The glycine transport inhibitor sarcosine is an inhibitory glycine receptor agonist

Hai Xia Zhang, Ariel Lyons-Warren, Liu Lin Thio

Research output: Contribution to journalArticle

25 Scopus citations

Abstract

Sarcosine is an endogenous amino acid that is a competitive inhibitor of the type I glycine transporter (GlyT1), an N-methyl-d-aspartate receptor (NMDAR) co-agonist, and an important intermediate in one-carbon metabolism. Its therapeutic potential for schizophrenia further underscores its clinical importance. The structural similarity between sarcosine and glycine and sarcosine's ability to serve as an NMDAR co-agonist led us to examine whether sarcosine is also an agonist at the inhibitory glycine receptor (GlyR). We examined this possibility using whole-cell recordings from cultured embryonic mouse hippocampal neurons and found that sarcosine evoked a dose-dependent, strychnine sensitive, Cl- current that cross-inhibited glycine currents. Sarcosine evoked this current with Li+ in the extracellular solution to block GlyT1, in neurons treated with the essentially irreversible GlyT1 inhibitor N[3-(4′-fluorophenyl)-3-(4′-phenylphenoxy)propyl]sarcosine (NFPS), and in neurons plated in the absence of glia. These results indicate that the sarcosine currents did not result from GlyT1 inhibition or heteroexchange. We conclude that sarcosine is a GlyR agonist.

Original languageEnglish
Pages (from-to)551-555
Number of pages5
JournalNeuropharmacology
Volume57
Issue number5-6
DOIs
StatePublished - Oct 1 2009

Keywords

  • Culture
  • Hippocampus
  • N-Methyl-d-aspartate
  • N[3-(4′-fluorophenyl)-3-(4′-phenylphenoxy)propyl]sarcosine
  • Patch clamp
  • Schizophrenia

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