粒细胞-巨噬细胞集落刺激因子与阿仑膦酸偶联物的促血特性

G. G. Shimina, A. V. Bateneva, E. S. Tsyplenkova, S. G. Gamaley, T. I. Esina, E. Volosnikova, E. Danilenko
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引用次数: 0

摘要

本研究的目的是评价重组人粒细胞-巨噬细胞集落刺激因子(rhGM-CSF)与阿仑膦酸(ALN)偶联物在细胞静态骨髓抑制模型中的促血活性,以及rhGM-CSF作为偶联物的一部分在小鼠骨组织和骨髓中的蓄积动力学。材料和方法。用1-乙基-3-[3-二甲氨基丙基]碳二亚胺或高碘酸盐氧化法固相合成得到的共轭物。通过给CBA/Calac小鼠注射环磷酰胺诱导的细胞抑制性骨髓抑制模型来评估血液刺激活性。RhGM-CSF制剂以90µg/kg的剂量皮下注射4-5天。注射周期结束后,对血液样本进行白细胞总数和分节中性粒细胞计数,对骨髓样本进行总核细胞计数。以有效剂量单次静脉给药后,在远交种CD-1小鼠中评估rhGM-CSF制剂的组织分布。采用酶免疫法测定大鼠血液、股组织和骨髓中rhGM-CSF的含量。RhGM-CSF与ALN的偶联物已被证明在偶联物的作用下保留了原始蛋白增加白细胞、分节血中性粒细胞和骨髓核细胞数量的能力。与rhGM-CSF相比,中性粒细胞产生的刺激在更早的时间被观察到。与原始蛋白相比,引入所有三种结合物后骨髓细胞总数的增加更为明显(增加34%)。AEG偶联物的血液刺激作用增强的同时,rhGM-CSF在小鼠骨组织和骨髓中的积累也更强烈。引入的rhGM-CSF在骨组织中存在24 h,与原蛋白相比,其在血液中的循环时间更长。所获得的数据使我们有可能得出结论,基于rhGM-CSF与ALN结合物的有效血液刺激药物的进一步开发工作是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HEMOSTIMULATING PROPERTIES OF THE CONJUGATES OF GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTOR WITH ALENDRONIC ACID
The aim of the work is to evaluate the hemostimulating activity of recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) conjugates with alendronic acid (ALN) in the model of cytostatic myelosuppression and the dynamics of rhGM-CSF accumulation as a part of the conjugate in the bone tissue and bone marrow of mice.Materials and methods. The conjugates obtained by a solid-phase synthesis using 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide or periodate oxidation, were used. A hemostimulating activity was evaluated in a model of a cytostatic myelosuppression induced by the administration of cyclophosphamide to CBA/Calac mice. RhGM-CSF preparations were injected subcutaneously for 4-5 days at the dose of 90 µg/kg. After the injections cycle had been completed, the total leukocyte and segmented neutrophil counts were carried out in the blood samples, and the total karyocyte count was carried out in the bone marrow samples.The tissue distribution of rhGM-CSF preparations was assessed in outbred CD-1 mice after a single intravenous administration at the effective dose. The content of rhGM-CSF in blood, femoral tissue and bone marrow was determined by enzyme immunoassay.Results. RhGM-CSF conjugates with ALN have been shown to retain the ability of the original protein to increase the number of leukocytes, segmented blood neutrophils, and bone marrow karyocytes under the action of conjugates. The stimulation of the neutrophil production used to be observed at earlier times than in the case of rhGM-CSF. The increase in the total number of bone marrow cells after the introduction of all three conjugates was more pronounced compared to the original protein (by 34%). The increased hemostimulatory effect of the AEG conjugate was accompanied by a more intense accumulation of rhGM-CSF in the bone tissue and bone marrow of mice. The rhGM-CSF introduced into the conjugate was detected in the bone tissue for 24 h and it circulated in the bloodstream for a longer time compared to the original protein.Conclusion. The data obtained make it possible to conclude that further work on the development of effective hemostimulating drugs based on rhGM-CSF conjugates with ALN, is promising.
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