Clarithromycin is an effective immunomodulator when administered late in experimental pyelonephritis by multidrug-resistant Pseudomonas aeruginosa

被引:19
作者
Giamarellos-Bourboulis, EJ [1 ]
Antonopoulou, A [1 ]
Raftogiannis, M [1 ]
Koutoukas, P [1 ]
Tsaganos, T [1 ]
Tziortzioti, V [1 ]
Panagou, C [1 ]
Adamis, T [1 ]
Giamarellou, H [1 ]
机构
[1] Univ Athens, Sch Med, Dept Internal Med 4, GR-10679 Athens, Greece
关键词
D O I
10.1186/1471-2334-6-31
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: To apply clarithromycin as an immunomodulatory treatment in experimental urosepsis by multidrug-resistant Pseudomonas aeruginosa. Methods: Acute pyelonephritis was induced in 40 rabbits after inoculation of the test isolate in the renal pelvis. Therapy was administered upon signs of sepsis in four groups: A, controls; B, intravenous clarithromycin; C, amikacin; and D, both agents. Survival and vital signs were recorded; blood was sampled for culture and estimation of pro-inflammatory mediators; monocytes were isolated for determination of apoptotic rate and ex vivo TNF alpha secretion. Quantitative cultures and biopsies of organs were performed after death. Results: Increased rectal temperature and oxygen saturation were found in groups B and D compared to A and C. Mean survival of groups A, B, C and D was 2.65, 7.15, 4.25 and 8.70 days respectively. No differences were noted between groups concerning bacterial load in blood and tissues and serum endotoxins. Serum MDA and total caspase-3 activity of monocytes of group D decreased following treatment compared to other groups. Negative correlation was detected between cytoplasmic caspase-3 and ex vivo secretion of TNF alpha of blood monocytes of group A; similar correlation was not found for any other group. Pathology scores of liver and lung of group B were lower than group A. Conclusion: Clarithromycin administered late in experimental urosepsis by multidrug-resistant P. aeruginosa prolonged survival and ameliorated clinical findings. Its effect is probably attributed to immunomodulatory intervention on blood monocytes.
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共 15 条
  • [1] Rapid, fluorimetric-liquid chromatographic determination of malondialdehyde in biological samples
    Agarwal, R
    Chase, SD
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 775 (01): : 121 - 126
  • [2] Immunological therapy of sepsis: experimental therapies
    Arndt, P
    Abraham, E
    [J]. INTENSIVE CARE MEDICINE, 2001, 27 (Suppl 1) : S104 - S115
  • [3] In vitro and in vivo influence of adjunct clarithromycin on the treatment of mucoid Pseudomonas aeruginosa
    Bui, KQ
    Banevicius, MA
    Nightingale, CH
    Quintiliani, R
    Nicolau, DP
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (01) : 57 - 62
  • [4] Anti-inflammatory effects of macrolide antibiotics
    Culic, O
    Erakovic, V
    Parnham, MJ
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 429 (1-3) : 209 - 229
  • [5] Serotype-related differences in inflammatory response to Streptococcus pneumoniae in experimental meningitis
    Engelhard, D
    Pomeranz, S
    Gallily, R
    Strauss, N
    Tuomanen, E
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (04) : 979 - 982
  • [6] Interleukin 8 receptor deficiency confers susceptibility to acute experimental pyelonephritis and may have a human counterpart
    Frendéus, B
    Godaly, G
    Hang, L
    Karpman, D
    Lundstedt, AC
    Svanborg, C
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (06) : 881 - 890
  • [7] Immunomodulatory clarithromycin treatment of experimental sepsis and acute pyelonephritis caused by multidrug-resistant Pseudomonas aeruginosa
    Giamarellos-Bourboulis, EJ
    Adamis, T
    Laoutaris, G
    Sabracos, L
    Koussoulas, V
    Mouktaroudi, M
    Perrea, D
    Karayannacos, PE
    Giamarellou, H
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) : 93 - 99
  • [8] Clarithromycin suppresses lipopolysaccharide-induced interleukin-8 production by human monocytes through AP-1 and NF-κB transcription factors
    Kikuchi, T
    Hagiwara, K
    Honda, Y
    Gomi, K
    Kobayashi, T
    Takahashi, H
    Tokue, Y
    Watanabe, A
    Nukiwa, T
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (05) : 745 - 755
  • [9] 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference
    Levy, MM
    Fink, MP
    Marshall, JC
    Abraham, E
    Angus, D
    Cook, D
    Cohen, J
    Opal, SM
    Vincent, JL
    Ramsay, G
    [J]. CRITICAL CARE MEDICINE, 2003, 31 (04) : 1250 - 1256
  • [10] *NAT COMM CLIN LAB, 2004, PERF STAND ANT S S24, V30