Ishii D N, Glazner G W, Pu S F
Department of Physiology, Colorado State University, Fort Collins 80523.
Pharmacol Ther. 1994 Apr-May;62(1-2):125-44. doi: 10.1016/0163-7258(94)90007-8.
Prolonged denervation results in atrophy of target organs and increased risk of permanent paralysis. A better understanding of the mechanism responsible for nerve regeneration may one day lead to improved rates of nerve regeneration and diminished risk of loss of function. Neurobiologists have known for decades that soluble neurotrophic activity is present in nerves and nerve targets. Until recently, the soluble molecules that regulate the rate of nerve regeneration have eluded identification. Insulin-like growth factor (IGF) gene expression is correlated with synapse formation during development and regeneration. IGFs are now identified as the first soluble nerve- and muscle-derived neurotrophic factors found to regulate the rate of peripheral nerve regeneration. The roles of IGFs and other neurotrophic factors in peripheral nerve regeneration, motor nerve terminal sprouting and synapse formation are reviewed.
长期去神经支配会导致靶器官萎缩,并增加永久性瘫痪的风险。更好地理解神经再生的机制,也许有一天能提高神经再生率,并降低功能丧失的风险。几十年来,神经生物学家已经知道神经和神经靶标中存在可溶性神经营养活性。直到最近,调节神经再生速度的可溶性分子仍未被鉴定出来。胰岛素样生长因子(IGF)基因表达与发育和再生过程中的突触形成相关。IGF现在被确定为第一种被发现可调节外周神经再生速度的可溶性神经和肌肉源性神经营养因子。本文综述了IGF和其他神经营养因子在外周神经再生、运动神经末梢发芽和突触形成中的作用。