Accepted Preprint first posted online on 1 July 2009
Journal of Endocrinology 2009;202:431.
Journal of Endocrinology (2009) In press
DOI: 10.1677/JOE-09-0132
© 2009 Society for Endocrinology
Exendin-4 protects dopaminergic neurons by inhibition of microglial activation and matrix metalloproteinase-3 expression in an animal model of Parkinsons disease
Sehee Kim,
Minho Moon and
Seungjoon Park
S Kim, Pharmacology, Kyunghee University School of Medicine,, Seoul, Korea, Republic of
M Moon, Pharmacology, Kyunghee University School of Medicine,, Seoul, Korea, Republic of
S Park, Pharmacology, Kyunghee University School of Medicine, Seoul, 130-701, Korea, Republic of
Correspondence: Seungjoon Park, Email: sjpark{at}khu.ac.kr
Exendin-4 is a naturally occurring more potent and stable analogue of glucagon-like peptide-1 (GLP-1) that selectively binds at the GLP-1 receptor. It has been recently demonstrated that GLP-1 receptor stimulation preserves dopaminergic neurons in cellular and rodent models of Parkinsons disease (PD). 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) causes nigrostriatal dopaminergic neurotoxicity in rodents; previous studies suggest that activated microglia actively participate in the pathogenesis of PD neurodegeneration. However, the role of microglia in the neuroprotective properties of exendin-4 is still unknown. Here we show that, in the mouse MPTP PD model, systemic administration of exendin-4 significantly attenuates the loss of substantia nigra pars compacta (SNpc) neurons and the striatal dopaminergic fibers. Exendin-4 prevents MPTP-induced microglial activation in the SNpc and striatum, and the expression of matrix metalloproteinase-3. In addition exendin-4 also suppressed MPTP-induced expression of pro-inflammatory molecules tumor necrosis factor
and interleukin-1β. Our data indicate that exendin-4 may act as a survival factor for dopaminergic neurons by functioning as a microglia-deactivating factor and suggest that exendin-4 may be a valuable therapeutic agent for neurodegenerative diseases such as PD.
Copyright © 2009 by the Society for Endocrinology.