Tore Seternes
Norwegian College of Fishery Science
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Publication
Featured researches published by Tore Seternes.
Proceedings of the National Academy of Sciences of the United States of America | 2002
Tore Seternes; Karen Kristine Sørensen; Bård Smedsrød
Studies over the last two decades have shown that mammalian nonmacrophagic liver endothelial cells clear the blood from numerous physiological and foreign waste macromolecules, such as polysaccharides and proteins released during extracellular matrix turnover, intracellular macromolecules, modified serum proteins, and bacterial and fungal proteins [Smedsrød, B., Pertoft, H., Gustafson, S. & Laurent, T. C. (1990) Biochem. J. 266, 313–327]. These macromolecules are released daily in gram-amounts in a normal human body and are effectively taken up and degraded by the liver endothelial cells. Recent studies show that bony fishes harbor a similar system of specialized nonmacrophagic scavenger endothelial cells in either kidney [Smedsrød, B., Gjøen, T., Sveinbjørnsson, B. & Berg, T. (1993) J. Fish Biol. 42, 279–291] or heart [Sørensen, K. K., Melkko, J. & Smedsrød, B. (1998) J. Exp. Biol. 201, 1707–1718], but not in liver. Using specific and extremely effective endocytosis, these fish scavenger endothelial cells function as their mammalian counterpart to eliminate soluble waste macromolecules from the circulation. We show here that species from all seven vertebrate classes carry a population of nonmacrophagic scavenger endothelial cells that efficiently eliminate an array of circulating waste macromolecules. Thus representing an important part of the vertebrate innate immune system, these scavenger endothelial cells display the following distribution in the different vertebrate classes: Gills in Agnatha and Chondrichtyes; heart or kidney in Osteichtyes; and liver in Amphibia, Reptilia, Aves, and Mammalia.
Scientific Reports | 2016
Tore Seternes; Tom Christian Tonheim; Anne Ingeborg Myhr; Roy A. Dalmo
The long-term persistence and activity of a naked plasmid DNA (pGL3-35S) containing a luc gene (reporter gene) controlled by a plant 35S CaMV promoter was studied in Atlantic salmon (Salmo salar L.) after injection. Atlantic salmon (mean weight 70 grams) were injected intramuscularly with 100 μg of plasmid DNA. Blood, different tissues and organs were sampled at different time points up to day 535 after injection. Southern blot analysis suggested the presence of extra-chromosomally open circular, linear and supercoiled topoforms of pGL3-35S at day 150 after injection. At day 536 open circular and supercoiled topoforms were detected. Luciferase activity was detected at the injection site up to 536 days post-injection of pGL3-35S, where it peaked at day 150 and decreased to approximately 17% of its maximum activity by day 536. Our study demonstrated that a plasmid containing the 35S promoter was able to induce expression of a reporter gene/protein in fish in vivo and that the plasmid DNA persisted for a prolonged time after intramuscular injection.
Clinical pharmacology in drug development | 2018
Magnus N. Hattrem; Morten J. Dille; Tore Seternes; Thorfinn Ege; Kurt I. Draget
The first aim of the present study was to evaluate the bioavailability of ibuprofen dispersed in a novel soft chewable formulation compared with a traditional ibuprofen tablet; its second was to map the quality of taste masking and patient product satisfaction. In a phase 1, single‐center, open‐label, randomized, crossover study, healthy subjects received a soft‐chew formulation or a hard tablet (reference), both containing 100 mg ibuprofen. Serial blood samples were collected over 24 hours to assess ibuprofen bioavailability. Taste and satisfaction after chewing the novel formulation 3 or 8 times were evaluated with a questionnaire. The soft‐chew formulation showed comparable bioavailability to the reference tablet. The highest peak plasma concentration was observed after 3 chews, and the relative bioavailability was approximately 8% higher compared to 8 chews. The overall flavor was well appreciated, and chewing 3 times was significantly preferred (P = .043) over chewing 8 times. Soft chewable drug formulations may improve compliance and potentially benefit several subpopulations who experience dysphagia.
European Journal of Lipid Science and Technology | 2011
Ingvild Johanne Haug; Lise B. Sagmo; Daniel Zeiss; Inge C. Olsen; Kurt I. Draget; Tore Seternes
Food Hydrocolloids | 2014
Magnus N. Hattrem; Morten J. Dille; Tore Seternes; Kurt I. Draget
The Journal of Experimental Biology | 2001
Tore Seternes; Roy A. Dalmo; James Hoffman; Jarl Bøgwald; Svetlana Zykova; Bård Smedsrød
Fish & Shellfish Immunology | 2008
Tom Christian Tonheim; Roy A. Dalmo; Jarl Bøgwald; Tore Seternes
Aquaculture | 2008
Frøydis Gillund; Roy A. Dalmo; Tom Christian Tonheim; Tore Seternes; Anne Ingeborg Myhr
Journal of Fish Diseases | 1998
Roy A. Dalmo; Tore Seternes; S. M. Arnesen; Trond Ø. Jørgensen; Jarl Bøgwald
Archive | 2009
Tore Seternes; Kurt Ingar Draget; Ingvild Johanne Haug