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克林霉素对β-内酰胺耐药菌中β-内酰胺酶产生的抑制作用。

Inhibitory effect of clindamycin on production of beta-lactamase in beta-lactam-resistant bacteria.

作者信息

Nishihata T, Kunieda S, Nakahama C, Soejima R

机构信息

Upjohn Tsukuba Research Laboratories, Ibaraki, Japan.

出版信息

Biol Pharm Bull. 1994 May;17(5):715-20. doi: 10.1248/bpb.17.715.

Abstract

The inhibitory effect of clindamycin on beta-lactamase biosynthesis was investigated in beta-lactam resistant bacteria with inducible and/or constitutive production of the enzyme(s). Clinical isolates of Enterobacter cloacae (E. cloacae) and Pseudomonas aeruginosa (P. aeruginosa) were examined. Three strains of each, against which sulbactam at 8 micrograms/ml reduced the minimum inhibitory concentration (MIC) of cefoperazone (CPZ) at least 4 fold, were studied in greater detail. Although clindamycin had no appreciable effect on bacteria growth at concentrations up to 50 micrograms/ml, it suppressed inducible beta-lactamase biosynthesis almost completely at a concentration of 20 micrograms/ml. There was also a significant reduction of constitutive enzyme biosynthesis by clindamycin at 50 micrograms/ml. Thus, it was estimated that a high concentration of clindamycin was required to suppress beta-lactamase biosynthesis in beta-lactamase producing bacteria of the constitutive type.

摘要

在具有诱导性和/或组成型β-内酰胺酶产生的β-内酰胺耐药菌中,研究了克林霉素对β-内酰胺酶生物合成的抑制作用。对阴沟肠杆菌(E. cloacae)和铜绿假单胞菌(P. aeruginosa)的临床分离株进行了检测。对每种细菌的三株菌株进行了更详细的研究,在这些菌株中,8微克/毫升的舒巴坦可使头孢哌酮(CPZ)的最低抑菌浓度(MIC)至少降低4倍。尽管在浓度高达50微克/毫升时,克林霉素对细菌生长没有明显影响,但在浓度为20微克/毫升时,它几乎完全抑制了诱导性β-内酰胺酶的生物合成。在50微克/毫升时,克林霉素也显著降低了组成型酶的生物合成。因此,据估计,在组成型产β-内酰胺酶的细菌中,需要高浓度的克林霉素来抑制β-内酰胺酶的生物合成。

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