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亚胺培南对临床分离细菌的体外及体内抗菌活性

In-vitro and in-vivo antibacterial activity of imipenem against clinical isolates of bacteria.

作者信息

Mitsuhashi S

出版信息

J Antimicrob Chemother. 1983 Dec;12 Suppl D:53-64. doi: 10.1093/jac/12.suppl_d.53.

Abstract

Imipenem, a derivative of thienamycin, a carbapenem antibiotic, has a broad spectrum of activity against aerobic (Gram-positive and Gram-negative) and anaerobic bacteria. It is quite stable to all tested beta-lactamases produced by various species of bacteria isolated from clinical specimens, whether plasmid or chromosomally mediated. One exception is its hydrolysis by the beta-lactamase produced by Pseudomonas maltophilia which is thus usually resistant to imipenem. Imipenem was found to be hydrolysed by renal dehydropeptidase-I residing on the luminal surface of the renal tubular epithelium. A dehydropeptidase-I inhibitor, cilastatin (MK-0791) was developed with specific inhibitory activity toward the renal dehydropeptidase-I and showed detectable effects in humans.

摘要

亚胺培南是碳青霉烯类抗生素硫霉素的衍生物,对需氧菌(革兰氏阳性菌和革兰氏阴性菌)和厌氧菌具有广谱抗菌活性。对于从临床标本中分离出的各种细菌产生的所有测试β-内酰胺酶,无论是质粒介导还是染色体介导的,它都相当稳定。一个例外是嗜麦芽窄食单胞菌产生的β-内酰胺酶可使其水解,因此该菌通常对亚胺培南耐药。发现亚胺培南可被存在于肾小管上皮腔面的肾脱氢肽酶-I水解。一种脱氢肽酶-I抑制剂西司他丁(MK-0791)被开发出来,它对肾脱氢肽酶-I具有特异性抑制活性,并在人体中显示出可检测到的效果。

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