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Quantification of D 1 and D 5 dopamine receptor localization in layers I, III, and V of Macaca mulatta prefrontal cortical area 9: Coexpression in dendritic spines and axon terminals
Author(s) -
BordelonGlausier Jill R.,
Khan Zafar U.,
Muly E. Chris
Publication year - 2008
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.21710
Subject(s) - dendritic spine , neuropil , neuroscience , biology , axon , prefrontal cortex , dopamine , receptor , dopamine receptor , central nervous system , cognition , hippocampal formation , biochemistry
D1 family receptors (D1R) in prefrontal cortex (PFC) are critical for normal cognition and are implicated in pathological states such as schizophrenia. The two D1R subtypes, D 1 and D 5 , cannot be pharmacologically distinguished but have important functional differences. To understand their contributions to cortical function, we quantified their localization in the neuropil of primate PFC. We identified different patterns of distribution for the two receptors that showed variation across cortical laminae. Although D 1 was enriched in spines and D 5 in dendrites, there was considerable overlap in their distribution within neuronal compartments. To determine whether the D 1 and D 5 receptors are localized to separate populations of synapses, we employed double‐labeling methods. We found the two receptors colocalized and quantified the overlap of their distribution in spines and axon terminals of prefrontal cortical area 9 in the Macaca mulatta monkey. The two receptors are found in partially overlapping populations, such that the D 5 receptor is found in a subpopulation of those spines and terminals that contain D 1 . These results indicate that dopamine activation of the two D1R subtypes does not modulate disparate populations of synapses onto dendritic spines in prefrontal cortical area 9; rather, dopamine can activate D 1 and D 5 receptors on the same spines, plus an additional group of spines that contains only D 1 . The implications of these results for the dose‐dependent relationship between D1R activation and PFC function are discussed. J. Comp. Neurol. 508:893–905, 2008. © 2008 Wiley‐Liss, Inc.