177 research outputs found
Seaweed against strontium and preussian blue against cesium
The fact that alginates bind strontium and cyanates bind cesium and are capable of removing these elements from living organisms is scientifically verified. Zeolites offer another possibility for exchange of these ions. Practical research should be initiated to find the right doses and procedure to decrease the body burden of radioactive isotopes in reindeer.Alger mot strontium och berlinerblått mot cesium.Abstract in Swedish / Sammanfattning: Mitt budskap år kort: Alger binder strontium, Berlinerblått binder cesium, Sätt fart på forskning och forsök
Planning theory and regulatory documents in practice : implementation of Stockholm's bycycle plan in Hjorthagen
MÄnga stÀder arbetar idag med att öka andelen resor som sker med cykel. Denna ambition finns ocksÄ i Stockholm, dÀr mÄlet Àr att Stockholm ska kunna konkurrera med Köpenhamn och Amsterdam som Àr vÀrldsledande inom omrÄdet. En del i stadens strategi för att öka andelen cykelresor Àr att utveckla och utöka cykelinfrastrukturen i staden och genom detta förbÀttra förutsÀttningarna för cyklister genom att tillhandahÄlla en cykelinfrastruktur som gör det enkelt och sÀkert att cykla i Stockholm. Ett antal strategidokument som anger riktningen för hur cykelinfrastrukturen ska utformas har dÀrför tagits fram av Stockholms stad.
Men i Stockholm finns en diskrepans mellan den bild av cykelinfrastrukturen som mÄlas upp i strategidokumenten och den bild den verkliga miljön ger. MÄlet för denna uppsats Àr att undersöka hur planeringsaktiva i Stockholm arbetar utifrÄn strategidokumenten, hur de förstÄr, tolkar och omsÀtter dessa och vad det i sin tur betyder för de cyklister som senare ska anvÀnda de miljöerna dessa skapar.
I detta arbete pĂ„visar jag att det finns skillnader i hur de olika planeringsaktiva involverade i en process tolkar och förstĂ„r strategidokumenten, och att detta pĂ„verkar deras syn pĂ„ mĂ„len för cykelinfrastrukturens utformning i en ny stadsdel. Jag menar ocksĂ„ att det har visat sig vara svĂ„rt att tillĂ€mpa cykelplanen pĂ„ ett konsekvent sĂ€tt dĂ„ olika hinder som anses oöverkomliga eller för svĂ„ra att avhjĂ€lpas uppkommer eller synliggörs under processens gĂ„ng. Cykelplanen har ocksĂ„ visat sig innehĂ„lla standardiserade lösningar som ibland stĂ„r i konflikt med de övergripande mĂ„lbilderna. Detta, tillsammans med en acceptans för undermĂ„liga lösningar, gör att den cykelinfrastruktur som anlĂ€ggs inte klarar av att leva upp till varken cykelplanens mĂ„lbild eller cyklisternas förvĂ€ntningar. Den diskrepans som finns mellan cykelinfrastrukturen i dokumenten och cykelinfrastrukturen i verkligheten kvarstĂ„r till stor del i det nya omrĂ„det, vilket i slutĂ€ndan drabbar de som vĂ€ljer att göra sin resa i Stockholm med cykel.Many cities are currently working to increase the amount of travels made by bike. This ambition is also shared by Stockholm, where the goal is to compete with cities like Copenhagen and Amsterdam who are world leading in this field. A part of the cityâs strategy to increase travels made by bike is to improve and expand the infrastructure for cycling in the city and provide an infrastructure that make it safe and easy to travel by bike in Stockholm. A number of strategy-documents to help set the course for how bicycle infrastructure should be designed has therefore been issued by the city of Stockholm.
However, in Stockholm there is a discrepancy between the picture drawn out in the documents and the experience in reality. The goal of this thesis is to examine how the people working within the field of planning in Stockholm understand, interpret and convert these strategies, and how this practice affects the bicyclists who will be using the environments created.
In this thesis I will show that there are differences in how the people working with the planning process interpret and understand these strategies, and that this affect their view of the goals for the bicycle infrastructure in shaping a new urban area. I will also show that it has been proven difficult to apply the strategies in a consistent manner, since obstacles viewed as insuperable or too hard to overcome, emerge or are made visible during the process of planning. The bicycle plan also contains standardized design solutions that are sometimes in conflict with the overall goals. This, in combination with the acceptance shown for inferior solutions, makes for a bicycle infrastructure that cannot live up to neither the goal of the bicycle plan nor the expectations of the bicyclists. The discrepancy between the bicycle infrastructure in the documents and in reality therefore remain in the new urban area, and this will ultimately come to affect those who will choose to travel by bike in Stockholm
Impact of pulsating infrared and red monochromatic light treatment on wound healing in horses.
Low Level Light Therapy (LLLT) is a treatment method where red light or near infrared (NIR) light is utilised for treating a variety of disorders including wounds. Wound healing in horses may be slow, especially on the distal limb, and there is an interest to shorten healing times. The purpose of the present study was to investigate how treatment with pulsating visible red light (λâ637 nm) and NIR light (λâ956 nm) affects wound healing time in healthy horses.
A circular skin wound (Ă=2 cm) was created on each side of the neck in healthy horses (n=8). One of the wounds was treated using light treatment and the other was left untreated, serving as negative control. Treatment duration was 4 minutes and 40 seconds (red light 95 seconds, NIR light 185 seconds) and was performed once daily day 0-4, 7-11, 14-18 and 21-25. The irradiance was measured to 2.3 mW/cm2 for red light and 6.4 mW/cm2 for NIR light.
The wounds were photographed and evaluated using digital planimetry day 0, 1, 2, 3, 4, 7, 14, 21, 28 and 35. The wound area did not differ between treated and control group on any day. The wounds where visually inspected daily and the time to complete healing was recorded. Control wounds were judged as completely healed after a mean time of 49,0 days (95%Ci=35,462,6) and treated wounds after 51,8 days (95%Ci=38,7-64,8). This is a significantly shorter time to complete healing for control wounds (p=0,026). The evaluators were blinded in respect to which wound was treated.
The results of this study do not indicate any positive effect of light treatment on healing of experimental skin wounds in horses.Low Level Light Therapy (LLLT) Ă€r en behandlingsmetod dĂ€r rött ljus eller ljus i den nĂ€ra infraröda (NIR) delen av spektrumet anvĂ€nds, bland annat i syfte att förkorta sĂ„rlĂ€kningstider. SĂ„rlĂ€kning pĂ„ hĂ€st kan ta lĂ„ng tid, sĂ€rskilt pĂ„ benens distala delar och ett intresse finns för metoder som kan förkorta lĂ€kningstiden. Syftet med denna studie Ă€r att undersöka om behandling med pulserande rött synligt ljus (λâ637 nm) och NIR ljus (λâ956 nm) pĂ„verkar sĂ„rlĂ€kningshastigheten hos friska hĂ€star.
Ett cirkulĂ€rt sĂ„r (Ă=2 cm) stansades ut pĂ„ vardera sida av halsen hos friska hĂ€star (n=8). Den ena sidans sĂ„r ljusbehandlades och den andra sidan lĂ€mnades som negativ kontroll. Behandlingen varade i 4 minuter och 40 sekunder (rött ljus 95 sekunder, NIR ljus 185 sekunder) och utfördes en gĂ„ng dagligen dag 0-4, 7-11, 14-18 och 21-25. Irradiansen för rött ljus mĂ€ttes till 2,3 mW/cm2 och för NIR ljus till 6,4 mW/cm2.
SÄren fotograferades och utvÀrderades med digital planimetri dag 0, 1, 2, 3, 4, 7, 14, 21, 28 och 35. SÄrarean skiljde inte mellan behandlings- och kontrollgrupp nÄgon av dagarna. SÄren inspekterades visuellt dagligen och tiden till fullstÀndig lÀkning noterades. KontrollsÄren bedömdes fullstÀndigt lÀkta efter i genomsnitt 49,0 dagar (95%Ci=35,4-62,6) och behandlade sÄr efter 51,8 dagar (95%Ci=38,7-64,8). Tiden till fullstÀndig lÀkning var signifikant kortare för kontrollsÄren (p=0,026). Personerna som utvÀrderade sÄrlÀkningen var blindade för vilka sÄr som var behandlade.
Ljusbehandling hade ingen pÄskyndande effekt pÄ lÀkning av experimentellt framkallade sÄr hos hÀst i denna studie
Visual evoked potentials (VEP) : development in the growing horse
VEP (visual evoked potentials) Àr en elektrofysiologisk metod som anvÀnds för att studera de högre synvÀgarnas (postretinal) funktion. Hos mÄnga djurslag sker en omfattande utveckling av VEP-kurvans utseende frÄn födseln fram till vuxen Älder. Syftet med denna studie Àr att undersöka hur hÀstens VEP, och dÀrmed synsinne, utvecklas i tidig Älder.
Arbetet bestÄr av en litteraturstudie och en experimentell del. I litteraturstudien sammanfattas vad som gjorts pÄ andra djurslag vad gÀller utvecklingen av VEP frÄn födseln och framÄt samt vad som gjorts gÀllande VEP pÄ hÀst. Den experimentella delen bestÄr i huvudsak av en jÀmförelse mellan VEP frÄn föl och VEP frÄn vuxna hÀstar, men det ingÄr Àven en jÀmförelse mellan sedering med tvÄ olika α2-agonister, xylazin och detomidin.
Resultaten visar att det utan större besvÀr gÄr att registrera VEP pÄ föl och att vÄgformen frÄn nyfödda föl (<48h gamla) visar stora likheter med VEP frÄn vuxna hÀstar. Fölen hade generellt högre amplituder som sedan verkade minska med stigande Älder. JÀmförelsen mellan sederingarna visade att det var svÄrare att fÄ ett adekvat sederingsdjup med xylazin, men med ett gott sederingsdjup gav det en kurvform som var jÀmförbar med detomidinsedering. Det Àr dock oklart exakt hur latenser och amplituder pÄverkas av sederingen, dÄ endast ett fÄtal hÀstar ingick i studien.
Slutsatsen Àr att hÀstars synsinne förefaller vara vÀl utvecklat redan vid mycket ung Älder. EvolutionÀra aspekter, effekten av sedering och möjliga anledningar till de högre amplituderna hos föl diskuteras.VEP (visual evoked potentials) is an electrophysiological method used for evaluating the postretinal pathways. In many species the VEP changes considerably and maturates during the first weeks/months of life. The purpose of this study was to examine how the equine VEP, and therefore postretinal function, changes from birth to adult age.
This thesis is composed of two parts. The first part is a review of pertinent studies regarding VEP in horses and the development of VEP in other species. The second part is an experimental part, which mainly consists of a comparison of the VEP between foals and adult horses. Furthermore, a comparison between sedation with two different α2-agonists, detomidine and xylazine, is made.
The results show that it is possible to register VEP from newly born foals (<48h of age) and that their basic waveform of the VEP is highly similar to the VEP of the adult horses. The amplitudes of the components in the foal-VEP were generally higher than the adult amplitudes. The comparison of sedation with detomidine and xylazin showed that it was more difficult obtaining an adequate sedation depth when using xylazine. When adequate xylazine sedation was achieved the two substances gave comparable waveforms. The exact impact on latencies and amplitudes could not be determined, because of the small sample size.
In conclusion horses seem to have a well-developed vision early in life. Evolutionary aspects, the effects of sedation and possible reasons for the higher amplitudes are discussed
Upper respiratory disease caused by feline herpesvirus type 1 and feline calicivirus : laboratory diagnostics, epidemiology and immunoprophylaxis
De vanligaste orsakerna till kattsnuva Àr infektion med felint herpesvirus typ 1 (FHV-1) eller felint calicivirus (FCV). BÄda virusen Àr vanligt förekommande Àven i den friska populationen och prevalensen Àr generellt högre i större djurgrupper. Efter infektion med FHV-1 lÀgger sig viruset ofta latent och kan Äteraktiveras av olika stressfaktorer. FCV kan utsöndras i flera Är efter infektion och detta utan att katterna visar kliniska symtom.
Smittspridning för FHV-1 sker frÀmst via direktkontakt med akut sjuka djur eller intermittent utsöndrande djur. FCV smittar direkt frÄn sjuka djur eller friska smittbÀrare men kan ocksÄ smitta via ytor. I tÀta kattpopulationer Àr troligen smittspridning via ytor en viktig smittvÀg Àven för FHV-1.
Polymeraskedjereaktion (PCR) och virusisolering (VI) anvÀnds idag för att detektera virus frÄn infekterade katter. En bra PCR kan upptÀcka fÀrre viruspartiklar Àn VI och Àr sÄledes bÄde kÀnsligare och snabbare. Eftersom det Àr vanligt med friska smittbÀrare betyder positivt
testsvar inte sĂ€kert att viruset Ă€r sjukdomsorsakande hos individen. Serologi har inte visat sig anvĂ€ndbart vid sjukdomsdiagnostisering, men höga antikroppstitrar kan tyda pĂ„ att individen Ă€r skyddad frĂ„n sjukdom. En korrelation mellan halten virusneutraliserande antikroppar (VNA) och skydd vid âchallengeâ förekommer, men Ă€r inte fullstĂ€ndig. Individer utan VNA kan ocksĂ„ vara skyddade, vilket tyder pĂ„ att cell-medierad immunitet ocksĂ„ Ă€r viktig.
Prevalensstudier i Europa visar siffror för FHV-1 i friska populationer sÄ lÄga som 0 % och sÄ höga som 11 %. För FCV Àr motsvarande siffror mellan 2,6 % och 29 % i den friska
populationen. Den stora skillnaden beror troligen pÄ hur studiepopulationen valts men ocksÄ pÄ flera faktorer sÄ som hur provet Àr taget och val av analysmetod.
Vaccinering ger inget fullstÀndigt skydd mot infektion och sjukdom men ger skydd genom en lindrigare symtombild vid infektion. Vaccinering ger ocksÄ en minskad virusutsöndring, men prevalensstudier tyder pÄ att den Àr otillrÀcklig för begrÀnsning av smittspridning. FCV
muterar ofta och antigeniciteten skiljer mycket mellan olika stammar, men alla anses tillhöra samma serotyp. Skillnaden i antigenicitet fÄr till följd att olika immunitet bildas beroende pÄ stam. Immunitet mot en stam ger bra skydd mot andra stammar om korsreaktiviteten mellan stammarna Àr hög. Val av vaccinstam kan sÄledes vara av betydelse för att skapa en sÄ bra immunitet som möjligt mot fÀltstammar. Nya studier tyder pÄ att bredare korsneutraliserande förmÄga och bÀttre skydd kan fÄs genom att kombinera flera stammar i samma vaccin.
Syftet med denna litteraturstudie Àr att undersöka vilka laboratoriediagnostiska metoder som finns tillgÀngliga för att undersöka förekomst av sjukdom och sjukdomens epidemiologi samt belysa vÀrdet av immunprofylax.The most common cause of upper respiratory disease in cats is infection with feline herpesvirus type 1 (FHV-1) or feline calicivirus (FCV). Both viruses are commonly found in
the healthy cat population and the prevalence is usually higher in larger cat groups. Following FHV-1-infection the virus often becomes latent and may be reactivated by stress. FCV may be shed for several years post infection without the presence of clinical signs. Transmission of
FHV-1 mainly occurs by direct contact with acutely ill animals or latently infected cats undergoing reactivation. FCV spreads mainly directly from sick cats or carriers, but may also spread via contaminated environment. Environmental contamination with FHV-1 is probably an important way of transmission in dense cat populations.
Polymerase chain reaction (PCR) and virus isolation (VI) are used for detecting virus in infected cats. A good PCR has the ability to detect smaller amounts of virions and is hence both more sensitive and faster. Since it is common with healthy cats shedding virus, a positive test does not automatically mean that the agent is disease-causing. Serology has not been found useful for diagnosing disease, but antibody level indicates if the cat is protected from disease or not. A correlation between virus-neutralizing antibodies (VNA) and protection against challenge infection exists but cats without VNA may also be protected,
indicating that cell-mediated immunity is an important factor.
Prevalence studies in Europe show a prevalence of FHV-1 in the healthy cat population between 0 % and 11 %. Corresponding figures for FCV are 2,6 % to 29 %. The substantial differences in results are probably due to how the study population is chosen but also to factors such as sampling technique and the method used for analysis.
Vaccination does not provide full protection against infection or disease but lessens the severity of clinical symptoms. Even though viral shedding is lower in vaccinated cats, prevalence studies indicate that this does not prevent transmission. FCV mutates quickly and the antigenicity differs between different strains, but all strains are considered to belong to the same serotype. The diverse antigenicity results in different immunity to the various strains.
Immunity to one strain offers protection to other strains corresponding to the degree of antigenic similarity. The selection of vaccine strain may therefore be of importance to create the best possible immunity to field strains. Recent studies indicate that combining various strains in vaccines can attain a broader cross-protecting ability.
The purpose of this literature review is to investigate which laboratory methods that are available for diagnosing disease and for investigating the epidemiology of the disease. In addition the value of immunoprophylaxis will be highlighted
RNA and DNA interactions with zwitterionic and charged lipid membranes â A DSC and QCM-D study
AbstractThe aim of the present study is to establish under which conditions tRNA associates with phospholipid bilayers, and to explore how this interaction influences the lipid bilayer. For this purpose we have studied the association of tRNA or DNA of different sizes and degrees of base pairing with a set of model membrane systems with varying charge densities, composed of zwitterionic phosphatidylcholines (PC) in mixtures with anionic phosphatidylserine (PS) or cationic dioctadecyl-dimethyl-ammoniumbromide (DODAB), and with fluid or solid acyl-chains (oleoyl, myristoyl and palmitoyl). To prove and quantify the attractive interaction between tRNA and model-lipid membrane we used quartz crystal microbalance with dissipation (QCM-D) monitoring to study the tRNA adsorption to deposit phospholipid bilayers from solutions containing monovalent (Na+) or divalent (Ca2+) cations. The influence of the adsorbed polynucleic acids on the lipid phase transitions and lipid segregation was studied by means of differential scanning calorimetry (DSC). The basic findings are: i) tRNA adsorbs to zwitterionic liquid-crystalline and gel-phase phospholipid bilayers. The interaction is weak and reversible, and cannot be explained only on the basis of electrostatic attraction. ii) The adsorbed amount of tRNA is higher for liquid-crystalline bilayers compared to gel-phase bilayers, while the presence of divalent cations show no significant effect on the tRNA adsorption. iii) The adsorption of tRNA can lead to segregation in the mixed 1,2-dimyristoyl-sn-glycerol-3-phosphatidylcholine (DMPC)-1,2-dimyristoyl-sn-glycero-3-phosphatidylserine (DMPS) and DMPCâDODAB bilayers, where tRNA is likely excluded from the anionic DMPS-rich domains in the first system, and associated with the cationic DODAB-rich domains in the second system. iv) The addition of shorter polynucleic acids influence the chain melting transition and induce segregation in a mixed DMPCâDMPS system, while larger polynucleic acids do not influence the melting transition in these system. The results in this study on tRNAâphospholipid interactions can have implications for understanding its biological function in, e.g., the cell nuclei, as well as in applications in biotechnology and medicine
Nitrofurantoin plasma- and urine exposure in eight healthy beagle dogs following standard nitrofurantoin dosing regimen
Bacterial cystitis is common in dogs and is usually treated with antibiotics. Nitrofurantoin is used for treatment of bacterial cystitis in humans and might provide a feasible treatment option in dogs. The aim of this study was to investigate the nitrofurantoin plasma concentration-time course and potential adverse effects in dogs. Nitro-furantoin (4.4-5.0 mg/kg) was administered orally to eight healthy beagles every 8 h for five days before repeated plasma and urine samples were collected. An additional four beagles served as untreated controls. The nitrofurantoin plasma and urine concentrations were measured using ultra high precision liquid chromatography coupled to tandem mass-spectrometry and further analysed using a non-compartmental pharmacokinetic model. In plasma, the median C-max was 2.1 mu g/mL, t(max) was 2 h, the terminal rate constant was 0.9 per h and the terminal half-life was 0.8 h. In urine, median C-max was 56 mu g/mL, t(max) was 1 h and the terminal half-life was 4.3 h. No adverse effects were observed clinically or in haematology or biochemistry. The data presented in this study combined with in vitro sensitivity data from common urine pathogens and the lack of observed adverse effects suggest that nitrofurantoin in a standard dosing regimen could be effective in sporadic bacterial cystitis treatment in dogs. Further clinical studies are highly warranted to verify the effectiveness in clinical cases
Plasma atropine concentrations associated with decreased intestinal motility in horses
IntroductionAtropine is an essential part of the treatment protocol for equine uveitis. Topical atropine administration has been associated with decreased intestinal motility and abdominal pain in horses. Experimental studies have indicated that frequent dosing is associated with a higher risk than dosing every 6 h. Unfortunately, no quantitative pharmacodynamic data for inhibition of the equine gut are published. Materials and methodsEight standardbred horses were assigned to receive either atropine or saline (control) to be infused over 30 min in a two-treatment cross-over design. Atropine concentrations in plasma were measured using ultra-high-performance liquid chromatography-tandem mass spectrometry. Intestinal motility was measured using borborygmi frequency and electrointestinography (EIG). Experimental data were analyzed using a non-linear mixed effects model. The model was then used to simulate different dosing regimens. ResultsAtropine significantly decreased borborygmi response and EIG response. Six horses developed clinical signs of abdominal pain. The pharmacokinetic typical values were 0.31, 1.38, 0.69, and 1.95 L/kg center dot h for the volumes of the central, the highly perfused, the scarcely perfused compartments, and the total body clearance, respectively. The pharmacodynamic typical values were 0.31 mu g/L and 0.6 and 207 nV(2)7 cpm for the plasma concentration at 50% of the maximum response and the maximum response and the baseline of cecal EIG response, respectively. Six different dosing regimens of topical atropine sulfate to the eye (0.4 and 1 mg every hour, every 3 h, and every 6 h) were simulated. ConclusionThe IV PK/PD data coupled with simulations predict that administration of 1 mg of topical atropine sulfate administered to the eye every hour or every 3 h will lead to atropine accumulation in plasma and decreased intestinal myoelectric activity. Administration every 6 h predicted a safe dosing regimen in full-sized horses. Clinical studies would be valuable to confirm the conclusions. For smaller equids and horses put at risk for colic due to othercauses, droplet bottles that deliver 40 mu l of 1% atropine sulfate per drop or less may be used to lower the risk further
Relationship between selected perinatal paratuberculosis management interventions and passive transfer of immunity in dairy calves
The objective of this cohort study was to assess the relationship between perinatal calf management practices relevant to the control of paratuberculosis and passive transfer of immunoglobulin in calves born in an endemically infected Irish dairy herd. Data from 176 calves were used to assess the effect of time spent in the calving area, individual versus non-designated calving and colostrum pasteurisation on serum total protein, zinc sulphate turbidity, globulin and Îł-glutamyltransferase. In addition, the effects of colostrum quality, volume of colostrum fed, method of colostrum administration and calving season on passive transfer were quantified. Serum samples were collected as part of routine herd health monitoring from calves aged between one and seven days. Multivariate linear and logistic regression models were used to assess the effect of each variable on the test result and failure of passive transfer as determined using a cut-off point for each diagnostic test. Colostrum pasteurisation and calving area were not significantly associated with passive transfer, whereas increased time spent in the calving pen was consistently associated with a detrimental effect. In addition, a strong seasonal effect was apparent, which appeared to be unrelated to colostrum quality and calf management. The authors are unaware of published studies documenting such a significant seasonal effect on passive transfer
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