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成熟和老年期靶组织及神经生长因子对大鼠交感神经密度的调节

Regulation of rat sympathetic nerve density by target tissues and NGF in maturity and old age.

作者信息

Thrasivoulou C, Cowen T

机构信息

Department of Anatomy and Developmental Biology, Royal Free Hospital School of Medicine, London, UK.

出版信息

Eur J Neurosci. 1995 Mar 1;7(3):381-7. doi: 10.1111/j.1460-9568.1995.tb00333.x.

Abstract

Previous studies in our laboratory using a transplantation model have shown that target tissues of some autonomic neurons, including cerebral blood vessels, exert a controlling influence on nerve fibre loss in old age. The present study was undertaken in order to discover whether the influence of targets extends to controlling age changes in specific populations of nerves. In old rats, we have demonstrated a significant decrease of approximately 50% in the sympathetic innervation of middle cerebral arteries, using tyrosine hydroxylase-like immunoreactivity. Following transplantation, tyrosine hydroxylase-like immunoreactive nerve density on both young and old implanted middle cerebral arteries mirrored the nerve densities seen in normal, non-transplanted vessels. Furthermore, implanted tissue from old donors became reinnervated with a nerve density approximately 50% less than that of young implanted vessels. Treatment of transplants with nerve growth factor, however, was able to reverse these age changes and restore the sympathetic innervation of aged middle cerebral arteries to levels above those seen in young middle cerebral arteries. These results suggest that the pattern and density of sympathetic innervation that the middle cerebral artery receives is determined by the target rather than by the neurons supplying the tissue. The ability of nerve growth factor to induce regrowth in sympathetic neurons innervating ageing target tissues implies that age-related neuronal atrophy may be due to reduced synthesis or availability of target-derived neurotrophic factors.

摘要

我们实验室之前使用移植模型进行的研究表明,包括脑血管在内的一些自主神经元的靶组织,对老年时的神经纤维损失具有控制作用。本研究旨在探究靶组织的影响是否扩展至控制特定神经群体的年龄变化。在老年大鼠中,我们利用酪氨酸羟化酶样免疫反应性,证明大脑中动脉的交感神经支配显著减少了约50%。移植后,年轻和老年植入大脑中动脉上的酪氨酸羟化酶样免疫反应性神经密度反映了正常未移植血管中的神经密度。此外,来自老年供体的植入组织重新获得神经支配,其神经密度比年轻植入血管低约50%。然而,用神经生长因子处理移植组织能够逆转这些年龄变化,并将老年大脑中动脉的交感神经支配恢复到高于年轻大脑中动脉的水平。这些结果表明,大脑中动脉接受的交感神经支配的模式和密度是由靶组织而非供应该组织的神经元决定的。神经生长因子诱导支配衰老靶组织的交感神经元再生的能力意味着,与年龄相关的神经元萎缩可能是由于靶源性神经营养因子的合成减少或可用性降低所致。

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