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Plumbagin, a novel Nrf2/ARE activator, protects against cerebral ischemia
Author(s) -
Son Tae Gen,
Camandola Simonetta,
Arumugam Thiruma V.,
Cutler Roy G.,
Telljohann Richard S.,
Mughal Mohamed R.,
Moore Tyson A.,
Luo Weiming,
Yu QianSheng,
Johnson Delinda A.,
Johnson Jeffrey A.,
Greig Nigel H.,
Mattson Mark P.
Publication year - 2010
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2009.06552.x
Subject(s) - plumbagin , neuroprotection , activator (genetics) , gene knockdown , pharmacology , oxidative stress , biology , small hairpin rna , microbiology and biotechnology , biochemistry , gene , genetics
J. Neurochem. (2010) 112 , 1316–1326. Abstract Many phytochemicals function as noxious agents that protect plants against insects and other damaging organisms. However, at subtoxic doses, the same phytochemicals may activate adaptive cellular stress response pathways that can protect cells against a variety of adverse conditions. We screened a panel of botanical pesticides using cultured human and rodent neuronal cell models, and identified plumbagin as a novel potent activator of the nuclear factor E2‐related factor 2 (Nrf2)/antioxidant response element (ARE) pathway. In vitro , plumbagin increases nuclear localization and transcriptional activity of Nrf2, and induces the expression of the Nrf2/ARE‐dependent genes, such as heme oxygenase 1 in human neuroblastoma cells. Plumbagin specifically activates the Nrf2/ARE pathway in primary mixed cultures from ARE‐human placental alkaline phosphatase reporter mice. Exposure of neuroblastoma cells and primary cortical neurons to plumbagin provides protection against subsequent oxidative and metabolic insults. The neuroprotective effects of plumbagin are abolished by RNA interference‐mediated knockdown of Nrf2 expression. In vivo , administration of plumbagin significantly reduces the amount of brain damage and ameliorates‐associated neurological deficits in a mouse model of focal ischemic stroke. Our findings establish precedence for the identification and characterization of neuroprotective phytochemicals based upon their ability to activate adaptive cellular stress response pathways.