Publications by authors named "A S Zhigulin"

Amidine-containing compounds are primarily known as antiprotozoal agents (pentamidine, diminazene, furamidine) or as serine protease inhibitors (nafamostat, sepimostat, camostat, gabexate). DAPI is widely recognized as a fluorescent DNA stain. Recently, it has been shown that these compounds also act as NMDA receptor inhibitors.

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Article Synopsis
  • - Recent research highlights the repurposing of NMDA receptor antagonists like ketamine for treating major depressive disorder, sparking renewed interest in studying NMDA receptors.
  • - A study used whole-cell patch-clamp methods to evaluate the effects of biguanide compounds on NMDA receptors in rat hippocampal neurons, finding that certain compounds like cycloguanil, proguanil, and phenformin effectively inhibited these receptors.
  • - The compounds were found to act as non-competitive inhibitors, with distinct mechanisms, suggesting their potential for treating neurodegenerative disorders linked to glutamatergic excitotoxicity and providing insights into NMDA receptor structure.
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N-methyl-D-aspartate (NMDA) receptors are inhibited by many amidine and guanidine compounds. In this work, we studied the mechanisms of their inhibition by sepimostat-an amidine-containing serine protease inhibitor with neuroprotective properties. Sepimostat inhibited native NMDA receptors in rat hippocampal CA1 pyramidal neurons with IC of 3.

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Article Synopsis
  • Proton-gated ASIC channels are found in central neurons and are thought to be important for neurophysiological functions, though their exact roles are not fully understood.
  • Acidification in the synaptic cleft affects glutamate receptors and ASICs differently, suggesting that ASICs might help balance post-synaptic responses during significant acidity levels.
  • Research involving rat brain neurons indicates variability in ASIC and glutamate receptor responses, highlighting the influence of pH, magnesium, and membrane voltage on synaptic transmission and plasticity.
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Febrile seizures (FSs) are a relatively common early-life condition that can cause CNS developmental disorders, but the specific mechanisms of action of FS are poorly understood. In this work, we used hyperthermia-induced FS in 10-day-old rats. We demonstrated that the efficiency of glutamatergic synaptic transmission decreased rapidly after FS by recording local field potentials.

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