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不同的机制调节出生后早期和幼年海马颗粒细胞中的抑制性突触后电流动力学。

Different mechanisms regulate IPSC kinetics in early postnatal and juvenile hippocampal granule cells.

作者信息

Draguhn A, Heinemann U

机构信息

Institut für Physiologie der Charité, Abt. Neurophysiologie, Berlin, Germany.

出版信息

J Neurophysiol. 1996 Dec;76(6):3983-93. doi: 10.1152/jn.1996.76.6.3983.

Abstract
  1. Monosynaptic inhibitory postsynaptic currents (IPSCs) were recorded from early postnatal and juvenile dentate granule cells in rat brain slices at room temperature. The focally evoked currents were mediated by gamma-aminobutyric acid-A (GABAA) receptors. 2. IPSCs were characterized by a steep rising phase and a slower, monoexponential decay time course. The decay time constant was potential dependent and average values ranged from 33 ms at a holding potential of -60 mV to 58 ms at a holding potential of +40 mV. 3. IPSCs were studied in tissue from animals between postnatal day (p) 3 and p25. All kinetic parameters as well as the mean current amplitude were unchanged during this ontogenetic period. 4. In juvenile granule cells from animals aged 13-16 days, addition of the GABA uptake blocker (R)-N-[4,4-bis (3-methyl-2-thienyl) but-3-en1-yl] nipecotic acid (tiagabine) (10 microM) prolonged the decaying phase of the IPSCs. The current decay remained monoexponential but the time constant increased to 250% of control values. Mean current amplitudes remained largely unchanged. 5. In contrast, tiagabine had no effect on IPSCs in early postnatal tissuĕ. The decay time constant remained unchanged in cells recorded from animals aged p4-p6. Other uptake blockers were also ineffective during the first postnatal week, whereas beta-alanine, NNC-711, and L-2,3-diaminoproprionic acid enhanced the decay time constant in the older tissue (p13-p16). 6. Hypoosmolaric extracellular solution was applied to restrict the extracellular space. In juvenile tissue (p13-p16), IPSCs were not affected by this treatment, whereas early postnatal granule cells (p4-p6) displayed clearly prolonged IPSC decay time constants (165% of control). 7. We conclude that the mechanism governing the kinetics of evoked IPSCs in granule cells changes during ontogenesis. Whereas in early postnatal tissue the transmitter leaves the postsynaptic site by diffusion, GABA uptake becomes time limiting after 2 wk of postnatal development.
摘要
  1. 在室温下,从新生大鼠和幼年大鼠脑片的齿状颗粒细胞记录单突触抑制性突触后电流(IPSCs)。局部诱发电流由γ-氨基丁酸-A(GABAA)受体介导。2. IPSCs的特征是上升相陡峭,衰减时间过程较慢且呈单指数形式。衰减时间常数取决于电位,在-60 mV的钳制电位下平均值为33 ms,在+40 mV的钳制电位下为58 ms。3. 对出生后第3天(p)至第25天动物的组织中的IPSCs进行了研究。在此个体发育期间,所有动力学参数以及平均电流幅度均未改变。4. 在13 - 16日龄动物的幼年颗粒细胞中,添加GABA摄取阻滞剂(R)-N-[4,4-双(3-甲基-2-噻吩基)丁-3-烯-1-基]烟碱酸(噻加宾)(10 microM)可延长IPSCs的衰减相。电流衰减仍为单指数形式,但时间常数增加至对照值的250%。平均电流幅度基本保持不变。5. 相比之下,噻加宾对新生组织中的IPSCs无影响。在出生后第4 - 6天动物记录的细胞中,衰减时间常数保持不变。其他摄取阻滞剂在出生后第一周也无效,而β-丙氨酸、NNC - 711和L - 2,3 - 二氨基丙酸可增加较老组织(p13 - p16)中的衰减时间常数。6. 应用低渗细胞外溶液来限制细胞外空间。在幼年组织(p13 - p16)中,IPSCs不受此处理的影响,而新生早期颗粒细胞(p4 - p6)的IPSC衰减时间常数明显延长(对照值的165%)。7. 我们得出结论,在个体发育过程中,颗粒细胞中诱发IPSCs动力学的机制发生变化。在新生早期组织中,递质通过扩散离开突触后位点,而在出生后发育2周后,GABA摄取成为时间限制因素。

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