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当归多糖通过抑制氧化应激和细胞凋亡拮抗 5-氟尿嘧啶所致脾损伤及脾功能障碍。

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

机构信息

Laboratory of Stem Cells and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China.

Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, China.

出版信息

Biomed Pharmacother. 2023 Jun;162:114602. doi: 10.1016/j.biopha.2023.114602. Epub 2023 Apr 3.

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.

摘要

当归多糖(ASP)是当归的主要活性成分,具有抗氧化和抗凋亡作用。本研究探讨了 ASP 对体内 5-FU 诱导的小鼠脾损伤和体外脾细胞损伤的拮抗作用及其可能的机制。结果表明,ASP 抑制了 5-FU 诱导的小鼠脾重和脏器指数下降,恢复了外周血白细胞和淋巴细胞数量,修复了脾结构紊乱和功能障碍,挽救了血清 IL-2、IL-6 和 IFN-γ 水平,并缓解了 5-FU 诱导的线粒体肿胀,减少了 MDA 和 ROS 等氧化剂的积累,同时增加了 GSH、SOD 和 CAT 的活性。其机制可能与 ASP 下调 Keap1 蛋白表达从而促进 Nrf2 的核转位有关。此外,ASP 减轻了体内脾和体外脾细胞的凋亡,并重新激活了 PI3K/AKT 信号通路。综上所述,ASP 对脾和脾细胞的保护作用可能与通过重新激活 Nrf2 和 PI3K/AKT 通路减少氧化应激和凋亡有关。本研究为减轻 5-FU 引起的脾损伤提供了一种新的保护剂,为改善化疗患者预后提供了新思路。

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