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N-甲基-D-天冬氨酸(NMDA)受体而非α-氨基-3-羟基-5-甲基-4-异恶唑丙酸/海人藻酸(AMPA/kainate)受体的拮抗作用可阻断由前额叶皮层电刺激诱导的多巴胺能神经元的爆发式放电。

Antagonism of NMDA receptors but not AMPA/kainate receptors blocks bursting in dopaminergic neurons induced by electrical stimulation of the prefrontal cortex.

作者信息

Tong Z Y, Overton P G, Clark D

机构信息

Department of Psychology, University of Wales, Swansea, United Kingdom.

出版信息

J Neural Transm (Vienna). 1996;103(8-9):889-904. doi: 10.1007/BF01291780.

Abstract

Evidence suggests that the prefrontal cortex (PFC) plays an important role in the burst activity of midbrain dopaminergic (DA) neurons. In particular, electrical stimulation of the PFC elicits patterns of activity in DA neurons, closely time-locked to the stimulation, which resemble natural bursts. Given that natural bursts are produced by the activity of excitatory amino acid (EAA)-ergic afferents, if PFC-induced time-locked bursts are homologues of natural bursts, EAA antagonists should attenuate them. Hence, the NMDA (N-methyl-D-aspartate) antagonist CPP (3-((+/-)-2-carboxypiperazin-4-yl)propyl-1-phosphonic acid) and the AMPA (D,L-alpha-amino-3-hydroxy-5-methyl-4-isoxalone propionic acid)/kainate antagonist CNQX (6-cyano-7-nitroquinoxaline-2,3-dione) were applied by iontophoresis to DA neurons exhibiting time-locked bursts during PFC stimulation. CPP produced a significant reduction in time-locked bursting. In contrast, CNQX (at currents which antagonised AMPA responses) did not. These effects of CPP and CNQX on time-locked bursting mirror the effects previously reported for these drugs on natural bursting. Since natural bursting and bursting induced by PFC stimulation are both blocked selectively by CPP, the present results increase the degree of analogy between the two burst phenomena, thereby adding extra support to the contention that the cortex is involved in producing the natural bursting in DA neurons.

摘要

有证据表明,前额叶皮层(PFC)在中脑多巴胺能(DA)神经元的爆发性活动中起重要作用。特别是,对PFC的电刺激会引发DA神经元的活动模式,与刺激紧密锁时,类似于自然爆发。鉴于自然爆发是由兴奋性氨基酸(EAA)能传入神经的活动产生的,如果PFC诱导的锁时爆发是自然爆发的同源物,EAA拮抗剂应该会减弱它们。因此,通过离子电泳将NMDA(N-甲基-D-天冬氨酸)拮抗剂CPP(3-((+/-)-2-羧基哌嗪-4-基)丙基-1-膦酸)和AMPA(D,L-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸)/海人藻酸拮抗剂CNQX(6-氰基-7-硝基喹喔啉-2,3-二酮)应用于在PFC刺激期间表现出锁时爆发的DA神经元。CPP使锁时爆发显著减少。相比之下,CNQX(在拮抗AMPA反应的电流下)则没有。CPP和CNQX对锁时爆发的这些作用反映了先前报道的这些药物对自然爆发的作用。由于自然爆发和PFC刺激诱导的爆发都被CPP选择性阻断,目前的结果增加了这两种爆发现象之间的相似程度,从而为皮层参与DA神经元自然爆发产生的观点提供了额外支持。

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