PVN Oxt mRNA levels increased in fluoxetine-treated female mice of both genotypes. The data suggests that the Avpr1b is required to drive the HPA axis response to acute antidepressant treatment and provides further evidence of a sexual dichotomy in the regulation of PVN Avp/Oxt gene expression following antidepressant administration. (C) 2007 Elsevier Ltd. All rights reserved.”
“Objective: Recombinant factor VIIa can decrease postoperative bleeding after cardiac surgery. However, the potential
for recombinant factor VIIa to cause early vascular graft occlusion at the site of new vascular anastomoses has not been fully explored. We hypothesized that recombinant factor VIIa would cause a dose-dependent reduction in vascular STAT inhibitor graft patency in rabbits.
Methods: Reversed end-to-end interpositional vein grafts were sutured into the carotid artery of heparinized rabbits, and then recombinant factor VIIa (300 mu g/kg, 90 mu g/kg, or 20 mu g/kg intravenously) or placebo was administered (n = 16/group). Graft patency was assessed at 24 hours using a vascular ultrasound probe. Factor VII activity levels
were measured using a prothrombin time-based Z-IETD-FMK mouse assay. In different rabbits, the patency of venous end-to-side anastomoses and simple carotid arterial repairs was assessed (recombinant factor VIIa, 300 mu g/kg vs placebo, n = 8/group). Data were analyzed using Fisher’s exact test, t tests, or analysis of variance.
Results: Physiologic variables (activated clotting time, hemoglobin, pH, Pao(2)) and vessel diameter were not different between BX-795 price groups. Vein graft patency was reduced (93.8%, 81.2%, 13.8%, and 6.3%) as factor VII activity levels increased (1.8 +/- 0.4, 4.4 +/- 2.1, 11.8 +/- 4.7, and 23.6 +/- 16.9 U/mL, respectively) with increasing doses of recombinant factor VIIa administered (0, 20, 90, and 300 mu g/kg, respectively, P < .05). Patency in the arterial repairs and end-to-side venous grafts was also reduced in recombinant factor VIIa-treated
rabbits (P < .05 for both).
Conclusions: This study suggests that recombinant factor VIIa is associated with a dose-dependent increase in fresh vascular graft occlusion. Higher doses of recombinant factor VIIa may be associated with increased thrombotic outcomes. (J Thorac Cardiovasc Surg 2011; 142: 418-23)”
“Biosensor research is a rapidly expanding field with an immense market potential spanning a broad spectrum of applications including biomedical diagnostics, environmental monitoring, veterinary and food quality control. Porous silicon (psi) is a nanostructured material poised to take centre stage in the biosensor development effort. This can be ascribed to the ease and speed of fabrication, remarkable optical and morphological properties of the material (including tuneable pore size and porosity), large internal surface area and the versatile surface chemistry.