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Angelica Sinensis polysaccharide antagonizes 5-Fluorouracil-induced spleen injury and dysfunction by suppressing oxidative stress and apoptosis.

Authors :
Du, Kunhang
Wang, Lu
Wang, Ziling
Xiao, Hanxianzhi
Hou, Jiying
Hu, Ling
Fan, Ningke
Wang, Yaping
Source :
Biomedicine & Pharmacotherapy. Jun2023, Vol. 162, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Angelica Sinensis polysaccharide (ASP), the main active component of Angelica sinensis, possesses antioxidative and anti-apoptotic properties. In this study, we have investigated the antagonistic effect of ASP on 5-FU-induced injury of mouse spleen in vivo and splenocytes in vitro, and its possible mechanism. Our results showed that ASP inhibited 5-FU-induced decreases in spleen weight and organ index in mice, restored the number of peripheral blood leukocytes and lymphocytes, repaired spleen structure disorder and functional impairment, rescued serum IL-2, IL-6, and IFN-γ levels, and relieved 5-FU-induced mitochondrial swelling, reduced the oxidant accumulation including MDA and ROS, whereas increasing the activities of GSH, SOD and CAT. The mechanism may be related to ASP downregulation of Keap1 protein expression thus motivating the nuclear translocation of Nrf2. Furthermore, ASP alleviated the apoptosis of spleens in vivo and splenocytes in vitro, and reactivated PI3K / AKT signalling. In conclusion, the protective effect of ASP on spleens and splenocytes may be related to the reduction of oxidative stress and apoptosis via reactivation of Nrf2 and PI3K/AKT pathways. This study has provided a new protective agent for minimizing the spleen injury caused by 5-FU and a new idea for improving the prognosis of chemotherapy patients. [Display omitted] • ASP restores spleen immune function by alleviating 5-FU-induced apoptosis and oxidative stress. • ASP ameliorates 5-FU-induced oxidative stress through activation of Nrf2. • ASP reactivates PI3K/AKT pathways inhibited by 5-FU to reduce apoptosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
162
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
163429399
Full Text :
https://doi.org/10.1016/j.biopha.2023.114602