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在豚鼠输精管中,交感神经组胺根据神经刺激频率发挥不同的突触前和突触后功能。

Sympathetic histamine exerts different pre- and post-synaptic functions according to the frequencies of nerve stimulation in guinea pig vas deferens.

作者信息

He Gonghao, Hu Jing, Ma Xue, Li Mingkai, Wang Hui, Meng Jingru, Jia Min, Luo Xiaoxing

机构信息

Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.

出版信息

J Neurochem. 2008 Aug;106(4):1710-9. doi: 10.1111/j.1471-4159.2008.05532.x. Epub 2008 Jun 28.

Abstract

Histamine (HA) was found to be present in the sympathetic nerve terminals of guinea pig hearts and vasa deferentia in our previous study; however, little is known about the functions of this neurogenic HA. In this study, we used guinea pig vasa deferentia to investigate the pre- and post-synaptic functions of HA evoked by different frequencies of sympathetic nerve stimulation. We found that sympathetic nerve stimulation could evoke HA release, which was independent to mast cell degranulator compound 48/80 and mast cell stabilizer cromolyn, but was highly sensitive to Na(+) channel blocker tetrodotoxin and chemical sympathectomy with 6-hydroxydopamine. The neurogenically released HA evoked by 12.5 Hz of nerve stimulation activated only pre-synaptic H(3) receptors and mediated pre-synaptic inhibitory effects, while under 25 or 50 Hz stimulation condition, HA simultaneously activated both pre-synaptic H(3) receptors and post-synaptic H(1) receptors. However, the direct contractile responses evoked by sympathetic HA via H(1) receptors were observed at 50 Hz. HA release and HA-mediated contractile responses upon sympathetic nerve stimulation were significantly inhibited by pre-treatment of histidine decarboxylase inhibitor alpha-fluoromethylhistidine. Furthermore, application of exogenous HA could mimic these pre- and post-synaptic effects. Our findings indicate that HA in sympathetic neurons acts as a neurotransmitter and its functions vary from pre-synaptic inhibition, to post-synaptic facilitation, to direct post-synaptic contractile responses according to sympathetic nerve stimulation frequencies.

摘要

在我们之前的研究中发现,组胺(HA)存在于豚鼠心脏和输精管的交感神经末梢;然而,对于这种神经源性HA的功能却知之甚少。在本研究中,我们使用豚鼠输精管来研究不同频率交感神经刺激诱发的HA的突触前和突触后功能。我们发现交感神经刺激可诱发HA释放,该释放与肥大细胞脱颗粒剂化合物48/80和肥大细胞稳定剂色甘酸无关,但对Na(+)通道阻滞剂河豚毒素和用6-羟基多巴胺进行的化学交感神经切除术高度敏感。12.5Hz神经刺激诱发的神经源性释放的HA仅激活突触前H(3)受体并介导突触前抑制作用,而在25或50Hz刺激条件下,HA同时激活突触前H(3)受体和突触后H(1)受体。然而,在50Hz时观察到交感神经HA通过H(1)受体诱发的直接收缩反应。组胺脱羧酶抑制剂α-氟甲基组氨酸预处理可显著抑制交感神经刺激时的HA释放和HA介导的收缩反应。此外,应用外源性HA可模拟这些突触前和突触后效应。我们的研究结果表明,交感神经元中的HA作为一种神经递质,其功能根据交感神经刺激频率从突触前抑制到突触后易化,再到直接的突触后收缩反应而有所不同。

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