SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "hsv:(MEDICIN OCH HÄLSOVETENSKAP) hsv:(Medicinska och farmaceutiska grundvetenskaper) hsv:(Farmaceutiska vetenskaper) srt2:(2000-2009);srt2:(2009);lar1:(lu)"

Sökning: hsv:(MEDICIN OCH HÄLSOVETENSKAP) hsv:(Medicinska och farmaceutiska grundvetenskaper) hsv:(Farmaceutiska vetenskaper) > (2000-2009) > (2009) > Lunds universitet

  • Resultat 1-10 av 21
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Rhodin, Malin M., et al. (författare)
  • Human renal function maturation : a quantitative description using weight and postmenstrual age
  • 2009
  • Ingår i: Pediatric nephrology (Berlin, West). - : Springer Science and Business Media LLC. - 0931-041X .- 1432-198X. ; 24:1, s. 67-76
  • Tidskriftsartikel (refereegranskat)abstract
    • This study pools published data to describe the increase in glomerular filtration rate (GFR) from very premature neonates to young adults. The data comprises measured GFR (using polyfructose, Cr-51-EDTA, mannitol or iohexol) from eight studies (n=923) and involved very premature neonates (22 weeks postmenstrual age) to adulthood (31 years). A nonlinear mixed effects approach (NONMEM) was used to examine the influences of size and maturation on renal function. Size was the primary covariate, and GFR was standardized for a body weight of 70 kg using an allometric power model. Postmenstrual age (PMA) was a better descriptor of maturational changes than postnatal age (PNA). A sigmoid hyperbolic model described the nonlinear relationship between GFR maturation and PMA. Assuming an allometric coefficient of 3/4, the fully mature (adult) GFR is predicted to be 121.2 mL/min per 70 kg [95% confidence interval (CI) 117-125]. Half of the adult value is reached at 47.7 post-menstrual weeks (95% CI 45.1-50.5), with a Hill coefficient of 3.40 (95% CI 3.03-3.80). At 1-year postnatal age, the GFR is predicted to be 90% of the adult GFR. Glomerular filtration rate can be predicted with a consistent relationship from early prematurity to adulthood. We propose that this offers a clinically useful definition of renal function in children and young adults that is independent of the predictable changes associated with age and size.
  •  
2.
  • Bengtsson, Jörgen, et al. (författare)
  • The influence of age on the distribution of morphine and morphine-3-glucuronide across the blood-brain barrier in sheep
  • 2009
  • Ingår i: British Journal of Pharmacology. - : Wiley. - 0007-1188 .- 1476-5381. ; 157:6, s. 1085-1096
  • Tidskriftsartikel (refereegranskat)abstract
    • Background and purpose  The effect of age on the distribution of morphine and morphine-3-glucuronide (M3G) across the blood-brain barrier (BBB) was studied in a sheep model utilizing intracerebral microdialysis. The effect of neonatal asphyxia on brain drug distribution was also studied. Experimental approach  Microdialysis probes were inserted into the cortex, striatum and blood of 11 lambs (127 gestation days) and six ewes. Morphine, 1 mg.kg(-1), was intravenously administered as a 10 min constant infusion. Microdialysis and blood samples were collected for up to 360 min and analysed using liquid chromatography-tandem mass spectrometry. The half-life, clearance, volume of distribution, unbound drug brain : blood distribution ratio (K(p,uu)) and unbound drug volume of distribution in brain (V(u,brain)) were estimated.  Key results  Morphine K(p,uu) was 1.19 and 1.89 for the sheep and premature lambs, respectively, indicating that active influx into the brain decreases with age. Induced asphyxia did not affect transport of morphine or M3G across the BBB. Morphine V(u,brain) measurements were higher in sheep than in premature lambs. The M3G K(p,uu) values were 0.27 and 0.17 in sheep and premature lambs, indicating a net efflux from the brain in both groups. Conclusions and implications  The morphine K(p,uu) was above unity, indicating active transport into the brain; influx was significantly higher in premature lambs than in adult sheep. These results in sheep differ from those in humans, rats, mice and pigs where a net efflux of morphine from the brain is observed.
  •  
3.
  • Jia, Juan, et al. (författare)
  • Lack of L-iduronic acid in heparan sulfate affects interaction with growth factors and cell signaling
  • 2009
  • Ingår i: Journal of Biological Chemistry. - 0021-9258 .- 1083-351X. ; 284:23, s. 15942-15950
  • Tidskriftsartikel (refereegranskat)abstract
    • Glucuronyl C5-epimerase (Hsepi) catalyzes the conversion of D-glucuronic acid to L-iduronic acid in heparan sulfate (HS) biosynthesis. Disruption of the Hsepi gene in mouse yielded a lethal phenotype with selective organ defects, but had remarkably little effect on other organ systems. We have approached the underlying mechanisms by examining the course and effects of FGF2 signaling in a mouse embryonic fibroblast (MEF) cell line derived from the Hsepi-/- mouse. The HS produced by these cells is devoid of IdoA residues, but shows upregulated N- and 6-O-sulfation compared to wildtype (WT) MEF HS. In medium fortified with 10% FCS the Hsepi-/- MEFs proliferated and migrated similar to WT cells. Under starvation conditions both cell types showed attenuated proliferation and migration, that could be restored by addition of FGF2 to WT cells whereas Hsepi-/- cells were resistant. Moreover, ERK phosphorylation following FGF2 stimulation was delayed in Hsepi-/- compared to WT cells. Assessment of HS-growth factor interaction by nitrocellulose filter trapping revealed strikingly aberrant binding property of FGF2 and glia-derived neurotropic factor (GDNF) to Hsepi-/- but not to WT HS. GDNF has a key role in kidney development, defective in Hsepi-/- mice. By contrast, Hsepi-/- and WT HS interacted similarly and in conventional mode with FGF10. These findings correlate defective function of growth factors with their mode of HS interaction, and may help explain the partly modest organ phenotypes observed after genetic ablation of selected enzymes in HS biosynthesis.
  •  
4.
  • Andersson, Roland, et al. (författare)
  • Treatment of acute pancreatitis: focus on medical care.
  • 2009
  • Ingår i: Drugs. - 0012-6667. ; 69:5, s. 505-514
  • Tidskriftsartikel (refereegranskat)abstract
    • Acute pancreatitis has an incidence of about 300 per 1 million individuals per year, of which 10-15% of patients develop the severe form of the disease. Novel management options, which have the potential to improve outcome, include initial proper fluid resuscitation, which maintains microcirculation and thereby potentially decreases ischaemia and reperfusion injury. The traditional treatment concept in acute pancreatitis, fasting and parenteral nutrition, has been challenged and early initiation of enteral feeding in severe pancreatitis and oral intake in mild acute pancreatitis is both feasible and provides some benefits. There are at present no data supporting immunonutritional supplements and probiotics should be avoided in patients with acute pancreatitis. There is also no evidence of any benefits provided by prophylactic antibacterials in patients with predicted severe acute pancreatitis. A variety of specific medical interventions have been investigated (e.g. intense blood glucose monitoring by insulin) but none has become clinically useful. Lessons can probably be learned from critical care in general, but studies are needed to verify these interventions in acute pancreatitis.
  •  
5.
  • Arup, Ulf, et al. (författare)
  • Professor Ingvar Kärnfelt - a birthday tribute
  • 2009
  • Ingår i: The Lichenologist. - Cambridge : Cambridge University Press. - 0024-2829 .- 1096-1135. ; 41:5, s. 453-456
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • On 19 July 2009 Ingvar Kärnefelt celebrated his 65th birthday. This could have meant that we, his former students, would be celebrating him in his retirement from his position as head of the Biological Museums at Lund University. We are grateful that this is not the case, as Ingvar will carry on, probably for at least one or two more years. Instead, we celebrate Ingvar because he is the main reason for all of us having studied lichenology in Lund. This special issue of The Lichenologist is dedicated to him as a birthday tribute in honour of his long and fruitful lichenological career. The main authors of all the papers in this issue are former students of Ingvar. For several of us he has not only acted as supervisor but later also as the director of the Botanical Museum where we meet him in our daily work.
  •  
6.
  •  
7.
  • Bysell, Helena, et al. (författare)
  • Binding and release of consensus peptides by poly(acrylic acid) microgels
  • 2009
  • Ingår i: Biomacromolecules. - : American Chemical Society. - 1525-7797 .- 1526-4602. ; 10:8, s. 2162-2168
  • Tidskriftsartikel (refereegranskat)abstract
    • The interaction between positively charged consensus peptides and  poly(acrylic acid) microgels was investigated with   micromanipulator-assisted light microscopy and confocal laser scanning   microscopy. Peptide binding and release was monitored by microgel   deswelling and swelling for monodisperse multiples of heparin-binding  Cardin and Weintraub motifs, (AKKARA)(n) (1 <= n <= 4) and   (ARKKAAKA)(n) (1 <= n <= 3), as well as the corresponding titratable   (AHHAHA)(4) and (AHHHAAHA)(3) peptides (A, K. R and H, refering to   alanine, lysine, arginine, and histidine, respectively). When fully   charged, these peptides distribute homogenously throughout the   microgels and display concentration-dependent deswelling, which   increases with increasing peptide length. Both (AKKARA)(4) and   (ARKKAAKA)(3) display potent and fast microgel deswelling but only   marginal subsequent electrolyte-induced desorption. In contrast,   reducing the peptide charge for (AHHAHA)(4) and (AHHHAAHA)(3) at  neutral and high pH, or the peptide length, substantially reduces the   peptide affinity for the microgels and facilitates rapid peptide release. Taken together, the results also show that quite short   peptides of moderate charge density interact strongly and cause   extensive gel deswelling of oppositely charged microgels, precluding   peptide release. They also show, however, that desirable triggered   release can be achieved with peptides of lower charge density.
  •  
8.
  • Collins, P. W., et al. (författare)
  • Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia A
  • 2009
  • Ingår i: Journal of Thrombosis and Haemostasis. - : Elsevier BV. - 1538-7933 .- 1538-7836. ; 7:3, s. 413-420
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: The role of prophylactic factor VIII (FVIII) to decrease hemophilic bleeding and arthropathy is well established. The rationale for this strategy is to convert patients with severe hemophilia A to a moderate clinical phenotype by reducing time spent with a FVIII level <1 IU dL(-1). Studies to date, however, have not demonstrated a strong link between FVIII level and the bleeding rate. OBJECTIVES: To assess the effect of FVIII level on break-through bleeding in patients with severe hemophilia A on prophylaxis. PATIENTS/METHODS: This study analysed data from 44 patients aged 1-6 and 99 patients aged 10-65 years with severe hemophilia A (FVIII <1 IU dL(-1)) who were treated with prophylactic FVIII as part of clinical studies assessing pharmacokinetics, safety and efficacy of a recombinant FVIII (Advate). Each patient had pharmacokinetic measurements and FVIII infusions recorded, and these were used to calculate time spent with a FVIII below 1, 2 and 5 IU dL(-1). RESULTS: The data demonstrate that increasing time with a FVIII below 1 IU dL(-1) is associated with increased total bleeds and hemarthroses. Lack of adherence to the intended frequency of FVIII infusion was the most important determinant of low FVIII and increased bleeding. In children aged 1-6 years, the rate of bleeding was also influenced by FVIII half-life and clearance. Conclusions: These data have important implications for the management of patients with severe hemophilia.
  •  
9.
  • Fatouros, Dimitrios G., et al. (författare)
  • Colloidal Structures in Media Simulating Intestinal Fed State Conditions with and Without Lipolysis Products
  • 2009
  • Ingår i: Pharmaceutical Research. - : Springer Science and Business Media LLC. - 1573-904X .- 0724-8741. ; 26:2, s. 361-374
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose. To study the ultrastructure of biorelevant media and digestion products of self-nanoemulsifying drug delivery system (SNEDDS) at high level BS/PL conditions. Methods. Cryogenic transmission electron microscopy (Cryo-TEM) was employed to visualize the colloid structures in the biorelevant media and lipolytic products generated during hydrolysis of a SNEDDS formulation. Their electrical properties were investigated by measuring their zeta-potential values. Results. In the biorelevant media, vesicles (either unilamellar or multilamellar) and bilayer fragments are visualized. Occasionally, vesicles with an internal deformed structure are recognized, suggesting surface tension or uneven lateral stress. Visualization studies of the intermediate colloidal phases produced during digestion of a SNEDDS using the in vitro lipolysis model revealed the formation of similar structures as previously reported. The zeta-potential of the media was negatively charged and decreased from -23 to -35 mV with increasing surfactant/lipid load. Lower zeta-potential values (-16 mV) obtained for the structures formed during the lipid hydrolysis of the SNEDDS were probably due to the presence of calcium, which shields the surface, thereby reducing the charge. Conclusions. The diversity of these vesicles in terms of size, lamellarity, and internal organization advocate their important role during lipid digestion in the gastrointestinal milieu.
  •  
10.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 21
Typ av publikation
tidskriftsartikel (20)
konferensbidrag (1)
Typ av innehåll
refereegranskat (20)
övrigt vetenskapligt/konstnärligt (1)
Författare/redaktör
Schmidtchen, Artur (7)
Malmsten, Martin (6)
Ley, David (2)
Andersson, Roland (1)
Mörgelin, Matthias (1)
Landén, Mikael, 1966 (1)
visa fler...
Borg, J. (1)
Nilsson, Staffan, 19 ... (1)
Fischer, K. (1)
Strömstedt, Adam A. (1)
Grubb, Anders (1)
Hellström, Ann, 1959 (1)
Larsson, Anette, 196 ... (1)
Marsal, Karel (1)
Li, Jin-Ping (1)
Lindahl, Ulf (1)
Sørensen, Ole E. (1)
Maccarana, Marco (1)
Nordström, Carl-Henr ... (1)
Lehnbom, Elin C. (1)
Bergenståhl, Björn (1)
Eriksson, Elias, 195 ... (1)
Hammarlund-Udenaes, ... (1)
Surewicz, Witold K. (1)
Nilsson, J. Lars G. (1)
Lindblad, Ulf, 1950 (1)
Larsson, Charlotte A (1)
Ring, Lena (1)
Thell, Arne (1)
Zhang, Xiao (1)
Ehinger, Mats (1)
Hansson, Stefan (1)
Råstam, Lennart (1)
Anckarsäter, Henrik, ... (1)
Niklasson, Aimon, 19 ... (1)
Henningsson, Susanne ... (1)
Karlsson, Stefan (1)
Tingstedt, Bobby (1)
Astermark, Jan (1)
Amer-Wåhlin, Isis (1)
Anderbrant, Olle (1)
Östrand, Fredrik (1)
Bergström, Gunnar, 1 ... (1)
Wassgren, Ann-Britt (1)
Hedenström, Erik (1)
Auger-Rozenberg, Mar ... (1)
Friberg, Lena E (1)
Rydengård, Victoria (1)
Söderström, Henrik, ... (1)
Wittgren, Bengt (1)
visa färre...
Lärosäte
Uppsala universitet (15)
Göteborgs universitet (4)
Karolinska Institutet (3)
Chalmers tekniska högskola (2)
Linköpings universitet (1)
visa fler...
Mittuniversitetet (1)
Södertörns högskola (1)
visa färre...
Språk
Engelska (21)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (21)
Naturvetenskap (3)
År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy