2019
DOI: 10.1016/j.biopha.2018.12.100
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CGY-1, a biflavonoid isolated from cardiocrinum giganteum seeds, improves memory deficits by modulating the cholinergic system in scopolamine-treated mice

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Cited by 6 publications
(5 citation statements)
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“…giganteum having antitussive properties. CGY-1 was further reported as a potent agent to improve memory deficit for the treatment of cognitive dysfunction [9]. Similarly, Xia et al [11] reported the isolation of a new biflavonoid, 3 -hydroxyrobustaflavone along with 3 -hydroxyamentoflavone, quercetin, apigenin, and kaempferol with antioxidative activities from the 95% ethanol extract of seeds of C. giganteum var.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…giganteum having antitussive properties. CGY-1 was further reported as a potent agent to improve memory deficit for the treatment of cognitive dysfunction [9]. Similarly, Xia et al [11] reported the isolation of a new biflavonoid, 3 -hydroxyrobustaflavone along with 3 -hydroxyamentoflavone, quercetin, apigenin, and kaempferol with antioxidative activities from the 95% ethanol extract of seeds of C. giganteum var.…”
Section: Resultsmentioning
confidence: 99%
“…Although the Cardiocrinum species have high value as food, medicinal, and ornamental plants [4,6], only a few studies have been performed regarding their chemical constituents. Some previous studies reported the flavonoids from the seeds of C. giganteum [9][10][11] and the starch composition of the bulbs of C. cordatum var. glehnii (F.Schmidt) H.Hara [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, scopolamine leads to increased oxidative stress, elevated inflammation, and blocking of the acetylcholine receptor in the brain [51][52][53]. Oxidative stress causes a significant increase in MDA levels, which is an index of lipid peroxidation, and decreases the expression levels of antioxidant enzymes.…”
Section: Discussionmentioning
confidence: 99%
“…Choi et al used the peptide of Aβ1-42 to inhibit the aggregation of Aβ1-42 in vitro by thioflavin T fluorescence analysis of biflavonoids (amentoflavone, bilobetin, sequoiaflavone, sotetsuflavone, podocarpuflavone, ginkgetin, isoginkgetin, and sciadopitysin), and found that amentoflavone has the strongest comprehensive strength in inhibiting the formation of Aβ1-42 fibers and reducing the formation of Aβ1-42 fibers among the eight biflavonoids, and it has great potential as a lead compound for treating Alzheimer’s disease [ 295 ]. CGY-1 [ 82 ], GB1, and other gambogic biflavonoids [ 296 ] also have the potential to treat Alzheimer’s disease.…”
Section: Pharmacology Of Biflavonoidsmentioning
confidence: 99%