Anti-Transferrin monoclonal antibody, clone 13B7

Objectives Caffeine is extensively consumed as a psychostimulant drug, acting on A(1)and A(2A)adenosine receptors blockade. Chronic exposure to caffeine during gestation and breast-feeding may be involved in infant rat's behavioral and biochemical alterations. Our goal was to evaluate the effect of chronic caffeine exposure during gestation and breast-feeding in the functionality of adenosine A(1)receptors in infant rats at P14. NTPDase and 5'-nucleotidase activities were also evaluated. Methods Mating of adult female Wistar rats was confirmed by presence of sperm in vaginal smears. Rats were divided into three groups on the first day of pregnancy: (1) control: tap water, (2) caffeine: 0.3 g/L until P14, and (3) washout caffeine: caffeine was changed to tap water at P7. Evaluation of nociceptive response was performed at P14 using hot plate (HP) and tail-flick latency (TFL) tests. A(1)receptor involvement was assessed using caffeine agonist (CPA) and antagonist (DPCPX). Enzymatic activities assays were conducted in the spinal cord. Results Gestational and breastfeeding exposure to caffeine (caffeine and washout groups) did not induce significant alterations in thermal nociceptive thresholds (HP and TF tests). Both caffeine groups did not show analgesic response induced by CPA when compared to the control group at P14, indicating chronic exposure to caffeine in the aforementioned periods inhibits the antinociceptive effects of the systemic A(1)receptor agonist administration. No effect was observed upon ectonucleotidase activities. Conclusions Our results demonstrate that chronic caffeine exposure in gestational and breastfeeding alters A1-mediated analgesic response in rats.

Objectives The aim of this study was to compare the push-out bond strength (POBS) of three calcium silicate-based cements (CSBC) after exposure to saline, sodium hypochlorite (NaOCl), ethylenediaminetetraacetic acid (EDTA), and a mixture of NaOCl and etidronic acid (NaOCl+HEBP) in simulated perforation. Materials and methods A total of 180 dentin slices were perforated and then filled with either Biodentine (BD), ProRoot MTA (PMTA), or Total Fill (TF). After 1 week, specimens in each group were divided into 4 subgroups (n = 15) according to the root canal irrigant (RCI) that their coronal surface was exposed to: saline, 5.25% NaOCl, 17% EDTA, or a mixture of 5.25% NaOCl and 9% HEBP (NaOCl+HEBP). A push-out test was performed, and the failure pattern was assessed. POBS data were analyzed with ANOVA and Tukey post hoc tests and the failure patterns with chi-square test. Results No differences were found when comparing the effect of RCI on the POBS of PMTA. BD showed significantly higher POBS values after exposure to NaOCl+HEBP (p < .05), and those of TF were significantly lower after exposure to EDTA (p < .05). No differences in the failure patterns were found among groups. Conclusion NaOCl+HEBP had no detrimental effect on the POBS of CSBC.