005). Mouse droppings were not associated with detection of Mus m1. Conclusion. – The prevalence of mouse allergen was substantial but their levels were most often very low. Mus m1 does not appear a major risk factor for asthma morbidity in PACA region. (C) 2014 Published by Elsevier Masson SAS.”
“The radiosensitizing effects of naturally occurring triterpenes were investigated
in human lung cancer cells. Several quinone methide-containing triterpenes (QMTs) enhanced the cytotoxic effect of Autophagy inhibitor ic50 ionizing radiation (IR) and of these QMTs, celastrol (CE) had the greatest enhancing effect on IR-induced cell death in vitro. Additionally, the quinone methide moiety of CE was shown to be essential for CE-mediated radiosensitization; in contrast, dihydrocelastrol (DHCE), does not contain this moiety. Reactive oxygen species (ROS) production by IR was augmented in combination with CE, which was responsible for CE-mediated radiosensitization. CE induced the thiol reactivity and inhibited the activities of antioxidant molecules, such as thioredoxin reductase and glutathione. In vivo, nude mouse xenografting data also revealed that tumor growth delay was greater in mice treated with CE plus IR, compared with those treated with CE or IR alone. When DHCE, instead
selleck compound of CE, was combined with IR, tumor growth delay was similar to that in IR alone-treated mice. These results demonstrate that CE synergistically enhances the effects of IR and suggest the novel anticancer therapeutic use of CE in combination with radiation therapy. (C) 2011 Elsevier DZNeP mw Ireland Ltd. All rights reserved.”
“Objectives Because a newly described salt-inducible kinase 1 (SIK1) network is responsible for increases in active cell sodium transport in response to
elevated intracellular sodium, we hypothesized that this network could mediate the effects of the mutant (hypertensive) form of alpha-adducin on Na(+),K(+)-ATPase activity.\n\nMethods Studies were performed in normotensive and hypertensive Milan rats and in a cell line of proximal tubule origin expressing transiently variants of alpha-adducin (human G460W/S586C;rat F316Y) that are associated with elevated blood pressure and result in increased Na(+),K(+)-ATPase activity. Na(+),K(+)-ATPase activity was determined as ouabain-sensitive rubidium transport.\n\nResults SIK1 activity (T182 phosphorylation) was significantly elevated in renal proximal tubule cells from Milan hypertensive rats (carrying a alpha-adducin mutation) when compared with normotensive controls. Similarly, SIK1 activity (T182 phosphorylation) was elevated in a normal renal proximal tubule cell line when transfected with the alpha-adducin variant carrying the human hypertensive mutation. Blocking the SIK1 network using negative mutants as well as different stages of its activation pathway prevented the effects induced by the hypertensive alpha-adducin.