Tetraenoic Species Are Conserved in Muscarinically Enhanced Inositide Turnover

Carbamylcholine enhances the labeling of phosphatidate and phosphatidylinositol from 32 P i in nerve endings. Approximately 74% of labeled phosphatidate and 85% of labeled phosphatidylinositol produced on muscarinic stimulation are accounted for by tetraenoic species, as detected by argentation TLC. Incubation of membranes derived from nerve endings with [Γ- 32 P]ATP under conditions of phosphodiesteratic degradation of endogenous polyphosphoinositides resulted in increased labeling of phosphatidate. Approximately 78% of the newly formed phosphatidate was in a tetraenoic fraction. It is concluded that in muscarinically stimulated nerve endings, the diacylglycerol moiety is conserved following diacylglycerol release from polyphosphoinositides through its resynthesis to inositol lipid via phosphatidate.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/65633/1/j.1471-4159.1985.tb05446.x.pd

The enzymatic exchange of the acyl group of acyl dihydroxyacetone phosphate with free fatty acids

Ehrlich ascites cell microsomes catalyze the exchange of the acyl group of acyl dihydroxyacetone phosphate with free fatty acids. The reaction does not require ATP and CoA.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/23003/1/0000571.pd

BIOSYNTHESIS OF PHOSPHATIDYLINOSITOL *

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73945/1/j.1749-6632.1970.tb56440.x.pd

Chemical constituents of Plumbago indica roots

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Coevolution of Glauber-like Ising dynamics on typical networks

We consider coevolution of site status and link structures from two different initial networks: a one dimensional Ising chain and a scale free network. The dynamics is governed by a preassigned stability parameter $S$, and a rewiring factor $\phi$, that determines whether the Ising spin at the chosen site flips or whether the node gets rewired to another node in the system. This dynamics has also been studied with Ising spins distributed randomly among nodes which lie on a network with preferential attachment. We have observed the steady state average stability and magnetisation for both kinds of systems to have an idea about the effect of initial network topology. Although the average stability shows almost similar behaviour, the magnetisation depends on the initial condition we start from. Apart from the local dynamics, the global effect on the dynamics has also been studied. These parameters show interesting variations for different values of $S$ and $\phi$, which helps in determining the steady-state condition for a given substrate.Comment: 8 pages, 10 figure

An Animal Cell Mutant With a Deficiency in Acyl/Alkyl-Dihydroxyacetone- Phosphate Reductase Activity. Effects on the Biosynthesis of Ether-Linked and Diacyl Glycerolipids

In the accompanying paper (James, P. F., and Zoeller, R. A. (1997) J. Biol. Chem. 272, 23532-23539), we reported the isolation of a series of mutants from the fibroblast-like cell line, CHO-K1, that are deficient in the incorporation of the long chain fatty alcohol, hexadecanol, into complex lipids. All but one of these mutants, FAA.K1B, were deficient in long-chain- fatty alcohol oxidase (FAO) activity. We have further characterized this FAO+ isolate. FAA.K1B cells displayed a 40% decrease in [9,103H]hexadecanol uptake when compared with the parent strain. Although incorporation of hexadecanol into the phospholipid fraction was decreased by 52%, the cells accumulated label in alkylglycerol (20-fold over wild type). The increase in 1-alkylglycerol labeling corresponded to a 4-fold increase in alkylglycerol mass. Short term labeling with 32P1 showed a 45-50% decrease in overall phospholipid biosynthesis in FAA.K1B. Both diacyl- and ether-linked species were affected, suggesting a general defect in phospholipid biosynthesis. Mutant cells were able to partially compensate for the decreased biosynthesis by decreasing the turnover of the phospholipid pools. The primary lesion in FAA.K1B was identified as a 95% reduction in acyl/alkyl-dihydroxyacetone- phospbate reductase activity. Whole cell homogenates from FAA.K1B were unable to reduce either acyl-dihydroxyacetone phosphate (DHAP) or alkyl-DHAP, supporting the notion that the reduction of these two compounds is catalyzed by a single enzyme. These data suggest that the biosynthesis of diacyl phospholipids, in Chinese hamster ovary cells, begins with the acylation of dihydroxyacetone phosphate as well as glycero-3-phosphate and that the \u27DHAP pathway\u27 contributes significantly to diacyl glycerolipid biosynthesis. Also, the severe reduction in acyl/alkyl-DHAP reductase activity in FAA.K1B resulted in only a moderate decrease in ether lipid biosynthesis. These latter data together with the observed increase in alkylglycerol levels sup port the existence of a shunt pathway that is able to partially bypass the enzymatic lesion

Effect of Pneumococcal Vaccine on Mortality and Cardiovascular Outcomes: A Systematic Review and Meta-Analysis

Various studies have suggested the possible cardiovascular (CV) protective effects of the pneumococcal vaccine (PV). Therefore, we conducted a meta-analysis to assess the association between recipients of PV with mortality and CV outcomes among patients with and without established cardiovascular disease. We performed a systematic literature search in PubMed, Embase, and Scopus for studies evaluating the effect of PV on mortality and CV outcomes. A total of 15 studies with 347,444 patients were included in the meta-analysis: 111,784 patients received PV (32%) and 235,660 patients were in the unvaccinated group (68%). Recipients of PV were associated with decreased all-cause mortality (HR, 0.76 (95% CI: 0.66 to 0.87), p &lt; 0.001). PV was associated with a decrease in the incidence of myocardial infarction (MI) (HR, 0.73 (95% CI: 0.56–0.96), p = 0.02), without significant reduction in CV mortality (HR, 0.87 (95% CI: 0.72–1.07), p = 0.18) and stroke (HR, 1.01 (95% CI: 0.93–1.10), p = 0.82). Our study found PV was associated with decreased risk of all-cause mortality and MI. Future RCTs will be necessary to confirm benefits associated with receipt of PV.</jats:p

Good practices for a literature survey are not followed by authors while preparing scientific manuscripts

The number of citations received by authors in scientific journals has become a major parameter to assess individual researchers and the journals themselves through the impact factor. A fair assessment therefore requires that the criteria for selecting references in a given manuscript should be unbiased with respect to the authors or the journals cited. In this paper, we advocate that authors should follow two mandatory principles to select papers (later reflected in the list of references) while studying the literature for a given research: i) consider similarity of content with the topics investigated, lest very related work should be reproduced or ignored; ii) perform a systematic search over the network of citations including seminal or very related papers. We use formalisms of complex networks for two datasets of papers from the arXiv repository to show that neither of these two criteria is fulfilled in practice

Combination of NH2OHHCl and NaIO4: A new and mild reagent for the synthesis of vicinal diiodo carbonyl compounds

The synthesis of vicinal diiodo carbonyl compounds from α,β-unsaturated carbonyl compounds has been carried out for the first time using the combination of NH2OHHCl and NaIO4 under mild reaction conditions at room temperature. The present methodology is also applicable for the synthesis of vicinal diiodo derivatives of nitrostyrene. The remarkable advantages of the present protocol are room temperature reaction, easy operation, good yields, fast reaction, transition metal-free and neutral reaction conditions. The present methodology is applicable to gram scale synthesis. © 2016 Arkat. All rights reserved

Bcl-2 protein family: Implications in vascular apoptosis and atherosclerosis

Apoptosis has been recognized as a central component in the pathogenesis of atherosclerosis, in addition to the other human pathologies such as cancer and diabetes. The pathophysiology of atherosclerosis is complex, involving both apoptosis and proliferation at different phases of its progression. Oxidative modification of lipids and inflammation differentially regulate the apoptotic and proliferative responses of vascular cells during progression of the atherosclerotic lesion. Bcl-2 proteins act as the major regulators of extrinsic and intrinsic apoptosis signalling pathways and more recently it has become evident that they mediate the apoptotic response of vascular cells in response to oxidation and inflammation either in a provocative or an inhibitory mode of action. Here we address Bcl-2 proteins as major therapeutic targets for the treatment of atherosclerosis and underscore the need for the novel preventive and therapeutic interventions against atherosclerosis, which should be designed in the light of molecular mechanisms regulating apoptosis of vascular cells in atherosclerotic lesions