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三磷酸肌醇受体相关蛋白 6 通道激活剂贯叶金丝桃素诱导线粒体释放锌和钙。

The TRPC6 channel activator hyperforin induces the release of zinc and calcium from mitochondria.

机构信息

UMR CNRS 5249, Grenoble, France.

出版信息

J Neurochem. 2010 Jan;112(1):204-13. doi: 10.1111/j.1471-4159.2009.06446.x. Epub 2009 Oct 21.

DOI:10.1111/j.1471-4159.2009.06446.x
PMID:19845832
Abstract

Hyperforin, an extract of the medicinal plant hypericum perforatum (also named St John's wort), possesses antidepressant properties. Recent data showed that it elevates the intracellular concentration of Ca(2+) by activating diacylglycerol-sensitive C-class of transient receptor potential (TRPC6) channels without activating the other isoforms (TRPC1, TRPC3, TRPC4, TRPC5, and TRPC7). This study was undertaken to further characterize the cellular neuronal responses induced by hyperforin. Experiments conducted on cortical neurons in primary culture and loaded with fluorescent probes for Ca(2+) (Fluo-4) and Zn(2+) (FluoZin-3) showed that it not only controls the activity of plasma membrane channels but it also mobilizes these two cations from internal pools. Experiments conducted on isolated brain mitochondria indicated that hyperforin, like the inhibitor of oxidative phosphorylation, carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP), collapses the mitochondrial membrane potential. Furthermore, it promotes the release of Ca(2+) and Zn(2+) from these organelles via a ruthenium red-sensitive transporter. In fact, hyperforin exerts complex actions on CNS neurons. This antidepressant not only triggers the entry of cations via plasma membrane TRPC6 channels but it displays protonophore-like properties. As hyperforin is now use to probe the functions of native TRPC6 channels, our data indicate that caution is required when interpreting results obtained with this antidepressant.

摘要

贯叶金丝桃素是药用植物贯叶连翘(也称为金丝桃)的提取物,具有抗抑郁作用。最近的数据表明,它通过激活二酰基甘油敏感的 C 类瞬时受体电位(TRPC6)通道而不激活其他亚型(TRPC1、TRPC3、TRPC4、TRPC5 和 TRPC7)来提高细胞内 Ca(2+)浓度。本研究旨在进一步研究贯叶金丝桃素诱导的神经元细胞反应。在原代培养的皮质神经元上进行的实验,并用荧光探针(Fluo-4 和 FluoZin-3)对 Ca(2+)和 Zn(2+)进行了负载,结果表明贯叶金丝桃素不仅控制质膜通道的活性,还能从内部池中动员这两种阳离子。在分离的脑线粒体上进行的实验表明,贯叶金丝桃素与氧化磷酸化抑制剂羰基氰化物 4-(三氟甲氧基)苯腙(FCCP)一样,会使线粒体膜电位崩溃。此外,它通过一种钌红敏感的转运蛋白促进这些细胞器中 Ca(2+)和 Zn(2+)的释放。事实上,贯叶金丝桃素对中枢神经系统神经元有复杂的作用。这种抗抑郁药不仅通过质膜 TRPC6 通道触发阳离子进入,而且还表现出质子载体样的特性。由于贯叶金丝桃素现在用于探测天然 TRPC6 通道的功能,我们的数据表明,在解释使用这种抗抑郁药获得的结果时需要谨慎。

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