Six-month continuous intraputamenal infusion toxicity study of recombinant methionyl human glial cell line-derived neurotrophic factor (r-metHuGDNF) in rhesus monkeys

被引:40
作者
Hovland, David N., Jr.
Boyd, Robert B.
Butt, Mark T.
Engelhardt, Jeffery A.
Moxness, Michael S.
Ma, Mark H.
Emery, Maurice G.
Ernst, Nadia B.
Reed, Randall P.
Zeller, Jillynne R.
Gash, Don M.
Masterman, Donna M.
Potter, Beth M.
Cosenza, Mary E.
Lightfoot, Ruth M.
机构
[1] Amgen Inc, Thousand Oaks, CA 91320 USA
[2] No Biomed Res Inc, Muskegon, MI USA
[3] Charles River Labs, Frederick, MD 21701 USA
[4] Univ Kentucky, Lexington, KY 40536 USA
关键词
GDNF; Parkinson's disease; toxicology; toxicity; cerebellum; Purkinje cello; monkey; infusions; putamen; rhesus;
D O I
10.1080/01926230701481899
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Recombinant human glial cell line-derived neurotrophic factor (r-metHuGDNF) is a potent neuronal growth and survival factor that has been considered for clinical use in the treatment of Parkinson's disease (PD). Here we present results of a 6-month toxicology study in rhesus monkeys conducted to support clinical evaluation of chronic intraputamenal infusion of r-metHuGDNF for PD. Monkeys (6-9/sex/group) were treated with 0 (vehicle). 15.30. or 100 mu g/day r-metHuGDNF by continuous unilateral intraputamenal infusion (150 mu l/day flow rate) for 6 months: a subset of animals (2-3/sex/group) underwent a subsequent 3-month treatment-free recovery period. Notable observations included reduced food consumption and body weight at 100 mu g/day and meningeal thickening underlying the medulla oblongata and/or overlying various spinal cord segments at 30 and 100 mu g/day. In addition. multifocal cerebellar Purkinje cell loss (with associated atrophy of the molecular layer and. in some cases, granule cell loss) was observed in 4 monkeys in the 100-mu g/day group. This cerebellar finding has not been observed in previous nonclinical studies evaluating r-metHuGDNF. The small number of affected animals precludes definitive conclusions regarding the pathogenesis of the cerebellar lesion, but the data support an association with r-metHuGDNF treatment.
引用
收藏
页码:676 / 692
页数:17
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