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眼内环磷酸腺苷(cAMP)水平升高可增强睫状神经营养因子诱导的成年大鼠视网膜神经节细胞轴突再生。

Intraocular elevation of cyclic AMP potentiates ciliary neurotrophic factor-induced regeneration of adult rat retinal ganglion cell axons.

作者信息

Cui Qi, Yip Henry K, Zhao Robert C H, So Kwok-Fai, Harvey Alan R

机构信息

School of Anatomy and Human Biology, Western Australian Institute for Medical Research, The University of Western Australia, 35 Stirling Highway, Crawley, WA 6009, Australia.

出版信息

Mol Cell Neurosci. 2003 Jan;22(1):49-61. doi: 10.1016/s1044-7431(02)00037-4.

Abstract

In vitro, cyclic AMP (cAMP) elevation alters neuronal responsiveness to diffusible growth factors and myelin-associated inhibitory molecules. Here we used an established in vivo model of adult central nervous system injury to investigate the effects of elevated cAMP on neuronal survival and axonal regeneration. We studied the effects of intraocular injections of neurotrophic factors and/or a cAMP analogue (CPT-cAMP) on the regeneration of axotomized rat retinal ganglion cell (RGC) axons into peripheral nerve autografts. Elevation of cAMP alone did not significantly increase RGC survival or the number of regenerating RGCs. Ciliary neurotrophic factor increased RGC viability and axonal regrowth, the latter effect substantially enhanced by coapplication with CPT-cAMP. Under these conditions over 60% of surviving RGCs regenerated their axons. Neurotrophin-4/5 injections also increased RGC viability, but there was reduced long-distance axonal regrowth into grafts, an effect partially ameliorated by cAMP elevation. Thus, cAMP can act cooperatively with appropriate neurotrophic factors to promote axonal regeneration in the injured adult mammalian central nervous system.

摘要

在体外,环磷酸腺苷(cAMP)水平升高会改变神经元对可扩散生长因子和髓磷脂相关抑制分子的反应性。在此,我们使用已建立的成年中枢神经系统损伤体内模型,来研究cAMP水平升高对神经元存活和轴突再生的影响。我们研究了眼内注射神经营养因子和/或一种cAMP类似物(CPT-cAMP)对切断轴突的大鼠视网膜神经节细胞(RGC)轴突向周围神经自体移植体再生的影响。单独提高cAMP水平并不会显著增加RGC的存活数量或再生RGC的数量。睫状神经营养因子可提高RGC的活力和轴突再生能力,与CPT-cAMP共同应用时,后一种作用会显著增强。在这些条件下,超过60%存活的RGC会使其轴突再生。注射神经营养因子-4/5也可提高RGC的活力,但进入移植体的长距离轴突再生减少,cAMP水平升高可部分改善这一效应。因此,cAMP可与适当的神经营养因子协同作用,促进成年哺乳动物受损中枢神经系统中的轴突再生。

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