Lapchak P A, Jiao S, Collins F, Miller P J
AMGEN Inc., Department of Neuroscience, Thousand Oaks, CA 91320, USA.
Brain Res. 1997 Jan 30;747(1):92-102. doi: 10.1016/s0006-8993(96)01265-6.
Glial cell line-derived neurotrophic factor (GDNF) has been shown to increase dopaminergic parameters in vitro and in vivo and can reduce parkinsonian behaviors in animal models of the disease. This study determined the potential of the lateral ventricle as an administration route for GDNF by examining the distribution and neurochemical consequences of a single intraventricular injection. Autoradiographic analysis showed that intraventricularly administered [125I]GDNF was distributed throughout the ventricular system at 1 and 24 h following injection. The cerebral cortex, septum, diagonal band, fimbria, striatum, hippocampus, hypothalamus, substantia nigra/ventral tegmental area, and cerebellum were also labeled. At 7 days, there was still labeling throughout the ventricular system, hypothalamus, substantia nigra, and cerebellum. Twenty-four hours following an intrastriatal injection of [125I]GDNF, label was observed in the substantia nigra/ventral tegmental area, demonstrating retrograde transport. The neurochemical effects of intraventricularly administered GDNF (0.1-100 micrograms) at 7 days post injection were also examined. GDNF significantly increased striatal (approximately 28%) and nigral (up to 40%) dopamine, as well as regulated the dopamine metabolites homovanillic acid and dihydroxyphenylacetic acid. Dopamine levels were unchanged in the frontal cortex. Dopamine content was significantly increased in the hypothalamus (up to 35%), an increase which may contribute to the inhibition of weight gain seen after administration of GDNF. Additionally, dopamine turnover was decreased or unchanged across the brain regions analyzed, which may indicate that in unlesioned rats, intraventricularly administered GDNF stimulates the synthesis and storage of dopamine. This study shows that intraventricularly injected GDNF can access basal ganglia structures, most notably the midbrain dopamine cell body region, and remains present in this area for at least 7 days following a single administration. GDNF differentially increases dopaminergic tone within a variety of brain structures, including the nigrostriatal pathway. These data support the potential effectiveness of intraventricular administered GDNF as a treatment for Parkinson's disease.
胶质细胞系源性神经营养因子(GDNF)已被证明在体外和体内均可增加多巴胺能参数,并可减轻帕金森病动物模型中的帕金森行为。本研究通过检查单次脑室内注射后的分布和神经化学后果,确定了侧脑室作为GDNF给药途径的潜力。放射自显影分析表明,脑室内注射的[125I]GDNF在注射后1小时和24小时分布于整个脑室系统。大脑皮层、隔区、斜角带、穹窿、纹状体、海马、下丘脑、黑质/腹侧被盖区和小脑也有标记。在7天时,整个脑室系统、下丘脑、黑质和小脑仍有标记。纹状体内注射[125I]GDNF 24小时后,在黑质/腹侧被盖区观察到标记,表明有逆行运输。还检查了注射后7天脑室内给予GDNF(0.1 - 100微克)的神经化学效应。GDNF显著增加纹状体(约28%)和黑质(高达40%)的多巴胺水平,并调节多巴胺代谢产物高香草酸和二羟基苯乙酸。额叶皮层的多巴胺水平未改变。下丘脑的多巴胺含量显著增加(高达35%),这一增加可能有助于解释给予GDNF后体重增加受到抑制的现象。此外,在所分析的脑区中,多巴胺周转率降低或未改变,这可能表明在未损伤的大鼠中,脑室内给予GDNF可刺激多巴胺的合成和储存。本研究表明,脑室内注射的GDNF可进入基底神经节结构,最显著的是中脑多巴胺细胞体区域,并且在单次给药后至少7天仍存在于该区域。GDNF在包括黑质纹状体通路在内的多种脑结构中差异性地增加多巴胺能张力。这些数据支持脑室内给予GDNF作为帕金森病治疗方法的潜在有效性。