These findings provide evidence for the mechanisms by which HSYA maintains EC survival under hypoxia.”
“Background. Deferoxamine mesylate is known to ameliorate tissue ischemia reperfusion injury. This study

was designed to explore the impact of deferoxamine mesylate preconditioning (DMP) on pancreatic tissue and its possible effects during orthotopic liver autotransplantation.\n\nMethods. A modified orthotopic liver autotransplantation model was used to simulate pancreatic ischemia reperfusion injury. Sprague-Dawley rats (0.25-0.30 kg) were randomly GANT61 divided into normal control, autotransplantation (AT), systemic deferoxamine mesylate preconditioning (SDMP), and partial deferoxamine mesylate conditioning (PDMC) groups. The SDMP group was injected with deferoxamine mesylate (75-90 mg; 300 mg/kg),

Ulixertinib via the celiac artery at 24 and 48 hours before surgery. During surgery, the PDMC group underwent liver perfusion by means of deferoxamine mesylate solution (20 ml; 0.6 mmol/L) rather than Ringer’s lactate solution, with no prior preconditioning. At 6, 24, and 48 hours after surgery, the rats were sacrificed to sample their pancreatic tissues for the expression of hypoxia-inducible factor-1 alpha (HIF-1 alpha) and malondialdehyde (MDA) content. The samples were subjected to blood chemistry analyses, light and transmission electron microscopic morphological studies, and quantitative measurement of HIF-1 alpha expression.\n\nResults. The serum levels

of amylase, lipase, and MDA in SDMP and PDMC groups were significantly lower than those in the AT group at 6, 24, and 48 hours after orthotopic liver autotransplantation (P < .05). Light and electron microscopic analyses showed much more severe pancreatic injury in the autotransplantation than in the SDMP and PDMC groups. The HIF-1 alpha expression was increased in the SDMP and PDMC groups more than in the autotransplantation group (P < .05).\n\nConclusions. Deferoxamine mesylate preconditioning protected pancreatic tissue in orthotopic liver autotransplantation GM6001 in rats. Inhibition of oxidative toxic reactions and up-regulated expression of HIF-1 alpha protein are possible mechanisms.”
“Evaluating the biomedical literature and health-related websites for quality are challenging information retrieval tasks. Current commonly used methods include impact factor for journals, PubMed’s clinical query filters and machine learning-based filter models for articles, and PageRank for websites. Previous work has focused on the average performance of these methods without considering the topic, and it is unknown how performance varies for specific topics or focused searches. Clinicians, researchers, and users should be aware when expected performance is not achieved for specific topics. The present work analyzes the behavior of these methods for a variety of topics.