Premium
Neuroprotective and anti‐inflammatory effects of morin in a murine model of Parkinson's disease
Author(s) -
Lee Kyung Moon,
Lee Yujeong,
Chun Hye Jeong,
Kim Ah Hyun,
Kim Ju Yeon,
Lee Joo Yeon,
Ishigami Akihito,
Lee Jaewon
Publication year - 2016
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.23764
Subject(s) - morin , neuroprotection , dopaminergic , substantia nigra , mptp , oxidative stress , parkinson's disease , striatum , reactive oxygen species , pharmacology , chemistry , inflammation , dopamine , neuroscience , biology , medicine , biochemistry , immunology , disease , pathology
Parkinson's disease (PD) is one of the most common neurodegenerative disorders and is characterized by loss of dopaminergic neurons in the substantia nigra (SN). Although the causes of PD are not understood, evidence suggests that oxidative stress, mitochondrial dysfunction, and inflammation are associated with its pathogenesis. Morin (3,5,7,2′,4′‐pentahydroxyflavone) is a flavonol found in wine and many herbs and fruits. Previous studies have suggested that morin prevents oxidative damage and inflammation and ameliorates mitochondrial dysfunction. The present study describes the neuroprotective effects of morin in a 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP)‐induced mouse model of PD, and we report the results of our investigation into its neuroprotective mechanism in primary neurons and astrocytes. In the mouse model, morin pretreatment ameliorated motor dysfunction, protected against dopaminergic neuronal losses in SN and striatum, and alleviated MPTP‐induced astrocyte activation. In vitro studies revealed that morin protected primary cultured neurons against 1‐methyl‐4‐phenylpyridine (MPP + )‐mediated reactive oxygen species production and mitochondrial membrane potential (MMP) disruption. In addition, morin effectively reduced MPP + ‐induced astroglial activation and nuclear translocation of nuclear factor‐κB in primary cultured astrocytes. These results indicate that morin acts via multiple neuroprotective mechanisms in our mouse model and suggest that morin be viewed as a potential treatment and preventative for PD. © 2016 Wiley Periodicals, Inc.