RESUMO
Data regarding the action of monensin on the concentrations of glycerophospholipids and cholesterol in bile of rats subjected to total biliary diversion for 3 h are reported. After monensin their concentration in bile drops significantly in the first 60 min collections with respect to the control. Differences seem to be produced between the rates of transport to the bile of glycerophospholipids and cholesterol, not sufficiently explained by the inhibition of bile salt uptake determined by monensin at the sinusoidal pole of the hepatocyte.
Assuntos
Ductos Biliares/fisiologia , Bile/metabolismo , Colesterol/metabolismo , Monensin/farmacologia , Ácidos Fosfatídicos/metabolismo , Animais , Ductos Biliares/cirurgia , Fístula Biliar , Transporte Biológico/efeitos dos fármacos , Feminino , Cinética , Ratos , Ratos EndogâmicosRESUMO
Retrospective studies have demonstrated that anti-annexin V (anti-AnxV) antibodies are linked to miscarriage. Their predictive value is, however, unknown. We have carried out a prospective study to evaluate the relationship between anti-AnxV antibodies and the pregnancy outcome. A serum sample was taken from 1038 consecutive healthy women at the beginning of pregnancy. IgG and IgM anti-AnxV antibodies were measured by an ELISA method. The cutoff value was set at 5 units for both IgG and IgM. Out of 1038 women, 116 (11.4%) had a miscarriage by the 22nd week; 10 were lost to follow-up, 10 had an induced abortion, 6 had a preterm delivery, and 896 carried their pregnancy through to term. An adverse outcome of the pregnancy proved to be directly related to the number of previous miscarriages (P = .008) and the age of the woman (P = .002). IgG and IgM anti-AnxV were present in 25% and 27% of the women who miscarried, and in 23% and 28% of those who gave birth (mean antibody concentration IgG, 4.2 vs. 4.4 U/mL; IgM, 3.7 vs. 3.5 U/mL). IgG and IgM anticardiolipin and anti-beta(2)GPI, together with antinuclear, antithyroperoxidase, and antithyroglobulin antibodies, were also measured in the 116 sera of the women with miscarriage and in an equal number of women who gave birth. Their positivity or level proved not to be useful in discriminating between the risk of miscarriage and term delivery. This large-scale prospective study demonstrates that the presence of IgG and IgM anti-AnxV antibodies, when measured in healthy women, does not give a positive predictive lead towards the possibility of a miscarriage, and it is not useful in evaluating the risk of miscarriage at the beginning of pregnancy.
Assuntos
Aborto Espontâneo/imunologia , Anexina A5/imunologia , Anticorpos Anti-Idiotípicos/imunologia , Imunoglobulina G/imunologia , Imunoglobulina M/imunologia , Adolescente , Adulto , Anticorpos Anticardiolipina/imunologia , Distribuição de Qui-Quadrado , Ensaio de Imunoadsorção Enzimática , Feminino , Glicoproteínas/imunologia , Humanos , Iodeto Peroxidase/imunologia , Modelos Logísticos , Idade Materna , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Gravidez , Resultado da Gravidez , Estudos Prospectivos , Curva ROC , Tireoglobulina/imunologia , beta 2-Glicoproteína IRESUMO
Reports of a possible correlation between anti-Scl-70 antibody concentration and clinical manifestations in systemic sclerosis patients have recently appeared in the scientific literature. The goal of our study was to evaluate, by means of a multicenter study, the analytical reliability of immunoassay systems in the quantitative measurement of Scl-70 antibodies. Three blind samples (H, M, L) at different anti-Scl-70 antibody concentrations, and a low concentration antibody serum (LPC) used as a common calibrator, were sent three times in a 6-month time span to 39 Italian clinical laboratories. Each laboratory was asked to calculate dosages following the enzyme-linked immunosorbent assay (ELISA) method they used and report the optical density values of each sample (ODs), of the cutoff serum provided by the manufacturer of the kit used (ODco) and of LPC (ODLPC). The overall analytical imprecision (between methods and between laboratories) of the three different determinations of the values respectively expressed in ODs, ODs/ODco and ODs/ODLPCratio was 47.1, 52.8 and 34.0% for sample H, 56.2, 47.4% and 34% for sample M and 84.6, 86.0 and 86.6% for sample L. The average intra-method analytical imprecision was, respectively, 20.7, 29.8 and 18.6% for sample H, 24.6, 26.5 and 19.3% for sample M, and 30.6, 28.1 and 20.2% for sample L. The commercial ELISA methods currently used to determine the presence of anti-Scl-70 autoantibodies show considerable differences in the quantitative determination. The best results for reproducibility analyses have been obtained when the values were expressed as a ratio between the ODs of the sample and of the common calibrator (ODs/ODLPC). Forward-looking clinical studies that can clarify the usefulness of quantitative determination of anti-Scl-70 antibodies in the monitoring of diffuse scleroderma patients can be performed only when standard serum with a known antibody concentration and calibration curves for quantitative ELISA measurements are made available.
Assuntos
Autoanticorpos/análise , Ensaio de Imunoadsorção Enzimática/métodos , Proteínas Nucleares/análise , Doenças Autoimunes/diagnóstico , Doenças Autoimunes/imunologia , Biomarcadores/análise , DNA Topoisomerases Tipo I , Humanos , Itália , Valor Preditivo dos Testes , Kit de Reagentes para Diagnóstico , Reprodutibilidade dos Testes , Estatística como AssuntoRESUMO
Glibenclamide, a second generation sulfonylurea, is an oral hypoglycemic drug. It seems to act mainly on the ATP-driven K(+)- channels of the beta-cells of pancreas determining insulin secretion. Because monensin, a Na+/H+ antiport, is able when administered to rats in vivo to inhibit insulin secretion, the action of glibenclamide is studied on glycemia and insulinemia to verify if it can antagonize the action of monensin. The results show that glibenclamide is able to partly reverse ionophore induced hyperglycemia and the inhibition of insulin secretion. These results might be interpreted as if glibenclamide only reverses the ATP-driven K(+)- channel dependent insulin secretion. Moreover the antagonist action of glibenclamide is slightly delayed when both drugs are administered together. The role of Na+/H+ antiport in basal insulin secretion is discussed.
Assuntos
Glibureto/farmacologia , Insulina/metabolismo , Monensin/antagonistas & inibidores , Animais , Glicemia/efeitos dos fármacos , Feminino , Hiperglicemia/induzido quimicamente , Insulina/sangue , Secreção de Insulina , Monensin/farmacologia , Ratos , Ratos Sprague-DawleyRESUMO
The effect of monensin, an electroneutral ionophore that exchanges Na+ for H+, is investigated on glucose and insulin concentration in serum of female rats. After monensin administration hyperglycemia is observed. Hyperglycemia is concentration and time dependent. In fact serum glucose starts increasing with 0.5 mg/kg b.w. of monensin and increases sharply till 2.5-3.0 mg/kg b.w. The timing of the appearance shows an increase already after few minutes and keeps increasing reaching its maximum between 30-120 minutes. Hyperglycemia is reversed by insulin; if not treated spontaneously it returns to normality in 4-5 hours. An inverse correlation is observed between insulinemia and glycemia. A significant fall in serum insulin concentration can be observed, with or without glucose-stimulation of insulin release, already after five minutes of treatment. Insulinemia returns to normal values after about two hours. The action of monensin on glycemia might therefore be a reversible inhibition of insulin secretion by the beta-cells of the pancreas.
Assuntos
Glicemia/metabolismo , Insulina/sangue , Monensin/farmacologia , Animais , Relação Dose-Resposta a Droga , Feminino , Insulina/metabolismo , Secreção de Insulina , Ratos , Ratos Endogâmicos , Fatores de TempoRESUMO
Bile derived from monensin treated bile-fistula rats has been analysed for bile acids content. Bile flow and bile acids decrease in bile following monensin treatment, in agreement with the disruption of the Na+ gradient determined by the ionophore and necessary for the vectorial Na+-cotransport of taurocholate at the sinusoidal pole of the hepatocyte.
Assuntos
Ácidos e Sais Biliares/metabolismo , Bile/metabolismo , Monensin/farmacologia , Animais , Bile/efeitos dos fármacos , Feminino , Cinética , Ratos , Ratos Endogâmicos , Valores de ReferênciaRESUMO
Growth hormone (GH) and prolactin (PRL) secretion after GH-releasing hormone (GHRH) and domperidone (DOM), an antidopaminergic drug which does not cross the blood-brain barrier (BBB), was evaluated in 8 healthy elderly men (65-91 years) and in 7 young adults (23-40 years). All received in random order at 2-day intervals: GHRH(1-40) (50 micrograms i.v.) bolus, DOM (5 mg/h) infusion, GHRH(1-40) (50 micrograms i.v.) plus DOM (5 mg/h i.v.), saline solution. In elderly men GH increase after GHRH was significantly lower than in young men. DOM alone did not change GH secretion in either of these groups, whereas it increased the GH response to GHRH only in young adults. PRL levels increased in both young and elderly men during both DOM and GHRH plus DOM, but the PRL release was more marked in young than in elderly men. Both integrated secretion of GH after GHRH and of PRL after DOM were inversely correlated to chronological age. Our data show an impairment of GH rise after GHRH and of PRL after DOM in elderly adults. It is also stressed that peripheral blockade of dopamine receptors by DOM is unable to amplify the GH response to GHRH only in elderly men. A reduction in GH release after GHRH might be related to aging, perhaps through a reduction of dopaminergic tonus.