[药芪酮茶碱毒性的实验研究(二)]。

M Koleva, N Donchev, B Borov, V Dzharova
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引用次数: 0

摘要

本文描述了在给药后第一个月和第三个月末对动物的肝、肺、心、脾、肠、脑、皮肤、睾丸(卵巢)进行形态学研究的结果。实验以雄性和雌性大鼠312只为实验对象,分为2个系列:I系列-口服剂量为100、300和6 mg/kg, II系列-腹腔剂量为30、75和150 mg/kg。经证实,PP以100mg /kg的口服剂量和30mg /kg的腹腔剂量给药3个月,不会引起所有被检查器官的结构变化。在口服剂量为300 mg/kg和腹腔剂量为75 mg/kg的影响下,在第三个月末出现肝、肺和脾的轻微营养不良变化。并结合药物外周血管扩张剂的药理作用对所得结果进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Experimental research on the toxicity of pharmapentoxifylline (II)].

The results from morphological studies on liver, lung, heart, spleen, intestine, brain, skin, testes (ovaries), obtained in the end of the first and third month of animals, treated with pharmapentoxiphyline (PP), are described. The experiments were carried out on 312 white rats (male and female), divided into 2 series: I series--oral usage of the preparation in doses of 100, 300 and 6 mg/kg, II series--intraperitoneal administration in doses of 30, 75 and 150 mg/kg. It was established that PP, administered for a period of 3 months orally in a dose of 100 mg/kg and intraperitoneally in a dose of 30 mg/kg did not induced changes in the structure of all examined organs. Slight dystrophic changes in liver, lung and spleen occurred in the end of the third month under the influence of an oral dose of 300 mg/kg and an intraperitoneal dose of 75 mg/kg. The obtained results are discussed in connection with the pharmacological action of drug-peripheral vasodilatator.

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