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Early Movement Restriction Affects FNDC5/Irisin and BDNF Levels in Rat Muscle and Brain
Orlane Dupuis1, Julien Girardie1, Mélanie Van Gaever1
1Univ. Lille, Univ. Artois, Univ. Littoral Côte d'Opale, ULR 7369, URePSSS-Unité de Recherche Pluridisciplinaire Sport Santé Société, F-59000 Lille, France.
Sensorimotor restriction in rats alters muscle-brain communication by affecting irisin (a muscle-secreted protein) levels in muscles and brain regions. This impacts early-life development and motor function.
Area of Science:
- Neuroscience
- Developmental Biology
- Muscle Physiology
Background:
- Environmental interaction is crucial for sensorimotor and cognitive development.
- Sensorimotor restriction (SMR) in early life impairs motor behavior and brain organization in rats.
- The muscle-brain dialogue, particularly involving myokines like irisin, is not well understood in the context of SMR.
Purpose of the Study:
- To investigate the impact of SMR on the muscle-brain communication axis.
- To examine the expression of FNDC5/irisin in muscles and brain structures during SMR.
- To assess the relationship between irisin and Brain-Derived Neurotrophic Factor (BDNF) levels under SMR conditions.
Main Methods:
- Rats were subjected to sensorimotor restriction from postnatal day 1 (P1) to P28.
- FNDC5/irisin expression was measured in hindlimb muscles and brain regions using Western blotting.
- Irisin levels in blood and cerebrospinal fluid were quantified via ELISA.
- BDNF levels were assessed in brain structures.
Main Results:
- SMR led to increased FNDC5/irisin levels in the soleus muscle starting at P21.
- Altered FNDC5/irisin expression was observed in several brain structures as early as P15.
- BDNF levels showed an increase in the hippocampus at P8, with limited overall effects.
Conclusions:
- Sensorimotor restriction significantly impacts FNDC5/irisin levels in a specific postural muscle and various brain regions.
- SMR has a notable effect on the muscle-brain dialogue involving irisin.
- The study indicates limited effects of SMR on BDNF expression within the brain.
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