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硫化氢决定了一氧化氮诱导的三叉神经传入神经的刺激。

Hydrogen sulfide determines HNO-induced stimulation of trigeminal afferents.

作者信息

Wild Vanessa, Messlinger Karl, Fischer Michael J M

机构信息

Institute of Physiology and Pathophysiology, University of Erlangen-Nürnberg, Erlangen, Germany.

Institute of Physiology and Pathophysiology, University of Erlangen-Nürnberg, Erlangen, Germany.

出版信息

Neurosci Lett. 2015 Aug 18;602:104-9. doi: 10.1016/j.neulet.2015.06.056. Epub 2015 Jul 3.

Abstract

Endogenous NO and hydrogen sulfide form HNO, which causes CGRP release via TRPA1 channel activation in sensory nerves. In the present study, stimulation of intact trigeminal afferent neuron preparations with NO donors, Na2S or both was analyzed by measuring CGRP release as an index of mass activation. Combined stimulation was able to activate all parts of the trigeminal system and acted synergistic compared to stimulation with both substances alone. To investigate the contribution of both substances, we varied their ratio and tracked intracellular calcium in isolated neurons. Our results demonstrate that hydrogen sulfide is the rate-limiting factor for HNO formation. CGRP has a key role in migraine pathophysiology and HNO formation at all sites of the trigeminal system should be considered for this novel means of activation.

摘要

内源性一氧化氮(NO)和硫化氢生成亚硝酸(HNO),后者通过激活感觉神经中的瞬时受体电位锚蛋白1(TRPA1)通道导致降钙素基因相关肽(CGRP)释放。在本研究中,通过测量CGRP释放作为整体激活指标,分析了用NO供体、硫化钠(Na2S)或两者刺激完整三叉神经传入神经元制剂的情况。联合刺激能够激活三叉神经系统的所有部分,并且与单独用两种物质刺激相比具有协同作用。为了研究这两种物质的作用,我们改变它们的比例并追踪分离神经元中的细胞内钙。我们的结果表明,硫化氢是HNO形成的限速因子。CGRP在偏头痛病理生理学中起关键作用,对于这种新的激活方式,应考虑三叉神经系统所有部位的HNO形成。

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