Objective: The aim of this study was to compare the effects of iron sucrose and iron dextran on the distribution and function of peripheral lymphocytes in healthy rats. Methods: 18 Wistar albino rats were divided into three groups. Group 1: control, group 2: iron sucrose and group 3: iron dextran group. Saline, iron sucrose and iron dextran were given as 1 ml/kg and 10 mg/kg intravenously to control, iron sucrose and iron dextran group, respectively. Peripheral blood samples were collected before injection and at 3, 6 and 24 hours after injection for flow cytometric and biochemical analysis. Demir Sükroz Ve Demir Dekstran’ın Sıçanlarda Periferik Kanda Lenfosit Dağılım Ve İşlevleri Üzerine Olan Etkilerinin Karşılaştırılması Results: The percentage of T suppressor lymphocytes in iron sucrose group showed significant increase at 6 and 24 hours, compared to control group. The percentage of T helper lymphocytes, activated T lymphocyte (CD3+/CD25+), antigen presenting cells and B lymphocyte, the ratio of CD4+ to CD8+ and IFN-γ level were found to be significantly decreased in iron sucrose group, compared to control and iron dextran group. Iron and transferrin saturation levels were significantly higher in iron sucrose group than others. Conclusion: This study showed that, iron sucrose, compared to iron dextran, had a negative effect on distribution of lymphocytes in healthy rats. These data support the development of further studies examining the effects of these iron preparations at low dosage and long duration on the effects of lymphocyte subpopulation
Objective: The aim of this study was to compare the effects of iron sucrose and iron dextran on the distribution and function of peripheral lymphocytes in healthy rats. Methods: 18 Wistar albino rats were divided into three groups. Group 1: control, group 2: iron sucrose and group 3: iron dextran group. Saline, iron sucrose and iron dextran were given as 1 ml/kg and 10 mg/kg intravenously to control, iron sucrose and iron dextran group, respectively. Peripheral blood samples were collected before injection and at 3, 6 and 24 hours after injection for flow cytometric and biochemical analysis. The percentage of T suppressor lymphocytes in iron sucrose group showed significant increase at 6 and 24 hours, compared to control group. The percentage of T helper lymphocytes, activated T lymphocytes (CD3+/CD25+), antigen presenting cells and B lymphocytes, the ratio of CD4+ to CD8+ and IFN-γ level were found to be significantly decreased in iron sucrose group, compared to control and iron dextran group. Iron and transferrin saturation levels were significantly higher in iron sucrose group than others. Conclusion: This study showed that, iron sucrose, compared to iron dextran, had a negative effect on the distribution of lymphocytes in healthy rats. These data support the development of further studies examining the effects of these iron preparations at low dosage and long duration on the effects of lymphocyte subpopulation
Field : Sağlık Bilimleri
Journal Type : Ulusal
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