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- 和 - 对 D-半乳糖诱导的免疫衰老和环磷酰胺诱导的免疫抑制的保护作用的植物生物类黄酮组成。

Botanical Bioflavonoid Composition from - and -Protected Mice against D-Galactose-Induced Immunosenescence, and Cyclophosphamide Induced Immune Suppression.

机构信息

Unigen Inc., 2121 South State Street, Suite #400, Tacoma, WA 98405, USA.

Department of Biology, Pacific Lutheran University, 12180 Park Ave. S, Tacoma, WA 98447, USA.

出版信息

Nutrients. 2024 Sep 18;16(18):3144. doi: 10.3390/nu16183144.

Abstract

Oxidative stress and chronic inflammation create a perpetual cycle in the elderly, where impaired immune function amplifies susceptibility to oxidative damage, and oxidative stress further weakens the immune response. This cycle is particularly detrimental to the respiratory system of the elderly, which is an easy target for constant exogenous harmful attacks during cold/flu season or under heavy air pollution. Herbal medicines that protect respiratory function are seen as safer alternatives to conventional therapies; however, there is limited availability of scientifically validated, safe, and effective natural supplements for these conditions. In this study, we evaluated a standardized bioflavonoid composition, UP446, that contains bioactives from the roots of and the heartwoods of as a natural and nutritional supplement for its antioxidative and immunoregulatory effects in oxidative stress-accelerated aging and chemically induced immune suppression mouse models. Immunosenescence was induced through the repeated subcutaneous inoculation of D-galactose (D-Gal) at a dose of 500 mg/kg/day in CD-1 mice. UP446 was administered orally at doses of 100 mg/kg and 200 mg/kg starting in the fifth week of immunosenescence induction. This study lasted a total of ten weeks. All mice received a quadrivalent influenza vaccine 2 weeks before termination. Whole blood, serum, spleen homogenate, and thymus tissues were processed for analysis. Cyclophosphamide (Cy)-induced immunosuppression was triggered by three consecutive injections of cyclophosphamide at 80 mg/kg/day, followed by the oral administration of UP446 for 18 days at doses of 100 mg/kg and 200 mg/kg. Blood was collected from each animal at necropsy, and serum was isolated for IgA and IgG ELISA analysis. UP446 was found to improve immune response, as evidenced by the stimulation of innate (NK cells) and adaptive immune responses (T cells and cytotoxic T cells), an increase in antioxidant capacity (glutathione peroxidase), the preservation of vital immune organs (the thymus), and a reduction in NFκB. UP446 also increased serum levels of IgA and IgG. The findings presented in this report demonstrate the antioxidative, anti-inflammatory, and immune-regulatory activities of UP446, suggesting its potential use in respiratory conditions involving immune stress due to aging, oxidative stress, and/or pathogenic challenges.

摘要

氧化应激和慢性炎症在老年人中形成了一个持久的循环,在此过程中,免疫功能受损会增加对氧化损伤的易感性,而氧化应激则进一步削弱免疫反应。这个循环对老年人的呼吸系统尤其不利,因为在寒冷/流感季节或在重度空气污染下,呼吸系统很容易受到持续的外源性有害攻击。保护呼吸功能的草药药物被视为传统疗法的更安全替代品;然而,对于这些病症,目前科学验证的、安全有效的天然补充剂的供应非常有限。在这项研究中,我们评估了一种标准化的生物类黄酮组合物 UP446,它包含 和 的根和心材中的生物活性物质,作为一种天然和营养补充剂,用于在氧化应激加速衰老和化学诱导免疫抑制的小鼠模型中发挥抗氧化和免疫调节作用。免疫衰老通过在 CD-1 小鼠中每天重复皮下接种 500mg/kg 的 D-半乳糖(D-Gal)来诱导。从免疫衰老诱导的第五周开始,以 100mg/kg 和 200mg/kg 的剂量口服给予 UP446。这项研究共持续了十周。所有小鼠在终止前两周接受了四价流感疫苗。处理全血、血清、脾匀浆和胸腺组织进行分析。环磷酰胺(Cy)诱导的免疫抑制通过连续三次注射 80mg/kg/day 的环磷酰胺来触发,随后以 100mg/kg 和 200mg/kg 的剂量口服给予 UP446 18 天。在解剖时从每个动物采集血液,并分离血清进行 IgA 和 IgG ELISA 分析。UP446 被发现改善了免疫反应,这表现在先天(NK 细胞)和适应性免疫反应(T 细胞和细胞毒性 T 细胞)的刺激、抗氧化能力(谷胱甘肽过氧化物酶)的增加、重要免疫器官(胸腺)的保存以及 NFκB 的减少。UP446 还增加了血清中 IgA 和 IgG 的水平。本报告中提出的研究结果表明 UP446 具有抗氧化、抗炎和免疫调节活性,提示其在涉及因衰老、氧化应激和/或致病挑战引起的免疫应激的呼吸道疾病中的潜在用途。

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