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灵芝多糖增强免疫抑制小鼠免疫效应细胞的功能。

Ganoderma lucidum polysaccharides enhance the function of immunological effector cells in immunosuppressed mice.

作者信息

Zhu Xiao-Ling, Chen Alex-F, Lin Zhi-Bin

机构信息

Department of Pharmacology, School of Basic Medical Science, Peking University Health Science Center, 38 Xueyuan Road, Beijing 100083, PR China. xiaolingzhu88yahoo.com.cn

出版信息

J Ethnopharmacol. 2007 May 4;111(2):219-26. doi: 10.1016/j.jep.2006.11.013. Epub 2006 Nov 21.

Abstract

The present study was designed to determine in vivo efficacy of Ganoderma lucidum polysaccharides (Gl-PS) for enhancing the activity of immunological effector cells in immunosuppressed mice. Mice were injected intraperitoneally (i.p.) once daily with low-dose (2.5mg/kg), intermediate-dose (25mg/kg), and high-dose (250 mg/kg) of Gl-PS, respectively, for 7 consecutive days 24h after i.p. injection of a immunosuppressing anti-tumor agent cyclophosphamide (Cy, 300 mg/kg). In Cy-treated mice, compared to vehicle, low-dose Gl-PS accelerated recovery of bone marrow cells, red blood cells and white blood cells, as well as splenic natural killer cells and natural killer T cells, and enhanced T and B cell proliferation responses on day 8, cytotoxic T lymphocyte activity on day 5, as well as NK cell and lymphokine activated killer cell activity on days 7-9. Furthermore, it promoted phagocytosis and cytotoxicity of macrophages on day 12. The above beneficial effects induced by the low-dose Gl-PS treatment did not result in any side effects. These results demonstrate the efficacious effects of low-dose Gl-PS treatment for enhancing the activity of immunological effector cells in immunosuppressed mice, and may provide a basis for applying this herb as an efficacious adjacent immunopotentiating therapy against cancer chemotherapy-induced immunosuppression.

摘要

本研究旨在确定灵芝多糖(Gl-PS)在增强免疫抑制小鼠免疫效应细胞活性方面的体内疗效。在腹腔注射免疫抑制抗肿瘤药物环磷酰胺(Cy,300mg/kg)24小时后,将小鼠分别连续7天每天腹腔注射低剂量(2.5mg/kg)、中剂量(25mg/kg)和高剂量(250mg/kg)的Gl-PS。在Cy处理的小鼠中,与赋形剂相比,低剂量Gl-PS加速了骨髓细胞、红细胞和白细胞以及脾脏自然杀伤细胞和自然杀伤T细胞的恢复,并增强了第8天的T和B细胞增殖反应、第5天的细胞毒性T淋巴细胞活性以及第7至9天的NK细胞和淋巴因子激活的杀伤细胞活性。此外,它在第12天促进了巨噬细胞的吞噬作用和细胞毒性。低剂量Gl-PS治疗诱导的上述有益效果未导致任何副作用。这些结果证明了低剂量Gl-PS治疗在增强免疫抑制小鼠免疫效应细胞活性方面的有效作用,并可能为将这种草药作为一种有效的辅助免疫增强疗法应用于对抗癌症化疗引起的免疫抑制提供依据。

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