Hymenin,a novel α-adrenoceptor blocking agent from the Okinawan marine spongeHymeniacidon sp.

Summary A novel bromine-containing alkaloid, hymenin, has been isolated from the Okinawan marine spongeHymeniacidon sp. as a potent -adrenoceptor blocking agent and its structure determined to be1 on the basis of the spectral data.     

Enzyme-linked immunosorbent assay for measuring serum IgE

Summary Serum IgE was measured by a sandwich method using polystyrene beads coated with anti-IgE -globulin and peroxidase labelled anti-IgE -globulin. The method was simple, and as sensitive as the radioimmunoassay.We are grateful for the skillful assistance of Mrs K. Kobayashi.     

Effects of thyrotrophic-releasing hormone (TRH) on thermoregulation in the rat

Summary At ambient temperatures (T_a) of both 8 and 22°C, intraventricular administration of TRH (10–80 g) produced a dose-dependent hypothermia in rats. The hypothermia was due to both decreased metabolic heat production and cutaneous vasodilatation. In contrast, at 30°C T_a, TRH increased metabolic heat production (due to behavioral excitation) and led to hyperthermia.This work was supported by the grants from the National Science Council of Republic of China and the Pjing-Ling Neurological Foundation (VGH, Taipei, Taiwan).     

Anti-oxidative effect of coenzyme Q10

Summary Coenzyme Q₁₀ is effective as an anti-oxidant like -tocopherol, especially in the heart.     

On the genesis of the soil mantle of the region of Manaus,Central Amazonia,Brazil

Summary The dynamics of the forest to the north of Manaus is tightly linked to that of the soil. The latosol that covers the plateau, which supports a dense forest, consists from top to bottom of: (a) a brown, clayey organic horizon (0.3 m), (b) a yellow horizon, very rich in clay but permeable (from 0.3 to 4 m), (c) a nodular horizon rich in Al and Fe oxides (from 4 to 9 m), and (d) a horizon which still preserves the sedimentary structures of the parent sandstone, where quartz is intensely dissolved and kaolinite crystallizes in pores. In perfectly flat areas, the clay of the organic horizon is destroyed by acidocomplexolysis, and the dissolved Al is transported vertically by the drainage water. A part of this Al is used to make the gibbsite nodules of horizon (c), and the rest is used to make kaolinite in horizon (d). Because aluminum is thus conserved within any vertical prism, the rate of destruction of horizon (a) is equivalent to the rate of advance of the kaolinization zone into the sediment: the latosol is said to be in equilibrium, the surface remains perfectly flat as it slowly sinks, the quantity of kaolinite increases with time, and the silica released by quartz dissolution in the whole profile is exported by drainage water to the water table. In contrast, near drainage axes, however small initially, the drainage becomes inclined toward the axis. Part of the Al released by acidocomplexolysis of horizon (a) is now exported to rivers, and Al is no longer conserved within any given prism. The rate of advance of the kaolinization zone (d) into the sediment now becomes less than the rate of destruction of horizon (a) and the surface sinks faster than that of the surrounding plateau. After this differential podzolization has gone on long enough, it creates a network of geochemical valleys characterized by convex slopes and bounded by sandy soils (campinas). The vegetation becomes sparser and sparser. At the end, only some bushes and lichens survive on the white sand.Acknowledgments. The authors are indebted to Dr E. Merino (Dept. of Geology, Indiana University) for helpful criticisms and suggestions. This research was carried out in I.N.P.A. (Instituto Nacional de Pesquisas da Amazonia) and was financially supported by the CNPq-CNRS/ORSTOM conv.     

Genetic and molecular approaches to synthesis and action of the yeast killer toxin

Summary The K1 killer toxin ofSaccharomyces cerevisiae is a secreted, virally-coded protein lethal to sensitive yeasts. Killer yeasts are immune to the toxin they produce. This killer system has been extensively examined from genetic and molecular perspectives. Here we review the biology of killer yeasts, and examine the synthesis and action of the protein toxin and the immunity component. We summarise the structure of the toxin precursor gene and its protein products, outline the proteolytic processing of the toxin subunits from the precursor, and their passage through the yeast secretory pathway. We then discuss the mode of action of the toxin, its lectin-like interaction with a cell wall glucan, and its probable role in forming channels in the yeast plasma membrane. In addition we describe models of how a toxin precursor species functions as the immunity component, probably by interfering with channel formation. We conclude with a review of the functional domains of the toxin structural gene as determined by site-directed mutagenesis. This work has identified regions associated with glucan binding, toxin activity, and immunity.     

PPARδ inhibits IL-1β-stimulated proliferation and migration of vascular smooth muscle cells via up-regulation of IL-1Ra

Activation of peroxisome proliferator-activated receptor (PPAR) δ by GW501516, a specific PPARδ ligand, significantly inhibited interleukin (IL)-1β-induced proliferation and migration of vascular smooth muscle cells (VSMCs). This effect of GW501516 was dependent on transforming growth factor-β, and was mediated through the up-regulation of IL-1 receptor antagonist. The inhibitory effect of GW501516 on VSMC proliferation was associated with cell cycle arrest at the G1 to S phase transition, which was accompanied by the induction of p21 and p53 along with decreased cyclin-dependent kinase 4 expression. Inhibition of cell migration by GW501516 was associated with the down-regulation of matrix metalloproteinase (MMP)-2 and MMP-9 in IL-1β-treated VSMCs. Inhibition of extracellular signal-regulated kinase significantly reduced the GW501516-mediated inhibition of IL-1β-stimulated VSMC proliferation. These results suggest that PPARδ plays an important role in the pathophysiology of diseases associated with the proliferation and migration of VSMCs.     

分数阶Fourier域多通道采样的滤波器组高效实现

研究了分数阶Fourier域周期非均匀采样以及多通道采样的滤波器组高效插值和重建方法．首先，根据分数阶Fourier变换的性质，得到了分数阶Fourier域插值和采样的恒等结构；然后根据该恒等结构，得到了从分数阶Fourier域多通道采样和周期非均匀采样中重建原始信号的滤波器组高效实现方法；最后建立了分数阶Fourier域多通道采样和分数阶Fourier域滤波器组的关系，并进一步说明可以通过分数阶Fourier域准确重建滤波器组，导出分数阶Fourier域新的采样和重建策略．