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maitotoxin,一种阳离子通道激活剂。

Maitotoxin, a cationic channel activator.

作者信息

Escobar L I, Salvador C, Martínez M, Vaca L

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, México, D.F.

出版信息

Neurobiology (Bp). 1998;6(1):59-74.

PMID:9713832
Abstract

Maitotoxin (MTX), a water soluble polyether obtained from the marine dinoflagellate Gambierdiscus toxicus is one of the entities responsible for Ciguatera, a form of seafood poisoning. This toxin is a potent activator of changes in the intracellular Ca2+ concentrations of cells from a wide variety of organisms. Evidence published in the last few years strongly suggests that this toxin has no ionophoretic activity. Molecular mechanics studies, shown for the first time in this review, models MTX as a molecular 'wire'. The present work compiles the few studies developed with electrophysiological techniques. All these reports indicate that MTX is activating a voltage independent, nonselective cationic channel, which in some preparations requires the presence of extracellular Ca2+ for channel activation. The conductance estimated from a variety of tissues is in the order of 12-40 pS. Thus far, no specific blocker has been identified for this channel. The nature of the MTX receptor remains a mistery.

摘要

maitotoxin(MTX)是一种从海洋甲藻纲毒冈比甲藻中提取的水溶性聚醚,是引起雪卡毒素中毒(一种海鲜中毒形式)的致病因素之一。这种毒素是多种生物体细胞内钙离子浓度变化的强效激活剂。过去几年发表的证据有力地表明,这种毒素没有离子载体活性。本综述首次展示的分子力学研究将MTX模拟为分子“导线”。目前的工作汇编了一些用电生理技术开展的研究。所有这些报告表明,MTX正在激活一个电压非依赖性、非选择性阳离子通道,在某些制剂中,该通道的激活需要细胞外钙离子的存在。从各种组织估计的电导约为12 - 40 pS。到目前为止,尚未确定该通道的特异性阻滞剂。MTX受体的性质仍然是个谜。

相似文献

1
Maitotoxin, a cationic channel activator.maitotoxin,一种阳离子通道激活剂。
Neurobiology (Bp). 1998;6(1):59-74.
2
Maitotoxin activates a nonselective cation channel and stimulates Ca2+ entry in MDCK renal epithelial cells.刺尾鱼毒素激活一种非选择性阳离子通道,并刺激钙离子进入犬肾上皮细胞。
Mol Pharmacol. 1994 Feb;45(2):300-5.
3
Calcium is permeable through a maitotoxin-activated nonselective cation channel in mouse L cells.钙可通过小鼠L细胞中由刺尾鱼毒素激活的非选择性阳离子通道通透。
Am J Physiol. 1996 Apr;270(4 Pt 1):C1145-52. doi: 10.1152/ajpcell.1996.270.4.C1145.
4
Studies on maitotoxin-induced intracellular Ca(2+) elevation in chinese hamster ovary cells stably transfected with cDNAs encoding for L-type Ca(2+) channel subunits.用编码L型钙离子通道亚基的cDNA稳定转染的中国仓鼠卵巢细胞中,海葵毒素诱导细胞内钙离子升高的研究。
J Pharmacol Exp Ther. 1999 Aug;290(2):725-30.
5
Maitotoxin potently promotes Ca2+ influx in mouse spermatogenic cells and sperm, and induces the acrosome reaction.刺尾鱼毒素可有效促进小鼠生精细胞和精子中的钙离子内流,并诱导顶体反应。
J Cell Physiol. 2006 Feb;206(2):449-56. doi: 10.1002/jcp.20487.
6
Characterization of the maitotoxin-activated cationic current from human skin fibroblasts.来自人皮肤成纤维细胞的刺尾鱼毒素激活的阳离子电流的特性分析。
J Physiol. 2002 Jan 1;538(Pt 1):79-86. doi: 10.1113/jphysiol.2001.013036.
7
Differential effects of ciguatoxin and maitotoxin in primary cultures of cortical neurons.雪卡毒素和刺尾鱼毒素对皮层神经元原代培养物的不同作用。
Chem Res Toxicol. 2014 Aug 18;27(8):1387-400. doi: 10.1021/tx5000969. Epub 2014 Jul 15.
8
Maitotoxin activates a nonselective cation channel and a P2Z/P2X(7)-like cytolytic pore in human skin fibroblasts.maitotoxin激活人皮肤成纤维细胞中的非选择性阳离子通道和P2Z/P2X(7)样溶细胞孔道
Am J Physiol. 1999 Oct;277(4):C755-65. doi: 10.1152/ajpcell.1999.277.4.C755.
9
Maitotoxin (MTX) activates a nonselective cation channel in Xenopus laevis oocytes.maitotoxin(MTX)可激活非洲爪蟾卵母细胞中的一种非选择性阳离子通道。
Pflugers Arch. 1998 Aug;436(3):329-37. doi: 10.1007/PL00008085.
10
Glucose and lactate regulate maitotoxin-activated Ca2+ entry in spermatogenic cells: the role of intracellular [Ca2+].葡萄糖和乳酸调节生精细胞中蜂毒素激活的 Ca2+内流:细胞内 Ca2+的作用。
FEBS Lett. 2010 Jul 16;584(14):3111-5. doi: 10.1016/j.febslet.2010.05.051. Epub 2010 Jun 2.

引用本文的文献

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Maitotoxin Is a Potential Selective Activator of the Endogenous Transient Receptor Potential Canonical Type 1 Channel in Xenopus laevis Oocytes.多管毒素是非洲爪蟾卵母细胞中内源性瞬时受体电位香草酸亚型1通道的潜在选择性激活剂。
Mar Drugs. 2017 Jun 25;15(7):198. doi: 10.3390/md15070198.
2
Caribbean maitotoxin elevates [Ca(2+)]i and activates non-selective cation channels in HIT-T15 cells.加勒比海雪卡毒素可提高 HIT-T15 细胞内钙离子浓度并激活非选择性阳离子通道。
World J Diabetes. 2013 Jun 15;4(3):70-5. doi: 10.4239/wjd.v4.i3.70.
3
Maitotoxin: An Inspiration for Synthesis.
maitotoxin:合成的灵感来源。
Isr J Chem. 2011 Apr;51(3-4):359-377. doi: 10.1002/ijch.201100003.
4
The opening of maitotoxin-sensitive calcium channels induces the acrosome reaction in human spermatozoa: differences from the zona pellucida.钙通道开放诱导人精子顶体反应:与透明带的不同。
Asian J Androl. 2011 Jan;13(1):159-65. doi: 10.1038/aja.2010.80. Epub 2010 Sep 13.
5
Impact of marine drugs on animal reproductive processes.海洋药物对动物生殖过程的影响。
Mar Drugs. 2009 Nov 6;7(4):539-64. doi: 10.3390/md7040539.
6
Twenty odd years of stretch-sensitive channels.二十多年来的牵张敏感通道。
Pflugers Arch. 2006 Dec;453(3):333-51. doi: 10.1007/s00424-006-0131-0. Epub 2006 Sep 21.
7
Involvement of ASK1 in Ca2+-induced p38 MAP kinase activation.凋亡信号调节激酶1参与钙离子诱导的p38丝裂原活化蛋白激酶激活。
EMBO Rep. 2004 Feb;5(2):161-6. doi: 10.1038/sj.embor.7400072. Epub 2004 Jan 16.
8
Characterization of the maitotoxin-activated cationic current from human skin fibroblasts.来自人皮肤成纤维细胞的刺尾鱼毒素激活的阳离子电流的特性分析。
J Physiol. 2002 Jan 1;538(Pt 1):79-86. doi: 10.1113/jphysiol.2001.013036.
9
Insulinotropic toxins as molecular probes for analysis of glucagon-likepeptide-1 receptor-mediated signal transduction in pancreatic beta-cells.促胰岛素毒素作为分析胰高血糖素样肽-1受体介导的胰岛β细胞信号转导的分子探针。
Biochimie. 2000 Sep-Oct;82(9-10):915-26. doi: 10.1016/s0300-9084(00)01171-8.