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. 2021 Mar 9;12(4):1211–1238. doi: 10.1093/advances/nmab007

TABLE 3.

In vitro neuroprotective role of ellagic acid against various types of stressors1

Stressor Experimental model EA concentration Observations References
Primary murine cortical microglia 10 μM/L Inhibited microglial activation via attenuation of TNF-α, and NFAT activity (105)
SH-SY5Y cells 2 mg/mL Prevented Aβ neurotoxicity by promoting Aβ aggregation into fibrils with significant oligomer loss (130)
0.1–0.4 mM Suppressed proinflammatory and disease aggravation markers (107)
D-gal SH-SY5Y cells 0.01–10μM Increased cell proliferation and GSH concentration, while decreasing concentrations of ROS, MDA, TNF-α, β-GAL, and AGEs (131)
ATRA and TPA SH-SY5Y cells 30–100 μM EA induced cell detachment, decreased cell viability, and induced apoptosis (132)
50 μM EA decreased cell detachment, loss of viability, and activation of apoptosis (133)
Cadmium Rat primary astrocytes 30 μM Decreased ROS production and astrocyte cell death (134)
Rotenone PC12 pheochromocytoma 10 μM Decreased ROS and RNS production, PARP1, HSP70, and α-synuclein aggregation (135)
OGD/R Primary culture of rat cortical neurons 10 and 30μg/mL Decreased the number of apoptotic/necrotic cells, and remedied the decrease in the ratio of Bcl-2/Bax expression (136)
Tumor Human glioblastoma and rat glioma cell line 5.5 mg or 10 mg Chitosan-EA composite films induced the accumulation of the tumor suppressor protein p53 and increased caspase-3 activation, which preceded induction of apoptosis (95)
5.5 mg or 10 mg EA induced apoptosis in cancer cells as well as suppressing angiogenesis in dose-dependent manner (94)
Antidepressant AChE, BuChE, and MAO-A EA exhibited appreciable MAO-A inhibition activity compared with cholinesterase inhibitors (88)

1Aβ, β-amyloid; AChE, acetylcholinesterase; AGE, advanced glycation end-product; ATRA, all-trans retinoic acid; BuChE, butyrylcholinesterase; D-gal, d-galactose; EA, ellagic acid; GSH, reduced glutathione; HSP70, heat shock protein 70; MAO-A, monoamine oxidase A; MDA, malondialdehyde; NFAT, nuclear factor of activated T-cells; OGD/R, oxygen-glucose deprivation and reoxygenation; PARP, poly(ADP-ribose) polymerase; RNS, reactive nitrogen species; ROS, reactive oxygen species; TPA, 12-O-tetradecanoylphorbol-13-acetate; β-GAL, β-galactose.