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Presence of Inhibitory Glycinergic Transmission in Medium Spiny Neurons in the Nucleus Accumbens.
Muñoz, Braulio; Yevenes, Gonzalo E; Förstera, Benjamin; Lovinger, David M; Aguayo, Luis G.
Afiliação
  • Muñoz B; Laboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepción, Chile.
  • Yevenes GE; Laboratory of Neuropharmacology, Department of Physiology, Universidad de Concepción, Concepción, Chile.
  • Förstera B; Laboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepción, Chile.
  • Lovinger DM; Laboratory for Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, United States.
  • Aguayo LG; Laboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepción, Chile.
Front Mol Neurosci ; 11: 228, 2018.
Article em En | MEDLINE | ID: mdl-30050406
ABSTRACT
It is believed that the rewarding actions of drugs are mediated by dysregulation of the mesolimbic dopaminergic system leading to increased levels of dopamine in the nucleus accumbens (nAc). It is widely recognized that GABAergic transmission is critical for neuronal inhibition within nAc. However, it is currently unknown if medium spiny neurons (MSNs) also receive inhibition by means of glycinergic synaptic inputs. We used a combination of proteomic and electrophysiology studies to characterize the presence of glycinergic input into MSNs from nAc demonstrating the presence of glycine transmission into nAc. In D1 MSNs, we found low frequency glycinergic miniature inhibitory postsynaptic currents (mIPSCs) which were blocked by 1 µM strychnine (STN), insensitive to low (10, 50 mM) and high (100 mM) ethanol (EtOH) concentrations, but sensitive to 30 µM propofol. Optogenetic experiments confirmed the existence of STN-sensitive glycinergic IPSCs and suggest a contribution of GABA and glycine neurotransmitters to the IPSCs in nAc. The study reveals the presence of glycinergic transmission in a non-spinal region and opens the possibility of a novel mechanism for the regulation of the reward pathway.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article