium influx via voltage-dependent calcium channels plays a crucial role in the regulation of cytosolic free calcium concentration and calcitonin secretion.

摘要

新型二氢吡啶Bay K 8644能以剂量依赖方式刺激大鼠甲状腺髓样癌细胞系rMTC 6 - 23分泌降钙素,并导致胞质游离钙浓度升高,这是通过喹啉-2测定的。这些效应被硝苯地平竞争性抑制,且在无细胞外钙的情况下完全消失。这些数据表明,通过电压依赖性钙通道的钙内流在调节胞质游离钙浓度和降钙素分泌中起关键作用。

相似文献

1
Effect of calcium channel agonist Bay K 8644 on calcitonin secretion from a rat C-cell line.钙通道激动剂Bay K 8644对大鼠C细胞系降钙素分泌的影响。
Biochem Biophys Res Commun. 1985 Jul 16;130(1):454-9. doi: 10.1016/0006-291x(85)90438-3.
2
Role of voltage-dependent calcium channels in secretion of calcitonin from human medullary thyroid carcinoma cells.电压依赖性钙通道在人甲状腺髓样癌细胞降钙素分泌中的作用。
Klin Wochenschr. 1989 Jun 15;67(12):635-9. doi: 10.1007/BF01718147.
3
In vitro secretion of calcitonin from a rat C cell line: effect of repetitive stimulation with the calcium channel agonist BAY K 8644.大鼠C细胞系降钙素的体外分泌:钙通道激动剂BAY K 8644重复刺激的作用。
Horm Metab Res. 1992 Jun;24(6):272-5. doi: 10.1055/s-2007-1003311.
4
Effects of the calcium channel activator BAY-K-8644 on in vitro secretion of calcitonin and parathyroid hormone.钙通道激活剂BAY-K-8644对降钙素和甲状旁腺激素体外分泌的影响。
Endocrinology. 1986 Feb;118(2):545-9. doi: 10.1210/endo-118-2-545.
5
Activation of protein kinase C by 1,4-dihydro-2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)-phenyl]-3-py rid ine carboxylic acid methyl ester (Bay K 8644), a calcium channel agonist, in alveolar type II cells.钙通道激动剂1,4-二氢-2,6-二甲基-5-硝基-4-[2-(三氟甲基)-苯基]-3-吡啶羧酸甲酯(Bay K 8644)对肺泡II型细胞中蛋白激酶C的激活作用。
Biochem Pharmacol. 1997 May 9;53(9):1307-13. doi: 10.1016/s0006-2952(96)00882-9.
6
The calcium channel agonist, Bay K 8644, inhibits renin release from rat kidney cortical slices.钙通道激动剂Bay K 8644可抑制大鼠肾皮质切片释放肾素。
Eur J Pharmacol. 1985 Nov 19;117(3):369-72. doi: 10.1016/0014-2999(85)90011-1.
7
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.
8
Interaction of dihydropyridine Ca2+ agonist Bay K 8644 with normal and transformed pituitary cells.
Am J Physiol. 1986 Jan;250(1 Pt 1):C95-102. doi: 10.1152/ajpcell.1986.250.1.C95.
9
The effect of dihydropyridine calcium agonists and antagonists on neuronal voltage sensitive calcium channels.二氢吡啶类钙激动剂和拮抗剂对神经元电压敏感性钙通道的作用。
Biochem Biophys Res Commun. 1986 Feb 13;134(3):1038-47. doi: 10.1016/0006-291x(86)90356-6.
10
The calcium agonist Bay K 8644 stimulates secretion from a pituitary cell line.
Biochem Biophys Res Commun. 1984 Aug 16;122(3):991-6. doi: 10.1016/0006-291x(84)91189-6.

引用本文的文献

1
Immunocytochemical characterization of two thyroid medullary carcinoma cell lines in vitro.两种甲状腺髓样癌细胞系的体外免疫细胞化学特征分析
Histochem J. 1995 Nov;27(11):859-68.
2
Role of voltage-dependent calcium channels in secretion of calcitonin from human medullary thyroid carcinoma cells.电压依赖性钙通道在人甲状腺髓样癌细胞降钙素分泌中的作用。
Klin Wochenschr. 1989 Jun 15;67(12):635-9. doi: 10.1007/BF01718147.
3
Regulation of calcitonin release from the 6.23 rat C-cell line by cyclic nucleotide analogues and pharmacological mediators.
环核苷酸类似物和药理介质对6.23大鼠C细胞系降钙素释放的调节
Experientia. 1991 Oct 15;47(10):1067-9. doi: 10.1007/BF01923344.
4
Membrane depolarization and intracellular Ca2+ increase caused by high external Ca2+ in a rat calcitonin-secreting cell line.高细胞外钙引起的大鼠降钙素分泌细胞系中的膜去极化和细胞内钙离子增加。
J Physiol. 1990 Dec;431:243-67. doi: 10.1113/jphysiol.1990.sp018329.