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Bactericidal activity of streptomycin, isoniazid, rifampin, ethambutol, and pyrazinamide alone and in combination against Mycobacterium Tuberculosis.

Log-phase cultures of Mycobacterium tuberculosis in Tween-albumin medium were exposed to streptomycin, isoniazid, rifampin, ethambutol, and pyrazinamide in concentrations in the range likely to be present in serum during treatment of patients. The bactericidal activity of the drugs was measured as the decrease in viable counts at 4 and 7 days. The activity of single drugs was highest for streptomycin and next highest for rifampin and isoniazid, but ethambutol only started to kill after 4 days. When exposed to 2 drugs, bactericidal synergism was found with streptomycin/isoniazid and isoniazid/ethambutol; additivity, with streptomycin/rifampin; indifference, with isoniazid rifampin and streptomycin/ethambutol; and antagonism, with rifampin/ethambutol and isoniazid/pyrazinamide. When cultures were exposed to the 3 drugs, isoniazid, rifampin, and ethambutol, marked antagonism was found between isoniazid and rifampin, whereas the addition of isoniazid or an increase in its concentration increased the bactericidal activity.

Drug Interactions

[Determination of the sensitivity of mycobacteria to pyrazinamide and nicotinamide (author's transl)].

Since pyrazinamide (PZA) has had a come-back in therapy of tuberculosis a simple and reliable method for sensitivity tests has been necessary. A comparison of resistance tests to PZA in acid Löwenstein-Jensen-medium and in fluid medium with those to nicotinamide (NSA) showed a clear superiority of the NSA method, recommended by BRANDER. Also in routine sensitivity tests the use of NSA instead of PZA has stood the test. Another advantage of the method is the possibility to integrate it in the simplified proportion method without any additional work.

Drug Resistance, Microbial

[Absorption and urinary elimination of pyrazinamid administered alone or in combination with isoniazid and rifampicin].

The aim of this work to study the PZA absorption in man its urinary excretion. The PZA was administered alone and in association with INH or/and Rifampicin. The PZA dosage in blood and urine and pyrazinoic acid in urine were performed in a sample of 80 patients divided into 4 groups. PZA dosage was also performed in blood from mice in the same experimental conditions. Our results showed that in man, the titres in serum gave higher peaks when PZA was given alone. Titres were significantly lower when PZA was associated with the two other drugs. The comparative study of PZA seral rates in men and women in one side and mice in the other, showed that the seral concentration was proportional to the body weight. Urinary excretion of Pyrazinamide and pyrazinoic acid showed a relation between the seral concentration and the urinary concentration. However, there was no correlation between the maximum seral concentration and urinary excretion of pyrazinoic acid.

Adult