The effect of five antibacterial agents on the physiological levels of serum nitric oxide in mice

被引:2
作者
Barsoumian, Hampartsoum [1 ]
El-Rami, Fadi [1 ]
Abdelnoor, Alexander M. [1 ]
机构
[1] Amer Univ Beirut, Fac Med, Dept Microbiol & Immunol, Beirut, Lebanon
关键词
Gentamicin; tobramycin; imipenem; tigecycline; isoniazid; nitric oxide; ESCHERICHIA-COLI; LIPOPOLYSACCHARIDE; RELEASE; ACTIVATION; ANTIBIOTICS; MINOCYCLINE; GENTAMICIN; ENDOTOXIN; BINDING; PROTEIN;
D O I
10.3109/08923973.2011.558095
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In addition to their action on microorganisms, antibacterial agents have been reported to affect host defense mechanisms. Nitric oxide (NO) that is produced by a number of cell types in the innate immune response is bactericidal, but when produced in excessive amounts it could be detrimental to the host. In this study, five antibacterial agents (gentamicin, tobramycin, imipenem, tigecycline, isoniazid) were compared with respect to their ability to affect NO production in mice. Groups of mice were injected with the different antibacterial agents, and at different time intervals post-injection serum NO levels were determined using the Griess reagent. All the antibacterial agents tested showed a significant effect in reducing NO levels in mice. It could be hypothesized that the excessive production of NO in infectious diseases is in most instances suppressed by the antibacterial agent(s) used.
引用
收藏
页码:652 / 655
页数:4
相关论文
共 26 条
[1]  
Al-Shami A. K., 1995, EOS-Rivista di Immunologia ed Immunofarmacologia, V15, P71
[2]   MyD88-dependent and MyD88-independent pathways in synergy, priming, and tolerance between TLR agonists [J].
Bagchi, Aranya ;
Herrup, Elizabeth A. ;
Warren, H. Shaw ;
Trigilio, James ;
Shin, Hae-Sook ;
Valentine, Catherine ;
Hellman, Judith .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :1164-1171
[3]  
BARSOUMIAN H, 2010, ADV BIOSCIENCE BIOTE, V1, P61
[4]   IN-VITRO ACTIVITY OF TOBRAMYCIN AND GENTAMICIN [J].
BRITT, MR ;
WILFERT, JN ;
SMITH, CB ;
GARIBALDI, RA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1972, 2 (03) :236-+
[5]   The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit [J].
Brodersen, DE ;
Clemons, WM ;
Carter, AP ;
Morgan-Warren, RJ ;
Wimberly, BT ;
Ramakrishnan, V .
CELL, 2000, 103 (07) :1143-1154
[6]   Doxycycline reduces lipopolysaccharide-induced inflammatory mediator secretion in macrophage and ex vivo human whole blood models [J].
Cazalis, Julia ;
Bodet, Charles ;
Gagnon, Guy ;
Grenier, Daniel .
JOURNAL OF PERIODONTOLOGY, 2008, 79 (09) :1762-1768
[7]   PHYSIOLOGICAL IMPORTANCE OF NITRIC-OXIDE [J].
COLLIER, J ;
VALLANCE, P .
BRITISH MEDICAL JOURNAL, 1991, 302 (6788) :1289-1290
[8]   The influence of antibiotic-induced filament formation on the release of endotoxin from Gram-negative bacteria [J].
Dofferhoff, ASM ;
Buys, J .
JOURNAL OF ENDOTOXIN RESEARCH, 1996, 3 (03) :187-194
[9]   Folimycin (concanamycin A) inhibits LPS-induced nitric oxide production and reduces surface localization of TLR4 in murine macrophages [J].
Eswarappa, Sandeepa M. ;
Basu, Nirmalya ;
Joy, Omana ;
Chakravortty, Dipshikha .
INNATE IMMUNITY, 2008, 14 (01) :13-24
[10]   Crucial role of interferon consensus sequence binding protein, but neither of interferon regulatory factor 1 nor of nitric oxide synthesis for protection against murine listeriosis [J].
Fehr, T ;
Schoedon, G ;
Odermatt, B ;
Holtschke, T ;
Schneemann, M ;
Bachmann, MF ;
Mak, TW ;
Horak, I ;
Zinkernagel, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (05) :921-931