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刺尾鱼毒素在体外刺激大鼠垂体前叶细胞的激素释放和钙通量。

Maitotoxin stimulates hormonal release and calcium flux in rat anterior pituitary cells in vitro.

作者信息

Schettini G, Koike K, Login I S, Judd A M, Cronin M J, Yasumoto T, MacLeod R M

出版信息

Am J Physiol. 1984 Oct;247(4 Pt 1):E520-5. doi: 10.1152/ajpendo.1984.247.4.E520.

DOI:10.1152/ajpendo.1984.247.4.E520
PMID:6496670
Abstract

The marine dinoflagellate toxin maitotoxin (MTX), an activator of calcium channels, stimulates the release of prolactin (PRL), growth hormone (GH), thyroid-stimulating hormone (TSH), and luteinizing hormone (LH) from monolayers of anterior pituitary cells in a dose-dependent manner. Maitotoxin significantly increased PRL, GH, and LH release within 1.5 min and TSH release within 3.5 min, and the stimulation continued for at least 1 h (P less than 0.01). MTX-stimulated hormonal release was blocked by the calcium channel blocker manganese (P less than 0.01). In freshly dispersed perifused pituitary cells in columns, exposure to MTX for 10 min markedly increased PRL, GH, TSH, and LH release for at least 1 h after withdrawal of the toxin. In other experiments, MTX significantly stimulated 45Ca2+ exchange by dispersed pituitary cells within 30 s, continuing for at least 30 min. We conclude that MTX increases anterior pituitary hormonal release, possibly by activating calcium channels, thereby increasing cellular calcium influx. Thus MTX may be a useful agent for investigating the involvement of Ca2+ in hormonal secretory processes.

摘要

海洋双鞭甲藻毒素——刺尾鱼毒素(MTX)是一种钙通道激活剂,它能以剂量依赖的方式刺激垂体前叶细胞单层释放催乳素(PRL)、生长激素(GH)、促甲状腺激素(TSH)和促黄体生成素(LH)。刺尾鱼毒素在1.5分钟内显著增加PRL、GH和LH的释放,在3.5分钟内增加TSH的释放,且这种刺激持续至少1小时(P<0.01)。MTX刺激的激素释放被钙通道阻滞剂锰阻断(P<0.01)。在柱中新鲜分散的灌流垂体细胞中,暴露于MTX 10分钟后,在撤除毒素后至少1小时内,PRL、GH、TSH和LH的释放显著增加。在其他实验中,MTX在30秒内显著刺激分散的垂体细胞进行45Ca2+交换,并持续至少30分钟。我们得出结论,MTX可能通过激活钙通道增加垂体前叶激素释放,从而增加细胞钙内流。因此,MTX可能是研究Ca2+在激素分泌过程中作用的有用试剂。

相似文献

1
Maitotoxin stimulates hormonal release and calcium flux in rat anterior pituitary cells in vitro.刺尾鱼毒素在体外刺激大鼠垂体前叶细胞的激素释放和钙通量。
Am J Physiol. 1984 Oct;247(4 Pt 1):E520-5. doi: 10.1152/ajpendo.1984.247.4.E520.
2
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Maitotoxin induces a calcium-dependent membrane depolarization in GH4C1 pituitary cells via activation of type L voltage-dependent calcium channels.刺尾鱼毒素通过激活L型电压依赖性钙通道,在GH4C1垂体细胞中诱导钙依赖性膜去极化。
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引用本文的文献

1
Maitotoxin activates cation channels distinct from the receptor-activated non-selective cation channels of HL-60 cells.maitotoxin激活的阳离子通道不同于HL-60细胞中受体激活的非选择性阳离子通道。
Biochem J. 1994 Jul 15;301 ( Pt 2)(Pt 2):437-41. doi: 10.1042/bj3010437.
2
Arachidonic acid elevates cytosolic free calcium concentration in rat anterior pituitary cells.花生四烯酸可提高大鼠垂体前叶细胞的胞质游离钙浓度。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Sep;338(3):303-9. doi: 10.1007/BF00173405.
3
The mechanism of action of maitotoxin in relation to Ca2+ movements in guinea-pig and rat cardiac muscles.
刺尾鱼毒素对豚鼠和大鼠心肌中钙离子运动的作用机制。
Br J Pharmacol. 1985 Oct;86(2):385-91. doi: 10.1111/j.1476-5381.1985.tb08907.x.
4
cAMP- and diacylglycerol-mediated pathways elevate cytosolic free calcium concentration via dihydropyridine-sensitive, omega-conotoxin-insensitive calcium channels in normal rat anterior pituitary cells.环磷酸腺苷(cAMP)和二酰基甘油介导的信号通路通过正常大鼠垂体前叶细胞中对二氢吡啶敏感、对ω-芋螺毒素不敏感的钙通道提高胞质游离钙浓度。
Naunyn Schmiedebergs Arch Pharmacol. 1989 Jan-Feb;339(1-2):1-7. doi: 10.1007/BF00165118.
5
Maitotoxin stimulates phosphoinositide breakdown in neuroblastoma hybrid NCB-20 cells.maitotoxin刺激神经母细胞瘤杂交细胞NCB - 20中的磷酸肌醇分解。
Cell Mol Neurobiol. 1987 Sep;7(3):317-22. doi: 10.1007/BF00711308.
6
Maitotoxin-activated single calcium channels in guinea-pig cardiac cells.海葵毒素激活豚鼠心脏细胞中的单个钙通道。
Br J Pharmacol. 1987 Nov;92(3):665-71. doi: 10.1111/j.1476-5381.1987.tb11370.x.
7
Ciguatoxin enhances quantal transmitter release from frog motor nerve terminals.雪卡毒素增强青蛙运动神经末梢的量子递质释放。
Br J Pharmacol. 1990 Apr;99(4):695-700. doi: 10.1111/j.1476-5381.1990.tb12991.x.