Metamodulation of presynaptic NMDA receptors: New perspectives for pharmacological interventions

Neuropharmacology. 2023 Aug 15:234:109570. doi: 10.1016/j.neuropharm.2023.109570. Epub 2023 May 3.

Abstract

Metamodulation shifted the scenario of the central neuromodulation from a simplified unimodal model to a multimodal one. It involves different receptors/membrane proteins physically associated or merely colocalized that act in concert to control the neuronal functions influencing each other. Defects or maladaptation of metamodulation would subserve neuropsychiatric disorders or even synaptic adaptations relevant to drug dependence. Therefore, this "vulnerability" represents a main issue to be deeply analyzed to predict its aetiopathogenesis, but also to propose targeted pharmaceutical interventions. The review focusses on presynaptic release-regulating NMDA receptors and on some of the mechanisms of their metamodulation described in the literature. Attention is paid to the interactors, including both ionotropic and metabotropic receptors, transporters and intracellular proteins, which metamodulate their responsiveness in physiological conditions but also undergo adaptation that are relevant to neurological dysfunctions. All these structures are attracting more and more the interest as promising druggable targets for the treatment of NMDA receptor-related central diseases: these substances would not exert on-off control of the colocalized NMDA receptors (as usually observed with NMDA receptor full agonists/antagonists), but rather modulate their functions, with the promise of limiting side effects that would favor their translation from preclinic to clinic. This article is part of the Special Issue on "The receptor-receptor interaction as a new target for therapy".

Keywords: Interactors; Metamodulation; NMDA receptor; Presynaptic; Therapeutics; Vulnerability.

Publication types

  • Review

MeSH terms

  • Neurons / metabolism
  • Receptors, N-Methyl-D-Aspartate* / metabolism
  • Receptors, Presynaptic* / metabolism
  • Signal Transduction

Substances

  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Presynaptic