Soy phytoestrogens are neuroprotective against stroke-like injury in vitro
Document Type
Article
Publication Date
2009
Abstract
Diets high in soy are neuroprotective in experimental stroke. This protective effect is hypothesized to be mediated by phytoestrogens contained in soy, because some of these compounds have neuroprotective effects in in vitro models of cell death. We tested the ability of the soy phytoestrogens genistein, daidzein, and the daidzein metabolite equol to protect embryonic rat primary cortical neurons from ischemic-like injury in vitro at doses typical of circulating concentrations in human populations (0.1-1 µM). All three phytoestrogens inhibited lactate dehydrogenase (LDH) release from cells exposed to glutamate toxicity or the calcium-ATPase inhibitor, thapsigargin. In cells exposed to hypoxia or oxygen-glucose deprivation (OGD), pretreatment with the phytoestrogens inhibited cell death in an estrogen receptor (ER) dependent manner. Although OGD results in multiple modes of cell death, examination of a-spectrin cleavage and caspase-3 activation revealed that the phytoestrogens were able to inhibit apoptotic cell death in this model. In addition, blockade of phosphoinositide 3-kinase prevented the protective effects of genistein and daidzein, and blockade of mitogen-activated protein kinase prevented genistein-dependent neuroprotection. These results suggest that pretreatment with dietary levels of soy phytoestrogens can mimic neuroprotective effects observed with estrogen and appear to use the same ER-kinase pathways to inhibit apoptotic cell death. © 2009 IBRO.
Publication Title
Neuroscience
Volume
158
Issue
2
First Page
602
Last Page
609
Recommended Citation
Schreifhofer, D. A, and Hardy, Lori Redmond, "Soy phytoestrogens are neuroprotective against stroke-like injury in vitro" (2009). PCOM Scholarly Works. 666.
https://digitalcommons.pcom.edu/scholarly_papers/666
Comments
This article was published in Neuroscience, Volume 158, Issue 2, Pages 602-609.
The published version is available at http://dx.doi.org/10.1016/j.neuroscience.2008.10.003.Copyright © 2009 Elsevier.