Hwang B H, Williams T H
Exp Neurol. 1985 May;88(2):336-48. doi: 10.1016/0014-4886(85)90196-7.
Regeneration in the central nervous system has been claimed to be very limited and abortive, although functional regeneration of some of its pathways after destruction has been observed. The exact mechanisms by which axons regenerate fully or fail to have functional regeneration remain to be studied further. We explored whether or not there is a regional difference in regeneration of central catecholaminergic (CA) neurons in the hypothalamus of young adult rats after 6-hydroxydopamine (6-OH-DA) treatment. Four days after treatment, the numbers of CA terminals and axons were significantly reduced in the paraventricular hypothalamic nucleus, periventricular hypothalamic nucleus, supraoptic commissure (SOC), and dorsomedial hypothalamic nucleus as assessed by a morphometric quantitation on fluorescence microscopy micrographs; CA axons were gradually increased in numbers after the treatment. The number of CA varicosities in the supraoptic commissure was restored to 96% of control 180 days after the 6-OH-DA lesion, whereas the actual numbers of CA varicosities in the paraventricular, periventricular, and dorsomedial hypothalamic nuclei were attained at 79, 79, and 68% of control values, respectively. Our results indicate that CA fibers in the supraoptic commissure possess more regenerative potential than the three other hypothalamic regions studied, suggesting a regional difference in CA nerve sprouting during neuroplasticity within the hypothalamus. The favorable regeneration of CA axons in the supraoptic commissure implies to us that some trophic features along that pathway, particularly near the third ventricle, may have been stimulated after chemical lesion using 6-OH-DA, and gradually released in the distal field of the supraoptic commissure to attract CA stumps to sprout. These factors may thus induce both regenerative sprouting and collateral sprouting resulting in vigorous regrowth of CA fibers in the supraoptic commissure.
尽管在中枢神经系统的某些通路遭到破坏后已观察到功能再生,但一般认为中枢神经系统中的再生非常有限且不完全。轴突完全再生或未能实现功能再生的确切机制仍有待进一步研究。我们探究了在给予成年幼鼠6-羟基多巴胺(6-OH-DA)处理后,下丘脑中枢儿茶酚胺能(CA)神经元的再生是否存在区域差异。处理后四天,通过荧光显微镜图像的形态计量学定量评估发现,室旁下丘脑核、室周下丘脑核、视上连合(SOC)和背内侧下丘脑核中的CA终末和轴突数量显著减少;处理后CA轴突数量逐渐增加。6-OH-DA损伤后180天,视上连合中CA曲张体的数量恢复到对照值的96%,而室旁、室周和背内侧下丘脑核中CA曲张体的实际数量分别达到对照值的79%、79%和68%。我们的结果表明,视上连合中的CA纤维比所研究的其他三个下丘脑区域具有更大的再生潜力,提示下丘脑内神经可塑性过程中CA神经发芽存在区域差异。视上连合中CA轴突的良好再生向我们表明,在使用6-OH-DA进行化学损伤后,该通路沿线,特别是靠近第三脑室的一些营养特性可能受到刺激,并在视上连合的远端区域逐渐释放,以吸引CA残端发芽。因此,这些因素可能诱导再生发芽和侧支发芽,从而导致视上连合中CA纤维的旺盛再生。