抗组胺药物对肺炎克雷伯菌抗生素疗效的调节作用

T. El-Banna, F. Sonbol, A. A. El-Aziz, Omnia Momtaz Al-Fakharany
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引用次数: 11

摘要

抗组胺药广泛应用于微生物感染的各种适应症。因此,本文研究了7种新旧两代抗组胺药对多重耐药肺炎克雷伯菌的抑菌活性。用琼脂稀释法测定了这些药物对30株多重耐药肺炎克雷伯菌的抑菌活性。异丙嗪、赛庚啶两种药物对肺炎克雷伯菌的抑菌活性均在400 ~ 1000 μg/ml之间(远高于其生物学水平)。而其他被试药物在试验条件下无体外抗菌活性。对不同抗生素对多重耐药肺炎克雷伯菌的相互作用进行了调查,发现大环内酯类药物、氨基糖苷类药物和喹诺酮类药物联用时协同作用主要,尤其是与异丙嗪、赛庚啶、西替利嗪和苯海拉明联用。还研究了被试药物对被试菌株抗生素外排的影响。在100 μg/ml浓度下,异丙嗪和赛庚啶是最有效的外排泵抑制剂。通过研究被测药物对肺炎克雷伯菌生物膜形成的影响,发现异丙嗪是最有效的生物膜形成抑制剂。以浓度依赖的方式减少肺炎克雷伯菌的生物膜形成,并在浓度为100 μg/ml时阻止生物膜的形成。在本研究中发现,使用100 μg/ml氯苯那敏可使肺炎克雷伯菌细胞由单独的棒状转化为长丝状。透射电子显微镜证实了这一点,记录了没有分离的隔膜形成。综上所述,本研究结果表明,在被试药物中,异丙嗪和赛庚啶对MDR肺炎克雷伯菌具有较高的抗菌活性。因此,有可能利用所获得的发现来引入克服不同传染病的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of Antibiotic Efficacy against Klebsiella pneumoniae byAntihistaminic Drugs
Antihistaminic drugs are widely used for various indications during microbial infection. Hence, this paper has investigated the antibacterial activity of seven antihistaminic drugs belonging to both old and new generations against multiresistant K. pneumonia isolates. The bacteriostatic activity of these tested drugs was investigated by determining their MIC by agar dilution technique against thirty multiresistant K. pneumoniae isolates. Two drugs namely promethazine, cyproheptadine showed antibacterial activity against the tested K. pneumoniae isolates with MIC values rangining from 400-1000 μg/ml (far more than their biological levels). In contrast, other tested drugs showed no in-vitro antibacterial activity under the conditions of test. Investigation of the interaction between the tested drugs and different antibiotics against multiresistant K. pneumoniae isolates revealed that synergism was major in case of combination with macrolides, aminoglycosides and quinolones especially with promethazine, cyproheptadine, cetirizine and diphenhydramine. The effect of tested drugs on antibiotic efflux by the tested isolates was also investigated. It was observed that promethazine and cyproheptadine were the most effective efflux pump inhibitor at a concentration of 100 μg/ml. Upon studying the effect of tested drugs on biofilm formation by K. pneumoniae, it was found that promethazine was the most effective inhibitor of biofilm formation. It reduced biofilm formation by K. pneumoniae in a concentration-dependent manner and prevented biofilm formation at a concentration of 100 μg/ml. In the present study, it was found that the use of 100 μg/ml chlorpheniramine resulted in the conversion of separate rod shape of K. pneumoniae cells into long filaments. This was confirmed by transmission electron microscope where septum formation with no separation was recorded. In conclusion, the data obtained in this work showed that, among the tested drugs promethazine and cyproheptadine exerted high antibacterial activity against MDR K. pneumoniae isolates. So, it is possible to take the advantages of the obtained findings to introduce new ways to overcome different infectious diseases.
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