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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 67 (1989), S. 1058-1060 
    ISSN: 1432-1440
    Keywords: Hyperuricemia ; Irtemazole ; Pharmacokinetics ; Uricosuric agents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A single 50 mg dose of irtemazole was given orally to ten healthy male volunteers. The onset of effects was tested. Plasma uric acid began to decrease 15 to 25 min after irtemazole was administrated. Renal uric acid excretion and uric acid clearance increased 10 to 20 min after drug administration. Maximal renal uric acid excretion (mean 197.4 mg/h) and maximal uric acid clearance (mean 78.4 ml/min) were reached after 15 to 55 min. No side effects were observed. The effects of irtemazole occur earlier than those of benzbromarone. The therapeutic effects of long-term therapy remain to be investigated.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1440
    Keywords: Human immunodeficiency virus infection ; Neopterin ; Beta2-microglobulin ; Cerebrospinal fluid ; Cerebral toxoplasmosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Elevated cerebrospinal fluid (CSF) levels of neopterin and beta2-microglobulin (\2MG) reflect activation of the cellular immune response in the central nervous system (CNS). In 118 consecutive subjects [15 controls and 103 patients with human immunodeficiency virus (HIV) infection classified according to the Walter Reed staging system (WR)], neopterin and β2MG were determined in paired samples of CSF and serum. The permeability of the blood-CSF barrier and local release of neopterin and β2MG were taken into account: The molecular weight and diameter were used to determine filtration at the blood-CSF barrier. CSF neopterin levels were increased in all stages of HIV infection. β2MG levels were elevated in WR2 and later stages. Neopterin, β2MG, and cell counts similarly showed peaks in WR2, as did neopterin and β2MG also in the later stages WR5 and WR6. Neurologically asymptomatic patients exhibited higher neopterin CSF levels than did controls (12.67 ± 11.6 vs. 2.34 ± 1.05 nmol/l, P 〈 0.001) and higher CSF β2MG (2.12 ± 1.25 vs. 1.3 ± 0.37 mg/l, P=0.001). Patients with HIV encephalopathy had higher levels of β2MG (3.75 ± 1.83 mg/1) than asymptomatic patients (P 〈 0.01). CSF levels of neopterin were markedly different in patients with HIV encephalopathy and toxoplasmosis (P 〈 0.01). A high quantity of local release of the markers neopterin and β2MG may reflect HIV infection of the CNS in early and late stages and additional release upon opportunistic infections.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 70 (1992), S. 1089-1091 
    ISSN: 1432-1440
    Keywords: HIV ; Pneumocystis carinii ; Prophylaxis ; Pentamidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The optimal dosage of pentamidine for prophylaxis of Pneumocystis carinii pneumonia (PcP) is unknown. We assessed the effects of 300 mg pentamidine inhaled every 2 weeks. Salbutamol was added for prevention of bronchoconstriction. A total of 128 consecutive HIV patients were enrolled, 21 of whom were excluded within 8 weeks; the remaining 107 patients, 66 on primary and 41 on secondary prophylaxis, were treated for 39 weeks (median; range 8–133). Two patients developed PcP. Side effects occurred in only 14 of 5082 inhalations. Three patients developed hypoglycemia after inhalations. Blood glucose levels determined in 34 patients before and after inhalation revealed a decline from 89 ± 23 mg/dl to 79 ±23 mg/dl (P 〈 0.005). A randomized prospective trial is necessary to evaluate the efficacy of 300 mg pentamidine inhaled every 4 or 2 weeks.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 38 (1990), S. 489-491 
    ISSN: 1432-1041
    Keywords: irtemazole ; dose-response relationship ; pharmacokinetics ; uricosuric drugs ; healthy volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Irtemazole 12.5 to 50 mg in 6 healthy, normouricaemic subjects caused a maximal decrease in plasma uric acid (after 8 to 12 h) of 46.5%. The uricosuric effect began during the first 60 min after drug administration and it lasted for 7 to 24 h. Renal uric acid excretion returned to its base line value after 8 to 16 h and uric acid clearance after 10.0 to 12.0 h. Doses of irtemazole between 12.5 and 37.5 mg produced a dose-related rise in the uricosuric effect. There was no essential difference between the uricosuric effect of 37.5 mg and 50 mg irtemazole. The D50 dose (that producing a half-maximal effect) was between 16.3 mg and 34.2 mg, (average 24.7 mg). The value of irtemazole in the management of hyperuricaemia and gout remains to be determined.
    Type of Medium: Electronic Resource
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