7 research outputs found
<i>Mtb</i> MazG is required for resistance to RNS shown <i>in vitro</i> and <i>ex vivo</i>.
<p>(<b>A</b>) <i>mazG</i>-null <i>Mtb</i> is susceptible to killing by acid nitrite. Exponential phase cultures (OD<sub>600</sub>âŒ0.5) were suspended in 7H9-OADC pH4.5 with or without 2.5 mM NaNO<sub>2</sub> and treated for 20 hours. wt, wild-type <i>Mtb</i>; Î<i>mazG</i>, <i>mazG</i>-null <i>Mtb</i>; compl, the complemented mutant. Data shown are mean ± S.E. of triplicates. * <i>p</i><0.05 <i>vs</i> wt. (<b>B</b>) Quantitative real-time PCR analyses of <i>mazG</i> and <i>dosR</i> from <i>Mtb</i> treated with DETA/NO or acid nitrite. All data were normalized to the levels of <i>sigA</i>. The <i>dosR</i> gene was used as a positive control <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003814#ppat.1003814-Voskuil1" target="_blank">[70]</a>. Results are expressed as the changes in expression levels compared to untreated samples. Mean ± S.E of three independent repeats. <b>C to E</b>, Survival of wild-type <i>Mtb</i>, the <i>mazG</i>-null mutant and the complemented mutant in resting (<b>C</b>), activated (<b>D</b>) or NMMA treated (<b>E</b>) cells of murine macrophage cell line RAW264.7. Shown is one representative result of two independent experiments.</p
Akupressur - Komplement till traditionell terapi vid postoperativt illamÄende och krÀkningar
Postoperativt illamÄende och krÀkningar, PONV, har sedan anestesins begynnelse vÄllat patienten stort lidande. TillstÄndet kan förlÀnga den postoperativa vistelsen och Àr en av de vanligaste orsakerna till oplanerad inlÀggning av patienter i samband med dagkirurgi. Syftet med föreliggande arbete var att undersöka den förebyggande effekten av akupressur som ensam intervention eller i kombination med viss farmakologisk antiemetisk terapi vid postoperativt illamÄende och krÀkningar hos vuxna patienter efter allmÀnkirurgi. En systematisk litteraturstudie genomfördes och tio vetenskapliga artiklar inkluderades och kvalitetsbedömdes. Sökning utfördes i databaserna PubMed, EBSCO HOST och Cochrane Library. Dessutom genomfördes manuell sökning. Resultatet visade att akupressur pÄ en speciell triggerpunkt, P6, har en förebyggande effekt mot PONV. Ondansetron och akupressur Àr lika effektivt mot PONV, medan Droperidol verkar ha bÀttre effekt Àn akupressur. Slutsatsen var att akupressur har en plats som profylaktisk antiemetika för att förebygga PONV.Postoperative nausea and vomiting (PONV) has since the beginning of anesthesia caused the patient great suffering. It can prolong the post-operative stay and is one of the most common reasons for unplanned admittance of patients in connection to day surgery.
The aim of this work was to study the preventive effect of acupressure as the lone intervention or in combination with certain pharmacological antiemetic therapies for post-operative nausea and vomiting in adult patients who have undergone general surgery. A systematic literature review was conducted and ten articles were included and each study subjected to a quality assessment. A PubMed, EBSCO HOST and Cochrane Library Database were conducted and a manual search of the literature references completed the search.
The results showed that acupressure at the P6 meridian point has a preventive effect against PONV and that Ondansetron and acupressure are similarly effective against PONV, while Droperidal seems to have a better effect than acupressure. The conclusion was that acupressure can be used prophylactic to prevent PONV
The antimutator role of MazG in <i>Msm</i> (A) and <i>Mtb</i> (B).
<p>Both the bacterial culture conditions and the methods for determination of mutation frequencies were illustrated in <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003814#s4" target="_blank"><b><i>Materials and Methods</i></b></a> in detail. The frequencies conferring resistance to rifampicin in wild-type (wt), <i>mazG</i>-null (Î<i>mazG</i>) and the complemented mutant (compl) strains were determined in exponential phase (OD<sub>600</sub>âŒ0.5) with or without oxidative stress and in the stationary growth phase. Oxidative stress was induced by treating exponential phase cultures with 10 mM H<sub>2</sub>O<sub>2</sub> for 5 h (<i>Msm</i>) or 24 h (<i>Mtb</i>). Stationary phase was at the 5<sup>th</sup>-day or 28<sup>th</sup>-day of culture for <i>Msm</i> or <i>Mtb</i>, respectively. (<b>C</b>) Survival rate of <i>Msm</i> and <i>Mtb</i> strains after exposure to H<sub>2</sub>O<sub>2</sub>. The numbers shown are mean ± S.E. of 3 independent experiments totaling 15 cultures of <i>Msm</i> and 6 of <i>Mtb</i>.</p
MazG is required for <i>Mtb</i> survival <i>in vivo</i> and the corresponding lung pathogenesis.
<p><b>A to B</b>, Bacterial loads in spleen (<b>A</b>) and lung (<b>B</b>) of mice infected with wild-type <i>Mtb</i> (wt), the <i>mazG</i>-null mutant (Î<i>mazG</i>) and the complemented mutant (compl). Data shown are mean ± S.E from 4 mice per group. (<b>C</b>) Lung sections taken from mice at 8-wk after infection and stained with hematoxylin and eosin. Inserted column shows mean ± S.E of lung inflammation of each group.</p
<i>mazG</i>-null <i>Msm</i> exhibited elevated CG to TA mutation under oxidative stress conditions and in the stationary phase of growth.
<p>Spontaneous rifampicin-resistant colonies were collected from 3 independent experiments (see Methods). Cluster I region of <i>rpoB</i> were PCR-amplified using <i>pfu</i> DNA polymerase and sequenced bi-directionally. All of the sequenced colonies contain single non-synonymous mutations (see also <b><a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003814#ppat.1003814.s003" target="_blank">Table S1</a> and <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003814#ppat.1003814.s004" target="_blank">S2</a></b>). wt, wild-type <i>Msm</i>; Î<i>mazG</i>, <i>mazG</i>-null <i>Msm</i>.</p
5-OH-dCTP is an <i>in vivo</i> substrate of mycobacterial MazG proved by chemical genetic analysis.
<p>The <i>Msm</i> competent cells were prepared as described in <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003814#s4" target="_blank"><b><i>Materials and Methods</i></b></a>, the nucleotides were incorporated by transformation. (<b>A</b>) <i>mazG</i>-null <i>Msm</i> (Î<i>mazG</i>) exhibited a dose-dependent 5-OH-dCTP induced mutagenesis. wt, wild-type <i>Msm</i>. The data shown are mean ± S.E. of four repeats. (<b>B</b>) The rifampicin-resistance mutation frequencies of wild-type <i>Msm</i>, the <i>mazG</i>-null mutant and the complemented mutant treated with 5-OH-dCTP and dCTP. Nucleotides were added at 100 ”M final concentration. Mean ± S.E of 12 independent transformations. **<i>p</i><0.01 <i>vs</i> wt, * <i>p</i><0.05 <i>vs</i> wt. (<b>C</b>) The rifampicin-resistance mutation frequencies of wild-type and <i>mazG</i>-null <i>Msm</i> treated with 100 ”M 2-OH-dATP, 5-CHO-dUTP and normal dNTPs. Mean ± S.E of 8 independent transformations. (<b>D</b>) <i>mazG</i>-null <i>Msm</i> is susceptible to killing by 5-OH-dCTP. Strains were treated with 100 ”M 5-OH-dCTP for 5 hours at 37°C. Shown is percent survival compared to an untreated control (100%). The data shown are mean ± S.E. of four repeats.</p