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2',3'-二脱氧腺苷的体内外抗菌活性

Antibacterial activity of 2',3'-dideoxyadenosine in vivo and in vitro.

作者信息

Beskid G, Eskin B, Cleeland R, Siebelist J, Cappetta A, Hill A D, Geiger R H

出版信息

Antimicrob Agents Chemother. 1981 Mar;19(3):424-8. doi: 10.1128/AAC.19.3.424.

Abstract

2',3'-Dideoxyadenosine (DDA) was shown not only to possess antibacterial activity in vitro against a variety of Enterobacteriaceae, but also to be effective in vivo, DDA was active in experimental mouse infections by the oral route against 5 Salmonella strains, 2 of 3 Arizona strains, 5 of 7 Citrobacter strains, 3 of 8 Klebsiella strains, 3 of 5 Escherichia strains, 1 of 3 Shigella strains, and 3 of 15 Serratia strains at concentrations generally well below the toxic level. Closely related compounds, with the exception of 2',3'-dideoxyinosine, were found to be inactive in vivo, indicating that a high degree of structural specificity was required for activity. The synthesis of deoxyribonucleic acid was inhibited by DDA in those strains susceptible in vitro to DDA, whereas ribonucleic acid and protein syntheses were not affected. The concentration of DDA which inhibited bacterial deoxyribonucleic acid synthesis by 50% was calculated based on the relative rates of deoxyribonucleic acid synthesis in ;the absence and in the presence of DDA. This value correlated well with the minimal inhibitory concentration determined by the in vitro broth dilution assay but not always with in vivo activity determined by the mouse protection test.

摘要

2',3'-二脱氧腺苷(DDA)不仅在体外对多种肠杆菌科细菌具有抗菌活性,而且在体内也有效。DDA通过口服途径对实验小鼠感染的5种沙门氏菌菌株、3种亚利桑那菌菌株中的2种、7种柠檬酸杆菌菌株中的5种、8种克雷伯菌菌株中的3种、5种大肠杆菌菌株中的3种、3种志贺菌菌株中的1种以及15种沙雷菌菌株中的3种具有活性,其浓度通常远低于毒性水平。除2',3'-二脱氧肌苷外,发现密切相关的化合物在体内无活性,这表明活性需要高度的结构特异性。在体外对DDA敏感的菌株中,DDA抑制了脱氧核糖核酸的合成,而核糖核酸和蛋白质合成未受影响。根据在无DDA和有DDA存在时脱氧核糖核酸合成的相对速率,计算出抑制细菌脱氧核糖核酸合成50%的DDA浓度。该值与体外肉汤稀释试验确定的最低抑菌浓度相关性良好,但与小鼠保护试验确定的体内活性并不总是相关。

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Antibacterial activity of 2',3'-dideoxyadenosine in vivo and in vitro.2',3'-二脱氧腺苷的体内外抗菌活性
Antimicrob Agents Chemother. 1981 Mar;19(3):424-8. doi: 10.1128/AAC.19.3.424.

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