Hypoxic pulmonary vasoconstric tion (HPV) is an important homeostatic mechanism in which increases of [Ca2+] i are primary events. In this study, primary cultured, human pulmonary artery smooth muscle cells (hPASMC) were used to examine the role of TRPC channels in mediating [Ca2+] i elevations during hypoxia. Hypoxia (PO2 about 20 mm Hg) evoked a transient [Ca2+] i elevation that was reduced by removal of extracellular calcium. Nifedipine and verapamil, blockers of vo ltage-gated calcium channels (VGCCs), attenuated th e hypoxia-induced [Ca2+] i elevation by about 30 %, suggesting the presence of alternate Ca2+ entry pathways. Expression of TRPC1 an d TRPC6 in hPASMC were found by RT-PCR and confirmed by Western blot analysis. Antagonists for TRPC, 2APB and SKF96365, significantly reduced hypoxia-induced [Ca2+] i elevation by almost 60 %. Both TRPC6 and TRPC1 were knocked down by siRNA, the loss of TRPC6 decreased hypoxic response down to 21 % of control, whereas the knockdown of TRPC1 reduced the hypoxia respon se to 85 %, suggesting that TRPC6 might play a central role in mediating hypoxia response in hPASMC. However, blockade of PLC pathway caused only small inhibition of the hypoxia response. In contrast, AICAR, the agonist of AMP-activated kinase (AMPK), induced a gradual [Ca2+] i elevation, whereas compound C, an antagonist of AMPK, almost abolished the hypoxia response. Ho wever, co-immunoprecipitation revealed that AMPK α was not colocalized with TRPC6. Our data supports a role for TRPC6 in mediation of the [Ca2+] i elevation in response to hypoxia in hPASMC and suggests that this response may be linked to cellular energy status via an activation of AMPK., C. Tang, W. K To, F. Meng, Y. Wang, Y. Gu., and Obsahuje bibliografii
The classification scheme for micaceous minerals is described. According to the size of mineral particles micas are divided into macrocrystalline compounds and microcrystalline clay micas. Macroc rystalline micas are differentiated into (a) Mg-Fe-Al micas, (b) Li-micas, (c) micas with other cations. Vertical boundary in the suggested scheme divides micas into trioctahedral and dioctahedral members. Additional subdivision is carried out on the basis of the extent of Si substitution in tetrahedral positions of their crystal lattice. Microcrystalline (<4μm) micas are subordinate to the crystallochemical scheme for macrocrystalline micas. List of mica species together with their varieties and synonyms is in Table 2., Karel Melka., and Obsahuje bibliografické odkazy
We obtain a sharp upper bound for the spectral radius of a nonnegative matrix. This result is used to present upper bounds for the adjacency spectral radius, the Laplacian spectral radius, the signless Laplacian spectral radius, the distance spectral radius, the distance Laplacian spectral radius, the distance signless Laplacian spectral radius of an undirected graph or a digraph. These results are new or generalize some known results., Lihua You, Yujie Shu, Xiao-Dong Zhang., and Obsahuje seznam literatury
We study higher local integrability of a weak solution to the steady Stokes problem. We consider the case of a pressure- and shear-rate-dependent viscosity, i.e., the elliptic part of the Stokes problem is assumed to be nonlinear and it depends on p and on the symmetric part of a gradient of u, namely, it is represented by a stress tensor T (Du, p):= v(p, |D|2)D which satisfies r-growth condition with r \in (1, 2]. In order to get the main result, we use Calderón-Zygmund theory and the method which was presented for example in the paper Caffarelli, Peral (1998)., Václav Mácha., and Obsahuje seznam literatury
The imbalance of an edge e = {u, v} in a graph is defined as i(e) = |d(u)−d(v)|, where d(·) is the vertex degree. The irregularity I(G) of G is then defined as the sum of imbalances over all edges of G. This concept was introduced by Albertson who proved that I(G)\leqslant 4n^{3}/27 (where n = |V(G)|) and obtained stronger bounds for bipartite and triangle-free graphs. Since then a number of additional bounds were given by various authors. In this paper we prove a new upper bound, which improves a bound found by Zhou and Luo in 2008. Our bound involves the Laplacian spectral radius λ., Felix Goldberg., and Obsahuje seznam literatury
Oxidative stress is an imbalance between free radicals and antioxidants, and is an important etiological factor in the development of hypertension. Recent experimental evidence suggests that subpressor doses of angiotensin II elevate oxidative stress and blood pressure. We aimed to investigate the oxidative stress related mechanism by which a subpressor dose of angiotensin II induces hypertension in a normotensive rat model. Normotensive male Wistar rats were infused with a subpressor dose of angiotensin II for 28 days. The control group was sham operated and infused with saline only. Plasma angiotensin II and H2O2 levels, whole-blood glutathione peroxidase, and AT-1a, Cu/Zn SOD, and p22phox mRNA expression in the aorta was assessed. Systolic and diastolic blood pressures were elevated in the experimental group. There was no change in angiotensin II levels, but a significant increase in AT-1a mRNA expression was found in the experimental group. mRNA expression of p22phox was increased significantly and Cu/Zn SOD decreased significantly in the experimental group. There was no significant change to the H2O2 and GPx levels. Angiotensin II manipulates the free radical-antioxidant balance in the vasculature by selectively increasing O2 - production and decreasing SOD activity and causes an oxidative stress induced elevation in blood pressure in the Wistar rat., M. M. Govender, A. Nadar., and Obsahuje bibliografii
Light is critical in determining plant structure and functioning in dune ecosystems, which are characterised by high incident and reflected radiation. Light variations demand great plasticity of the photosynthetic apparatus. This study assessed the phenotypic plasticity of foredune species by analysing their light response and dark recovery curves measured under field conditions. We also addressed the question how coexisting species, structurally distinct, differed in their photochemical efficiency in response to short-term changes in light. Finally, we examined how the varying intensity of stressors operating along a dune gradient affected responses to light. The species differed in light use strategies but showed similar patterns of the dark recovery. Species differences in photochemistry varied seasonally, with species being winter specialists, summer specialist or generalists. Some aspects of their photochemistry varied significantly along the gradient. Unexpectedly, other traits did not vary as predicted. For example, changes in light efficiency of plants along the gradient were not consistent with assumed directional changes in the severity of stressors. The different light use strategies observed in coexisting species did not conform to the prediction that stressors constrain the range of possible functional designs in harsh environments. However, the species followed very similar patterns of post-illumination recovery, which suggests that evolutionary pressures might be acting to maintain similar recovery mechanisms. Our results indicated that dune gradients might be nondirectional, which determines unpredictable patterns of variation in leaf traits along the dune gradient. Seasonal differences in the relative performance may allow species to coexist where otherwise one species would exclude the other., R. Bermúdez, R. Retuerto., and Obsahuje bibliografii
Fiedler and Markham (1994) proved {\left( {\frac{{\det \hat H}}{k}} \right)^k} \geqslant \det H, where H = (H_{ij})_{i,j}^{n}_{=1} is a positive semidefinite matrix partitioned into n × n blocks with each block k × k and \hat H = \left( {tr{H_{ij}}} \right)_{i,j = 1}^n. We revisit this inequality mainly using some terminology from quantum information theory. Analogous results are included. For example, under the same condition, we prove \det \left( {{I_n} + \hat H} \right) \geqslant \det {\left( {{I_{nk}} + kH} \right)^{{1 \mathord{\left/ {\vphantom {1 k}} \right. \kern-\nulldelimiterspace} k}}}., Minghua Lin., and Obsahuje seznam literatury