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Umbelliferone Enhances Immune Function in Cyclophosphamide-Induced Immunosuppressed Mice via Histidine and Purine Metabolism Regulation

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机构: [1]The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050000, China [2]Tianjin University, Tianjin, 300072, China [3]Department of Pharmacy, Tianjin Second People's Hospital, Tianjin, 300192, China [4]First School of Clinical Medicine, Yunnan University of Chinese Medicine, Kunming, 650500, China [5]Yunnan University of Chinese Medicine, Kunming, 650500, China [6]Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China [7]Tianjin Nankai Hospital, Tianjin Medical University, Tianjin, 300100, China [8]Tianjin Key Laboratory of Acute Abdomen Disease Associated Organ Injury and ITCWM Repair, Tianjin, 300100, China [9]Institute of Integrative Medicine for Acute Abdominal Diseases, Tianjin, 300100, China
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关键词: Immunosuppression cyclophosphamide untargeted metabolomics histidine and purine metabolism umbelliferone oxidative stress apoptosis

摘要:
Chemotherapy-induced immunosuppression significantly impacts patient's quality of life. Umbelliferone (UMB) is known for its anti-inflammatory, antioxidant, and anti-apoptotic properties, but its effects on cyclophosphamide (CTX)-induced immunosuppression need further study.We established a CTX-induced immunosuppressed mouse model and administered varying doses of UMB. Immune function was assessed by evaluating white blood cells, lymphocytes, thymus and spleen indices, and CD4+/CD8+ T cell ratios. Serum levels of IL-2, IFN-γ, IgA, IgM, and IgG, along with macrophage phagocytic activity, NK cytotoxicity, and lymphocyte proliferation, were measured. Untargeted metabolomics was used to identify key pathways regulated by UMB, and RT-qPCR and Western blotting were performed to analyze the expression of related enzymes and metabolites.UMB intervention increased white blood cells, lymphocytes, thymus and spleen indices, and CD4+/CD8+ T cell ratios in CTX-immunosuppressed mice. It reversed reduced levels of serum IL-2, IFN-γ, IgA, IgM, and IgG and improved macrophage phagocytic activity, NK cytotoxicity, and lymphocyte proliferation. Key pathways identified by metabolomics included histidine and purine metabolism. UMB improved levels of histamine, L-glutamate, L-aspartate, xanthine, dAMP, deoxyinosine, xanthosine, and cGMP and upregulated HDC, ASPA, and PNP while downregulating XDH, PDE5, ROS, and MDA in spleen tissue. UMB enhanced SOD activity and GSH levels and reduced apoptosis, as indicated by lower TUNEL-positive expression.UMB enhanced immune function in CTX-immunosuppressed mice through the regulation of histidine and purine metabolism, exhibiting antioxidant and anti-apoptotic effects. These findings highlight the potential of UMB in mitigating immunosuppression.Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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出版当年[2025]版
大类 | 4 区 医学
小类 | 4 区 生化与分子生物学 4 区 药学
最新[2025]版
大类 | 4 区 医学
小类 | 4 区 生化与分子生物学 4 区 药学
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第一作者机构: [1]The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050000, China [2]Tianjin University, Tianjin, 300072, China
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通讯机构: [2]Tianjin University, Tianjin, 300072, China [3]Department of Pharmacy, Tianjin Second People's Hospital, Tianjin, 300192, China [7]Tianjin Nankai Hospital, Tianjin Medical University, Tianjin, 300100, China [8]Tianjin Key Laboratory of Acute Abdomen Disease Associated Organ Injury and ITCWM Repair, Tianjin, 300100, China [9]Institute of Integrative Medicine for Acute Abdominal Diseases, Tianjin, 300100, China
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