Literature DB >> 15236467

An electron microscope immunocytochemical study of GABA(B) R2 receptors in the monkey basal ganglia: a comparative analysis with GABA(B) R1 receptor distribution.

Ali Charara1, Adriana Galvan, Masaaki Kuwajima, Randy A Hall, Yoland Smith.   

Abstract

Functional gamma-aminobutyric acid (GABA)(B) receptors are heterodimers made up of GABA(B) R1 and GABA(B) R2 subunits. The subcellular localization of GABA(B) R2 receptors remains poorly known in the central nervous system. Therefore, we performed an ultrastructural analysis of the localization of GABA(B) R2 receptor immunoreactivity in the monkey basal ganglia. Furthermore, to characterize better the neuronal sites at which GABA(B) R1 and GABA(B) R2 may interact to form functional receptors, we compared the relative distribution of immunoreactivity of the two GABA(B) receptors in various basal ganglia nuclei. Light to moderate GABA(B) R2 immunoreactivity was found in cell bodies and neuropil elements in all basal ganglia nuclei. At the electron microscope level, GABA(B) R2 immunoreactivity was commonly expressed postsynaptically, although immunoreactive preterminal axonal segments were also frequently encountered, particularly in the globus pallidus and substantia nigra, where they accounted for the third of the total number of GABA(B) R2-containing elements. A few labeled terminals that displayed the ultrastructural features of glutamatergic boutons were occasionally found in most basal ganglia nuclei, except for the subthalamic nucleus, which was devoid of GABA(B) R2-immunoreactive boutons. The relative distribution of GABA(B) R2 immunoreactivity in the monkey basal ganglia was largely consistent with that of GABA(B) R1, but some exceptions were found, most noticeably in the globus pallidus and substantia nigra, which contained a significantly larger proportion of presynaptic elements labeled for GABA(B) R1 than GABA(B) R2. These findings suggest the possible coexistence and heterodimerization of GABA(B) R1 and GABA(B) R2 at various pre- and postsynaptic sites, but also raise the possibility that the formation of functional GABA(B) receptors in specific compartments of basal ganglia neurons relies on mechanisms other than GABA(B) R1/R2 heterodimerization. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15236467     DOI: 10.1002/cne.20210

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  8 in total

1.  Ultrastructural localization and function of dopamine D1-like receptors in the substantia nigra pars reticulata and the internal segment of the globus pallidus of parkinsonian monkeys.

Authors:  Michele A Kliem; Jean-Francois Pare; Zafar U Khan; Thomas Wichmann; Yoland Smith
Journal:  Eur J Neurosci       Date:  2010-03       Impact factor: 3.386

Review 2.  Glutamate and GABA receptors and transporters in the basal ganglia: what does their subsynaptic localization reveal about their function?

Authors:  A Galvan; M Kuwajima; Y Smith
Journal:  Neuroscience       Date:  2006-10-23       Impact factor: 3.590

3.  Localization and function of dopamine receptors in the subthalamic nucleus of normal and parkinsonian monkeys.

Authors:  Adriana Galvan; Xing Hu; Karen S Rommelfanger; Jean-Francois Pare; Zafar U Khan; Yoland Smith; Thomas Wichmann
Journal:  J Neurophysiol       Date:  2014-04-23       Impact factor: 2.714

4.  Localization and pharmacological modulation of GABA-B receptors in the globus pallidus of parkinsonian monkeys.

Authors:  Adriana Galvan; Xing Hu; Yoland Smith; Thomas Wichmann
Journal:  Exp Neurol       Date:  2011-03-16       Impact factor: 5.330

5.  Localization and function of GABA transporters in the globus pallidus of parkinsonian monkeys.

Authors:  Adriana Galvan; Xing Hu; Yoland Smith; Thomas Wichmann
Journal:  Exp Neurol       Date:  2010-02-04       Impact factor: 5.330

6.  Postnatal induction and localization of R7BP, a membrane-anchoring protein for regulator of G protein signaling 7 family-Gbeta5 complexes in brain.

Authors:  D Grabowska; M Jayaraman; K M Kaltenbronn; S L Sandiford; Q Wang; S Jenkins; V Z Slepak; Y Smith; K J Blumer
Journal:  Neuroscience       Date:  2007-12-08       Impact factor: 3.590

7.  Immunogold electron microscopic evidence of in situ formation of homo- and heteromeric purinergic adenosine A1 and P2Y2 receptors in rat brain.

Authors:  Kazunori Namba; Tokiko Suzuki; Hiroyasu Nakata
Journal:  BMC Res Notes       Date:  2010-11-29

8.  In vivo optogenetic control of striatal and thalamic neurons in non-human primates.

Authors:  Adriana Galvan; Xing Hu; Yoland Smith; Thomas Wichmann
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

  8 in total

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