Effects of CPAP on oxidative stress and nitrate efficiency in sleep apnoea: a randomised trial.

Background: Previous studies have presented contradictory data concerning obstructive sleep apnoea syndrome (OSAS), lipid oxidation and nitric oxide (NO) bioavailability. This study was undertaken to (1) compare the concentration of 8-isoprostane and total nitrate and nitrite (NOx) in plasma of middle-aged men with OSAS and no other known co-morbidity and healthy controls of the same age, gender and body mass index; and (2) test the hypothesis that nasal continuous positive airway pressure (CPAP) therapy attenuates oxidative stress and nitrate deficiency. Methods: A prospective, randomised, placebo controlled, double-blind, crossover study was performed in 31 consecutive middle-aged men with newly diagnosed OSAS and 15 healthy control subjects. Patients with OSAS were randomised to receive sham CPAP or effective CPAP for 12 weeks. Blood pressure, urinary catecholamine levels and plasma 8-isoprostane and NOx concentrations were obtained before and after both treatment modalities. Results: Patients with OSAS had significantly higher 8-isoprostane levels (median (IQR) 42.5 (29.2-78.2) vs 20.0 (12.5-52.5) pg/ml, p = 0.041, Mann-Whitney test) and lower NOx levels (264 (165-650) vs 590 (251- 1465) mmol/l, p = 0.022) than healthy subjects. Body mass index, blood pressure and urinary catecholamines were unchanged by CPAP therapy, but 8-isoprostane concentrations decreased (38.5 (24.2-58.7) pg/ml at baseline vs 22.5 (16.2-35.3) pg/ml on CPAP, p = 0.0001) and NOx levels increased (280 (177-707) vs 1373 (981-1517) mmol/l, p = 0.0001) after CPAP. Conclusions: OSAS is associated with an increase in oxidative stress and a decrease in NOx that is normalised

The measurement of ice velocity, mass balance and thinning-rate on Johnsons Glacier, Livingston Island, South Shetland Islands, Antarctica

A network of twenty stakes was set up on Johnsons Glacier in order to determine its dynamics. During the austral summers from 1994-95 to 1997-98, we estimated surface velocities, mass balances and ice thickness variations. Horizontal velocity increased dow nstream from 1 m a- 1 near the ice divides to 40 m a- 1 near the ice terminus. The accumulation zone showed low accumulation rates (maximum of 0,6 m a- 1 (ice)), whereas in the lower part of the glacier, ablation rates were 4,3 m a- 1 (ice). Over the 3-year study period, both in the accumulation and ablation zones, we detected a reduction in the ice surface level ranging from 2 to 10 m from the annual ve rt ical velocities and ice-thinning data, the mass balance was obtained and compared with the mass balance field values, resulting in similar estimates. Flux values were calculated using cross-section data and horizontal velocities, and compared with the results obtained by means of mass balance and ice thinning data using the continuity equation. The two methods gave similar results.

LWC-SYVÄPAINOHIOKKEEN LAADUN OPTIMOINTI

Työn tavoitteena oli hiokkeen laatua optimoimalla löytää keinoja pohjapaperin opasiteetin parantamiseksi. Tehtaalla oli havaittu hiokkeen palstautumislujuuden pudonneen ja pian tämän jälkeen oli paperikoneella nostettu sellun jauhatustehoa mikä puolestaan vaikuttaa negatiivisesti pohjapaperin opasiteettiin. Päähuomio hiokkeen laadun optimoinnissa keskitettiin tästä syystä palstautumislujuuden tason nostamiseen. Kirjallisuuden mukaan tärkein hiokkeen palstautumislujuuteen ja myös opasiteettiin vaikuttava tekijä on massan hienoaines. Hiokkeen hienoainespitoisuuden lisäämistä tutkittiin tässä työssä seuraavalla kolmella tavalla: rejektijauhatuksen optimointi, kivenalusmassan CSF-tason alentaminen ja jälkijauhatustehon lisääminen. Työn toisena tavoitteena oli varmistaa rejektilinjan kapasiteetin riittävyys, erityisesti rejektilajitin 6:n osalta. Taustana tälle tarkastelulle oli mahdollisen lisälajittimen investointitarve RL 6:n rinnalle. Rejektijauhatuksen optimoinnissa tutkittiin jauhatustehon, eri terämallien ja kahden rinnakkaisen rejektijauhimen (yhden sijasta) vaikutusta jauhetun rejektimassan ominaisuuksiin. Pidättävillä rejektijauhimen terillä jauhetusta massasta tuli pitkäkuituisempaa kuin referenssiterillä, joissa staattori oli pumppaava ja roottori pidättävä. Mutta vaikka pidättävillä terillä jauhettu massa oli pitkäkuituisempaa ja sisälsi vähemmän hienoainetta oli sen palstautumislujuus samaa luokkaa kuin referenssiterillä jauhetun massan. Kahden rinnakkaisen jauhimen ajomallilla saatiin laadultaan kaikein heikointa massaa. Kaikissa koeajoissa saatiin rejektimassan palstautumislujuutta parannettua jauhatustehoa lisäämällä. Kivenalusmassan CSF-tasoa alentamalla ei valmiin annosteluhiokkeen palstautumislujuus alentunut vaikka hiokkeen hienoainespitoisuus kasvoi hieman. Mutta vaikka hiokkeen palstautumislujuus ei kasvanutkaan niin koejaksolla, joka oli pituudeltaan hieman yli kuukauden, pohjapaperin opasiteetti kuitenkin parani hieman ja sellun jauhatustehoa voitiin paperikoneella pudottaa hieman. Palstautumislujuuskartoituksen, jossa otettiin näytteitä hiomon eri prosessivaiheista, mukaan jälkijauhatus oli yksittäisenä prosessivaiheena eniten hiokkeen palstautumislujuuteen vaikuttava prosessivaihe. Jälkijauhatuskoeajosta saatiinkiin parhaimmat tulokset hienoainespitoisuuden ja palstautumislujuuden nousun suhteen. Rejektilajittelun massarejektisuhteiden määritysten ja rejektilajitin 6:n kapasiteettikokeen mukaan rejektilajittelu toimii nykyisellä tuotantomäärällä halutunlaisesti ja rejektilajitin 6:n osalta tuotantoa on vielä varaa nostaakin.

Contribution of Intronic miR-338-3p and Its Hosting Gene AATK to Compensatory β-Cell Mass Expansion.

The elucidation of the mechanisms directing β-cell mass regeneration and maintenance is of interest, because the deficit of β-cell mass contributes to diabetes onset and progression. We previously found that the level of the microRNA (miRNA) miR-338-3p is decreased in pancreatic islets from rodent models displaying insulin resistance and compensatory β-cell mass expansion, including pregnant rats, diet-induced obese mice, and db/db mice. Transfection of rat islet cells with oligonucleotides that specifically block miR-338-3p activity increased the fraction of proliferating β-cells in vitro and promoted survival under proapoptotic conditions without affecting the capacity of β-cells to release insulin in response to glucose. Here, we evaluated the role of miR-338-3p in vivo by injecting mice with an adeno-associated viral vector permitting specific sequestration of this miRNA in β-cells. We found that the adeno-associated viral construct increased the fraction of proliferating β-cells confirming the data obtained in vitro. miR-338-3p is generated from an intron of the gene coding for apoptosis-associated tyrosine kinase (AATK). Similarly to miR-338-3p, we found that AATK is down-regulated in rat and human islets and INS832/13 β-cells in the presence of the cAMP-raising agents exendin-4, estradiol, and a G-protein-coupled Receptor 30 agonist. Moreover, AATK expression is reduced in islets of insulin resistant animal models and selective silencing of AATK in INS832/13 cells by RNA interference promoted β-cell proliferation. The results point to a coordinated reduction of miR-338-3p and AATK under insulin resistance conditions and provide evidence for a cooperative action of the miRNA and its hosting gene in compensatory β-cell mass expansion.

Use of the dried blood spot sampling process coupled with fast gas chromatography and negative-ion chemical ionization tandem mass spectrometry: application to fluoxetine, norfluoxetine, reboxetine, and paroxetine analysis.

The objective of this work was to combine the advantages of the dried blood spot (DBS) sampling process with the highly sensitive and selective negative-ion chemical ionization tandem mass spectrometry (NICI-MS-MS) to analyze for recent antidepressants including fluoxetine, norfluoxetine, reboxetine, and paroxetine from micro whole blood samples (i.e., 10 microL). Before analysis, DBS samples were punched out, and antidepressants were simultaneously extracted and derivatized in a single step by use of pentafluoropropionic acid anhydride and 0.02% triethylamine in butyl chloride for 30 min at 60 degrees C under ultrasonication. Derivatives were then separated on a gas chromatograph coupled with a triple-quadrupole mass spectrometer operating in negative selected reaction monitoring mode for a total run time of 5 min. To establish the validity of the method, trueness, precision, and selectivity were determined on the basis of the guidelines of the "Société Française des Sciences et des Techniques Pharmaceutiques" (SFSTP). The assay was found to be linear in the concentration ranges 1 to 500 ng mL(-1) for fluoxetine and norfluoxetine and 20 to 500 ng mL(-1) for reboxetine and paroxetine. Despite the small sampling volume, the limit of detection was estimated at 20 pg mL(-1) for all the analytes. The stability of DBS was also evaluated at -20 degrees C, 4 degrees C, 25 degrees C, and 40 degrees C for up to 30 days. Furthermore, the method was successfully applied to a pharmacokinetic investigation performed on a healthy volunteer after oral administration of a single 40-mg dose of fluoxetine. Thus, this validated DBS method combines an extractive-derivative single step with a fast and sensitive GC-NICI-MS-MS technique. Using microliter blood samples, this procedure offers a patient-friendly tool in many biomedical fields such as checking treatment adherence, therapeutic drug monitoring, toxicological analyses, or pharmacokinetic studies.

Nestepakkauskartongin runkokerroksen rakenteen optimointi

Diplomityön tavoitteena oli optimoida KA4:n nestepakkauskartongin runkokerroksen massakoostumus ja rakenne kartonkikoneen uusinnan jälkeen. Työssä tutkittiin Natura 285 –laatua, jota käytetään yhden litran vetoisissa maitopurkeissa. Pääasiallisena tavoitteena oli lisätä CTMP:n osuutta ja vähentää mäntysellun osuutta rungossa siten, että kartongin laatu ei heikkene. Työn kirjallisuusosassa perehdyttiin nestepakkauskartongin kriittisiin ominaisuuksiin ja CTMP:n vaikutuksiin runkokerroksessa. Rainanmuodostusta ja kuituverkoston lujuuden syntymistä käsiteltiin omina kokonaisuuksinaan. CTMP:n freeness-tason huomattava vähentäminen kasvattaa kartongin z-lujuutta ja palstautumislujuutta merkittävästi. Samalla höyrynkulutus kuitenkin kasvaa ja kartongin jäykkyys laskee jonkin verran paksuuden vähenemisen seurauksena. CTMP:n freeness-tason alentaminen arvosta 420 ml CSF arvoon 380 ml CSF ei alenna bulkkia merkittävästi. CTMP:n määrän kasvattaminen yli 60 %:in keskikerroksessa alentaa palstautumislujuutta ja z-lujuutta merkittävästi. Runkokerroksen mäntysellun korvaaminen koivusellulla parantaa kartongin sileyttä merkittävästi vakiopaksuudessa. Runkokerroksen massakomponenttien jauhatuksen lisäämisestä huolimatta z-lujuus ja palstautumislujuus laskevat vastaavasti huomattavan paljon. Koivusellun käytöllä valmiin pakkauksen ominaisuudet eivät heikkene, mutta painatusominaisuudet paranevat. CTMP-laitoksen pääjauhinten uudella LE-terämallilla saavutetaan huomattava energian säästö vanhaan terämalliin verrattuna. Kuidun keskipituus laskee jonkin verran LE-terien ikääntyessä ja samalla kuitujen sitoutumiskyky heikkenee.

Energiansäästäminen, sen toteutus ja vaikutukset lannoitteita valmistavalla tehtaalla

Suomen täytyy vähentää kasvihuonekaasupäästöt vuoden 1990 tasolle vuosien 2008–2012 velvoitekauden aikana. Suomen kansallisen ilmasto-ohjelman mukaan noin puolet vaadittavasta vähennystavoitteesta voidaan saavuttaa lisäämällä biopolttoaineiden käyttöä ja säästämällä energiaa. Kemira Agro Oy:n Uudenkaupungin tehtaiden energiansäästäminen on alkanut sen liityttyä teollisuuden vapaaehtoiseen energiansäästösopimukseen vuonna 1999. Sopimus velvoittaa vähentämään energian ja veden kulutusta sekä raportoimaan vuosittaisista kulutuksista. Työssä on esitelty energiansäästämisen eteneminen yrityksessä sopimuksen hyväksymisestä energiansäästöanalyysin toteutukseen asti. Työssä on etsitty energiaa säästäviä ratkaisuja lannoitetehtaan käyttöön tehtaan tuotantoprosesseissa. Tuotanto-osastoille on laskettu energiataseet, joiden avulla on piirretty energiavirtoja kuvaavat sankey – diagrammit. Työssä on esitetty perusidea energiansäästön toteuttamiseksi ja alustavat kustannusarviot. Löydetyillä kohteilla voidaan säästää tehtaan sähkönkulutusta yhteensä 19 GWh/a ja lisätä tuotantoa. Ionivaihdettua vettä voidaan säästää noin 6000 m3/a. Laskelmat on esitetty cd-romilla liitteessä 31.

Residues of b-lactams and quinolones in tissues and milk samples. Confirmatory analysis by liquid chromatography-mass spectrometry

The aim of this work is to optimize and validate methods for the multiresidue determination of series of families of antibiotics as quinolones, penicillins and cephalosporins included in European regulation in food samples using LC-MS/MS. Different extraction techniques and clean-up applied to antibiotics in meat were compared. The quality parameters were established according with EU guideline. The developed method was applied to 49 positive raw milk samples from animal medicated with different antibiotics; the 63% of the analyzed samples were found to be compliant. ___________________________________________________________________________________________

Metabolomic assays of amoxicillin, cephapirin and ceftiofur in chicken muscle. Application to treated chicken samples by liquid chromatography quadrupole time-of-flight mass spectrometry

The aim of this study was to identity metabolites and transformation products (TPs) in chicken muscle from amoxicillin (AMX), cephapirin (PIR) and ceftiofur (TIO), which are antibiotics of the β-lactam family. Liquid chromatography coupled to quadrupole time-of-flight (QqTOF) mass spectrometry was utilized due to its high resolution, high mass accuracy and MS/MS capacity for elemental composition determination and structural elucidation. Amoxicilloic acid (AMA) and amoxicillin diketopiperazine (DKP) were found as transformation products from AMX. Desacetylcephapirin (DAC) was detected as a metabolite of PIR. Desfuroylceftiofur (DFC) and its conjugated compound with cysteine (DFC-S-Cys) were detected as a result of TIO in contact with chicken muscle tissue. The metabolites and transformation products were also monitored during the in vivo AMX treatment and slaughtering period. It was found that two days were enough to eliminate AMX and associated metabolites/transformation products after the end of administration.

Effect of GA3, KNO3, and removing of basal point of seeds on germination of sweet granadilla (Passiflora ligularis Juss) and yellow passion fruit (Passiflora edulis f. flavicarpa)

Passiflora seeds germinate erratically presenting difficulties for their handling in a greenhouse. The effect of removing of basal point of seeds (RB) and pre-imbibition of seeds of sweet granadilla and yellow passion fruit in 50, 100, 200, and 400 mg mL-1 solutions of gibberellic acid (GA3) or 0.1% KNO3 solution was studied. The experiment was conducted in greenhouses in La Plata, Colombia. Two accessions PrJ1 and PrJ2 of sweet granadilla were evaluated. There were calculated the final percentage of germination (PG), mean germination time (MGT), and the mean germination rate (MGR). The leaf area and dry mass of seedlings were measured 22 days after sowing (das); with this data, specific leaf area and relation root/shoot were calculated. In all cases, the highest germination percentages were achieved treating seeds with KNO3 (89, 92, and 87% for yellow passion fruit, PrJ2, and PrJ1, respectively), but the increase in MGR (3.3 germinated seeds per day) and the decrease in MGT (16 days) were only significant for PrJ1. RB had a significant reduction of PG in all cases (28, 12, and 33% for passion fruit, PrJ2 and PrJ1, respectively). With the increase in the concentration of GA3, PG was reduced for two accessions of sweet granadilla, for yellow passion fruit this trend was not clear, no treatment with GA3 showed significant differences with the control. Leaf area (24.07 cm2) and dry mass of seedlings (135 mg) were significantly higher than seeds previously treated with KNO3 only for PrJ1.The solution of KNO3 0,1% is recommended to improve the germination and initial growth of granadilla seedlings.

The role of ubiquitin specific peptidase 15 (USP 15) in human glioblastoma

Glioblastoma (GBM) is the most common and most aggressive malignant primary brain tumour. Despite the aggressiveness of the applied therapy, the prognosis remains poor with a median survival to of about 15 months. It is important to identify new candidate genes that could have clinical application in this disease. Previous gene expression studies from human GBM samples in our laboratory, revealed Ubiquitin Specific Peptidase 15 (USP15) as a gene with low expression, significantly associated with genomic deletions of the chromosomal region encompassing the USP15 locus. USP15 belongs to the ubiquitin-specific protease (USPs) family of which the main role is the reversion of ubiquitination and thereby stabilization of substrates. Previously, USP15 has been suggested to have a tumour suppressor function via its substrates APC and Caspase 3. We established GBM cell lines that stably express USP15 wt or its catalytic mutant. USP15 expression impairs cell growth by inhibiting cell cycle progression. On the other hand USP15 depletion in GBM cell lines induces cell cycle progression and proliferation. In order to identify the molecular pathways in which USP15 is implicated we aimed to identify protein-binding partners in the GBM cell line LN-229 by Mass spectrometry. As a result we identified eight new proteins that interact with USP15. These proteins are involved in important cellular processes like cytokinesis, cell cycle, cellular migration, and apoptosis. Three of these protein interactions were confirmed by co-immunoprecipitation in four GBM cell lines LN-229, LN428, LN18, LN-Z308. One of the binding proteins is HECTD1 E3 ligase of which the murine homologue promotes the APC-Axin interaction to negatively regulate the Wnt pathway. USP15 can de-ubiquitinate HECTD1 in the LN229 cell line while its depletion led to decrease of HECTD1 in GBM cell lines suggesting stabilizing role for USP15. Moreover, HECTD1 stable expression in LN229 inhibits cell cycle, while its depletion induces cell cycle progression. These results suggest that the USP15-HECTD1 interaction might enhance the antiproliferative effect of HECTD1 in GBM cell lines. Using the TOPflash/FOPflash luciferase system we showed that HECTD1 and USP15 overexpression can attenuate WNT pathway activity, and decrease the Axin2 expression. These data indicate that this new protein interaction of USP15 with HECTD1 results in negative regulation of the WNT pathway in GBM cell lines. Further investigation of the regulation of this interaction or of the protein binding network of HECTD1 in GBM may allow the discovery of new therapeutic targets. Finally PTPIP51 and KIF15 are the other two identified protein partners of USP15. These two proteins are involved in cell proliferation and their depletion in LN-229 cell line led to induction of cell cycle progression. USP15 displays a stabilizing role for them. Hence, these results show that the tumour suppressive role of USP15 in GBM cell line via different molecular mechanisms indicating the multidimensional function of USP15. Résumé Le glioblastome (GBM) est la tumeur primaire la plus fréquente et la plus agressive du cervau caractérisée par une survie médiane d'environ à 15 mois. De précédant travaux effectués au sein de notre laboratoire portant sur l'étude de l'expression de gènes pour des échantillons humains de GBM ont montré que le gène Ubiquitin Specific Peptidase 15 (USP1S) était significativement associée à une délétion locales à 25% des cas. Initialement, les substrats protéiques APC et CaspaseS de USP15 ont conduit à considérer cette protéine comme un suppresseur de tumeur. USP15 appartient à la famille protèsse spécifique de l'ubiquitine (USPs) dont le rôle principal est la réversion de l'ubiquitination et la stabilisation de substrats. Par conséquent, nous avons établi des lignées de cellules de glioblastome qui expriment de manière stable USP15 ou bien son mutant catalytique. Ainsi, nous avons ainsi démontré que l'expression de l'USP15 empêche la croissance cellulaire en inhibant la progression du cycle cellulaire. Inversement, la suppression de l'expression du gène USP15 dans les lignées cellulaires de glioblastome induit la progression du cycle cellulaire et la prolifération. Afin d'identifier les voies moléculaires dans lesquelles sont impliquées USP15, nous avons cherché à identifier les partenaires de liaisons protéiques par spectrométrie de masse dans la lignée cellulaire LN-229. Ainsi, huit nouvelles protéines interagissant avec USP15 ont été identifiées dont la ligase E3 HECTD1. L'homologue murin de Hectdl favorise l'interaction APC-Axin en régulant négativement la voie de signalisation de Wnt. USP15 interagit en désubiquitinant HECTD1 dans la lignée cellulaire LN-229 et provoque ainsi l'atténuation de l'activité de cette voie de signalisation. En conclusion, HECTD1, en interagissant avec USP15, joue un rôle de suppresseur de tumeur dans les lignées cellulaire de GBM.