首页> 外文期刊>American Journal of Physiology >Inhibitory effects of galanin on evoked (Ca2+)i responses in cultured myenteric neurons.
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Inhibitory effects of galanin on evoked (Ca2+)i responses in cultured myenteric neurons.

机译:甘丙肽对培养的肌层神经元诱发的(Ca2 +)i反应的抑制作用。

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Galanin modulates gastrointestinal motility by inhibiting the release of ACh from enteric neurons. It is, however, not known whether galanin also inhibits neuronal cholinergic transmission postsynaptically and whether galanin also reduces the action of other excitatory neurotransmitters. The aim of the present study was thus to investigate the effect of galanin on the evoked intracellular Ca(2+) concentration ([Ca(2+)](i)) responses in myenteric neurons. Cultured myenteric neurons from small intestine of adult guinea pigs were loaded with the Ca(2+) indicator fluo-3 AM, and the [Ca(2+)](i) responses following the application of different stimuli were quantified by confocal microscopy and expressed as a percentage of the response to high-K(+) solution (75 mM). Trains of electrical pulses (2 s, 10 Hz) were applied to stimulate the neuronal fibers before and after a 30-s superfusion with galanin (10(-6) M). Substance P (SP), 5-HT, 1,1-dimethyl-4-phenyl-piperazinium iodide (DMPP), and carbachol were used as direct postsynaptic stimuli (10(-5) M, 30 s) and were applied alone or after galanin perfusion. Galanin significantly reduced the responses induced by electrical fiber stimulation (43 +/- 2 to 35 +/- 3%, P = 0.01), SP (15.4 +/- 1 to 8.0 +/- 0.3%, P < 0.01), and 5-HT (26 +/- 2 to 21.4 +/- 1.5%, P < 0.05). On the contrary, galanin did not affect the responses induced by local application of DMPP and carbachol. We conclude that in cultured myenteric neurons, galanin inhibits the excitatory responses induced by electrical stimulation, SP, and 5-HT. Finally, the inhibitory effect of galanin on electrical stimulation, but not on DMPP- and carbachol-induced responses, suggests that, at least for the cholinergic component, galanin acts at the presynaptic level.
机译:甘丙肽通过抑制ACh从肠神经元的释放来调节胃肠蠕动。然而,尚不知道甘丙肽是否也突触抑制神经元胆碱能传递,甘丙肽是否也降低其他兴奋性神经递质的作用。因此,本研究的目的是研究甘丙肽对肌层神经元中诱发的细胞内Ca(2+)浓度([Ca(2 +)](i))反应的影响。从成年豚鼠小肠的培养的肠系膜神经元上加载Ca(2+)指示剂fluo-3 AM,并通过共聚焦显微镜定量分析不同刺激后的[Ca(2 +)](i)反应。表示为对高K(+)溶液(75 mM)的响应的百分比。在与甘丙肽(10(-6)M)融合30秒之前和之后,施加电脉冲序列(2 s,10 Hz)刺激神经元纤维。物质P(SP),5-HT,1,1-二甲基-4-苯基碘化哌嗪鎓(DMPP)和卡巴胆碱被用作直接突触后刺激(10(-5)M,30 s),可以单独使用或甘丙肽灌注后。甘丙肽显着降低了电刺激(43 +/- 2至35 +/- 3%,P = 0.01),SP(15.4 +/- 1至8.0 +/- 0.3%,P <0.01)和5-HT(26 +/- 2至21.4 +/- 1.5%,P <0.05)。相反,甘丙肽不影响DMPP和卡巴胆碱局部应用引起的反应。我们得出的结论是,在培养的肌层神经元中,甘丙肽抑制由电刺激,SP和5-HT诱导的兴奋性反应。最后,甘丙肽对电刺激的抑制作用,但对DMPP和卡巴胆碱诱导的应答没有抑制作用,这表明,至少对于胆碱能成分,甘丙肽在突触前起作用。

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