Cellular effects induced by some synthetic prostaglandins obtained at ICCF-Bucharest.

Romanian journal of virology Pub Date : 1997-01-01
A Pleşa, F Cocu, R Repanovici
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引用次数: 0

Abstract

Four prostaglandin compounds synthetized at ICCF [chloprostenol triacetate (a), the isopropylic ester of the chloprostenol analogue (b), a PGA2 sulprostone analogue (c) and a PGE2 analogue (d)] were tested with respect to the cytotoxic effect, by successive studies on chicken embryo fibroblasts (CEF) and on human cells (HeLa). It was established that (b) and (d) display a high cytotoxicity, while (a) and (c) were relatively well tolerated by the cell layer. The spectrofluorometric determinations showed that these drugs did not induce modifications at the cell membrane level. The treatment with 4 micrograms/ml PGs (a) and (c) of HeLa cells inoculated with Sendai virus produced a significant decrease of TCID50/ml 24 hrs after drug introduction into the culture medium, from 10(6.5) to 10(4.5) and to 10(3.25), respectively.

在ICCF-Bucharest获得的一些合成前列腺素诱导的细胞效应。
通过对鸡胚成纤维细胞(CEF)和人细胞(HeLa)的连续研究,研究了在ICCF合成的四种前列腺素化合物[氯前列腺醇三醋酸酯(a),氯前列腺醇类似物的异丙酯(b), PGA2磺胺酮类似物(c)和PGE2类似物(d)]对细胞毒性的影响。(b)和(d)表现出较高的细胞毒性,而(a)和(c)对细胞层的耐受性相对较好。荧光光谱测定表明,这些药物在细胞膜水平上没有引起修饰。4微克/ml pg (a)和4微克/ml pg (c)处理仙台病毒接种的HeLa细胞,在药物进入培养基24小时后,TCID50/ml显著降低,分别从10(6.5)降至10(4.5)和10(3.25)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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