2020
DOI: 10.1007/s11356-020-09516-3
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Protective effects of thymoquinone against acrylamide-induced liver, kidney and brain oxidative damage in rats

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Cited by 70 publications
(30 citation statements)
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“…The first investigational evidence was provided in 2010, when a β-secretase inhibitor, GRL-8234, was employed to treat Tg2576 transgenic mice, and resulted in improved cognitive effects [ 54 ]. Moreover, soluble Aβ levels were also found to be retarded in mice [ 55 , 56 ] following GRL-8234 administration [ 54 ]. A significant reduction in Aβ plaque load was also observed in aged mice treated with GRL-8234 [ 57 ].…”
Section: Therapeutic Agents Targeting Amyloid Cascade Eventsmentioning
confidence: 99%
“…The first investigational evidence was provided in 2010, when a β-secretase inhibitor, GRL-8234, was employed to treat Tg2576 transgenic mice, and resulted in improved cognitive effects [ 54 ]. Moreover, soluble Aβ levels were also found to be retarded in mice [ 55 , 56 ] following GRL-8234 administration [ 54 ]. A significant reduction in Aβ plaque load was also observed in aged mice treated with GRL-8234 [ 57 ].…”
Section: Therapeutic Agents Targeting Amyloid Cascade Eventsmentioning
confidence: 99%
“…Plant products have potent protective effects against toxic insults [ [20] , [21] , [22] ]. However, several researchers have shown that many medicinal plants have potential toxicity on cellular and biochemical parameters of blood [ 23 , 24 ] and histopathology of various internal organs like the liver and kidney [ [25] , [26] , [27] , [28] , [29] ].…”
Section: Introductionmentioning
confidence: 99%
“…4 Recent studies showed that acrylamide caused oxidative brain damage by increasing Malondialdehyde (MDA) production in the brain tissue and reducing endogenous glutathione (GSH) concentrations as well as activities of antioxidant enzymes. [5][6][7][8] Moreover, it has been demonstrated that acrylamide produced neurotoxic effects by increasing the production of both oxidants and proinflammatory cytokines such as interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α). [6][7][8][9] These literature data suggest that antioxidant and anti-inflammatory drugs can be useful in the treatment of the neurotoxicity of acrylamide.…”
Section: Introductionmentioning
confidence: 99%