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老年胶质细胞源性神经营养因子杂合小鼠的去甲肾上腺素能系统

The Noradrenergic System of Aged GDNF Heterozygous Mice.

作者信息

Zaman V, Li Z, Middaugh L, Ramamoorthy S, Rohrer B, Nelson M E, Tomac A C, Hoffer B J, Gerhardt G A, Granholm A Ch

机构信息

Department of Physiology and Neuroscience and the Center on Aging, Medical University of South Carolina, Charleston, SC 29425.

Department of Neurology, Medical University of South Carolina, Charleston, SC 29425.

出版信息

Cell Transplant. 2003 Apr;12(3):291-303. doi: 10.3727/000000003108746740.

Abstract

Glial cell line-derived neurotrophic factor (GDNF) is a trophic factor for noradrenergic (NE) neurons of the pontine nucleus locus coeruleus (LC). Decreased function of the LC-NE neurons has been found during normal aging and in neurodegenerative disorders. We have previously shown that GDNF participates in the differentiation of LC-NE neurons during development. However, the continued role of GDNF for LC-NE neurons during maturation and aging has not been addressed. We examined alterations in aged mice that were heterozygous for the GDNF gene (Gdnf+/-). Wild-type (Gdnf+/+) and Gdnf+/- mice (18 months old) were tested for locomotor activity and brain tissues were collected for measuring norepinephrine levels and uptake, as well as for morphological analysis. Spontaneous locomotion was reduced in Gdnf+/- mice in comparison with Gdnf+/+ mice. The reduced locomotor activity of Gdnf +/- mice was accompanied by reductions in NE transporter activity in the cerebellum and brain stem as well as decreased norepinephrine tissue levels in the LC. Tyrosine hydroxylase (TH) immunostaining demonstrated morphological alterations of LC-NE cell bodies and abnormal TH-positive fibers in the hippocampus, cerebellum, and frontal cortex of Gdnf+/- mice. These findings suggest that the LC-NE system of Gdnf+/- mice is impaired and suggest that GDNF plays an important role in continued maintenance of this neuronal system throughout life.

摘要

胶质细胞系源性神经营养因子(GDNF)是脑桥核蓝斑(LC)中去甲肾上腺素能(NE)神经元的一种营养因子。在正常衰老过程和神经退行性疾病中,已发现LC-NE神经元的功能下降。我们之前已经表明,GDNF在发育过程中参与LC-NE神经元的分化。然而,GDNF在成熟和衰老过程中对LC-NE神经元的持续作用尚未得到探讨。我们检测了GDNF基因杂合(Gdnf+/-)的老年小鼠的变化。对野生型(Gdnf+/+)和Gdnf+/-小鼠(18个月大)进行运动活性测试,并收集脑组织以测量去甲肾上腺素水平和摄取情况,以及进行形态学分析。与Gdnf+/+小鼠相比,Gdnf+/-小鼠的自发运动减少。Gdnf+/-小鼠运动活性降低伴随着小脑和脑干中NE转运体活性降低以及LC中去甲肾上腺素组织水平降低。酪氨酸羟化酶(TH)免疫染色显示Gdnf+/-小鼠的LC-NE细胞体形态改变以及海马、小脑和额叶皮质中异常的TH阳性纤维。这些发现表明Gdnf+/-小鼠的LC-NE系统受损,并表明GDNF在整个生命过程中对该神经元系统的持续维持起着重要作用。

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