首页> 美国卫生研究院文献>The Journal of Physiology >GABAA and glutamate receptor involvement in dendrodendritic synaptic interactions from salamander olfactory bulb.
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GABAA and glutamate receptor involvement in dendrodendritic synaptic interactions from salamander olfactory bulb.

机译:GABAA和谷氨酸受体参与sal sal嗅球的树突突触相互作用。

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摘要

1. Whole-cell patch clamp and optical recording techniques were applied to the same in vitro salamander olfactory bulb preparations to study the postsynaptic responses of single mitral/tufted cells in the context of the surrounding neural activity in which they are embedded. Mitral/tufted cells were identified by intracellular filling with biocytin. 2. Single mitral/tufted cells were under a tonic GABAA receptor-mediated inhibitory influence as revealed by the recording of bicuculline methiodide (BMI)/picrotoxin-sensitive inhibitory postsynaptic currents (IPSCs) in symmetrical chloride conditions at a holding potential of -70 mV. Depolarizing voltage steps (100 ms) applied to single cells or electrical stimulation of the olfactory nerve or medial olfactory tract evoked a prolonged increase in the frequency of GABAergic IPSCs. 3. The frequency of spontaneous and driven IPSCs was reduced with application of the glutamate receptor antagonists 6-cyano-2,3-dihydroxy-7-nitro-quionoxaline (CNQX) or 2-amino-5-phosphonopentanoic acid (AP5) whereas olfactory nerve- or medial olfactory tract-driven IPSC frequency was enhanced with removal of bathing Mg2+, indicating that GABAergic interneurones were driven by mitral/tufted cells at both non-NMDA and NMDA receptors. 4. Olfactory nerve or medial olfactory tract stimulation evoked widely distributed changes in fluorescence in preparations stained with the voltage-sensitive dye RH414. The optical response predominantly consisted of a decrease in fluorescence, indicative of depolarization. The presence of the dye did not obviously affect mitral/tufted cell postsynaptic responses. 5. BMI enhanced the amplitude and duration of optical signals related to depolarization within the bulb and in regions central to the bulb. In the presence of BMI, depolarizing activity appeared to spread hundreds of micrometres into regions of the bulb not activated in control conditions showing explicitly that GABAA receptors in the bulb participate in lateral inhibition. 6. CNQX and AP5 attenuated the optical signals within the bulb supporting the contention that in these conditions, optical signals arise mainly from granule cell dendritic activity. Furthermore, AP5 or removal of bath Mg2+ reduced or enlarged the spatial distribution of activity respectively, suggesting that in some cases the NMDA receptor may be involved in generating or stabilizing spatial patterns of activity. 7. It is concluded that in the salamander olfactory bulb, both GABAA- and glutamate receptor-mediated synaptic transmission shape the different temporal and spatial patterns of neural activity associated with olfactory coding.
机译:1.将全细胞膜片钳和光学记录技术应用于相同的体外sal嗅球制备物中,以研究单个二尖瓣/簇状细胞在嵌入它们的周围神经活动的背景下的突触后反应。通过细胞内填充生物胞素鉴定二尖瓣/簇状细胞。 2.单二尖瓣/簇状细胞在强直性GABA A受体介导的抑制作用下,如在对称氯化物条件下在-70 mV的保持电位下记录双甲硫氨酸(BMI)/对微毒素敏感的抑制性突触后电流(IPSC)所揭示的那样。 。应用于单细胞的消极电压阶跃(100毫秒)或嗅觉神经或嗅觉神经的电刺激引起了GABA能IPSC频率的长期增加。 3.使用谷氨酸受体拮抗剂6-氰基-2,3-二羟基-7-硝基喹喔啉(CNQX)或2-氨基-5-膦基戊酸(AP5)可以降低自发和驱动IPSC的频率。神经或内嗅道驱动的IPSC频率随着沐浴Mg2 +的去除而增加,表明GABA能的中间神经元由非NMDA和NMDA受体处的二尖瓣/簇状细胞驱动。 4.在用压敏染料RH414染色的制剂中,嗅觉神经或嗅觉刺激引起荧光的广泛分布变化。光学响应主要由荧光的减少组成,表明去极化。染料的存在并不明显影响二尖瓣/簇状细胞突触后反应。 5. BMI增强了与灯泡内部以及灯泡中心区域中的去极化相关的光信号的幅度和持续时间。在存在BMI的情况下,去极化活性似乎在控制条件下未激活的鳞茎区域中扩散了数百微米,这清楚地表明了鳞茎中的GABAA受体参与了侧向抑制。 6. CNQX和AP5减弱了灯泡内的光信号,从而支持了以下观点:在这些条件下,光信号主要来自颗粒细胞树突活动。此外,AP5或去除浴液Mg2 +会分别减少或扩大活动的空间分布,这表明在某些情况下NMDA受体可能参与生成或稳定活动的空间模式。 7.结论是,在the嗅球中,GABAA和谷氨酸受体介导的突触传递均塑造了与嗅觉编码相关的神经活动的不同时空模式。

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