Chitosan promotes immune responses, ameliorating total mature white blood cell numbers, but increases glutamic oxaloacetic transaminase and glutamic pyruvic transaminase, and ameliorates lactate dehydrogenase levels in leukemia mice in vivo
Autor: | Shu Fen Peng, Chia‑Hui Liu, Yung Luen Shih, Ming Yang Yeh, Lung‑Yuan Wu, Hsueh Yu Chung, Wen Wen Huang, Jing Gung Chung, Jia You Liu, Hsu Feng Lu, Jason Chou |
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Rok vydání: | 2017 |
Předmět: |
Cytotoxicity
Immunologic Male 0301 basic medicine Cancer Research glutamic pyruvic transaminase Lymphocyte Activation Biochemistry immune response Leukocyte Count Mice chemistry.chemical_compound 0302 clinical medicine Immunity Cellular Mice Inbred BALB C Leukemia biology Alanine Transaminase Articles Killer Cells Natural medicine.anatomical_structure Oncology 030220 oncology & carcinogenesis Molecular Medicine medicine.medical_specialty Phagocytosis Spleen Peripheral blood mononuclear cell 03 medical and health sciences Immune system Adjuvants Immunologic Cell Line Tumor Internal medicine Lactate dehydrogenase White blood cell Genetics medicine Animals Aspartate Aminotransferases Molecular Biology Chitosan L-Lactate Dehydrogenase glutamic oxaloacetic transaminase lactate dehydrogenase medicine.disease Molecular biology 030104 developmental biology Endocrinology Alanine transaminase chemistry biology.protein |
Zdroj: | Molecular Medicine Reports |
ISSN: | 1791-3004 1791-2997 |
DOI: | 10.3892/mmr.2017.6923 |
Popis: | The aim of the present study was to investigate the effect of chitosan (a naturally derived polymer) on the immune responses and glutamic oxaloacetic transaminase (GOT), glutamic pyruvic transaminase (GPT) and lactate dehydrogenase (LDH) levels in WEHI-3 cell-generated leukemia mice. Mice were divided into control, WEHI-3 control, acetic acid (vehicle)-treated, and 5 and 20 mg/kg chitosan-treated groups. Mice were subsequently weighed, blood was collected, and liver and spleen samples were isolated and weighed. Blood samples were measured for cell markers, the spleen underwent phagocytosis and natural killer (NK) cell activity examination, and cell proliferation was analyzed by flow cytometry. Chitosan did not significantly affect the weights of body, liver and spleen at 5 and 20 mg/kg treatment. Chitosan increased the percentage of CD3 (T cells marker), decreased the levels of CD19 (B-cell marker) and CD11b at 5 mg/kg treatment, and decreased the levels of Mac-3 at 5 and 20 mg/kg treatment. Chitosan significantly increased macrophage phagocytosis of PBMCs, but did not significantly affect macrophage phagocytosis in the peritoneal cavity. Chitosan treatment did not significantly affect the cytotoxic activity of NK cells, and also did not affect T- and B-cell proliferation. Chitosan significantly increased total white blood cell numbers, and GOT and GPT activities were both significantly increased. However, chitosan did not significantly affect LDH activity in leukemia mice. Chitosan may aid in future studies on improving immune responses in the treatment of leukemia. |
Databáze: | OpenAIRE |
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