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Kunihiko Ikeguchi

Researcher at Jichi Medical University

Publications -  29
Citations -  1794

Kunihiko Ikeguchi is an academic researcher from Jichi Medical University. The author has contributed to research in topics: Tyrosine hydroxylase & Adeno-associated virus. The author has an hindex of 17, co-authored 29 publications receiving 1709 citations. Previous affiliations of Kunihiko Ikeguchi include Mitsubishi Tanabe Pharma.

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A phase I study of aromatic L-amino acid decarboxylase gene therapy for Parkinson's disease.

TL;DR: The findings provide class IV evidence regarding the safety and efficacy of AADC gene therapy and warrant further evaluation in a randomized, controlled, phase 2 setting.
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Neuroprotective effects of glial cell line-derived neurotrophic factor mediated by an adeno-associated virus vector in a transgenic animal model of amyotrophic lateral sclerosis.

TL;DR: It is shown here that AAV-GDNF leads to substantial and long-lasting expression of transgenic GDNF in a large number of myofibers with its accumulation at the sites of neuromuscular junctions, indicating that A AV-mediated GDNF delivery to the muscle is a promising means of gene therapy for ALS.
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Triple Transduction with Adeno-Associated Virus Vectors Expressing Tyrosine Hydroxylase, Aromatic-L-Amino-Acid Decarboxylase, and GTP Cyclohydrolase I for Gene Therapy of Parkinson's Disease

TL;DR: Results suggest that GCH, in addition to TH and AADC, is important for effective gene therapy of PD, and triple transduction enhanced BH4 and dopamine production in denervated striatum of parkinsonian rats and improved the rotational behavior of the rats more efficiently than did double transduction.
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Behavioral recovery in a primate model of Parkinson's disease by triple transduction of striatal cells with adeno-associated viral vectors expressing dopamine-synthesizing enzymes

TL;DR: The results show that AAV vectors efficiently introduce DA-synthesizing enzyme genes into the striatum of primates with restoration of motor functions and this triple transduction method may offer a potential therapeutic strategy for PD.
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Delayed delivery of AAV-GDNF prevents nigral neurodegeneration and promotes functional recovery in a rat model of Parkinson's disease

TL;DR: Significant behavioral recovery was observed from 4–20 weeks following AAV-GDNFflag injection, indicating that a delayed delivery of GDNF gene using AAV vector is efficacious even 4 weeks after the onset of progressive degeneration in a rat model of PD.