Quinn S D, De Boni U
Faculty of Medicine, Department of Physiology, University of Toronto, Ontario, Canada.
In Vitro Cell Dev Biol. 1991 Jan;27(1):55-62. doi: 10.1007/BF02630895.
This study demonstrates that retinoic acid (RA), an active metabolite of vitamin A, can act to enhance regeneration of neurites, at physiologic concentrations, in vitro. Explanted fragments of mouse dorsal root ganglia (DRG) and mouse and human spinal cord (SC) were maintained, in vitro, for periods up to 11 d. Murine DRG neurons were exposed to RA concentrations ranging from 100 microM to 1 nM, whereas neurons within murine and human SC explants were exposed to 10 microM to 10 nM RA. Results show that RA significantly (P less than 0.001) increases mean neurite length but not neurite number. Specifically, murine DRG neurons showed increases in mean neurite length of 30.7% with individual explants showing increases of up to 133.5%. Murine and human SC showed mean enhancements of 43.4 and 58.1%, respectively, but did so at lower concentrations of RA. The results indicate that RA may play a potentially critical role in neuronal regeneration.
本研究表明,视黄酸(RA)作为维生素A的一种活性代谢产物,在生理浓度下可在体外促进神经突的再生。将小鼠背根神经节(DRG)以及小鼠和人类脊髓(SC)的外植片段在体外培养长达11天。将小鼠DRG神经元暴露于浓度范围为100微摩尔/升至1纳摩尔/升的RA中,而将小鼠和人类SC外植体中的神经元暴露于10微摩尔/升至10纳摩尔/升的RA中。结果显示,RA显著(P<0.001)增加了平均神经突长度,但未增加神经突数量。具体而言,小鼠DRG神经元的平均神经突长度增加了30.7%,个别外植体的增加幅度高达133.5%。小鼠和人类SC的平均增强幅度分别为43.4%和58.1%,但在较低浓度的RA下即可实现。结果表明,RA可能在神经元再生中发挥潜在的关键作用。