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西格玛-1受体拮抗剂氟哌啶醇减弱巨噬细胞中储存依赖性钙内流。

Sigma-1 Receptor Antagonist Haloperidol Attenuates Store-Dependent Ca Entry in Macrophages.

作者信息

Krutetskaya Z I, Milenina L S, Naumova A A, Butov S N, Antonov V G, Nozdrachev A D

机构信息

St. Petersburg State University, St. Petersburg, 199034, Russia.

出版信息

Dokl Biochem Biophys. 2018 May;480(1):162-165. doi: 10.1134/S1607672918030109. Epub 2018 Jul 14.

DOI:10.1134/S1607672918030109
PMID:30008101
Abstract

Using Fura-2AM microfluorimetry, we have shown for the first time that preincubation of macrophages with sigma-1 receptor antagonist haloperidol leads to a significant inhibition of the store-dependent Ca entry induced by endoplasmic Ca-ATPase inhibitors thapsigargin or cyclopiazonic acid in rat peritoneal macrophages. The results suggest the involvement of the sigma-1 receptor in the regulation of storedependent Ca entry in macrophages.

摘要

利用Fura-2AM显微荧光测定法,我们首次证明,用西格玛-1受体拮抗剂氟哌啶醇对巨噬细胞进行预孵育,会显著抑制内质网Ca-ATP酶抑制剂毒胡萝卜素或环匹阿尼酸在大鼠腹膜巨噬细胞中诱导的储存依赖性Ca内流。结果表明西格玛-1受体参与巨噬细胞中储存依赖性Ca内流的调节。

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本文引用的文献

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The σ receptor agonist (+)-pentazocine increases store-operated Ca entry in MCF7σ and SK-N-SH cell lines.σ受体激动剂(+)-喷他佐辛可增加MCF7σ和SK-N-SH细胞系中储存式钙内流。
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Sigma1 receptors inhibit store-operated Ca2+ entry by attenuating coupling of STIM1 to Orai1.σ1受体通过减弱STIM1与Orai1的偶联来抑制钙库操纵的Ca2+内流。
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Store-Operated Calcium Channels.储存式钙通道
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Inhibition of endothelial cell Ca²⁺ entry and transient receptor potential channels by Sigma-1 receptor ligands.Sigma-1 受体配体对内皮细胞钙离子内流和瞬时受体电位通道的抑制作用。
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The sigma-1 receptor chaperone as an inter-organelle signaling modulator.sigma-1 受体伴侣作为细胞器间信号调节剂。
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Haloperidol moderately inhibits cardiovascular L-type calcium current.氟哌啶醇适度抑制心血管L型钙电流。
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Irreversible blockade of sigma-1 receptors by haloperidol and its metabolites in guinea pig brain and SH-SY5Y human neuroblastoma cells.氟哌啶醇及其代谢产物对豚鼠脑和SH-SY5Y人神经母细胞瘤细胞中σ-1受体的不可逆阻断作用。
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