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重组人白血病抑制因子可诱导非人类灵长类动物产生急性期蛋白并提高血小板计数。

Recombinant human leukemia inhibitory factor induces acute phase proteins and raises the blood platelet counts in nonhuman primates.

作者信息

Mayer P, Geissler K, Ward M, Metcalf D

机构信息

Sandoz Research Institute, Vienna, Austria.

出版信息

Blood. 1993 Jun 15;81(12):3226-33.

PMID:7685199
Abstract

Recombinant human leukemia inhibitory factor (rhLIF) produced by Escherichia coli was administered subcutaneously (sc) to rhesus monkeys at doses of 2, 10, and 50 micrograms/kg body weight/d for 14 days to assess its biologic activities in vivo. Serum levels of positively regulated acute phase proteins (APP) (C-reactive protein, alpha 1-antitrypsin, haptoglobin, and ceruloplasmin) were increased, whereas the negatively regulated APP prealbumin decreased in response to rhLIF treatment. During the second week of treatment, blood platelet counts began to increase, resulting in a maximum of a twofold increase above normal levels a week after termination of the rhLIF treatment. No changes were seen in total and differential white blood cell counts in blood progenitor levels and in red blood cell numbers. The low- and medium-dose rhLIF treatments were tolerated without significant side effects. The animals treated with the high dose showed a reduction in body weight of approximately 10%. In conclusion, rhLIF was shown to stimulate APP and to increase the number of platelets in circulation in nonhuman primates.

摘要

将大肠杆菌产生的重组人白血病抑制因子(rhLIF)以2、10和50微克/千克体重/天的剂量皮下注射给恒河猴,持续14天,以评估其体内生物活性。阳性调节的急性期蛋白(APP)(C反应蛋白、α1抗胰蛋白酶、触珠蛋白和铜蓝蛋白)的血清水平升高,而阴性调节的APP前白蛋白则因rhLIF治疗而降低。在治疗的第二周,血小板计数开始增加,在rhLIF治疗终止一周后,最高比正常水平增加两倍。血液祖细胞水平的总白细胞计数和分类白细胞计数以及红细胞数量均未见变化。低剂量和中剂量的rhLIF治疗耐受性良好,无明显副作用。高剂量治疗的动物体重减轻了约10%。总之,rhLIF被证明能刺激APP并增加非人类灵长类动物循环中的血小板数量。

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