2021
DOI: 10.1016/j.exger.2021.111400
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Shenqi Yizhi Granule attenuates Aβ1–42 induced cognitive dysfunction via inhibiting JAK2/STAT3 activated astrocyte reactivity

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Cited by 6 publications
(3 citation statements)
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“…SQYG treatment exhibited significant neuroprotective effects on the hippocampus of 5XFAD mice through modulating multiple pathological processes, such as synaptic transmission, signal transduction, and amino acid metabolism ( Ren et al, 2020 ). Other relevant mechanisms involve inhibiting response of astrocytes regulated by the JAK2/STAT3 signaling pathway, which has been proven in an Aβ 1-42 -induced rat model of AD ( Li P. et al, 2021 ). Other possible molecular mechanisms of SQYG were investigated through an integration strategy of network pharmacology and molecular docking.…”
Section: Herbal Medicine and Admentioning
confidence: 99%
“…SQYG treatment exhibited significant neuroprotective effects on the hippocampus of 5XFAD mice through modulating multiple pathological processes, such as synaptic transmission, signal transduction, and amino acid metabolism ( Ren et al, 2020 ). Other relevant mechanisms involve inhibiting response of astrocytes regulated by the JAK2/STAT3 signaling pathway, which has been proven in an Aβ 1-42 -induced rat model of AD ( Li P. et al, 2021 ). Other possible molecular mechanisms of SQYG were investigated through an integration strategy of network pharmacology and molecular docking.…”
Section: Herbal Medicine and Admentioning
confidence: 99%
“…Bunge, Scutellaria baicalensis Georgi, Salvia miltiorrhiza Bunge, and Alisma plantago-aquatica L with a ratio of 2 : 4 : 3 : 3 : 2. The main active compounds of SQYG included ginsenoside Rb1, ginsenoside Rg1, ginsenoside Rd, baicalin, cryptotanshinone, and tanshinone IIA [ 10 ]. These active compounds have a wide range of activities, including neuron cells protection, synaptoprotective effect, antioxidation, promoting energy metabolism, anti-inflammation, lipid composition regulation, and metal ion homeostasis, which are all key points in AD therapy [ 11 , 12 ].…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies have shown that SQYG ameliorated the cognitive impairments in APP/PS1 mice by inhibiting neuronal loss, soluble A β deposition, tau hyperphosphorylation, and inflammation [ 14 ]. The hippocampus of 5XFAD transgenic mice treated with SQYG presented fewer A β deposits and reduced A β 1–42 levels [ 10 ]. The neuroprotective mechanisms of SQYG on the hippocampus of 5XFAD mice were related to modulation of multiple pathological processes, including energy metabolism, stress response, cytoskeleton, synaptic transmission, signal transduction, and amino acid metabolism [ 15 ].…”
Section: Introductionmentioning
confidence: 99%