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Antidepressants modulate glycine action in rat hippocampus

机译:抗抑郁药调节大鼠海马中的甘氨酸作用

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摘要

Antidepressants are drugs that relieve symptoms of depressive disorders. Fluoxetine, tianeptine, and milnacipran are different types of antidepressants, and they have widely been used for relieving of depression symptoms. In the present study, the effects of fluoxetine, tianeptine, and milnacipran on the glycine-induced ion current by nystatin-perforated patch clamp and on the amplitude of field potential in the hippocampal CA1 region by multichannel extracellular recording, MED64, system, were studied. In the present results, fluoxetine, tianeptine, and milnacipran reduced glycine-induced ion current in the hippocampal CA1 neurons in nystatin-perforated patch clamp method. These drugs enhanced the amplitude of the field potential in the hippocampal CA1 region in MED64 system. These results suggest that antidepressants may increase neuronal activity by enhancing field potential through inhibition on glycine-induced ion current.
机译:抗抑郁药是缓解抑郁症症状的药物。氟西汀,噻吩汀和米那普仑是不同类型的抗抑郁药,它们已广泛用于缓解抑郁症症状。在本研究中,通过多通道细胞外记录,MED64系统,研究了氟西汀,丁肽和米那普仑对制霉菌素穿孔的膜片钳对甘氨酸诱导的离子电流的影响以及对海马CA1区场电位振幅的影响。 。在目前的结果中,氟西汀,田奈汀和米那普仑通过制霉菌素穿孔的膜片钳方法降低了海马CA1神经元中甘氨酸诱导的离子电流。这些药物增强了MED64系统中海马CA1区场电位的幅度。这些结果表明,抗抑郁药可以通过抑制甘氨酸诱导的离子电流来增强电场潜能,从而增加神经元的活性。

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