Aug 2026· Journal of Agricultural and Food Chemistry· Vol 74 33, pp.
26311-26331
· 0 citations· 50 references
Medicine
TL;DR
In APP/PS1 mice, compound 11 dose-dependently improved cognitive function, reduced Aβ plaques, and attenuated glial inflammation, supporting its promising neuroprotective potential.
Abstract
An investigation of the seeds of Astragalus complanatus (SAC), a homologous food-medicine plant in China, yielded 29 compounds, including four new terpenoids, astranoids A-D (1, 2, 6, 23), and one new stigmastane steroid, astrasteroid (12). Structural elucidation was achieved using NMR, HRESIMS, quantum-chemical ECD, and NMR computations, and X-ray crystallography. Astranoid A (1) features a novel 5/6/6/6/5 pentacyclic skeleton with cis-fused A/B rings. All isolates were evaluated for nitric oxide inhibition in LPS-stimulated BV-2 cells. 7-oxo-β-sitosterol (11) demonstrated potent antineuroinflammatory activity with an IC50 of 6.09 ± 0.49 μM. This compound suppressed proinflammatory cytokines, NF-κB translocation, and iNOS/COX-2 expression, activated Nrf2/HO-1 in HT22 cells, and protected neurons from Aβ-induced inflammatory injury. In APP/PS1 mice, compound 11 dose-dependently improved cognitive function, reduced Aβ plaques, and attenuated glial inflammation, supporting its promising neuroprotective potential.
Findings indicate that flavonoids from SAC, particularly rhamnocitrin (15), are promising natural neuroprotective candidates for food-based health applications.
Angeloylgomisin O (31) exhibited anti-neuroinflammatory activity by inhibiting lipopolysaccharide (LPS)-induced overproduction of nitric oxide (NO) in BV-2 microglial cells and exhibited notable neuroprotective effects against oxygen-glucose deprivation/reoxygenation (OGD/R)-induced injuries in SH-SY5Y cells.
Fengbei Gong, Pei-Kun Tian, Ning-Yuan Gong et al.· Phytochemistry· 0 citations
It is demonstrated that diarylheptanoids are the major anti-inflammatory components in A. maximum fruits, which not only validates the ethnopharmacological use of this herb, but also provides new anti-inflammatory agents derived from natural products.
Phytochemical investigation of the methanol extract of L. wallichii roots led to the isolation and structural elucidation of four previously undescribed compounds and eight known analogues, positioning them as promising anti-inflammatory and anti-cancer agents.
Ninh Khac Thanh Tung, Oanh Thị Tú Nguyễn, Giáp Hữu Trần et al.· Phytochemistry· 0 citations
Callilongiflocin A (1) exhibited the most potent effects, significantly suppressing the production of NO, pro-inflammatory cytokines interleukin (IL)-6 and tumor necrosis factor-α (TNF-α), and the overexpression of inducible NO synthase (iNOS) in a concentration-dependent manner.
Ting Liu, Xiao-Lu Wu, Lianchun Li et al.· Phytochemistry· 0 citations
Among them, compound 1 displayed the most potent anti-inflammatory activity, with an IC50 value of 9.05 ± 1.60 μM, comparable to that of the positive control dexamethasone.
Jing-Yi Yue, Yu-Jia Lu, Yang Yu et al.· Records of Natural Products· 0 citations
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