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Functional and morphological characterization of glutamate transporters in the rat locus coeruleus
Author(s) -
Medrano M C,
Gerrikagoitia I,
MartínezMillán L,
Mendiguren A,
Pineda J
Publication year - 2013
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.12235
Subject(s) - glutamate receptor , locus coeruleus , ionotropic effect , glutamatergic , ampa receptor , synaptic cleft , chemistry , biology , excitatory postsynaptic potential , metabotropic glutamate receptor 6 , biochemistry , receptor , neuroscience , central nervous system
Background and Purpose Excitatory amino acid transporters ( EAAT s) in the CNS contribute to the clearance of glutamate released during neurotransmission. The aim of this study was to explore the role of EAATs in the regulation of locus coeruleus ( LC ) neurons by glutamate. Experimental Approach We measured the effect of different EAAT subtype inhibitors/enhancers on glutamate‐ and KCl ‐induced activation of LC neurons in rat slices. EAAT2 –3 expression in the LC was also characterized by immunohistochemistry. Key Results The EAAT2 –5 inhibitor DL‐threo‐β‐benzyloxaspartic acid (100 μM), but not the EAAT2 , 4, 5 inhibitor L‐trans‐pyrrolidine‐2,4‐dicarboxylic acid (100 μM) or the EAAT2 inhibitor dihydrokainic acid ( DHK ; 100 μM), enhanced the glutamate‐ and KCl ‐induced activation of the firing rate of LC neurons. These effects were blocked by ionotropic, but not metabotrobic, glutamate receptor antagonists. DHK (100 μM) was the only EAAT inhibitor that increased the spontaneous firing rate of LC cells, an effect that was due to inhibition of EAAT2 and subsequent AMPA receptor activation. Chronic treatment with ceftriaxone (200 mg·kg −1 i.p., once daily, 7 days), an EAAT2 expression enhancer, increased the actions of glutamate and DHK , suggesting a functional impact of EAAT2 up‐regulation on the glutamatergic system. Immuhistochemical data revealed the presence of EAAT2 and EAAT3 surrounding noradrenergic neurons and EAAT2 on glial cells in the LC . Conclusions and Implications These results remark the importance of EAAT2 and EAAT3 in the regulation of rat LC by glutamate. Neuronal EAAT3 would be responsible for terminating the action of synaptically released glutamate, whereas glial EAAT2 would regulate tonic glutamate concentrations in this nucleus.