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Updated: Jul 16, 2026

Inducing Long-Term Plasticity of Intrinsic Neuronal Excitability in Neurons of the Dorsal Lateral Geniculate Nucleus
Published on: September 20, 2024
Growth factors and plasticity.
Stéphane V Sizonenko1, Nathalie Bednarek, Pierre Gressens
1Service du Développement et de la Croissance, Département de Pédiatrie, Faculté de Médecine, Geneva, Switzerland.
Neuroprotective agents can prevent brain lesion progression and promote repair in developing brains. Promising preclinical data suggest melatonin and erythropoietin may advance to clinical trials for treating perinatal brain damage.
Area of Science:
- Neuroscience
- Developmental Biology
- Pharmacology
Background:
- Brain lesions in developing individuals present challenges for both prevention and treatment.
- While early intervention is ideal, targeting delayed cell death and enhancing post-lesion plasticity are key therapeutic goals.
Purpose of the Study:
- To review neurotrophic agents and their potential for treating perinatal brain damage.
- To evaluate the efficacy of trophic factors in limiting delayed cell death and promoting neural repair.
Main Methods:
- Review of preclinical studies on trophic factors in animal models of perinatal brain injury.
- Analysis of agents like melatonin and brain-derived neurotrophic factor for their effects on cell death and plasticity.
Main Results:
- Several trophic factors demonstrate potential in limiting delayed cell death in animal models.
- Melatonin and brain-derived neurotrophic factor show promise in enhancing post-lesion plasticity after neonatal excitotoxic white-matter damage.
Conclusions:
- Trophic factors offer a promising avenue for neuroprotection and repair in developing brains.
- Further preclinical research is necessary, but melatonin and erythropoietin are potential candidates for clinical trials.
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