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首页> 外文期刊>Archives of Toxicology >Intermittent convection-enhanced delivery of GDNF into rhesus monkey putamen: absence of local or cerebellar toxicity
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Intermittent convection-enhanced delivery of GDNF into rhesus monkey putamen: absence of local or cerebellar toxicity

机译:间歇对流 - 增强GDNF进入恒河猴腐败:没有局部或小脑毒性

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Glial cell line-derived neurotrophic factor (GDNF) has demonstrated neurorestorative and neuroprotective effects in rodent and nonhuman primate models of Parkinson's disease. However, continuous intraputamenal infusion of GDNF (100 A mu g/day) resulted in multifocal cerebellar Purkinje cell loss in a 6-month toxicity study in rhesus monkeys. It was hypothesized that continuous leakage of GDNF into the cerebrospinal fluid compartment during the infusions led to down-regulation of GDNF receptors on Purkinje cells, and that subsequent acute withdrawal of GDNF then mediated the observed cerebellar lesions. Here we present the results of a 9-month toxicity study in which rhesus monkeys received intermittent intraputamenal infusions via convection-enhanced delivery. Animals were treated with GDNF (87.1 A mu g; N = 14) or vehicle (N = 6) once every 4 weeks for a total of 40 weeks (11 treatments). Four of the GDNF-treated animals were utilized in a satellite study assessing the impact of concomitant catheter repositioning prior to treatment. In the main study, eight animals (5 GDNF, 3 control) were euthanized at the end of the treatment period, along with the four satellite study animals, while the remaining eight animals (5 GDNF, 3 control) were euthanized at the end of a 12-week recovery period. There were no GDNF-related adverse effects and in particular, no GDNF-related microscopic findings in the brain, spinal cord, dorsal root ganglia, or trigeminal ganglia. Therefore, 87.1 A mu g/4 weeks is considered the no observed adverse effect level for GDNF in rhesus monkeys receiving intermittent, convection-enhanced delivery of GDNF for 9 months.
机译:神经胶质细胞系衍生的神经营养因子(GDNF)已经证明了帕金森病的啮齿动物和非人类动物的神经口腔和神经保护作用。然而,连续的血小板输注GDNF(100 a mu g /日)导致恒河猴毒性研究中的6个月毒性研究中的多焦点小脑缺血细胞损失。假设在输注期间GDNF在脑脊液池中的连续泄漏导致留下细胞上的GDNF受体的下调,随后GDNF的急性戒断,然后介导观察到的小脑病变。在这里,我们介绍了9个月的毒性研究结果,其中恒河猴通过对流增强的交付接受了间歇性的血上的输注。每4周用GDNF(87.1 a mu g; n = 14)或载体(n = 6)处理动物,共为40周(11种处理)。在卫星研究中使用了四种GDNF处理的动物,评估治疗前伴随导管重新定位的影响。在主要研究中,在治疗期结束时,八只动物(5GDNF,3个对照)以及四种卫星研究动物,而剩下的八只动物(5GDNF,3个对照)在结束时被安乐死为期12周的恢复期。没有GDNF相关的不良反应,特别是脑,脊髓,背根神经节或三叉神经节的GDNF相关的显微镜发现。因此,87.1 a mu g / 4周被认为是在接受间歇性,对流增强的GDNF递送9个月的恒河猴中GDNF的未观察到的不良反应水平。

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