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

机译:突触前多巴胺D2样受体抑制兴奋性传递到大鼠腹侧被膜多巴胺能神经元

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摘要

class="enumerated" style="list-style-type:decimal">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 μm CNQX in the presence of bicuculline (20 μm), strychnine (0.5 μm) and D-amino-5-phosphonopentanoic acid (D-AP5, 25 μm).Bath application of DA reduced the amplitude of EPSCs up to 65.1 ± 9.52% in a concentration-dependent manner between 0.3–1000 μm (IC50, 16.0 μm) without affecting the holding current at −60 mV measured using a Cs+-filled electrode.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 μm), but not by the D1-like receptor antagonist SCH 23390 (KB, 228.6 μm).Dopamine (30 μm) 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.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.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 使用全细胞膜片钳技术在大鼠中脑切片中检查了多巴胺(DA)对腹侧被盖区(VTA)中非NMDA谷氨酸能传递到多巴胺能神经元的影响。 VTA内局部刺激引起的多巴胺能神经元中的EPSC在存在双小分子(20μm),士丁碱(0.5μm)和D-氨基-5-膦基戊酸(D-AP5,25μm)的情况下被5μmCNQX可逆地阻断。 DA的应用在0.3–1000μm(IC50,16.0μm)之间以浓度依赖的方式将EPSC的幅度降低了65.1±9.52%,而不会影响在−60 mV时的保持电流使用Cs + 填充电极。 DA对诱发的EPSC的作用是通过D2样受体激动剂喹吡罗模拟的,而不是通过D1样受体激动剂SKF 81297模仿的。 ,并被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。 多巴胺(30μm)减少自发微型EPSCs的平均频率而不影响其平均幅度,并且DA诱导的mEPSCs效应取决于外部Ca 2 + 浓度 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,其激活可通过减少Ca 2 + 流入来抑制谷氨酸释放。 / li>

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