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Neuroprotective diarylheptanoids from the leaves and twigs of juglans sinensis against glutamate-induced toxicity in HT22 cells.

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TLDR
A new diarylheptanoid, juglanin C(1), was isolated from the 80 % methanolic extract of the leaves and twigs of JUGLANS SINENSIS and compounds 1 and 2 significantly showed neuroprotective activities against glutamate-induced toxicity in HT22 cells.
Abstract
A new diarylheptanoid, juglanin C ( 1), was isolated from the 80 % methanolic extract of the leaves and twigs of JUGLANS SINENSIS with three known diarylheptanoids, juglanin A ( 2), juglanin B ( 3), and (5R)-5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1(4-hydroxyphenyl)-3-heptanone ( 4), using bioactivity-guided fractionation and chromatographic techniques. Among the isolated diarylheptanoids, compounds 1 and 2 significantly showed neuroprotective activities against glutamate-induced toxicity in HT22 cells. These two diarylheptanoids significantly reduced the overproduction of cellular peroxide in glutamate-injured HT22 cells. Moreover, these two diarylheptanoids significantly maintained antioxidative defense systems, including glutathione, glutathione reductase, and glutathione peroxidase, under glutamate-induced oxidative stress in HT22 cells.

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Tacrine-silibinin codrug shows neuro- and hepatoprotective effects in vitro and pro-cognitive and hepatoprotective effects in vivo.

TL;DR: The tacrine-silibinin codrug shows high AChE and BChE inhibition, neuroprotective effects, lacks tacrine's hepatotoxicity in vitro and in vivo, and shows the same pro-cognitive effects in vivo as tacrine, being superior to the physical mixture of tacrine and silibInin in all these regards.
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Involvement of heme oxygenase-1 expression in neuroprotection by piceatannol, a natural analog and a metabolite of resveratrol, against glutamate-mediated oxidative injury in HT22 neuronal cells.

TL;DR: Results suggest that piceatannol, similar to resveratrol, is capable of protecting HT22 neuronal cells against glutamate-induced cell death, at least in part, by inducing Nrf2-dependent HO-1 expression.
Journal ArticleDOI

Characterization of diarylheptanoids: An emerging class of bioactive natural products.

TL;DR: Diarylheptanoids are a class of secondary plant metabolites with a wide variety of bioactivity and research on their phytochemistry and phytoanalysis is rapidly growing and the number of identified structures bearing the aryl‐C7‐aryl skeleton is at present approaching 500.
References
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Assays of glutathione peroxidase

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Journal ArticleDOI

Oxidative stress, glutamate, and neurodegenerative disorders

TL;DR: Two broad mechanisms--oxidative stress and excessive activation of glutamate receptors--are converging and represent sequential as well as interacting processes that provide a final common pathway for cell vulnerability in the brain.
Journal ArticleDOI

Purification and characterization of the flavoenzyme glutathione reductase from rat liver.

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