Browse publications by year: 2013

  1. Anuar TS, Ghani MK, Azreen SN, Salleh FM, Moktar N
    Parasit Vectors, 2013;6:40.
    PMID: 23433099 DOI: 10.1186/1756-3305-6-40
    Blastocystis has been described as the most common intestinal parasite in humans and has an increased impact on public health. However, the transmission of this parasite has not been conclusively determined.
    MeSH terms: Adolescent; Adult; Aged; Child; Child, Preschool; Cross-Sectional Studies; Feces/parasitology; Female; Humans; Malaysia/epidemiology; Male; Microscopy; Middle Aged; Parasitology/methods; Risk Factors; Prevalence; Blastocystis Infections/epidemiology*; Blastocystis Infections/transmission*; Blastocystis/isolation & purification*; Population Groups; Young Adult
  2. Sambasevam KP, Mohamad S, Sarih NM, Ismail NA
    Int J Mol Sci, 2013;14(2):3671-82.
    PMID: 23434664 DOI: 10.3390/ijms14023671
    A β-cyclodextrin (β-Cyd) inclusion complex containing azomethine as a guest was prepared by kneading method with aliquot addition of ethanol. The product was characterized by Fourier Transform Infrared (FTIR) spectrometer, 1H Nuclear Magnetic Resonance (1H NMR) and Thermogravimetric Analyzer (TGA), which proves the formation of the inclusion complex where the benzyl part of azomethine has been encapsulated by the hydrophobic cavity of β-Cyd. The interaction of β-Cyd and azomethine was also analyzed by means of spectrometry by UV-Vis spectrophotometer to determine the formation constant. The formation constant was calculated by using a modified Benesi-Hildebrand equation at 25 °C. The apparent formation constant obtained was 1.29 × 104 L/mol. Besides that, the stoichiometry ratio was also determined to be 1:1 for the inclusion complex of β-Cyd with azomethine.
    MeSH terms: Ethanol; Azo Compounds; Fourier Analysis; Magnetic Resonance Spectroscopy; Thiosemicarbazones; beta-Cyclodextrins
  3. Ahmad TA, Jubri Z, Rajab NF, Rahim KA, Yusof YA, Makpol S
    Molecules, 2013 Feb 11;18(2):2200-11.
    PMID: 23434870 DOI: 10.3390/molecules18022200
    The present study was designed to determine the radioprotective effects of Malaysian Gelam honey on gene expression and enzyme activity of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) of human diploid fibroblasts (HDFs) subjected to gamma-irradiation. Six groups of HDFs were studied: untreated control, irradiated HDFs, Gelam honey-treated HDFs and HDF treated with Gelam honey pre-, during- and post-irradiation. HDFs were treated with 6 mg/mL of sterilized Gelam honey (w/v) for 24 h and exposed to 1 Gray (Gy) of gamma rays at the dose rate of 0.25 Gy/min. Gamma-irradiation was shown to down-regulate SOD1, SOD2, CAT and GPx1 gene expressions (p < 0.05). Conversely, HDFs treated with Gelam honey alone showed up-regulation of all genes studied. Similarly, SOD, CAT and GPx enzyme activities in HDFs decreased with gamma-irradiation and increased when cells were treated with Gelam honey (p < 0.05). Furthermore, of the three different stages of study treatment, pre-treatment with Gelam honey caused up-regulation of SOD1, SOD2 and CAT genes expression and increased the activity of SOD and CAT. As a conclusion, Gelam honey modulates the expression of antioxidant enzymes at gene and protein levels in irradiated HDFs indicating its potential as a radioprotectant agent.
    MeSH terms: Antioxidants/metabolism*; Catalase/genetics; Catalase/metabolism; Child; Diploidy*; Fibroblasts/drug effects*; Fibroblasts/enzymology*; Fibroblasts/radiation effects; Gamma Rays*; Glutathione Peroxidase/genetics; Glutathione Peroxidase/metabolism; Honey*; Humans; Male; Radiation-Protective Agents/pharmacology*; Superoxide Dismutase/genetics; Superoxide Dismutase/metabolism; Gene Expression Regulation, Enzymologic/drug effects; Gene Expression Regulation, Enzymologic/radiation effects
  4. Zen DI, Saidin N, Damanhuri SS, Harun SW, Ahmad H, Ismail MA, et al.
    Appl Opt, 2013 Feb 20;52(6):1226-9.
    PMID: 23434993 DOI: 10.1364/AO.52.001226
    We demonstrate mode locking of a thulium-bismuth codoped fiber laser (TBFL) operating at 1901.6 nm, using a graphene-based saturable absorber (SA). In this work, a single layer graphene is mechanically exfoliated using the scotch tape method and directly transferred onto the surface of a fiber pigtail to fabricate the SA. The obtained Raman spectrum characteristic indicates that the graphene on the core surface has a single layer. At 1552 nm pump power of 869 mW, the mode-locked TBFL self starts to generate an optical pulse train with a repetition rate of 16.7 MHz and pulse width of 0.37 ps. This is a simple, low-cost, stable, and convenient laser oscillator for applications where eye-safe and low-photon-energy light sources are required, such as sensing and biomedical diagnostics.
    MeSH terms: Absorption; Bismuth/chemistry*; Equipment Design; Graphite/chemistry; Lasers; Oscillometry/methods; Spectrum Analysis, Raman/methods; Surface Properties; Thulium/chemistry*; Time Factors; Biosensing Techniques*; Optical Fibers
  5. Harun NH, Misron N, Sidek RM, Aris I, Ahmad D, Wakiwaka H, et al.
    Sensors (Basel), 2013;13(2):2254-66.
    PMID: 23435051 DOI: 10.3390/s130202254
    From the Malaysian harvester's perspective, the determination of the ripeness of the oil palm (FFB) is a critical factor to maximize palm oil production. A preliminary study of a novel oil palm fruit sensor to detect the maturity of oil palm fruit bunches is presented. To optimize the functionality of the sensor, the frequency characteristics of air coils of various diameters are investigated to determine their inductance and resonant characteristics. Sixteen samples from two categories, namely ripe oil palm fruitlets and unripe oil palm fruitlets, are tested from 100 Hz up to 100 MHz frequency. The results showed the inductance and resonant characteristics of the air coil sensors display significant changes among the samples of each category. The investigations on the frequency characteristics of the sensor air coils are studied to observe the effect of variations in the coil diameter. The effect of coil diameter yields a significant 0.02643 MHz difference between unripe samples to air and 0.01084 MHz for ripe samples to air. The designed sensor exhibits significant potential in determining the maturity of oil palm fruits.
    MeSH terms: Agriculture/instrumentation; Agriculture/methods*; Air; Fruit/growth & development*; Plant Oils/chemistry*; Arecaceae/growth & development*
  6. Hossain MS, Rahman NN, Balakrishnan V, Puvanesuaran VR, Sarker MZ, Kadir MO
    Int J Environ Res Public Health, 2013 Jan 31;10(2):556-67.
    PMID: 23435587 DOI: 10.3390/ijerph10020556
    The present study was undertaken to determine the bacterial agents present in various clinical solid wastes, general waste and clinical sharp waste. The waste was collected from different wards/units in a healthcare facility in Penang Island, Malaysia. The presence of bacterial agents in clinical and general waste was determined using the conventional bacteria identification methods. Several pathogenic bacteria including opportunistic bacterial agent such as Pseudomonas aeruginosa, Salmonella spp., Klebsiella pneumoniae, Serratia marcescens, Acinetobacter baumannii, Staphylococcus aureus, Staphylococcus epidermidis, Enterococcus faecalis, Streptococcus pyogenes were detected in clinical solid wastes. The presence of specific pathogenic bacterial strains in clinical sharp waste was determined using 16s rDNA analysis. In this study, several nosocomial pathogenic bacteria strains of Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Lysinibacillus sphaericus, Serratia marcescens, and Staphylococcus aureus were detected in clinical sharp waste. The present study suggests that waste generated from healthcare facilities should be sterilized at the point of generation in order to eliminate nosocomial infections from the general waste or either of the clinical wastes.
    MeSH terms: Bacteria/genetics; Bacteria/isolation & purification*; Bacterial Infections/epidemiology*; Cross Infection/epidemiology*; DNA, Bacterial/genetics; Health Facilities; Humans; Malaysia/epidemiology; Waste Management/methods*; Risk Assessment; Solid Waste/analysis*
  7. Shaharir SS, Remli R, Marwan AA, Said MS, Kong NCT
    Lupus, 2013 Apr;22(5):492-6.
    PMID: 23435619 DOI: 10.1177/0961203313478303
    INTRODUCTION:Posterior reversible encephalopathy syndrome (PRES) is a rare neurological disorder which is increasingly recognized to occur in systemic lupus erythematosus (SLE).
    OBJECTIVE: The purpose of this study was to identify the characteristics of SLE patients with PRES and the associated factors of the poor outcome among them.
    METHODS: We investigated SLE patients who developed PRES between 2005-2011 at the Universiti Kebangsaan Malaysia Medical Centre. A comprehensive literature search was done to find all published cases of PRES in SLE. Pooled analysis was conducted to identify the factors associated with poor outcome.
    RESULTS: There were 103 cases of PRES in SLE published in the literature but only 87 cases were included in the analysis in view of incomplete individual data in the remaining cases. The majority of the cases were Asians (74.2%), female (95.4%) with mean age of 26.3 ± 8.8 years. PRES was highly associated with active disease (97.5%), hypertension (91.7%) and renal involvement (85.1%). We found that 79 patients had a full recovery (90.8%) with a mean onset of full clinical recovery in 5.6 ± 4.1 days. On univariate analysis and logistic regression analysis the predictors of poor outcome, defined as incomplete clinical recovery or death, were intracranial hemorrhage, odds ratio (OR) 14 (1.1-187.2), p=0.04 and brainstem involvement in PRES, OR 10.9 (1.3-90.6), p=0.003.
    CONCLUSION: Intracranial hemorrhage and brainstem involvement were the two important predictors of poor outcome of PRES. Larger prospective studies are needed to further delineate the risk of poor outcome among them.
    MeSH terms: Adolescent; Adult; Female; Hospitals, University; Humans; Lupus Erythematosus, Systemic/complications*; Malaysia; Male; Retrospective Studies; Logistic Models; Posterior Leukoencephalopathy Syndrome/complications*; Young Adult
  8. Camalxaman SN, Zeenathul NA, Quah YW, Loh HS, Zuridah H, Hani H, et al.
    In Vitro Cell Dev Biol Anim, 2013 Mar;49(3):238-44.
    PMID: 23435855 DOI: 10.1007/s11626-012-9553-5
    Endothelial cells have been implicated as key cells in promoting the pathogenesis and spread of cytomegalovirus (CMV) infection. This study describes the isolation and culture of rat brain endothelial cells (RBEC) and further evaluates the infectious potential of a Malaysian rat CMV (RCMV ALL-03) in these cultured cells. Brain tissues were mechanically fragmented, exposed to enzymatic digestion, purified by gradient density centrifugation, and cultured in vitro. Morphological characteristics and expression of von Willebrand factor (factor VIII-related antigen) verified the cells were of endothelial origin. RBEC were found to be permissive to the virus by cytopathic effects with detectable plaques formed within 7 d of infection. This was confirmed by electron microscopy examination which proved the existence of the viral particles in the infected cells. The susceptibility of the virus to these target cells under the experimental conditions described in this report provides a platform for developing a cell-culture-based experimental model for studies of RCMV pathogenesis and allows stimulation of further studies on host cell responses imposed by congenital viral infections.
    MeSH terms: Animals; Brain/metabolism; Brain/pathology; Brain/virology; Cytomegalovirus Infections/metabolism; Cytomegalovirus Infections/pathology; Cytomegalovirus Infections/virology; Cytopathogenic Effect, Viral; Disease Susceptibility; Endothelium, Vascular/metabolism; Endothelium, Vascular/pathology; Endothelium, Vascular/virology; Fibroblasts/cytology; Fibroblasts/metabolism; Fibroblasts/virology; von Willebrand Factor/metabolism; Muromegalovirus/isolation & purification*; Muromegalovirus/metabolism; Muromegalovirus/pathogenicity; Endothelial Cells/metabolism*; Endothelial Cells/pathology; Endothelial Cells/virology; Rats
  9. Yunus NA, Nili H, Green NG
    Electrophoresis, 2013 Apr;34(7):969-78.
    PMID: 23436439 DOI: 10.1002/elps.201200466
    Dielectrophoresis is the movement of particles in nonuniform electric fields and has been of interest for application to manipulation and separation at and below the microscale. This technique has the advantages of being noninvasive, nondestructive, and noncontact, with the movement of particle achieved by means of electric fields generated by miniaturized electrodes and microfluidic systems. Although the majority of applications have been above the microscale, there is increasing interest in application to colloidal particles around a micron and smaller. This paper begins with a review of colloidal and nanoscale dielectrophoresis with specific attention paid to separation applications. An innovative design of integrated microelectrode array and its application to flow-through, continuous separation of colloidal particles is then presented. The details of the angled chevron microelectrode array and the test microfluidic system are then discussed. The variation in device operation with applied signal voltage is presented and discussed in terms of separation efficiency, demonstrating 99.9% separation of a mixture of colloidal latex spheres.
    MeSH terms: Colloids/isolation & purification*; Colloids/chemistry; Electrophoresis/instrumentation*; Electrophoresis/methods*; Image Processing, Computer-Assisted; Microelectrodes; Microspheres*; Microfluidic Analytical Techniques/instrumentation*; Microfluidic Analytical Techniques/methods*; Nanoparticles/chemistry*
  10. Looi CY, Arya A, Cheah FK, Muharram B, Leong KH, Mohamad K, et al.
    PLoS One, 2013;8(2):e56643.
    PMID: 23437193 DOI: 10.1371/journal.pone.0056643
    Centratherum anthelminticum (L.) seeds (CA) is a well known medicinal herb in Indian sub-continent. We recently reported anti-oxidant property of chloroform fraction of Centratherum anthelminticum (L.) seeds (CACF) by inhibiting tumor necrosis factor-α (TNF-α)-induced growth of human breast cancer cells. However, the active compounds in CACF have not been investigated previously.
    MeSH terms: Antineoplastic Agents/administration & dosage; Breast Neoplasms/drug therapy*; Breast Neoplasms/pathology; Female; Humans; Mitochondria/drug effects; Plant Extracts/chemistry*; Seeds/chemistry; Sesquiterpenes/administration & dosage; Sesquiterpenes/isolation & purification; Tumor Necrosis Factor-alpha/metabolism; Apoptosis/drug effects; Reactive Oxygen Species/metabolism; Caspases/drug effects; Caspases/metabolism; Cell Proliferation/drug effects; Membrane Potential, Mitochondrial/drug effects; DNA Fragmentation/drug effects; Cell Cycle Checkpoints/drug effects; MCF-7 Cells
  11. Chung PY, Chung LY, Navaratnam P
    PLoS One, 2013;8(2):e56687.
    PMID: 23437212 DOI: 10.1371/journal.pone.0056687
    Staphylococcus aureus is an important human pathogen in both hospital and the community that has demonstrated resistance to all currently available antibiotics over the last two decades. Multidrug-resistant isolates of methicillin-resistant S. aureus (MRSA) exhibiting decreased susceptibilities to glycopeptides has also emerged, representing a crucial challenge for antimicrobial therapy and infection control. The availability of complete whole-genome nucleotide sequence data of various strains of S. aureus presents an opportunity to explore novel compounds and their targets to address the challenges presented by antimicrobial drug resistance in this organism. Study compounds α-amyrin [3β-hydroxy-urs-12-en-3-ol (AM)], betulinic acid [3β-hydroxy-20(29)-lupaene-28-oic acid (BA)] and betulinaldehyde [3β-hydroxy-20(29)-lupen-28-al (BE)] belong to pentacyclic triterpenoids and were reported to exhibit antimicrobial activities against bacteria and fungi, including S. aureus. The MIC values of these compounds against a reference strain of methicillin-resistant S. aureus (MRSA) (ATCC 43300) ranged from 64 µg/ml to 512 µg/ml. However, the response mechanisms of S. aureus to these compounds are still poorly understood. The transcription profile of reference strain of MRSA treated with sub-inhibitory concentrations of the three compounds was determined using Affymetrix GeneChips. The findings showed that these compounds regulate multiple desirable targets in cell division, two-component system, ABC transporters, fatty acid biosynthesis, peptidoglycan biosynthesis, aminoacyl-tRNA synthetase, ribosome and β-lactam resistance pathways which could be further explored in the development of therapeutic agents for the treatment of S. aureus infections.
    MeSH terms: Anti-Bacterial Agents/administration & dosage; Drug Resistance, Microbial/drug effects; Humans; Oleanolic Acid/administration & dosage; Oleanolic Acid/analogs & derivatives*; Staphylococcal Infections/drug therapy*; Staphylococcal Infections/genetics; Staphylococcal Infections/microbiology; Triterpenes/administration & dosage*; Gene Expression Regulation, Bacterial/drug effects; Gene Expression Profiling; Methicillin-Resistant Staphylococcus aureus/drug effects*; Methicillin-Resistant Staphylococcus aureus/genetics; Methicillin-Resistant Staphylococcus aureus/pathogenicity
  12. Lee ST, Wong PF, He H, Hooper JD, Mustafa MR
    PLoS One, 2013;8(2):e57708.
    PMID: 23437404 DOI: 10.1371/journal.pone.0057708
    Nuclear factor-kappa B (NF-κB) plays a role in prostate cancer and agents that suppress its activation may inhibit development or progression of this malignancy. Alpha (α)-tomatine is the major saponin present in tomato (Lycopersicon esculentum) and we have previously reported that it suppresses tumor necrosis factor-alpha (TNF-α)-induced nuclear translocation of nuclear factor-kappa B (NF-κB) in androgen-independent prostate cancer PC-3 cells and also potently induces apoptosis of these cells. However, the precise mechanism by which α-tomatine suppresses NF-κB nuclear translocation is yet to be elucidated and the anti-tumor activity of this agent in vivo has not been examined.
    MeSH terms: Adenocarcinoma/drug therapy*; Adenocarcinoma/genetics; Adenocarcinoma/metabolism; Adenocarcinoma/pathology; Animals; Antineoplastic Agents, Phytogenic/pharmacology*; Choristoma; Humans; Male; Neoplasm Transplantation; Phosphorylation/drug effects; Prostatic Neoplasms/drug therapy*; Prostatic Neoplasms/genetics; Prostatic Neoplasms/metabolism; Prostatic Neoplasms/pathology; Tomatine/analogs & derivatives*; Tomatine/pharmacology; Signal Transduction/drug effects; Gene Expression Regulation, Neoplastic/drug effects*; NF-kappa B/antagonists & inhibitors; NF-kappa B/genetics*; NF-kappa B/metabolism; Apoptosis/drug effects; Protein Subunits/antagonists & inhibitors; Protein Subunits/genetics*; Protein Subunits/metabolism; Protein Transport/drug effects; Cell Proliferation/drug effects; Apoptosis Regulatory Proteins/antagonists & inhibitors; Apoptosis Regulatory Proteins/genetics; Apoptosis Regulatory Proteins/metabolism; Mice; I-kappa B Kinase/antagonists & inhibitors; I-kappa B Kinase/genetics; I-kappa B Kinase/metabolism
  13. Shepard DS, Undurraga EA, Halasa YA
    PLoS Negl Trop Dis, 2013;7(2):e2055.
    PMID: 23437406 DOI: 10.1371/journal.pntd.0002055
    BACKGROUND: Dengue poses a substantial economic and disease burden in Southeast Asia (SEA). Quantifying this burden is critical to set policy priorities and disease-control strategies.

    METHODS AND FINDINGS: We estimated the economic and disease burden of dengue in 12 countries in SEA: Bhutan, Brunei, Cambodia, East-Timor, Indonesia, Laos, Malaysia, Myanmar, Philippines, Singapore, Thailand, and Viet Nam. We obtained reported cases from multiple sources--surveillance data, World Health Organization (WHO), and published studies--and adjusted for underreporting using expansion factors from previous literature. We obtained unit costs per episode through a systematic literature review, and completed missing data using linear regressions. We excluded costs such as prevention and vector control, and long-term sequelae of dengue. Over the decade of 2001-2010, we obtained an annual average of 2.9 million (m) dengue episodes and 5,906 deaths. The annual economic burden (with 95% certainty levels) was US$950m (US$610m-US$1,384m) or about US$1.65 (US$1.06-US$2.41) per capita. The annual number of disability-adjusted life years (DALYs), based on the original 1994 definition, was 214,000 (120,000-299,000), which is equivalent to 372 (210-520) DALYs per million inhabitants.

    CONCLUSION: Dengue poses a substantial economic and disease burden in SEA with a DALY burden per million inhabitants in the region. This burden is higher than that of 17 other conditions, including Japanese encephalitis, upper respiratory infections, and hepatitis B.

    MeSH terms: Asia, Southeastern/epidemiology; Dengue/economics*; Dengue/mortality; Dengue/epidemiology*; Humans; Survival Analysis; Health Care Costs; Cost of Illness*
  14. Undurraga EA, Halasa YA, Shepard DS
    PLoS Negl Trop Dis, 2013;7(2):e2056.
    PMID: 23437407 DOI: 10.1371/journal.pntd.0002056
    BACKGROUND: Dengue virus infection is the most common arthropod-borne disease of humans and its geographical range and infection rates are increasing. Health policy decisions require information about the disease burden, but surveillance systems usually underreport the total number of cases. These may be estimated by multiplying reported cases by an expansion factor (EF).

    METHODS AND FINDINGS: As a key step to estimate the economic and disease burden of dengue in Southeast Asia (SEA), we projected dengue cases from 2001 through 2010 using EFs. We conducted a systematic literature review (1995-2011) and identified 11 published articles reporting original, empirically derived EFs or the necessary data, and 11 additional relevant studies. To estimate EFs for total cases in countries where no empirical studies were available, we extrapolated data based on the statistically significant inverse relationship between an index of a country's health system quality and its observed reporting rate. We compiled an average 386,000 dengue episodes reported annually to surveillance systems in the region, and projected about 2.92 million dengue episodes. We conducted a probabilistic sensitivity analysis, simultaneously varying the most important parameters in 20,000 Monte Carlo simulations, and derived 95% certainty level of 2.73-3.38 million dengue episodes. We estimated an overall EF in SEA of 7.6 (95% certainty level: 7.0-8.8) dengue cases for every case reported, with an EF range of 3.8 for Malaysia to 19.0 in East Timor.

    CONCLUSION: Studies that make no adjustment for underreporting would seriously understate the burden and cost of dengue in SEA and elsewhere. As the sites of the empirical studies we identified were not randomly chosen, the exact extent of underreporting remains uncertain. Nevertheless, the results reported here, based on a systematic analysis of the available literature, show general consistency and provide a reasonable empirical basis to adjust for underreporting.

    MeSH terms: Asia, Southeastern/epidemiology; Dengue/drug therapy; Dengue/epidemiology*; Humans; Cost of Illness*; Disease Notification/statistics & numerical data
  15. Rani AQ, Sasongko TH, Sulong S, Bunyan D, Salmi AR, Zilfalil BA, et al.
    J. Neurogenet., 2013 Jun;27(1-2):11-5.
    PMID: 23438214 DOI: 10.3109/01677063.2012.762580
    We undertook the clinical feature examination and dystrophin analysis using multiplex ligation-dependent probe amplification (MLPA) and direct DNA sequencing of selected exons in a cohort of 35 Malaysian Duchenne/Becker muscular dystrophy (DMD/BMD) patients. We found 27 patients with deletions of one or more exons, 2 patients with one exon duplication, 2 patients with nucleotide deletion, and 4 patients with nonsense mutations (including 1 patient with two nonsense mutations in the same exon). Although most cases showed compliance to the reading frame rule, we found two unrelated DMD patients with an in-frame deletion of the gene. Two novel mutations have been detected in the Dystrophin gene and our results were compatible with other studies where the majority of the mutations (62.8%) are located in the distal hotspot. However, the frequency of the mutations in our patient varied as compared with those found in other populations.
    MeSH terms: Adolescent; Child; Child, Preschool; Creatine Kinase/blood; DNA Mutational Analysis; Female; Genotype; Humans; Malaysia; Male; Mutation/genetics*; Cohort Studies; Dystrophin/genetics*; Sequence Analysis, DNA; Genetic Predisposition to Disease/genetics*; Muscular Dystrophy, Duchenne/blood; Muscular Dystrophy, Duchenne/genetics*
  16. Shamsabadi FT, Khoddami A, Fard SG, Abdullah R, Othman HH, Mohamed S
    Nutr Cancer, 2013;65(2):255-62.
    PMID: 23441613 DOI: 10.1080/01635581.2013.756528
    The tropical edible red seaweed (Eucheuma cottonii L.) is rich in nutrients and polyphenolic compounds that may suppress cancer through its antioxidant and antiproliferative properties. The study reports on rat mammary tumor suppression and tissue antioxidant status modulation by E. cottonii ethanol extract (ECE). The effect of orally administered ECE (100 mg/kg body-weight) was compared with that of tamoxifen (10 mg/kg body-weight). Rat was induced to develop mammary tumor with subcutaneous injection of LA-7 cells (6 × 10(6) cells/rat). The ECE was more effective than tamoxifen in suppressing tumor growth (27%), improving tissues (plasma, liver, and kidney) malondialdehyde concentrations, superoxide dismutase activity and erythrocyte glutathione concentrations (P < 0.05). Unlike tamoxifen, the ECE displayed little toxicity to the liver and kidneys. The ECE exhibited strong anticancer effect with enzyme modulating properties, suggesting its potential as a suppressing agent for mammary gland tumor.
    MeSH terms: Administration, Oral; Rhodophyta*; Animals; Antineoplastic Agents, Phytogenic/adverse effects; Antineoplastic Agents, Phytogenic/pharmacology; Drug Screening Assays, Antitumor/methods; Female; Kidney/drug effects; Kidney/metabolism; Liver/drug effects; Liver/metabolism; Malondialdehyde/metabolism; Mammary Neoplasms, Experimental/drug therapy*; Mammary Neoplasms, Experimental/pathology; Plant Extracts/pharmacology*; Seaweed*; Superoxide Dismutase/metabolism; Tamoxifen/pharmacology*; Rats, Sprague-Dawley; Antineoplastic Agents, Hormonal/pharmacology; Rats
  17. Velu SS, Di Meo F, Trouillas P, Sancho-Garcia JC, Weber JF
    J Nat Prod, 2013 Apr 26;76(4):538-46.
    PMID: 23441649 DOI: 10.1021/np300705p
    Oligostilbenoids (e.g., ampelopsin F, viniferin, pallidol) result from homogeneous or heterogeneous coupling of monomeric stilbenoid units, leading to various chemical structures. Oligostilbenoid synthesis is regio- and stereocontrolled. To tackle this regio- and stereocontrol, a supramolecular chemistry approach is required that can be achieved by quantum chemistry. The stability of noncovalent π-stacks, formed between two stilbenoid units prior to oxidation, is accurately evaluated with density functional theory (DFT) including dispersive effects (within the DFT-D formalism). These noncovalent arrangements drive the regiocontrol. The rest of the chemical pathway is a succession of dearomatization and rearomatization stages. The thermodynamics and kinetics of the processes are calculated with classical hybrid functionals. This study allows discrimination between the two main possible chemical pathways, namely, radical-neutral and radical-radical reactions. The former appears more likely, thermodynamics and kinetics being in perfect agreement with the experimental 1:2 ratio obtained for ampelopsin F:pallidol analogues, respectively.
    MeSH terms: Algorithms; Models, Theoretical*; Molecular Conformation; Stereoisomerism; Stilbenes/chemical synthesis; Stilbenes/chemistry*; Thermodynamics; Molecular Structure
  18. Yeap SS, Hew FL, Lee JK, Goh EM, Chee W, Mumtaz M, et al.
    Int J Rheum Dis, 2013 Feb;16(1):30-40.
    PMID: 23441770 DOI: 10.1111/1756-185x.12037
    AIM: This Clinical Guidance is aimed to help practitioners assess, diagnose and manage their patients with osteoporosis (OP), using the best available evidence.
    METHODS: A literature search using PubMed (MEDLINE) and The Cochrane Library identified all relevant articles on OP and its assessment, diagnosis and treatment, from 2005, to update from the previous edition published in 2006. The studies were assessed and the level of evidence assigned; for each statement, studies with the highest level of evidence were used to frame the recommendation.
    RESULTS: This article summarizes the diagnostic and treatment pathways for OP, highlighting the new data that have changed the way we assess and treat OP. Instead of starting treatment based on bone mineral density alone, there has been a move to assessing 10-year fracture risk before treatment, using tools such as the Fracture Risk Assessment Tool (FRAX). There has been a re-evaluation on calcium supplementation and more emphasis on the importance of vitamin D. There has been concern about the potential adverse effects of the long-term usage of bisphosphonates, which we have discussed fully. New drugs that have been licensed since 2006 in Malaysia have been included.
    CONCLUSIONS: Adequate intake of calcium (1000 mg from both diet and supplements) and vitamin D (800 IU) daily remain important in the treatment of OP. However, in confirmed OP, pharmacological therapy with anti-resorptives is the mainstay of treatment. Patients need to be regularly assessed while on medication and treatment adjusted as required.
    MeSH terms: Combined Modality Therapy; Female; Humans; Malaysia; Male; Risk Factors; Vitamin D/administration & dosage; Bone Density; Osteoporosis, Postmenopausal/physiopathology; Osteoporosis, Postmenopausal/therapy*; Practice Guidelines as Topic*; Calcium Compounds/administration & dosage; Risk Assessment; Dietary Supplements; Bone Density Conservation Agents/therapeutic use; Osteoporotic Fractures
  19. Hassan Y, Kassab Y, Abd Aziz N, Akram H, Ismail O
    J Clin Pharm Ther, 2013 Apr;38(2):97-100.
    PMID: 23441979 DOI: 10.1111/jcpt.12027
    Pharmacists have the knowledge regarding optimal use of medications and the ability to influence physician prescribing. Successful interventions by a pharmacist to implement cardioprotective medications to a coronary artery disease patient's regimen would not only improve the patient's quality of care but may also increase his or her likelihood of survival. Therefore, the aim of this study was to (i) evaluate the effectiveness of pharmacist initiated interventions in increasing the prescription rates of acute coronary syndrome (ACS) secondary prevention pharmacotherapy at discharge, and to (ii) evaluate the acceptance rate of these interventions by prescribers.
    MeSH terms: Adrenergic beta-Antagonists/therapeutic use; Angiotensin-Converting Enzyme Inhibitors/therapeutic use; Cardiotonic Agents/therapeutic use*; Cross-Sectional Studies; Female; Humans; Male; Middle Aged; Patient Discharge; Pharmacists*; Retrospective Studies; Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use; Acute Coronary Syndrome/drug therapy*; Acute Coronary Syndrome/prevention & control*; Secondary Prevention/methods*; Prescriptions; Angiotensin Receptor Antagonists/therapeutic use
  20. Chai WL, Moharamzadeh K, van Noort R, Emanuelsson L, Palmquist A, Brook IM
    J Periodontal Res, 2013 Oct;48(5):663-70.
    PMID: 23442017 DOI: 10.1111/jre.12062
    Studies of peri-implant soft tissue on in vivo models are commonly based on histological sections prepared using undecalcified or 'fracture' techniques. These techniques require the cutting or removal of implant during the specimen preparation process. The aim of this study is to explore a new impression technique that does not require any cutting or removal of implant for contour analysis of soft tissue around four types of titanium (Ti) surface roughness using an in vitro three-dimensional oral mucosal model (3D OMM).
    MeSH terms: Cell Adhesion/physiology; Cell Line; Dental Impression Materials/chemistry; Dental Impression Technique; Dental Materials/chemistry; Dental Polishing/methods; Epithelial Cells/cytology; Fibroblasts/cytology; Gingiva/cytology*; Humans; Mouth Mucosa/cytology; Surface Properties; Time Factors; Titanium/chemistry; Keratinocytes/cytology; Dental Implants*; Histocytological Preparation Techniques; Dental Prosthesis Design*; Coculture Techniques; Tissue Engineering/methods; Dental Etching/methods; Tissue Scaffolds; Electrochemical Techniques; Acellular Dermis
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