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胶质细胞源性神经营养因子的点源浓度可能解释了II期临床试验的失败。

Point source concentration of GDNF may explain failure of phase II clinical trial.

作者信息

Salvatore Michael F, Ai Yi, Fischer Brent, Zhang Amanda M, Grondin Richard C, Zhang Zhiming, Gerhardt Greg A, Gash Don M

机构信息

Department of Anatomy and Neurobiology and The Morris K. Udall Parkinson's Disease Research Center of Excellence, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Exp Neurol. 2006 Dec;202(2):497-505. doi: 10.1016/j.expneurol.2006.07.015. Epub 2006 Sep 7.

Abstract

Significant differences have been reported in results from three clinical trials evaluating intraputamenal infusion of glial cell line-derived neurotrophic factor (GDNF) for the treatment of Parkinson's disease. To determine if problems in drug bioavailability could have contributed to the discrepancies between studies, we have analyzed the distribution of intraputamenally infused GDNF in the rhesus monkey brain using the delivery system and infusion protocol followed in a phase 2 clinical trial that failed to achieve its primary endpoint. I125-GDNF was unilaterally infused into the putamen of three adult rhesus monkeys for 7 days. Three age- and sex-matched animals received vehicle infusions following identical procedures. GDNF levels in the brain, peripheral organs, blood and CSF were quantified and mapped by GDNF immunocytochemistry, GDNF ELISAs and I125 measurements. Infused GDNF was found to be unevenly concentrated around the catheter, with tissue levels dropping exponentially with increasing distance from the point source of the single opening in the catheter tip. The volume of distribution of GDNF around the catheter, as determined by immunocytochemistry, varied over four-fold between animals ranging from 87 to 369 mm3. The concentration of GDNF around the catheter tip and limited diffusion into surrounding brain parenchyma support the hypothesis that drug bioavailability was limited to a small portion (2-9%) of the human putamen in the clinical trial using this catheter and infusion protocol.

摘要

在三项评估向壳核内输注胶质细胞源性神经营养因子(GDNF)治疗帕金森病的临床试验中,已报告了显著不同的结果。为确定药物生物利用度方面的问题是否可能导致了研究之间的差异,我们使用了在一项未能达到其主要终点的2期临床试验中所采用的给药系统和输注方案,分析了向恒河猴脑内壳核输注的GDNF的分布情况。将I125-GDNF单侧注入三只成年恒河猴的壳核中,持续7天。三只年龄和性别匹配的动物按照相同程序接受载体输注。通过GDNF免疫细胞化学、GDNF酶联免疫吸附测定和I125测量对脑、外周器官、血液和脑脊液中的GDNF水平进行定量和定位。发现注入的GDNF在导管周围分布不均,组织水平随着距导管尖端单个开口的点源距离增加而呈指数下降。通过免疫细胞化学确定,导管周围GDNF的分布体积在不同动物之间变化超过四倍,范围从87到369立方毫米。导管尖端周围GDNF的浓度以及向周围脑实质的有限扩散支持了这样的假设,即在使用该导管和输注方案的临床试验中,药物生物利用度仅限于人类壳核的一小部分(2 - 9%)。

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