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  • 1
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Both short-term and long-term effects of the β-sympathomimetic drugs isoprenaline and terbutaline on the urinary excretion of histamine and its two main metabolites were evaluated in patients with systemic mastocytosis. In a short-term study isoprenaline and terbutaline were given intravenously during five hours to three and two patients, respectively. Compared with placebo infusion Nt-methyl-histamine excretion fell during terbutaline administration, whereas during isoprenaline no changes were observed. In a long-term study three patients received a treatment with orally administered terbutaline for 24 days. In one patient a slight reduction of the excretion of the histamine metabolites was found. In another patient the excretion of histamine and its metabolites, decreased especially during the eight days observation period after the end of the treatment. In this study we saw occasionally large and rapid changes occurring simultaneously in all three urinary parameters of histamine release. In conclusion, terbutaline can reduce histamine release in systemic mastocytosis. However, because of the small symptomatic and biochemical effects found in our patients, the clinical significance of β-sympathomimetic drug treatment in this disease has yet to be established.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Type 1 (insulin-dependent) diabetes mellitus ; evening primrose oil ; fatty acids ; α-tocopherol ; erythropoiesis ; platelet function
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In addition to their usual diet, nine Type 1 (insulin-dependent) diabetic men and ten male control subjects took 20 g d,ga-tocopheryl acetate enriched evening primrose oil (14.45 g 18∶2c,ω6, 1.73g 18∶3c,ω6, 400 mg d,α-tocopheryl acetate) daily for one week. At start, diabetic patients had more 14∶0, 15∶0 and 18∶ 2c,ω6, and less 16∶0, 16∶1c,ω7, 18∶1c,ω7, 18∶3c,ω6, 20∶3c,ω9, 20∶3c,ω6, 20∶4c,ω6 and 22∶6c,ω3 in plasma, erythrocytes and/or platelets. Furthermore, they had lower 16∶1c,ω7/16∶0, 18∶1c,ω7/16∶0, and 20∶4c,ω6/20∶3c,ω6 ratios and a higher 20∶3c,ω6/18∶3c,ω6 ratio. In diabetic patients, α-tocopherol levels in erythrocytes were lower, whereas those in plasma were normal. In both groups, oil intake changed fatty acid profiles. Most markedly, 20∶3c,ω6 increased, whereas the ratios 20∶3c,ω6/ 18∶3c,ω6 and 20∶4c,ω6/20∶3c,ω6 decreased. 20∶4c,ω6 increased in control subjects, but not in diabetic patients. Erythrocytes and platelets responded differently in their fatty acid profiles, α-tocopherol rose in plasma and, although less for diabetic patients, in erythrocytes. In diabetic patients as well as in control subjects, erythrocyte count, haemoglobin level, mean corpuscular haemoglobin content and concentration increased and glycosylated haemoglobin percentage decreased without an apparent decline in blood glucose levels. Plasma β-thromboglobulin and platelet factor 4 decreased, especially in diabetic patients. In conclusion, diabetic patients had abnormal fatty acid patterns, suggesting an impaired Δ 9, Δ 6 and Δ 5 desaturation and an enhanced chainelongation, and had lower erythrocyte a-tocopherol levels; and short-term high dose intake of evening primrose oil increased 20∶3c,ω6 in both groups, but 20∶4c,ω6 only in control subjects, gave fatty acid responses which were different for erythrocytes and platelets, enhanced erythropoiesis, and lowered indices of in vivo platelet activation.
    Type of Medium: Electronic Resource
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