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DQ-2556的体外和体内活性及其作用方式。

In vitro and in vivo activities of DQ-2556 and its mode of action.

作者信息

Tanaka M, Otsuki M, Nishino T

机构信息

Exploratory Research Laboratories I, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Antimicrob Agents Chemother. 1992 Dec;36(12):2595-601. doi: 10.1128/AAC.36.12.2595.

Abstract

DQ-2556 is a recently developed cephalosporin with a broad spectrum of antibacterial activity against both gram-positive and gram-negative bacteria. Its in vitro activity was roughly comparable to those of cefuzonam and cefpirome and greater than those of ceftazidime, cefepime, and cefclidin against gram-positive bacteria. Against gram-negative bacteria, DQ-2556 showed almost the same activity as those shown by cefpirome and cefepime. The activity was largely unaffected by culture medium pH or the addition of human serum. The protective effect of DQ-2556 in experimental gram-positive pathogen and Escherichia coli infections in mice was greater than those of ceftazidime, cefuzonam, cefepime, and cefclidin and was similar to that of cefpirome. Against Pseudomonas aeruginosa and Acinetobacter calcoaceticus infections, DQ-2556 was more active than cefuzonam and had activity similar to or less than those of ceftazidime, cefpirome, cefepime, and cefclidin. When cells of E. coli were exposed to various concentrations of DQ-2556, filamentous cells were observed at concentrations of 0.0008 micrograms/ml and greater, spheroplasts started to form at 0.025 micrograms/ml, and subsequent cell lysis was observed. The affinity of DQ-2556 to PBP 3 of E. coli, which participates in septum formation, as suggested by morphological observation, was two times greater than that of ceftazidime. DQ-2556 also had high affinities for PBPs 1B and 1A of E. coli. These results suggest that DQ-2556 is worthy for subsequent clinical trials.

摘要

DQ - 2556是一种最近研发的头孢菌素,对革兰氏阳性菌和革兰氏阴性菌均具有广谱抗菌活性。其体外活性与头孢唑南和头孢匹罗大致相当,对革兰氏阳性菌的活性大于头孢他啶、头孢吡肟和头孢利定。对于革兰氏阴性菌,DQ - 2556显示出与头孢匹罗和头孢吡肟几乎相同的活性。该活性在很大程度上不受培养基pH值或人血清添加的影响。在小鼠实验性革兰氏阳性病原菌和大肠杆菌感染中,DQ - 2556的保护作用大于头孢他啶、头孢唑南、头孢吡肟和头孢利定,与头孢匹罗相似。对于铜绿假单胞菌和醋酸钙不动杆菌感染,DQ - 2556比头孢唑南更具活性,其活性与头孢他啶、头孢匹罗、头孢吡肟和头孢利定相似或更低。当大肠杆菌细胞暴露于不同浓度的DQ - 2556时,在浓度为0.0008微克/毫升及以上时观察到丝状细胞,在0.025微克/毫升时开始形成原生质球,随后观察到细胞裂解。形态学观察表明,参与隔膜形成的大肠杆菌PBP 3对DQ - 2556的亲和力是头孢他啶的两倍。DQ - 2556对大肠杆菌的PBPs 1B和1A也具有高亲和力。这些结果表明DQ - 2556值得进行后续临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d352/245513/2ff31251794b/aac00045-0050-a.jpg

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