A D2 class dopamine receptor transactivates a receptor tyrosine kinase to inhibit NMDA receptor transmission

被引:178
作者
Kotecha, SA
Oak, JN
Jackson, MF
Perez, Y
Orser, BA
Van Tol, HHM
MacDonald, JF [1 ]
机构
[1] Univ Toronto, Fac Med, Dept Physiol, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Fac Med, Dept Pharmacol, Toronto, ON, Canada
[3] Univ Toronto, Fac Med, Dept Psychiat, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Fac Med, Dept Anesthesiol, Toronto, ON, Canada
[5] Univ Toronto, Fac Med, Inst Med Sci, Toronto, ON, Canada
[6] Univ Toronto, Fac Med, Ctr Addict & Mental Hlth, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0896-6273(02)00859-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Receptor tyrosine kinases (RTKs) are membrane spanning proteins with intrinsic kinase activity. Although these receptors are known to be involved in proliferation and differentiation of cells, their roles in regulating central synaptic transmission are largely unknown. In CA1 pyramidal neurons, activation of D2 class dopamine receptors depressed excitatory transmission mediated by the NMDA subtype of glutamate receptor. This depression resulted from the quinpirole-induced release of intracellular Ca2+ and enhanced Ca2+-dependent inactivation of NMDA receptors. The dopamine receptor-mediated depression was dependent on the "transactivation" of PDGFRbeta. Therefore, RTK transactivation provides a novel mechanism of communication between dopaminergic and glutamatergic systems and might help to explain how,reciprocal changes in these systems could be linked to the deficits in cognition, memory, and attention observed in schizophrenia and attention deficit hyperactivity disorder.
引用
收藏
页码:1111 / 1122
页数:12
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