554 research outputs found

    The effects of antiretroviral treatment on liver function enzymes among HIV-infected out patients attending the Central Hospital of Yaounde, Cameroon

    Get PDF
    The emergence of liver diseases as one of the major causes of death in people infected with HIV has paralleled the introduction of more effective antiretroviral therapies. This study was carried out with the aim of determining the effects of antiretroviral treatment on liver enzymes (SGOT and SGPT) in patients placed on antiretroviral therapy. A prospective cross-sectional 3 years study was carried out among patients confirmed to be HIV positive and who were to be placed on antiretroviral drugs at the HIV/AIDS out patient clinic of the Yaoundé Central Hospital, . Cameroon. Levels of transaminases of patients were measured in four phases using the International Federation of Clinical Chemistry (IFCC) protocol. Of the 150 patients who participated in the study, 54.0 %( 81/150) presented with transaminitis at the final phase of the study with respect to aspartate aminotransferase (AST), 77.78% (63/81) of whose AST levels only increased after initiation of highly active antiretroviral therapy (HAART). 22.67% (34/150) presented with transaminitis with respect to alanine aminotransferase (ALT). At the final phase, 70.58% of whose ALT levels only increased after HAART initiation. Increase in blood transaminase levels was statistically independent on age group and the drug combinations. Increase in AST levels was associated with an increase in ALT levels upon treatment (r = 0.58). There was a significant positive linear relationship between duration of treatment and concentration of transaminases over the years (r= 0.9). We therefore concluded that highly active antiretroviral therapy (HAART) is associated with low level hepatotoxicity at therapy initiation, regardless of drug class or combination.Keywords: Antiretroviral treatment, Liver function enzymes, Hepatotoxicity, Highly active antiretroviral therap

    Long-Term Potentiation in Isolated Dendritic Spines

    Get PDF
    BACKGROUND:In brain, N-methyl-D-aspartate (NMDA) receptor (NMDAR) activation can induce long-lasting changes in synaptic alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate (AMPA) receptor (AMPAR) levels. These changes are believed to underlie the expression of several forms of synaptic plasticity, including long-term potentiation (LTP). Such plasticity is generally believed to reflect the regulated trafficking of AMPARs within dendritic spines. However, recent work suggests that the movement of molecules and organelles between the spine and the adjacent dendritic shaft can critically influence synaptic plasticity. To determine whether such movement is strictly required for plasticity, we have developed a novel system to examine AMPAR trafficking in brain synaptosomes, consisting of isolated and apposed pre- and postsynaptic elements. METHODOLOGY/PRINCIPAL FINDINGS:We report here that synaptosomes can undergo LTP-like plasticity in response to stimuli that mimic synaptic NMDAR activation. Indeed, KCl-evoked release of endogenous glutamate from presynaptic terminals, in the presence of the NMDAR co-agonist glycine, leads to a long-lasting increase in surface AMPAR levels, as measured by [(3)H]-AMPA binding; the increase is prevented by an NMDAR antagonist 2-amino-5-phosphonopentanoic acid (AP5). Importantly, we observe an increase in the levels of GluR1 and GluR2 AMPAR subunits in the postsynaptic density (PSD) fraction, without changes in total AMPAR levels, consistent with the trafficking of AMPARs from internal synaptosomal compartments into synaptic sites. This plasticity is reversible, as the application of AMPA after LTP depotentiates synaptosomes. Moreover, depotentiation requires proteasome-dependent protein degradation. CONCLUSIONS/SIGNIFICANCE:Together, the results indicate that the minimal machinery required for LTP is present and functions locally within isolated dendritic spines

    Effect of Selected Agrochemicals on Protozoans and Algae Isolated from Mosquito Larval Habitats in Bamenda

    Get PDF
    The present study establishes the in-vitro effect of some selected agrochemicals(Glycot, Lamida and Pencozeb) on protozoans and some algae isolated from mosquito larval habitats in Bamenda urban zone, Cameroon. A convenience sampling technique was used in which water samples were randomly collected from 125 mosquito larval habitats from Bamenda urban zone. Out of the 123 samples tested, 41(33.33%) samples were found to be positive. Dinoflagellates predorminated with a frequency of 20(16.26%). One genera of protozoa(chillodenella) pathogenic to mosquito larvae was seen. Hook worm, Faciola, Paramecium and Trichomonas were found to be of medical importance while Euglena, Diatoms and Dinoflagellates were found to be of agricultural importance. All the protozoans and algae tested were susceptible to Lamida and Penncozeb, but resistant to glycot at all concentrations tested. Conclusively, the susceptibility of Chillodenella spp to Lamida and Penncozeb suggest their interference with natural biological control for mosquito population and also distortion of the ecosystem. Keywords: Agrochemicals, protozoans and algae , mosquito larval habitat

    Coloring translates and homothets of a convex body

    Full text link
    We obtain improved upper bounds and new lower bounds on the chromatic number as a linear function of the clique number, for the intersection graphs (and their complements) of finite families of translates and homothets of a convex body in \RR^n.Comment: 11 pages, 2 figure

    Calculation of nanowire thermal conductivity using complete phonon dispersion relations

    Full text link
    The lattice thermal conductivity of crystalline Si nanowires is calculated. The calculation uses complete phonon dispersions, and does not require any externally imposed frequency cutoffs. No adjustment to nanowire thermal conductivity measurements is required. Good agreement with experimental results for nanowires wider than 35 nm is obtained. A formulation in terms of the transmission function is given. Also, the use of a simpler, nondispersive "Callaway formula", is discussed from the complete dispersions perspective.Comment: 4 pages, 3 figures. Accepted in Phys. Rev.

    Canonical Representatives of Morphic Permutations

    Get PDF
    An infinite permutation can be defined as a linear ordering of the set of natural numbers. In particular, an infinite permutation can be constructed with an aperiodic infinite word over {0,,q1}\{0,\ldots,q-1\} as the lexicographic order of the shifts of the word. In this paper, we discuss the question if an infinite permutation defined this way admits a canonical representative, that is, can be defined by a sequence of numbers from [0, 1], such that the frequency of its elements in any interval is equal to the length of that interval. We show that a canonical representative exists if and only if the word is uniquely ergodic, and that is why we use the term ergodic permutations. We also discuss ways to construct the canonical representative of a permutation defined by a morphic word and generalize the construction of Makarov, 2009, for the Thue-Morse permutation to a wider class of infinite words.Comment: Springer. WORDS 2015, Sep 2015, Kiel, Germany. Combinatorics on Words: 10th International Conference. arXiv admin note: text overlap with arXiv:1503.0618

    Minimum Degree up to Local Complementation: Bounds, Parameterized Complexity, and Exact Algorithms

    Full text link
    The local minimum degree of a graph is the minimum degree that can be reached by means of local complementation. For any n, there exist graphs of order n which have a local minimum degree at least 0.189n, or at least 0.110n when restricted to bipartite graphs. Regarding the upper bound, we show that for any graph of order n, its local minimum degree is at most 3n/8+o(n) and n/4+o(n) for bipartite graphs, improving the known n/2 upper bound. We also prove that the local minimum degree is smaller than half of the vertex cover number (up to a logarithmic term). The local minimum degree problem is NP-Complete and hard to approximate. We show that this problem, even when restricted to bipartite graphs, is in W[2] and FPT-equivalent to the EvenSet problem, which W[1]-hardness is a long standing open question. Finally, we show that the local minimum degree is computed by a O*(1.938^n)-algorithm, and a O*(1.466^n)-algorithm for the bipartite graphs

    EphA4 signaling regulates phospholipase Cgamma1 activation, cofilin membrane association, and dendritic spine morphology

    Full text link
    Specialized postsynaptic structures known as dendritic spines are the primary sites of glutamatergic innervation at synapses of the CNS. Previous studies have shown that spines rapidly remodel their actin cytoskeleton to modify their shape and this has been associated with changes in synaptic physiology. However, the receptors and signaling intermediates that restructure the actin network in spines are only beginning to be identified. We reported previously that the EphA4 receptor tyrosine kinase regulates spine morphology. However, the signaling pathways downstream of EphA4 that induce spine retraction on ephrin ligand binding remain poorly understood. Here, we demonstrate that ephrin stimulation of EphA4 leads to the recruitment and activation of phospholipase Cgamma1 (PLCgamma1) in heterologous cells and in hippocampal slices. This interaction occurs through an Src homology 2 domain of PLCgamma1 and requires the EphA4 juxtamembrane tyrosines. In the brain, PLCgamma1 is found in multiple compartments of synaptosomes and is readily found in postsynaptic density fractions. Consistent with this, PLC activity is required for the maintenance of spine morphology and ephrin-induced spine retraction. Remarkably, EphA4 and PLC activity modulate the association of the actin depolymerizing/severing factor cofilin with the plasma membrane. Because cofilin has been implicated previously in the structural plasticity of spines, this signaling may enable cofilin to depolymerize actin filaments and restructure spines at sites of ephrin-EphA4 contact

    Electrical conductivity of plasmas of DB white dwarf atmospheres

    Full text link
    The static electrical conductivity of non-ideal, dense, partially ionized helium plasma was calculated over a wide range of plasma parameters: temperatures 1104KT1105K1\cdot 10^{4}\textrm{K} \lesssim T \lesssim 1\cdot 10^{5}\textrm{K} and mass density 1×106g/cm3ρ2g/cm31 \times 10^{-6} \textrm{g}/\textrm{cm}^{3} \lesssim \rho \lesssim 2 \textrm{g}/\textrm{cm}^{3}. Calculations of electrical conductivity of plasma for the considered range of plasma parameters are of interest for DB white dwarf atmospheres with effective temperatures 1104KTeff3104K1\cdot 10^{4}\textrm{K} \lesssim T_{eff} \lesssim 3\cdot 10^{4}\textrm{K}. Electrical conductivity of plasma was calculated by using the modified random phase approximation and semiclassical method, adapted for the case of dense, partially ionized plasma. The results were compared with the unique existing experimental data, including the results related to the region of dense plasmas. In spite of low accuracy of the experimental data, the existing agreement with them indicates that results obtained in this paper are correct
    corecore