金合欢烯脂质体对环磷酰胺诱导的 BALB/c 小鼠免疫抑制的免疫调节和抗氧化作用

IF 3.9
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引用次数: 0

摘要

简介环磷酰胺(CP)是一种常用的化疗药物,可导致一系列副作用,如免疫抑制、骨髓抑制、白细胞减少和氧化应激。本研究旨在探讨具有免疫调节和抗氧化特性的金合欢素(AUR)对受 CP 抑制的小鼠免疫功能的影响:60 只雄性 BALB/c 小鼠接受了为期 10 天的治疗。在第 1、3 和 9 天,CP 以 80 毫克/千克的 IP 剂量诱导免疫抑制。小鼠被分为五组:对照组、CP 组、CP + 脂质体 AUR 0.2 mg/kg 组(AUR 0.2)、CP + 脂质体 AUR 0.25 mg/kg 组(AUR 0.25)和脂质体载体组。对小鼠体重、免疫器官重量指数(脾脏和胸腺)、脾脏和胸腺组织病理学、炎症细胞因子水平(IL2、IL10、IL4、IFN-γ)、TH1/TH2 平衡比、IgG 和 IgM 免疫球蛋白水平、白细胞计数、血小板、中性粒细胞、淋巴细胞以及氧化活性(MDA、SOD 和总抗氧化剂)等多项指标进行了测定:与对照组相比,CP 治疗组的小鼠体重明显下降。相比之下,接受 AUR 治疗的小鼠体重保持不变,与对照组没有明显差异。AUR 0.25 减少了氯化石蜡对脾脏和胸腺的损害。此外,与 CP 组相比,AUR 0.25 显著降低了 IL4 和 IL10 的水平(p = 0.04),接近对照组的水平。此外,与 CP 组相比,AUR 0.25 组的 IL2 和 IFN-γ 水平明显升高(p = 0.04),达到与对照组相似的水平。与 CP 组相比,AUR 还使血清 IgM 和 IgG 水平增加了 2 到 3 倍,接近对照组的水平。AUR 0.25 组的 MDA 水平降至正常和对照组水平。AUR 0.25 还显示出 SOD 和总抗氧化剂水平的提高。此外,与 CP 组相比,AUR 组的白细胞、血小板、中性粒细胞和淋巴细胞显著增加,达到与对照组相似的正常水平。与 CP 组相比,AUR 组的 TH1/TH2 比率显著增加了 2.5 倍(p = 0.002):这些结果表明,AUR 可通过 TH1/TH2 的平衡增强体液和细胞免疫系统的功能,提高免疫球蛋白的水平,以及增强抗氧化活性和细胞毒性的保护作用,从而抵御 CP 的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunomodulatory and antioxidant effect of liposomal auraptene against cyclophosphamide-induced immunosuppression in BALB/c mice

Introduction

Cyclophosphamide (CP), which is a commonly used chemotherapy drug, can lead to a range of side effects such as immunosuppression, bone marrow suppression, leukopenia, and oxidative stress. This study aims to explore the effects of Auraptene (AUR), which has immunomodulatory and antioxidant properties, on immune function in mice that are experiencing suppression induced by CP.

Materials and methods

The experiment involved 60 male BALB/c mice that underwent a 10-day treatment. On days 1, 3, and 9, CP was given at 80 mg/kg IP doses to induce immunosuppression. The mice were divided into five groups: Control group, CP group, CP + liposomal AUR 0.2 mg/kg (AUR 0.2), CP + liposomal AUR 0.25 mg/kg (AUR 0.25), and liposomal vehicle group. Various parameters were measured, including mouse weight, immune organ weight index (spleen and thymus), spleen and thymus histopathology, levels of inflammatory cytokines (IL2, IL10, IL4, IFN-γ), TH1/TH2 balance ratio, IgG and IgM immunoglobulin levels, white blood cell count, platelets, neutrophils, lymphocytes, and oxidative activity measured by MDA, SOD, and Total Antioxidant.

Results

In the group treated with CP, the mice showed a significant decrease in weight compared to the control group. In contrast, the group treated with AUR maintained their weight and did not show a significant difference from the control group. AUR 0.25 reduced the damage to the spleen and thymus caused by CP. Additionally, AUR 0.25 demonstrated a significant decrease in IL4 and IL10 levels compared to the CP group (p = 0.04), approaching the levels of the control group. Furthermore, IL2 and IFN-γ levels in the AUR 0.25 group significantly increased (p = 0.04) compared to the CP group, reaching levels similar to the control group. AUR also increased serum IgM and IgG levels two to three times compared to the CP group, approaching the levels of the control group. MDA levels in the AUR 0.25 group decreased to normal and control levels. AUR 0.25 also showed increased SOD and Total Antioxidant levels. Additionally, white blood cells, platelets, neutrophils, and lymphocytes in the AUR group significantly increased compared to the CP group, reaching normal levels similar to the control group. The TH1/TH2 ratio in the AUR group exhibited a significant increase of two and a half times (p = 0.002) compared to the CP group.

Conclusion

These results show that AUR protects against the side effects of CP by increasing the function of the humoral and cellular immune system through the balance of TH1/TH2 and increasing the level of immunoglobulins, as well as increasing the antioxidant activity and the protective role of cytotoxicity.

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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
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