A novel systemically active caspase inhibitor attenuates the toxicities of MPTP, malonate, and 3NP in vivo

Yang, L; Sugama, S; Mischak, RP; Kiaei, M; Bizat, N; Brouillet, E; Joh, TH; Beal, MF

HERO ID

4933492

Reference Type

Journal Article

Year

2004

Language

English

PMID

15474362

HERO ID 4933492
In Press No
Year 2004
Title A novel systemically active caspase inhibitor attenuates the toxicities of MPTP, malonate, and 3NP in vivo
Authors Yang, L; Sugama, S; Mischak, RP; Kiaei, M; Bizat, N; Brouillet, E; Joh, TH; Beal, MF
Journal Neurobiology of Disease
Volume 17
Issue 2 (November 2004)
Page Numbers 250-259
Abstract Molecular machinery involved in apoptosis plays a role in neuronal death in neurodegenerative disorders such as Parkinson's disease (PD) and Huntington's disease (HD). Several caspase inhibitors, such as the well-known peptidyl inhibitor carbobenzoxy-Val-Ala-Asp-fluoromethylketone (zVADfmk), can protect neurons from apoptotic death caused by mitochondrial toxins. However, the poor penetrability of zVADfmk into brain and toxicity limits its use therapeutically. In the present study, a novel peptidyl broad-spectrum caspase inhibitor, Q-VD-OPH, which offers improvements in potency, stability, and toxicity over zVADfmk, showed significant protection against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), 3-nitropropionic acid (3NP), and malonate toxicities. Q-VD-OPH significantly reduced dopamine depletion in striatum produced by MPTP administration and prevented MPTP-induced loss of dopaminergic neurons in the substantia nigra. It significantly reduced the size of striatal lesions produced by intrastriatal malonate injections and systemic administration of 3NP. Western blots performed on tissues from the midbrain following administration of MPTP or the striatum in 3NP-treated animals showed increases of the active forms of caspase-9 and caspase-8, as well as the caspase-8-mediated proapoptotic protein Bid, which were inhibited Q-VD-OPH treatment. These findings suggest that systematically active broad-spectrum caspase inhibitors maybe useful in the treatment of neurodegenerative diseases such as PD and HD.
Doi 10.1016/j.nbd.2004.07.021
Pmid 15474362
Wosid 000224757500013
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Index Medicus
Is Peer Review Yes
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