药物庆大霉素- b在抗肿瘤治疗条件下对小鼠机体形态功能状态影响的评价

V.A. Gritsyuk, G.A. Vostroilova, A.A. Korchagina, N.A. Khokhlova, D.I. Shabanov, A.V. Nekrasov
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引用次数: 0

摘要

本实验旨在研究庆大霉素- b在阿霉素作用下对埃利希腹水癌(EAC)小鼠机体形态功能状态的影响。在肿瘤生长第10天,我们研究了药物对EAC小鼠腹腔肿瘤细胞浓度以及血液中白细胞及其个体群的单独和联合影响;此外,对肿瘤动物在使用阿霉素和Gentabiferon-B后的寿命进行了估计。通过测定腹水中EAC细胞的浓度,确定了联合用药并没有降低阿霉素对肿瘤细胞的特异性细胞毒作用。与未处理EAC小鼠相比,该组动物体内肿瘤细胞数量减少49.3%。在实验中,用阿霉素和庆大霉素- b治疗的动物的预期寿命比用庆大霉素- b单药治疗的肿瘤小鼠的预期寿命增加55.8%。联合药物治疗诱导EAC小鼠血液淋巴细胞浓度相对于单独暴露于阿霉素后淋巴细胞数量增加39.5%。结果表明,阿霉素与庆大霉素- b联合使用的抗肿瘤活性和庆大霉素- b在肿瘤进展条件下的免疫调节作用得以保留。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF THE EFFECT OF THE DRUG GENTABIFERON-B ON THE MORPHOFUNCTIONAL STATE OF THE MICE BODY UNDER THE CONDITIONS OF ANTITUMOR THERAPY
The objective of this work was to study the effect of Gentabiferon-B on the morphofunctional state of the organism of mice with Ehrlich ascites carcinoma (EAC) under the effect of doxorubicin. We studied the individual and combined effects of drugs on the concentration of tumor cells in the peritoneal cavity, as well as leukocytes and their individual populations in the blood of mice with EAC on day 10 of tumor growth; in addition, the longevity in the animals with a tumor was estimated after the use of doxorubicin and Gentabiferon-B. It was established that the combined use of drugs did not reduce the specific cytotoxic effect of doxorubicin in relation to tumor cells, which was assessed by the concentration of EAC cells in ascite. The number of tumor cells in the animals of this group was by 49.3% lower than the concentration of neoplasm cells in mice with EAC without treatment. In the experiment, an increase by 55.8% in the life expectancy of the animals treated with doxorubicin and Gentabiferon-B was observed relative to mice with a tumor after monotherapy with Gentabiferon-B. Combined drug therapy induced an increase in the concentration of blood lymphocytes by 39.5% relative to the number of these cells in mice with EAC after exposure to doxorubicin alone. The results obtained allows to assume that the efficacy of the antitumor activity of doxorubicin in its combined use with Gentabiferon-B and the immunomodulatory effect of Gentabiferon-B in conditions of tumor progression are preserved.
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