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1.
J Antimicrob Chemother ; 46(3): 391-5, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10980165

RESUMO

Subinhibitory concentrations of bacitracin, vancomycin and other inhibitors of cell wall synthesis reversed to varying extents the intrinsic resistance of Mycobacterium tuberculosis to clarithromycin. Ethambutol reversed clarithromycin resistance in all of the M. tuberculosis strains studied regardless of their susceptibility to this drug.


Assuntos
Antibacterianos/farmacologia , Parede Celular/efeitos dos fármacos , Claritromicina/farmacologia , Mycobacterium tuberculosis/efeitos dos fármacos , Antituberculosos/farmacologia , Parede Celular/metabolismo , Resistência Microbiana a Medicamentos , Sinergismo Farmacológico , Etambutol/farmacologia , Humanos , Testes de Sensibilidade Microbiana , Tuberculose/microbiologia
2.
Int J Antimicrob Agents ; 16(1): 69-71, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11185417

RESUMO

The comparative activity of five phenothiazines against multidrug-resistant strains of Mycobacterium tuberculosis (MDRTB) was studied using the Bactec 460 system. The order of antimycobacterial activity of the phenothiazines was: chlorpromazine = thioridazine > promethazine > promazine = desipramine. However, the levels required for an MIC 50 exceeded 1 mg/l and are beyond those that are clinically achievable. As phenothiazines are concentrated by macrophages that phagocytose and have in situ activity against mycobacteria, these agents may be considered for use as adjuvants for the management of freshly diagnosed tuberculosis in patients from populations with a high prevalence of MDRTB.


Assuntos
Antituberculosos/farmacologia , Mycobacterium tuberculosis/efeitos dos fármacos , Fenotiazinas/farmacologia , Tuberculose Resistente a Múltiplos Medicamentos/microbiologia , Resistência Microbiana a Medicamentos , Resistência a Múltiplos Medicamentos , Humanos , Testes de Sensibilidade Microbiana/métodos , Mycobacterium tuberculosis/crescimento & desenvolvimento
3.
Antimicrob Agents Chemother ; 41(8): 1837-9, 1997 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-9257775

RESUMO

Heterologous mycobactins and the synthetic FR160 [N4-nonyl,N1,N8-bis(2,3-dihydroxybenzoyl) spermidine hydrobromide (C3 0H4 6N3, O6 Br)] promoted growth in Mycobacterium aurum in low concentrations. They were otherwise highly inhibitory, as opposed to homologous mycobactin, which was strictly growth promoting. Desferrioxamine B (Desferal) had no significant effect on growth.


Assuntos
Desferroxamina/farmacologia , Mycobacterium/efeitos dos fármacos , Oxazóis/farmacologia , Sideróforos/farmacologia , Espermidina/análogos & derivados , Divisão Celular/efeitos dos fármacos , Estudos de Avaliação como Assunto , Espermidina/farmacologia , Fatores de Tempo
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