Cholecalciferol (Vitamin D3) Improves Myelination and Recovery after Nerve Injury

被引:121
作者
Chabas, Jean-Francois [1 ,2 ]
Stephan, Delphine [1 ]
Marqueste, Tanguy [3 ]
Garcia, Stephane [4 ,5 ]
Lavaut, Marie-Noelle [4 ,5 ]
Catherine Nguyen [6 ]
Legre, Regis [2 ]
Khrestchatisky, Michel [1 ]
Decherchi, Patrick [3 ]
Feron, Francois [1 ]
机构
[1] Aix Marseille Univ, CNRS, NICN UMR 7259, Marseille, France
[2] Hop Conception, APHM, Serv Chirurg Main, Marseille, France
[3] Aix Marseille Univ, CNRS, ISM UMR 7287, Marseille, France
[4] Aix Marseille Univ, Assistance Publ Hop Marseille, Serv Hosp Anat & Cytol Pathol Humaines, Marseille, France
[5] Aix Marseille Univ, INSERM, U1068, Marseille, France
[6] Aix Marseille Univ, INSERM, TAGC UMR U1090, Marseille, France
关键词
TIBIALIS-ANTERIOR MUSCLE; 1,25-DIHYDROXYVITAMIN D-3; GROWTH-FACTOR; AFFERENT ACTIVITIES; MESSENGER-RNA; D DEFICIENCY; D-RECEPTOR; RAT; BRAIN; PROTEIN;
D O I
10.1371/journal.pone.0065034
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previously, we demonstrated i) that ergocalciferol (vitamin D-2) increases axon diameter and potentiates nerve regeneration in a rat model of transected peripheral nerve and ii) that cholecalciferol (vitamin D-3) improves breathing and hyper-reflexia in a rat model of paraplegia. However, before bringing this molecule to the clinic, it was of prime importance i) to assess which form - ergocalciferol versus cholecalciferol - and which dose were the most efficient and ii) to identify the molecular pathways activated by this pleiotropic molecule. The rat left peroneal nerve was cut out on a length of 10 mm and autografted in an inverted position. Animals were treated with either cholecalciferol or ergocalciferol, at the dose of 100 or 500 IU/kg/day, or excipient (Vehicle), and compared to unlesioned rats (Control). Functional recovery of hindlimb was measured weekly, during 12 weeks, using the peroneal functional index. Ventilatory, motor and sensitive responses of the regenerated axons were recorded and histological analysis was performed. In parallel, to identify the genes regulated by vitamin D in dorsal root ganglia and/or Schwann cells, we performed an in vitro transcriptome study. We observed that cholecalciferol is more efficient than ergocalciferol and, when delivered at a high dose (500 IU/kg/day), cholecalciferol induces a significant locomotor and electrophysiological recovery. We also demonstrated that cholecalciferol increases i) the number of preserved or newly formed axons in the proximal end, ii) the mean axon diameter in the distal end, and iii) neurite myelination in both distal and proximal ends. Finally, we found a modified expression of several genes involved in axogenesis and myelination, after 24 hours of vitamin supplementation. Our study is the first to demonstrate that vitamin D acts on myelination via the activation of several myelin-associated genes. It paves the way for future randomised controlled clinical trials for peripheral nerve or spinal cord repair.
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页数:15
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