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突触前多巴胺D2样受体抑制对大鼠腹侧被盖区多巴胺能神经元的兴奋性传递。

Presynaptic dopamine D2-like receptors inhibit excitatory transmission onto rat ventral tegmental dopaminergic neurones.

作者信息

Koga E, Momiyama T

机构信息

Department of Physiology, Nagasaki University School of Medicine, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.

出版信息

J Physiol. 2000 Feb 15;523 Pt 1(Pt 1):163-73. doi: 10.1111/j.1469-7793.2000.t01-2-00163.x.

Abstract
  1. The effects of dopamine (DA) on non-NMDA glutamatergic transmission onto dopaminergic neurones in the ventral tegmental area (VTA) were examined in rat midbrain slices using the whole-cell patch-clamp technique. EPSCs in dopaminergic neurones evoked by focal stimulation within the VTA were reversibly blocked by 5 microM CNQX in the presence of bicuculline (20 microM), strychnine (0.5 microM) and D-amino-5-phosphonopentanoic acid (D-AP5, 25 microM). 2. Bath application of DA reduced the amplitude of EPSCs up to 65.1 +/- 9. 52% in a concentration-dependent manner between 0.3-1000 microM (IC50, 16.0 microM) without affecting the holding current at -60 mV measured using a Cs+-filled electrode. 3. The effect of DA on evoked EPSCs was mimicked by the D2-like receptor agonist quinpirole but not by the D1-like receptor agonist SKF 81297, and was antagonized by the D2-like receptor antagonist sulpiride (KB, 0.96 microM), but not by the D1-like receptor antagonist SCH 23390 (KB, 228.6 microM). 4. Dopamine (30 microM) reduced the mean frequency of spontaneous miniature EPSCs (mEPSCs) without affecting their mean amplitude, and the DA-induced effect on the mEPSCs was dependent on the external Ca2+ concentration. 5. These results suggest that afferent glutamatergic fibres which terminate on VTA dopaminergic neurones possess presynaptic D2-like receptors, activation of which inhibits glutamate release by reducing Ca2+ influx.
摘要
  1. 采用全细胞膜片钳技术,在大鼠中脑切片中研究了多巴胺(DA)对腹侧被盖区(VTA)多巴胺能神经元上非NMDA谷氨酸能传递的影响。在存在荷包牡丹碱(20μM)、士的宁(0.5μM)和D - 氨基 - 5 - 膦酰戊酸(D - AP5,25μM)的情况下,VTA内局部刺激诱发的多巴胺能神经元中的兴奋性突触后电流(EPSCs)被5μM CNQX可逆性阻断。2. 浴槽中应用DA以浓度依赖性方式使EPSCs的幅度降低高达65.1±9.52%,浓度范围为0.3 - 1000μM(IC50,16.0μM),且不影响使用Cs⁺填充电极在 - 60mV测量的钳制电流。3. DA对诱发的EPSCs的作用可被D2样受体激动剂喹吡罗模拟,但不能被D1样受体激动剂SKF 81297模拟,且被D2样受体拮抗剂舒必利(KB,0.96μM)拮抗,但不被D1样受体拮抗剂SCH 23390(KB,228.6μM)拮抗。4. 多巴胺(30μM)降低了自发性微小兴奋性突触后电流(mEPSCs)的平均频率,但不影响其平均幅度,且DA对mEPSCs的诱导作用依赖于细胞外Ca²⁺浓度。5. 这些结果表明,终止于VTA多巴胺能神经元的传入谷氨酸能纤维具有突触前D2样受体,其激活通过减少Ca²⁺内流来抑制谷氨酸释放。

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