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Kanggan Granule Ameliorates Dexamethasone-Induced Immunosuppression in Mice

Kanggan Granule Ameliorates Dexamethasone-Induced Immunosuppression in Mice

作     者:Yumiao Gan Manxia Gu Dongling Liu Hongjing Zhou Chenye Zeng Tingting Yang Hui Li Funeng Geng Junrong Du 

作者机构:Department of Pharmacology West China School of Pharmacy Key Laboratory of Drug Targeting and Drug Delivery System Sichuan University Chengdu China Sichuan Engineering Research Center for Medicinal Animals Chengdu China 

出 版 物:《Journal of Biosciences and Medicines》 (生物科学与医学(英文))

年 卷 期:2019年第7卷第3期

页      面:80-91页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主  题:Kanggan Granule Immunomodulatory Nonspecific Immunity Humoral Immunity Cellular Immunity 

摘      要:Objective: This study was to investigate the effect of the Chinese herbal compound Kanggan granule (KG) on immune function in a mouse model of immunosuppression and its possible mechanism of action. Method: ICR mice were randomly divided into a normal control group (untreated non-immunosuppressed, Control), untreated immunosuppressed group (Model), positive control group (immunosuppressed and treated with 1.6 g/kg astragalus granule [AG]), high-dose KG group (immunosuppressed and treated with 24 g/kg, KG-24), and low-dose KG group (immunosuppressed and treated with 6 g/kg, KG-6). Each group received intragastric administration once daily for 7 days. Immunosuppression was induced by an intraperitoneal injection of dexamethasone (25 mg/kg) once daily beginning on day 1 for 3 days. To illuminate the mechanism of immunomodulatory, we studied the effects of KG on nonspecific immunity, humoral immunity and cellular immunity in mice respectively. Results: KG improved organ weights and improved the phagocytic ability of mononuclear macrophages in immunosuppressed mice (p p 0.05). The proliferation of spleen lymphocytes and number of peripheral blood leukocytes were enhanced after KG treatment in immunosuppressed mice (p +/CD8+ ratio in immunosuppressed mice (p p Conclusions: KG can improve immune function in immunosuppressed mice. Nonspecific immunity, humoral immunity, and cellular immunity were all enhanced.

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