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Synapse
February 8, 2026Physiology0 citations

mRNA translation and proteasomal degradation in health and neurological disease

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AIAlinny Rosendo IsaacUniversidade Federal do Rio de JaneiroDCDanielle CozachencoBWBeatriz de A WagnerUniversidade Federal do Rio de Janeiro

Key Points

  • To explore the mechanisms of protein synthesis and degradation related to neurological diseases.
  • Review of existing literature on proteostasis and molecular pathways
  • Discussion of pharmacological interventions
  • Analysis of protein synthesis and degradation mechanisms
  • Identified disruptions in proteostasis linked to various neurological diseases
  • Highlighted potential pharmacological strategies to restore proteostasis
  • Outlined future directions for research in the field.

Abstract

The homeostasis of cellular proteins, i.e., proteostasis, is critical for neuronal function and brain processes. Proteostasis comprises a set of cellular mechanisms that control protein synthesis, folding, post-translational modification and degradation. Mounting evidence indicates that disruptions in such mechanisms may underlie several neurological diseases, including neurodevelopmental, neurodegenerative and psychiatric diseases. In this review, we discuss molecular pathways involved in protein synthesis and degradation that are altered in several brain diseases, possible pharmacological approaches to correct these defects, and future perspectives for the field.

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Cite This Study

Isaac et al. (2026) studied this question.

synapsesocial.com/papers/698828fd0fc35cd7a8848e5chttps://doi.org/10.1152/physiol.00023.2025
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