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大鼠海马抑制性细胞上的兴奋性突触连接可能涉及单个递质释放位点。

Excitatory synaptic connections onto rat hippocampal inhibitory cells may involve a single transmitter release site.

作者信息

Arancio O, Korn H, Gulyas A, Freund T, Miles R

机构信息

Laboratoire de Neurobiologie Cellulaire, Institut Pasteur, Paris, France.

出版信息

J Physiol. 1994 Dec 1;481 ( Pt 2)(Pt 2):395-405. doi: 10.1113/jphysiol.1994.sp020448.

DOI:10.1113/jphysiol.1994.sp020448
PMID:7738832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1155938/
Abstract
  1. Whole-cell tight-seal records of excitatory postsynaptic currents (EPSCs) were made from inhibitory cells in the CA3 region of thin hippocampal slices. We tested the hypothesis that excitatory synaptic connections made on inhibitory cells involve few transmitter release sites. 2. EPSCs impinging on inhibitory cells had a time to peak of 0.4-3.8 ms and an amplitude of 8-90 pA at a holding potential of -60 mV. They were suppressed by the excitatory amino acid antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and DL-2-amino-5-phosphonovaleric acid (APV). 3. Addition of tetrodotoxin (TTX) and Co2+ to the external solution reduced the frequency of EPSCs from 0.90 to 0.25 s-1 (n = 24 cells). In the majority of cells EPSC amplitude distributions were not significantly changed. 4. Increasing Ca2+ and reducing Mg2+ in the external solution, in order to enhance the probability of transmitter release, did not change EPSC amplitude distributions. In contrast, amplitude histograms for IPSCs recorded from pyramidal cells were shifted to higher mean values in this solution. 5. EPSCs were elicited in inhibitory cells by electrical stimulation via a glass pipette placed near to pyramidal cells in stratum pyramidale. EPSCs elicited by weak stimuli had similar amplitude distributions to excitatory synaptic events recorded in the presence of TTX and Co2+. 6. These findings suggest excitatory synaptic connections made with CA3 inhibitory cells involve few or possibly just one transmitter release site.
摘要
  1. 全细胞紧密封接记录兴奋性突触后电流(EPSCs),是在薄海马切片CA3区的抑制性细胞上进行的。我们检验了这样一个假设:在抑制性细胞上形成的兴奋性突触连接涉及很少的递质释放位点。2. 在-60 mV的钳制电位下,作用于抑制性细胞的EPSCs的峰值时间为0.4 - 3.8毫秒,幅度为8 - 90皮安。它们被兴奋性氨基酸拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)和DL-2-氨基-5-膦酸戊酸(APV)所抑制。3. 向细胞外溶液中加入河豚毒素(TTX)和Co2+,使EPSCs的频率从0.90次/秒降至0.25次/秒(n = 24个细胞)。在大多数细胞中,EPSC幅度分布没有显著变化。4. 为了提高递质释放的概率,增加细胞外溶液中的Ca2+并降低Mg2+,并没有改变EPSC幅度分布。相比之下,在这种溶液中,从锥体细胞记录到的IPSCs的幅度直方图向更高的平均值偏移。5. 通过置于锥体层靠近锥体细胞的玻璃微电极进行电刺激,在抑制性细胞中诱发EPSCs。弱刺激诱发的EPSCs与在TTX和Co2+存在下记录到的兴奋性突触事件具有相似的幅度分布。6. 这些发现表明,与CA3抑制性细胞形成的兴奋性突触连接涉及很少或可能只有一个递质释放位点。

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