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1.
World Allergy Organ J ; 10(1): 3, 2017.
Article in English | MEDLINE | ID: mdl-28232856

ABSTRACT

BACKGROUND: Galacto-oligosaccharides (GOS) are prebiotics added to commercial milk formula of infants and mothers. In recent years, cases of allergy related to GOS in atopic children have been reported in the South East Asian region. CASE PRESENTATIONS: We describe a series of pregnant (n = 4) and lactating mothers (n = 2) who developed anaphylactic reactions after consumption of maternal milk formula containing GOS. All six subjects had pre-existing atopy and a positive skin prick test to GOS and 5/5 of the subjects who were tested had positive basophil activation tests to GOS. All of the mothers and their babies had normal neonatal outcomes after the reactions. CONCLUSIONS: The supplementation of GOS into milk and beverages in the Asian region should take into account the rare chance of allergenicity of GOS in the atopic population.

2.
Allergol Immunopathol (Madr) ; 39(5): 291-4, 2011.
Article in English | MEDLINE | ID: mdl-21272988

ABSTRACT

BACKGROUND: Studies on serum IgE levels during pregnancy are limited. OBJECTIVE: To investigate the course of serum total IgE levels during pregnancy and postpartum. METHODS: 159 pregnant subjects provided 218 serum samples during various stages of pregnancy and the postpartum period. Serum total IgE geometric means were compared at various trimesters and postpartum. In addition, the postpartum IgE data were analysed according to the method of delivery. Analysis was also done according to history of allergy. RESULTS: The geometric mean serum total IgE was 20.5 IU/ml in the first trimester, 20.8 IU/ml in the second and 22.2 IU/ml in the third. Postpartum serum IgE level showed a lower mean, 14.9 IU/ml during the early postpartum period (less than 30 days) compared to 30.3 IU/ml during the late postpartum period (30 days-25 weeks). However this was not statistically significant. Serum IgE in the postpartum period also did not differ according to method of delivery. A history of allergy was positive in 98 samples, negative in 61 and unclear in 59. Using analysis of variance, none of these three groups showed significant change in serum total IgE level during pregnancy or postpartum. CONCLUSION: In this cross-sectional study, serum total IgE levels showed no statistically significant changes during pregnancy or postpartum. This finding would be of greater weight if reproduced in a larger number of subjects with multiple serial samples at fixed regular time intervals during pregnancy and postpartum.


Subject(s)
Immunoglobulin E/blood , Postpartum Period/blood , Pregnancy Complications/blood , Adolescent , Adult , Cross-Sectional Studies , Delivery, Obstetric , Female , Humans , Postpartum Period/immunology , Pregnancy , Pregnancy Complications/immunology , Pregnancy Trimesters , Young Adult
3.
J Med Chem ; 44(1): 78-93, 2001 Jan 04.
Article in English | MEDLINE | ID: mdl-11141091

ABSTRACT

Database searching and compound screening identified 1-benzyl-3-(3-dimethylaminopropyloxy)indazole (benzydamine, 3) as a potent activator of the nitric oxide receptor, soluble guanylate cyclase. A comprehensive structure-activity relationship study surrounding 3 clearly showed that the indazole C-3 dimethylaminopropyloxy substituent was critical for enzyme activity. However replacement of the indazole ring of 3 by appropriately substituted pyrazoles maintained enzyme activity. Compounds were evaluated for inhibition of platelet aggregation and showed a general lipophilicity requirement. Aryl-substituted pyrazoles 32, 34, and 43 demonstrated potent activation of soluble guanylate cyclase and potent inhibition of platelet aggregation. Pharmacokinetic studies in rats showed that compound 32 exhibits modest oral bioavailability (12%). Furthermore 32 has an excellent selectivity profile notably showing no significant inhibition of phosphodiesterases or nitric oxide synthases.


Subject(s)
Guanylate Cyclase/metabolism , Indazoles/chemical synthesis , Nitric Oxide/metabolism , Pyrazoles/chemical synthesis , Animals , Enzyme Activation , Humans , In Vitro Techniques , Indazoles/chemistry , Indazoles/pharmacokinetics , Indazoles/pharmacology , Male , Platelet Aggregation Inhibitors/chemical synthesis , Platelet Aggregation Inhibitors/chemistry , Platelet Aggregation Inhibitors/pharmacokinetics , Platelet Aggregation Inhibitors/pharmacology , Pyrazoles/chemistry , Pyrazoles/pharmacokinetics , Pyrazoles/pharmacology , Rats , Rats, Sprague-Dawley , Solubility , Structure-Activity Relationship
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