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Effects of baclofen on synaptically-induced cell firing in the rat hippocampal slice.

机译:巴氯芬对大鼠海马切片突触诱导的细胞放电的影响。

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摘要

The effects of baclofen on the synaptically-induced firing of pyramidal and granule cell populations were tested in the rat hippocampal slice. Population spikes were evoked by stimulating excitatory pathways in the presence and absence of bath-applied drug. (+/-)-Baclofen (20 microM) completely blocked the firing of CA1 or CA3 hippocampal pyramidal cells subsequent to stimulation of projections that originate in area CA3. In contrast, the firing of dentate granule cells evoked by stimulation of the perforant path fibres was depressed by only 46% and baclofen did not affect the monosynaptic firing of CA3 pyramidal cells evoked by mossy fibre stimulation. These results are consistent with the effects of baclofen on the corresponding extracellularly-recorded excitatory postsynaptic potentials (e.p.s.ps). The Schaffer collateral-commissural population spike in area CA1 was depressed by (-)-baclofen (EC50 = 2.8 microM), GABA (EC50 = 2.2 mM) and 3-aminopropanesulphonic acid (3-APS) (EC50 = 0.34 mM). (-)-Baclofen was 180 times as potent as (+)-baclofen. Bicuculline methiodide (100 microM) did not reverse the depressant action of (-)-baclofen. GABA-induced depressions were antagonized to only a small degree, whilst the effect of 3-APS was readily reversed. Raising the concentration of bicuculline from 100 microM to 500 microM did not further reverse the action of GABA. The effects of (-)-baclofen and 3-APS on the relationship between extracellular e.p.s.p. and population spike were tested by stimulation of the Schaffer collateral-commissural fibres in area CA1. (-)-Baclofen shifted the 'input/output' curve to the right at a concentration of 1 microM, but less or not at all at 3 microM. In contrast, increasing the concentration of 3-APS shifted this curve farther to the right.
机译:在大鼠海马切片中测试了巴氯芬对突触诱导的锥体细胞和颗粒细胞群放电的影响。在存在和不存在浴用药物的情况下,通过刺激兴奋性途径引起群体高峰。 (+/-)-Baclofen(20 microM)在刺激源自CA3区域的投射后完全阻断了CA1或CA3海马锥体细胞的放电。相反,刺激穿孔路径纤维引起的齿状颗粒细胞的放电仅降低了46%,而巴氯芬不影响苔藓纤维刺激引起的CA3锥体细胞的单突触放电。这些结果与巴氯芬对相应的细胞外记录的兴奋性突触后电位(e.p.s.ps)的作用一致。 (1)-baclofen(EC50 = 2.8 microM),GABA(EC50 = 2.2 mM)和3-氨基丙磺酸(3-APS)(EC50 = 0.34 mM)抑制了CA1区的Schaffer侧腹-连合人口高峰。 (-)-巴氯芬的效力是(+)-巴氯芬的180倍。甲硫氨酸小分子(100 microM)不能逆转(-)-baclofen的抑制作用。 GABA诱导的抑郁症仅在很小的程度上被拮抗,而3-APS的作用则容易逆转。将双小分子的浓度从100 microM提高到500 microM并没有进一步逆转GABA的作用。 (-)-baclofen和3-APS对细胞外e.p.s.p.通过刺激CA1区的Schaffer侧连合纤维测试人口和峰值。 (-)-Baclofen在1 microM的浓度下将“输入/输出”曲线向右移动,但在3 microM的浓度下几乎没有或根本没有。相反,增加3-APS的浓度会使该曲线向右移动。

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    Ault, B.; Nadler, J. V.;

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  • 年度 1983
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