Morphine Withdrawal Increases Glutamate Uptake and Surface Expression of Glutamate Transporter GLT1 at Hippocampal Synapses

• DOI: 10.1523/jneurosci.23-11-04775.2003
• Publication Date: 2018-04-13T22:30:28Z
• Authors: Nan-Jie Xu; Lan Bao; Hua-Ping Fan; Guo-Bin Bao; Lu Pu; Ying-Jin Lu; Chun-Fu Wu; Xu Zhang; Gang Pei
• Keywords: Male; Neurons; 0301 basic medicine; Morphine; Symporters; Amino Acid Transport System X-AG; Presynaptic Terminals; Glutamic Acid; Hippocampus; Rats; Substance Withdrawal Syndrome; Rats, Sprague-Dawley; Glutamate Plasma Membrane Transport Proteins; Protein Transport; 03 medical and health sciences; Excitatory Amino Acid Transporter 3; Excitatory Amino Acid Transporter 2; Astrocytes; Animals; RNA, Messenger; Morphine Dependence; Cells, Cultured

Opiate abuse causes adaptive changes in several processes of synaptic transmission in which the glutamatergic system appears a critical element involved in opiate tolerance and dependence, but the underlying mechanisms remain unclear. In the present study, we found that glutamate uptake in hippocampal synaptosomes was significantly increased (by 70% in chronic morphine-treated rats) during the morphine withdrawal period, likely attributable to an increase in the number of functional glutamate transporters. Immunoblot analysis showed that expression of GLT1 (glutamate transporter subtype 1) was identified to be upregulated in synaptosomes but not in total tissues, suggesting a redistribution of glutamate transporter expression. Moreover, the increase in glutamate uptake was reproduced in cultured neurons during morphine withdrawal, and the increase of uptake in neurons could be blocked by dihydrokainate, a specific inhibitor of GLT1. Cell surface biotinylation and immunoblot analysis showed that morphine withdrawal produced an increase in GLT1 expression rather than EAAC1 (excitatory amino acids carrier 1), a neuronal subtype, at the cultured neuronal cell surface, whereas no significant change was observed in that of cultured astrocytes. Electron microscopy also revealed that GLT1 expression was markedly increased in the nerve terminals of hippocampus and associated with the plasma membranein vivo. These results suggest that GLT1 in hippocampal neurons can be induced to translocate to the nerve terminals and express on the cell surface during morphine withdrawal. The translocation of GLT1 at synapses during morphine withdrawal provides a neuronal mechanism for modulation of excitatory neurotransmission during opiate abuse.