Suppr超能文献

一氧化氮是轴突切断的C型背根神经节神经元中钠离子电流的自分泌调节因子。

Nitric oxide is an autocrine regulator of Na(+) currents in axotomized C-type DRG neurons.

作者信息

Renganathan M, Cummins T R, Hormuzdiar W N, Black J A, Waxman S G

机构信息

Department of Neurology, Yale Medical School, New Haven 06510, USA.

出版信息

J Neurophysiol. 2000 Apr;83(4):2431-42. doi: 10.1152/jn.2000.83.4.2431.

Abstract

In this study, we examined whether nitric oxide synthase (NOS) is upregulated in small dorsal root ganglion (DRG) neurons after axotomy and, if so, whether the upregulation of NOS modulates Na(+) currents in these cells. We identified axotomized C-type DRG neurons using a fluorescent label, hydroxystilbamine methanesulfonate and found that sciatic nerve transection upregulates NOS activity in 60% of these neurons. Fast-inactivating tetrodotoxin-sensitive (TTX-S) Na(+) ("fast") current and slowly inactivating tetrodotoxin-resistant (TTX-R) Na(+) ("slow") current were present in control noninjured neurons with current densities of 1.08 +/- 0. 09 nA/pF and 1.03 +/- 0.10 nA/pF, respectively (means +/- SE). In some control neurons, a persistent TTX-R Na(+) current was observed with current amplitude as much as approximately 50% of the TTX-S Na(+) current amplitude and 100% of the TTX-R Na(+) current amplitude. Seven to 10 days after axotomy, current density of the fast and slow Na(+) currents was reduced to 0.58 +/- 0.05 nA/pF (P < 0.01) and 0.2 +/- 0.05 nA/pF (P < 0.001), respectively. Persistent TTX-R Na(+) current was not observed in axotomized neurons. Nitric oxide (NO) produced by the upregulation of NOS can block Na(+) currents. To examine the role of NOS upregulation on the reduction of the three types of Na(+) currents in axotomized neurons, axotomized DRG neurons were incubated with 1 mM N(G)-nitro-L-arginine methyl ester (L-NAME), a NOS inhibitor. The current density of fast and slow Na(+) channels in these neurons increased to 0.82 +/- 0.08 nA/pF (P < 0.01) and 0.34 +/- 0.04 nA/pF (P < 0.05), respectively. However, we did not observe any persistent TTX-R current in axotomized neurons incubated with L-NAME. These results demonstrate that endogenous NO/NO-related species block both fast and slow Na(+) current in DRG neurons and suggest that NO functions as an autocrine regulator of Na(+) currents in injured DRG neurons.

摘要

在本研究中,我们检测了轴突切断后小背根神经节(DRG)神经元中一氧化氮合酶(NOS)是否上调,若上调,NOS的上调是否会调节这些细胞中的钠电流。我们使用荧光标记物甲磺酸羟基芪胺来识别轴突切断的C型DRG神经元,发现坐骨神经横断可使60%的此类神经元的NOS活性上调。对照未损伤神经元中存在快速失活的河豚毒素敏感(TTX-S)钠(“快”)电流和缓慢失活的河豚毒素抵抗(TTX-R)钠(“慢”)电流,其电流密度分别为1.08±0.09 nA/pF和1.03±0.10 nA/pF(均值±标准误)。在一些对照神经元中,观察到一种持续的TTX-R钠电流,其电流幅度高达TTX-S钠电流幅度的约50%以及TTX-R钠电流幅度的100%。轴突切断后7至10天,快钠电流和慢钠电流的电流密度分别降至0.58±0.05 nA/pF(P<0.01)和0.2±0.05 nA/pF(P<0.001)。在轴突切断的神经元中未观察到持续的TTX-R钠电流。NOS上调产生的一氧化氮(NO)可阻断钠电流。为检测NOS上调在轴突切断神经元中三种钠电流减少中的作用,将轴突切断的DRG神经元与1 mM N-硝基-L-精氨酸甲酯(L-NAME,一种NOS抑制剂)一起孵育。这些神经元中快钠通道和慢钠通道的电流密度分别增加至0.82±0.08 nA/pF(P<0.01)和0.34±0.04 nA/pF(P<0.05)。然而,在与L-NAME一起孵育的轴突切断神经元中,我们未观察到任何持续的TTX-R电流。这些结果表明内源性NO/NO相关物质可阻断DRG神经元中的快钠电流和慢钠电流,并提示NO在受损DRG神经元中作为钠电流的自分泌调节因子发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验