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A Pharmacokinetic–Pharmacodynamic Study of Protosappanoside D, a Component Derived from Biancaea decapetala Extracts, for Its Anti-Inflammatory Effects.
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- المؤلفون: Zhou, Zuying1,2 (AUTHOR); Zhou, Yang1,2 (AUTHOR); Wang, Pu2,3 (AUTHOR); Zhou, Ting1,2 (AUTHOR); Chi, Mingyan2 (AUTHOR); Li, Yueting1,3 (AUTHOR); Zhou, Meng3 (AUTHOR); Yang, Shuai1 (AUTHOR); Wang, Aimin3 (AUTHOR); Zheng, Lin1,2 (AUTHOR); Huang, Yong1,2 (AUTHOR)
- المصدر:
International Journal of Molecular Sciences. Apr2025, Vol. 26 Issue 8, p3694. 19p.
- معلومة اضافية
- نبذة مختصرة :
Biancaea decapetala (Roth) O. Deg. (Fabaceae), traditionally used by the Hmong people to treat rheumatoid arthritis (RA), has not been extensively studied for the correlation between its anti-inflammatory activity and its active components. Protosappanoside D (PTD), a new component, has been isolated for the first time from the extract of Biancaea decapetala. This study focused on the anti-arthritic and anti-inflammatory effects of Biancaea decapetala extracts (BDE) and PTD, along with their pharmacokinetic–pharmacodynamic (PK-PD) analysis. In the adjuvant-induced arthritis (AA) rat model, HE staining and cytokine assays showed that BDE alleviated joint damage and reduced inflammatory cytokines, similar to the positive control. In the LPS-induced inflammatory cell model, both BDE and PTD demonstrated anti-inflammatory effects by inhibiting the secretion of inflammatory factors. A PK-PD analysis of BDE in AA rats and inflammatory cells, as well as an analysis of PTD as a monomer, was conducted. The results indicated that PTD had different regulatory effects on cytokines like TNF-α, with a certain lag and sustained effects. These findings suggest the potential of BDE and PTD as treatments for rheumatoid arthritis, though further in vivo studies and clinical trials are needed. [ABSTRACT FROM AUTHOR]
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