2019
DOI: 10.1007/s11356-019-05862-z
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Soybean isoflavone ameliorates cognitive impairment, neuroinflammation, and amyloid β accumulation in a rat model of Alzheimer’s disease

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Cited by 36 publications
(21 citation statements)
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“…Regarding neurodegenerative diseases isoflavones have shown protective properties. An extract of soybean isoflavone reduced the elevated oxidative stress parameters and reversed the overproduction of Aβ in rats with colchicine-induced neuronal damage [ 334 ]. In the same way, daidzein alone or mixed with genistein and glycitin isoflavones could reverse the cognitive impairments produced by scopolamine injection by activating the cholinergic system and the BDNF/ERK/CREB signaling pathway in mice [ 335 , 336 ], thus reinforcing the idea that soy isoflavones may be a good candidate for the treatment of neurodegenerative diseases.…”
Section: Isoflavonesmentioning
confidence: 99%
“…Regarding neurodegenerative diseases isoflavones have shown protective properties. An extract of soybean isoflavone reduced the elevated oxidative stress parameters and reversed the overproduction of Aβ in rats with colchicine-induced neuronal damage [ 334 ]. In the same way, daidzein alone or mixed with genistein and glycitin isoflavones could reverse the cognitive impairments produced by scopolamine injection by activating the cholinergic system and the BDNF/ERK/CREB signaling pathway in mice [ 335 , 336 ], thus reinforcing the idea that soy isoflavones may be a good candidate for the treatment of neurodegenerative diseases.…”
Section: Isoflavonesmentioning
confidence: 99%
“…Soybean isoflavone (SI) is a bioactive secondary metabolite formed during soybean growth. Studies have shown that SI can protect the cardiovascular system through its antioxidant effects [ 195 197 ]. SI enhanced the activity of SOD, decreased the level of thiobarbituric acid reactant in plasma, and enhanced the antioxidant capacity of plasma, as well as the activity of GSH-PX in erythrocytes [ 198 ].…”
Section: Application Of Antioxidant Natural Drugs For Cardiovasculmentioning
confidence: 99%
“…S2A-B). Except the changes in GSK3β activity and tau pT231 phosphorylation levels, the abnormal deposition of Aβ produced by the sequential cleavage of β-site AβPP-cleaving enzyme (BACE1) and γ-secretase from AβPP is a major pathological feature of AD [32]. Evidence has also suggested that an imbalance in Aβ metabolic enzymes, including BACE1 for Aβ production, insulin-degrading enzyme (IDE) and neprilysin (NEP) for Aβ clearance, causes Aβ deposition [33,34].…”
Section: Ps128 Supplementation Prevented the Increase In Gsk3β Activity And Aβ Production In 3 × Tg-ad Mice Treated With Icv-stzmentioning
confidence: 99%