原生物类黄酮复合物对环磷酰胺诱导的免疫紊乱的纠正作用

I. Goldina, E. Markova, I. Orlovskaya, L. Toporkova, V. Kozlov
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摘要

我们的目的是评估一种原始生物类黄酮复合物在环磷酰胺(Cy)诱导的实验性免疫紊乱中的免疫调节特性。我们研究了实验动物在cy诱导免疫抑制过程中胸腺和脾脏的形态计量指标、血液白细胞计数、淋巴器官细胞增殖活性、对T细胞依赖性抗原的延迟超敏反应以及生物类黄酮治疗后骨髓干细胞的分化活性。将生物类黄酮复合物的悬浮液引入12- 14周龄雄性小鼠(СВАхC57Bl/6)F1,每日剂量为2mg /只(80 mg/kg),每只,每只,通过胃导管,持续14天。单次腹腔注射Cy可产生细胞抑制免疫抑制作用。用Н3 -胸腺嘧啶掺入标准方法测定脾脏和胸腺细胞的增殖活性。细胞免疫反应是通过对绵羊红细胞反应的迟发性超敏反应发展程度来测定的。通过在甲基纤维素培养基中培养骨髓细胞来评估造血祖细胞的数量。实验表明,在生物类黄酮复合物治疗过程中,Cy诱导的免疫抑制作用在外周血淋巴器官的绝对质量和相对质量以及白细胞数量方面有所缓解。此外,我们已经证明,Cy治疗对脾细胞自发活性、丝裂原诱导的胸腺细胞和脾细胞增殖的影响降低,延迟型超敏反应的强度达到了完整动物的值。随着生物类黄酮的使用,我们发现了早期造血祖细胞的增加。减轻cy对细胞免疫应答的抑制作用,提高免疫细胞的增殖速率,刺激造血干细胞功能,表明原生物类黄酮复合物具有足够的调节免疫和造血功能的能力,从而为其作为恶性疾病患者辅助治疗的潜在应用提供了实验证据。
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Corrective effects of original bioflavonoid complex in the cyclophosphamide-induced immunity disorders
Our aim was to evaluate immunomodulatory properties of an original bioflavonoid complex in experimental immune disturbances induced by cyclophosphamide (Cy). We have studied morphometric indexes of thymus and spleen, as well as blood leukocyte counts, cell proliferative activity in lymphoid organs, delayed hypersensitivity responses to T cell-dependent antigen, along with differentiation activity of bone marrow stem cells in experimental animals during Cy-induced immune suppression after a course of bioflavonoid treatment. Suspension of the bioflafonoid complex was introduced to the male mice (СВАхC57Bl/6)F1 aged 12- 14 weeks at a daily dose of 2 mg/animal (80 mg/kg), per os, using gastric catheter, over 14 days. Cytostatic immunosuppression was produced by a single intraperitoneal Cy injection. Proliferative activity of spleen and thymic cells was determined by standard method with Н3 -thymidine incorporation in the 72-h cell culture. Cellular immune response was assayed by the degree of delayed-type hypersensitivity development in response to sheep erythrocytes. The number of hematopoietic progenitors was evaluated by culturing bone marrow cells in methylcellulose-based medium. The experiments have shown mitigation of immunosuppressive effects induced by Cy, in the course of bioflavonoid complex treatment, with respect to absolute and relative mass of lymphoid organs and leukocyte numbers in peripheral blood. Moreover, we have demonstrated decreased effects of Cy treatment upon the spontaneous activity of spleen cells, mitogen-induced thymocyte and splenocyte proliferation, intensivity of delayed-type hypersensitivity response that reached the values of intact animals. Following the course of bioflavonoids, we have revealed an increase in early hematopoietic progenitors. Alleviation of Cy-induced suppressive effects upon cellular immune response, proliferation rates of immune cells, as well as stimulation of hematopoietic stem cell functions suggest a sufficient capacity of the original bioflavonoid complex for modulation of immunity and hematopoiesis, thus presenting experimental proofs for its potential usage as an adjuvant treatment of the patients with malignant diseases.
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