PKU is a reversible neurodegenerative process within the nigrostriatum that begins as early as 4 weeks of age in Pah enu2 mice

• Published in: Brain research Vol. 1127; pp. 136 - 150
• Main Authors: Embury, Jennifer E., Charron, Catherine E., Martynyuk, Anatoly, Zori, Andreas G., Liu, Bin, Ali, Syed F., Rowland, Neil E., Laipis, Philip J.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 2007
• Subjects: Adeno-associated virus; Gene therapy; Monoamines; Oxidative stress; Phenylketonuria; RS; Oxidative stress; VTA; SNPc; PHE; Monoamines; rAAV-mPAH-WPRE; STR; SN; H 20 2; Phenylketonuria; Adeno-associated virus; DAB; DOPAC; BDNF; INOS; TYR; GFAP; HVA; PD; TH; CX; 5-HIAA; AAV; PAH; HPA; MPTP; PKU; 5-HT; Gene therapy; DA
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/j.brainres.2006.09.101

Phenylketonuria (PKU) is a common genetic disorder in humans that arises from deficient activity of phenylalanine hydroxylase (PAH), which catalyzes the conversion of phenylalanine to tyrosine. There is a resultant hyperphenylalanemia with subsequent impairment in cognitive abilities, executive functions and motor coordination. The neuropathogenesis of the disease has not been completely elucidated, however, oxidative stress is considered to be a key feature of the disease process. Hyperphenylalanemia also adversely affects monoaminergic metabolism in the brain. For this reason we chose to evaluate the nigrostriatum of Pah enu2 mice, to determine if alterations of monoamine metabolism resulted in morphologic nigrostriatal pathology. Furthermore, we believe that recent developments in adeno-associated virus (AAV)-based vectors have greatly increased the potential for long-term gene therapy and may be a viable alternative to dietary treatment for this metabolic disorder. In this study we identified neurodegenerative changes with regenerative responses in the nigrostriatum of Pah enu2 mice that are consistent with oxidative injury and occurred as early as 4 weeks of age. These neuropathologic changes were reversed following portal vein delivery of a recombinant adeno-associated virus-mouse phenylalanine hydroxylase-woodchuck hepatitis virus post-transcriptional response element (rAAV-mPAH-WPRE) vector to Pah enu2 mice and corresponded to rapid reduction of serum Phe levels.