“
“delta-Elemene, an antitumor component, is a chemical compound isolated from Curcuma wenyujin, a Chinese traditional herb. We examined whether delta-elemene could affect apoptosis in human lung carcinoma mucoepidermoid NCI-11292 cells, and test whether and how the over-expression of B-cell lymphoma-2 (Bcl-2) and B-cell lymphoma extra large (Bcl-xL) could off-set the effect of delta-elemene on cell growth. The result demonstrated that delta-elemene

significantly induced apoptosis of NCI-H292, as shown by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium selleck bromide (MTT) assay, DNA fragmentation measurement, Annexin V (AnV) binding of externalized phosphatidylserine and the mitochondrial probe JC-1 using flow cytometry. Treatment of NCI-H292 with delta-elemene increased both p38 mitogen-activated protein kinase (MAPK) and inducible nitric oxide synthese (iNOS) levels, suggesting these two molecules maybe relate learn more to the apoptotic effect of delta-elemene. The cells with Bcl-2 or Bcl-xL over-expression showed an elevation of nuclear factor kappa B (NF-kappa B) activity, accompanying a significant reduction of delta-elemene-induced apoptosis. Furthermore, inhibition of NF-kappa B by IkB alpha SR, which is a powerful inhibitor of NF-kappa

B, restored the ability of delta-elemene to induce apoptosis in the cells transfected with Bcl-2. These data strongly indicated that the apoptotic effect of delta-elemene on NCI-H292 was closely associated with the activity of NF-kappa B, which was up-regulated by Bcl-2 and Bcl-xL. In conclusion, delta-elemene induced apoptosis in NCI-H292 cells. The apoptotic effect of delta-elemene could be significantly offset by over-expression of either Bcl-2 or Bcl-xL. Bcl-2 and Bcl-xL were able to increase the activity of NF-kappa B, which was a known anti-apoptotic molecule in human lung cancer cells.”
“This study explored arterial

remodelling in fetuses growth restricted by hypoxia. Chronically catheterized Momelotinib fetal sheep were made moderately or severely hypoxic by placental embolization for 15 days starting at gestational age 116-118 (term similar to 147 days). Cross-sections of the aorta were analysed for collagen and elastin content using histological procedures, while immunofluorescence was applied to measure markers of vascular smooth muscle cell (VSMC) type. In frozen aortae quantitative PCR was used to measure mRNA levels of extracellular matrix (ECM) precursor proteins as well as molecular regulators of developmental and pathological remodelling. Relative to Control (n = 6), aortic wall thickness was increased by 23% in the Moderate group (n = 5) and 33% (P < 0.01) in the Severe group (n = 5). Relative to Control, the Severe group exhibited a 5-fold increase in total collagen content (P < 0.01) that paralleled increases in mRNA levels of procollagen I (P < 0.05) and III and transforming growth factor beta (TGF-beta(1)) (P < 0.05).