Table 7.
Author and Year | Cell Culture | Intervention Time | Concentration | Condition/Disease | Mechanism in Nrf2 |
---|---|---|---|---|---|
Hao et al. [282] | Cells ARPE-19 | 24 h | 15 μM | Prevent macular degeneration | ↑ antioxidant genes, catalytic subunit glutamate-cysteine ligase (GCLc), SOD and HO-1, ↓ ROS |
Kil et al. [274] | Endothelial cells | ECs were pre-incubated for 6 h with Pic before 12 h exposure to 3 mM Hcy | 10 μM | Prevent endothelial cell apoptosis | Induced HO-1 expression, ↓ ROS |
Achy-Brou et al. [283] | RAW 264.7 macrophages cells | 24 and 48 h | 3, 10, 20 or 30 μM | Cytotoxicity and ability to reduce NO | Are cytotoxic to transformed RAW 264.7 macrophages inhibit ↓ NO expression via Nrf2 |
Zhu et al. [284] | Human keratinocyte cells (HaCaT cell line) | 24 h | 15 μM | Preventing the proliferation of acne vulgaris | ↓ NF-κB, ↑ HO-1 and NQO1 |
Li et al. [280] | H9C2 rat cardiac myoblasts | 48 h | 10 μM | Diabetic cardiomyopathy | ↓ IL-6 and TNF-α, ↑ Nrf2 expression, via Nrf2/HO-1, SOD |
Hosoda et al. [206] | C2C12 myoblasts | 24 h | 10 μM | Antioxidant and antiapoptotic effects | ↓ ROS, ↑ HO-1 |
Wang et al. [285] | Highly differentiated rat adrenal pheochromocytoma cells (PC12 cells) | 24 h | 2.5; 10 and 40 μM | Cerebral ischemia–reperfusion injury | ↓ MDA and LDH, ↑ HO-1 and NQO1 |
↑: increased; ↓: decreased; Ecs: endothelial cells; PIC = piceatannol Nrf2: nuclear factor erythroid 2-related factor; ROS: reactive oxygen species; HO-1: heme oxygenase-1; NF-κB: nuclear factor kappa B; NQO1: quinone oxidoreductase 1; MDA: malondialdehyde; SOD: superoxide dismutase; GCLC: glutamate-cysteine ligase catalytic subunit; TNF-α: tumor necrosis factor-α; IL-6: interleukin-6; iNOS: induced nitric oxide synthase; LDH: lactate dehydrogenase; PMs: primary peritoneal macrophages; LPS: lipopolysaccharide; HaCaT: cell line of aneuploid immortal keratinocytes from adult human skin; NO: nitric oxide.