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藜芦定的纯化、溶解度及pKa值

Purification, solubility, and pKa of veratridine.

作者信息

McKinney L C, Chakraverty S, De Weer P

出版信息

Anal Biochem. 1986 Feb 15;153(1):33-8. doi: 10.1016/0003-2697(86)90056-4.

DOI:10.1016/0003-2697(86)90056-4
PMID:3963380
Abstract

The alkaloid neurotoxin veratridine is widely used by cell physiologists to increase membrane sodium permeability. The compound is only sporadically available from commercial sources, but can be purified (Kupchan et al., 1953, J. Amer. Chem. Soc. 75, 5519-5524) from veratrine, a mixture of several alkaloids. We describe here a purification procedure only slightly modified from that of Kupchan et al., and include important details not mentioned in the original paper. Ultraviolet and infrared spectra are presented. We have also determined the pKa and solubility of veratridine in 150 mM NaCl at 25 degrees C. The solubility is steeply pH dependent, ranging from 0.61 +/- 0.02 mM above pH 12 to 18.5 mM at pH 8.07. The pKa, determined from the solubility versus pH curve, was found to be 9.54 +/- 0.02.

摘要

生物碱神经毒素藜芦定被细胞生理学家广泛用于增加细胞膜对钠的通透性。该化合物仅偶尔能从商业渠道获得,但可从藜芦碱(几种生物碱的混合物)中纯化得到(库普昌等人,1953年,《美国化学会志》75卷,5519 - 5524页)。我们在此描述一种仅对库普昌等人的方法稍作修改的纯化程序,并包含原始论文中未提及的重要细节。给出了紫外和红外光谱。我们还测定了藜芦定在25℃下于150 mM氯化钠中的pKa和溶解度。溶解度强烈依赖于pH值,在pH值高于12时为0.61±0.02 mM,在pH 8.07时为18.5 mM。由溶解度与pH值曲线确定的pKa为9.54±0.02。

相似文献

1
Purification, solubility, and pKa of veratridine.藜芦定的纯化、溶解度及pKa值
Anal Biochem. 1986 Feb 15;153(1):33-8. doi: 10.1016/0003-2697(86)90056-4.
2
The effect of temperature on veratridine action in squid giant axons.温度对鱿鱼巨轴突中藜芦碱作用的影响。
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Sodium permeability of frog skeletal muscle in absence and presence of veratridine.在有无藜芦定情况下青蛙骨骼肌的钠通透性
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Rapid and slow gating of veratridine-modified sodium channels in frog myelinated nerve.青蛙有髓神经中藜芦碱修饰的钠通道的快速和慢速门控
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引用本文的文献

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Pharmaceutics. 2022 Mar 9;14(3):598. doi: 10.3390/pharmaceutics14030598.
2
Late cardiac sodium current can be assessed using automated patch-clamp.晚期心脏钠电流可通过自动膜片钳技术进行评估。
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Antagonism by local anesthetics of sodium channel activators in the presence of scorpion toxins: two mechanisms for competitive inhibition.
在存在蝎毒素的情况下局部麻醉药对钠通道激活剂的拮抗作用:竞争性抑制的两种机制。
Cell Mol Neurobiol. 2004 Aug;24(4):565-77. doi: 10.1023/b:cemn.0000023630.16308.54.
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Point mutations in segment I-S6 render voltage-gated Na+ channels resistant to batrachotoxin.第I-S6段中的点突变使电压门控性钠通道对蟾毒素产生抗性。
Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2653-8. doi: 10.1073/pnas.95.5.2653.
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Mutually exclusive action of cationic veratridine and cevadine at an intracellular site of the cardiac sodium channel.阳离子藜芦定和瑟瓦定在心脏钠通道细胞内位点的互斥作用。
J Gen Physiol. 1992 May;99(5):699-720. doi: 10.1085/jgp.99.5.699.
6
Relation between veratridine reaction dynamics and macroscopic Na current in single cardiac cells.单个心肌细胞中藜芦定反应动力学与宏观钠电流之间的关系。
J Gen Physiol. 1992 May;99(5):683-97. doi: 10.1085/jgp.99.5.683.