首页> 外文期刊>Arzneimittel-Forschung: =Drug Research >Investigation of serum minimal inhibitory concentrations of some benzimidazole, imidazole and benzothiazole derivatives and their effects on liver and renal functions.
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Investigation of serum minimal inhibitory concentrations of some benzimidazole, imidazole and benzothiazole derivatives and their effects on liver and renal functions.

机译:研究某些苯并咪唑,咪唑和苯并噻唑衍生物的血清最低抑菌浓度及其对肝肾功能的影响。

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摘要

In previous studies many benzimidazole, imidazole and benzothiazole derivatives had been synthesized and their antimicrobial activities were tested in vitro conditions. Four of these compounds showed minimal inhibitory concentrations (MIC) of 5-25 micrograms/ml against standard strains and clinical isolates. In order to determine whether these four compounds can be used for therapeutic purpose, their serum MIC values and side effects on hepatic and renal functions were determined. Different concentrations of the compounds were tested on Wistar rats. Compound 1 was administered orally, intramuscularly and intravenously; compounds 2, 3 and 4 were given orally and intramuscularly. Blood samples were taken 4 and 24 h after administration of the compounds. Serum MIC values were investigated by bioassay and serum levels of biochemical parameters by autoanalyzer. None of the tested compounds showed antimicrobial activity at their serum concentrations. Although creatinine activity was found at normal levels in all experiments, compounds 1 and 2 caused a significant increase in blood urea nitrogen (BUN) level. The values of aspartate aminotransferase and/or alanine aminotransferase and/or alkaline phosphatase which are characteristic for liver function were generally found at high levels. According to these results, it can be concluded that the tested compounds caused damage in liver and biliary tracts without antimicrobial activity by their serum concentrations.
机译:在以前的研究中,已经合成了许多苯并咪唑,咪唑和苯并噻唑衍生物,并在体外条件下测试了它们的抗菌活性。这些化合物中有四种对标准菌株和临床分离株的最小抑菌浓度(MIC)为5-25微克/毫升。为了确定这四种化合物是否可用于治疗目的,测定了它们的血清MIC值以及对肝和肾功能的副作用。在Wistar大鼠上测试了不同浓度的化合物。化合物1经口服,肌内和静脉内给药。化合物2、3和4口服和肌肉注射。化合物给药后4和24小时采集血样。通过生物测定研究血清MIC值,通过自动分析仪研究血清生化参数水平。所测试的化合物均未在其血清浓度下显示出抗菌活性。尽管在所有实验中均发现肌酐活性处于正常水平,但化合物1和2导致血尿素氮(BUN)水平显着增加。通常发现高水平的肝功能特征的天冬氨酸转氨酶和/或丙氨酸转氨酶和/或碱性磷酸酶。根据这些结果,可以得出结论,受试化合物通过其血清浓度引起肝和胆道损害而无抗微生物活性。

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