Effects of Omega-3 Fatty Acids on Immune Cells
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Omega-3 Fatty Acids As First-Line Treatment in Paediatric Depression
Se Clinical Study Protocol OMEGA-3 FATTY ACIDS AS FIRST-LINE TREATMENT IN PAEDIATRIC DEPRESSION. A phase III, 36-week, multi-centre, double-blind, placebo-controlled randomized superiority Study. The Omega-3-pMDD Study Study Type: Intervention with Investigational Medicinal Product (IMP) Study Categorisation: Clinical Trial with IMP Category C Study Registration: Swiss Federal Complementary Database Clinicaltrials.gov Study Identifier: SNF 33IC30_166826 Sponsor, Sponsor- Gregor Berger Investigator and Principal Investigator: Department of Child and Adolescent Psychiatry University Hospital of Psychiatry University of Zurich Neumünsterallee 9 Omega-3-pMDD, Version 3 of 13.07.2017 Page 1 of 108 CH 8032 Zürich Switzerland Phone: +41 43 499 26 71 Mobile: +41 76 464 61 54 E-Mail: [email protected] Investigational Product: Omega-3 fatty acids (1000mg EPA / 500mg DHA in > in 13 years old and 500mg EPA / 250mg DHA in < in 13 years old) Protocol Version and Version3 of 13..07.2017 Date: CONFIDENTIAL The information contained in this document is confidential and the property of the Department of Child and Adolescent Psychiatry of the University of Zurich. The information may not - in full or in part - be transmitted, reproduced, published, or disclosed to others than the applicable Independent Ethics Committee(s) and Competent Authority(ies) without prior written authorization from the Department of Child and Adolescent Psychiatry of the University of Zurich, except to the extent necessary to obtain informed consent from those participants who will participate in the study. Omega-3-pMDD, Version 3 of 13.07.2017 Page 2 of 108 SIGNATURE PAGES Study number Swiss Federal Complementary Database Study Title Omega-3 fatty acids as first-line treatment in Paediatric Depression. -
Lipid Bilayer, with the Nonpolar Regions of the Lipids Facing Inward
Chapter 7 Membranes: Their Structure, Function, and Chemistry Lectures by Kathleen Fitzpatrick Simon Fraser University © 2012 Pearson Education, Inc. Membranes: Their Structure, Function, and Chemistry • Membranes define the boundaries of a cell, and its internal compartments • Membranes play multiple roles in the life of a cell © 2012 Pearson Education, Inc. Figure 7-1A © 2012 Pearson Education, Inc. Figure 7-1B © 2012 Pearson Education, Inc. The Functions of Membranes • 1. Define boundaries of a cell and organelles and act as permeability barriers • 2. Serve as sites for biological functions such as electron transport • 3. Possess transport proteins that regulate the movement of substances into and out of cells and organelles © 2012 Pearson Education, Inc. The Functions of Membranes (continued) • 4. Contain protein molecules that act as receptors to detect external signals • 5. Provide mechanisms for cell-to-cell contact, adhesion, and communication © 2012 Pearson Education, Inc. Figure 7-2 © 2012 Pearson Education, Inc. Models of Membrane Structure: An Experimental Approach • The development of electron microscopy in the 1950s was important for understanding membrane structure • The fluid mosaic model is thought to be descriptive of all biological membranes • The model envisions a membrane as two fluid layers of lipids with proteins within and on the layers © 2012 Pearson Education, Inc. Overton and Langmuir: Lipids Are Important Components of Membranes • In the 1890s Overton observed the easy penetration of lipid-soluble substances into cells and concluded that the cell surface had some kind of lipid “coat” on it • Langmuir studied phospholipids and found that they were amphipathic and reasoned that they must orient on water with the hydrophobic tails away from the water © 2012 Pearson Education, Inc. -
Downloaded from GEO
bioRxiv preprint doi: https://doi.org/10.1101/2020.08.17.252007; this version posted November 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Oxylipin metabolism is controlled by mitochondrial b-oxidation during bacterial inflammation. Mariya Misheva1, Konstantinos Kotzamanis1*, Luke C Davies1*, Victoria J Tyrrell1, Patricia R S Rodrigues1, Gloria A Benavides2, Christine Hinz1, Robert C Murphy3, Paul Kennedy4, Philip R Taylor1,5, Marcela Rosas1, Simon A Jones1, Sumukh Deshpande1, Robert Andrews1, Magdalena A Czubala1, Mark Gurney1, Maceler Aldrovandi1, Sven W Meckelmann1, Peter Ghazal1, Victor Darley-Usmar2, Daniel White1, and Valerie B O’Donnell1 1Systems Immunity Research Institute and Division of Infection and Immunity, and School of Medicine, Cardiff University, UK, 2Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA, 3Department of Pharmacology, University of Colorado Denver, Aurora, CO 80045, USA, 4Cayman Chemical 1180 E Ellsworth Rd, Ann Arbor, MI 48108, United States, 5UK Dementia Research Institute at Cardiff, Cardiff University, UK Address correspondence: Valerie O’Donnell, [email protected] or Daniel White, [email protected], Systems Immunity Research Institute, Cardiff University *Both authors contributed equally to the study 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.08.17.252007; this version posted November 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
A Novel Resolvin-Based Strategy for Limiting Acetaminophen Hepatotoxicity
A Novel Resolvin-Based Strategy for Limiting Acetaminophen Hepatotoxicity The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Patel, Suraj J, Jay Luther, Stefan Bohr, Arvin Iracheta-Vellve, Matthew Li, Kevin R King, Raymond T Chung, and Martin L Yarmush. 2016. “A Novel Resolvin-Based Strategy for Limiting Acetaminophen Hepatotoxicity.” Clinical and Translational Gastroenterology 7 (3): e153. doi:10.1038/ctg.2016.13. http://dx.doi.org/10.1038/ctg.2016.13. Published Version doi:10.1038/ctg.2016.13 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:26860020 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Citation: Clinical and Translational Gastroenterology (2016) 7, e153; doi:10.1038/ctg.2016.13 & 2016 the American College of Gastroenterology All rights reserved 2155-384X/16 www.nature.com/ctg A Novel Resolvin-Based Strategy for Limiting Acetaminophen Hepatotoxicity Suraj J. Patel, MD, PhD1,2,5, Jay Luther, MD3,5, Stefan Bohr, MD1, Arvin Iracheta-Vellve, BS1, Matthew Li, PhD1, Kevin R. King, MD, PhD1, Raymond T. Chung, MD3 and Martin L. Yarmush, MD, PhD1,2,4 OBJECTIVES: Acetaminophen (APAP)-induced hepatotoxicity is a major cause of morbidity and mortality. The current pharmacologic treatment for APAP hepatotoxicity, N-acetyl cysteine (NAC), targets the initial metabolite-driven injury but does not directly affect the host inflammatory response. -
Frequencies Between Serial Killer Typology And
FREQUENCIES BETWEEN SERIAL KILLER TYPOLOGY AND THEORIZED ETIOLOGICAL FACTORS A dissertation presented to the faculty of ANTIOCH UNIVERSITY SANTA BARBARA in partial fulfillment of the requirements for the degree of DOCTOR OF PSYCHOLOGY in CLINICAL PSYCHOLOGY By Leryn Rose-Doggett Messori March 2016 FREQUENCIES BETWEEN SERIAL KILLER TYPOLOGY AND THEORIZED ETIOLOGICAL FACTORS This dissertation, by Leryn Rose-Doggett Messori, has been approved by the committee members signed below who recommend that it be accepted by the faculty of Antioch University Santa Barbara in partial fulfillment of requirements for the degree of DOCTOR OF PSYCHOLOGY Dissertation Committee: _______________________________ Ron Pilato, Psy.D. Chairperson _______________________________ Brett Kia-Keating, Ed.D. Second Faculty _______________________________ Maxann Shwartz, Ph.D. External Expert ii © Copyright by Leryn Rose-Doggett Messori, 2016 All Rights Reserved iii ABSTRACT FREQUENCIES BETWEEN SERIAL KILLER TYPOLOGY AND THEORIZED ETIOLOGICAL FACTORS LERYN ROSE-DOGGETT MESSORI Antioch University Santa Barbara Santa Barbara, CA This study examined the association between serial killer typologies and previously proposed etiological factors within serial killer case histories. Stratified sampling based on race and gender was used to identify thirty-six serial killers for this study. The percentage of serial killers within each race and gender category included in the study was taken from current serial killer demographic statistics between 1950 and 2010. Detailed data -
The Omega Course
The Omega Course A six-session course designed to help older people to face up to the challenges ageing. With Bible-based teaching and questions to encourage debate and discussion. Written by Peter Sanderson Adapted by Lesley Bell From an idea suggested by Don Blevin. O ehalf of “t. Pauls Churh, Kigsto Hill. Free to use. INTRODUCTION: The aims of the course (for course leaders). People are living longer. This fact presents social, economic and political challenges to both society and government. What about the Church? How do we support older people in the church family? How can we help them face the many issues that longevity brings? What part can they play in serving the church? Are they an under-used resource? What about people who are not practicing Christians? How do they approach old age and dying? How do we share the good news of Jesus with them? We recognise the invaluable work done by Evergreens* and the way the church seeks to accept and empower its Senior Citizens in many ways. But some are looking for more teaching and discussion on this matter so that they can live well and, when the time comes, die well! The Alpha Course has been inspirational in bringing many to the beginning of a walk of faith. Because of Alpha, millions world-wide have begun to follow Jesus. But we want to explore, through the Omega Course, ways to help people end their lives in a faith-filled way. A course for both Christians and non- believers. The Bible raises the issue of old age. -
Senior Softball World Championships 2020 St
Senior Softball World Championships 2020 St. George, Utah September 17 - 19, 2020 Rev. 08/28/2020 Men's 60+ Major Plus Division • 4 Teams Win Loss 3 0 1 LPC 60's/Dudley (CA) 122Omega IT Services, LLC (VA) 0 3 3 Samurai (CA) 2 1 4 Texas Crush Sixties Thursday • September 17, 2020 • The Canyons Softball Complex • St. George Field address ► 1890 West 2000 North - St George, UT 84770 Time # Runs Team Name Field # Runs Team Name 9:30 AM 317 Samurai (CA) 2132 LPC 60's/Dudley (CA) 11:00 AM 220 Omega IT Services, LLC (VA) 2426 Texas Crush Sixties 12:30 PM 423 Texas Crush Sixties 23 7 Samurai (CA) USA NATIONAL CHAMPIONSHIP GAME • LPC 60's/Dudley (West) vs. Omega IT Services, LLC (East) 2:00 PM 124 LPC 60's/Dudley (CA) 22 8 Omega IT Services, LLC (VA) Friday • September 18, 2020 • The Canyons Softball Complex • St. George Time # Runs Team Name Field # Runs Team Name 12:30 PM 226 Omega IT Services, LLC (VA) 6311 Samurai (CA) 12:30 PM 130 LPC 60's/Dudley (CA) 7429 Texas Crush Sixties Seeding for 60-Major Plus Double Elimination bracket commencing Friday afternoon • See bracket for details Format: Full (3-game) Round Robin to seed 60-Major+ Double Elimination bracket Home Runs - Major+ = 9 per team per game, Outs NOTE SSUSA Official Rulebook §9.5 (Retrieving Home Run Balls) will be strictly enforced. Pitch Count - All batters start with 1-1 count (WITH courtesy foul) per SSUSA Rulebook §6.2 (Pitch Count) Run Rules - 7 runs per ½ inning at bat (except open inning) Time Limits - RR = 65 + open inn. -
The Walking Dead,” Which Starts Its Final We Are Covid-19 Safe-Practice Compliant Season Sunday on AMC
Las Cruces Transportation August 20 - 26, 2021 YOUR RIDE. YOUR WAY. Las Cruces Shuttle – Taxi Charter – Courier Veteran Owned and Operated Since 1985. Jeffrey Dean Morgan Call us to make is among the stars of a reservation today! “The Walking Dead,” which starts its final We are Covid-19 Safe-Practice Compliant season Sunday on AMC. Call us at 800-288-1784 or for more details 2 x 5.5” ad visit www.lascrucesshuttle.com PHARMACY Providing local, full-service pharmacy needs for all types of facilities. • Assisted Living • Hospice • Long-term care • DD Waiver • Skilled Nursing and more Life for ‘The Walking Dead’ is Call us today! 575-288-1412 Ask your provider if they utilize the many benefits of XR Innovations, such as: Blister or multi-dose packaging, OTC’s & FREE Delivery. almost up as Season 11 starts Learn more about what we do at www.rxinnovationslc.net2 x 4” ad 2 Your Bulletin TV & Entertainment pullout section August 20 - 26, 2021 What’s Available NOW On “Movie: We Broke Up” “Movie: The Virtuoso” “Movie: Vacation Friends” “Movie: Four Good Days” From director Jeff Rosenberg (“Hacks,” Anson Mount (“Hell on Wheels”) heads a From director Clay Tarver (“Silicon Glenn Close reunited with her “Albert “Relative Obscurity”) comes this 2021 talented cast in this 2021 actioner that casts Valley”) comes this comedy movie about Nobbs” director Rodrigo Garcia for this comedy about Lori and Doug (Aya Cash, him as a professional assassin who grapples a straight-laced couple who let loose on a 2020 drama that casts her as Deb, a mother “You’re the Worst,” and William Jackson with his conscience and an assortment of week of uninhibited fun and debauchery who must help her addict daughter Molly Harper, “The Good Place”), who break up enemies as he tries to complete his latest after befriending a thrill-seeking couple (Mila Kunis, “Black Swan”) through four days before her sister’s wedding but decide job. -
The Role of N-3 PUFA-Derived Fatty Acid Derivatives and Their Oxygenated Metabolites in the Modulation of Inflammation
The role of n-3 PUFA-derived fatty acid derivatives and their oxygenated metabolites in the modulation of inflammation de Bus, I., Witkamp, R., Zuilhof, H., Albada, B., & Balvers, M. This is a "Post-Print" accepted manuscript, which has been Published in "Prostaglandins and Other Lipid Mediators" This version is distributed under a non-commercial no derivatives Creative Commons (CC-BY-NC-ND) user license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited and not used for commercial purposes. Further, the restriction applies that if you remix, transform, or build upon the material, you may not distribute the modified material. Please cite this publication as follows: de Bus, I., Witkamp, R., Zuilhof, H., Albada, B., & Balvers, M. (2019). The role of n-3 PUFA-derived fatty acid derivatives and their oxygenated metabolites in the modulation of inflammation. Prostaglandins and Other Lipid Mediators, 144, [106351]. https://doi.org/10.1016/j.prostaglandins.2019.106351 You can download the published version at: https://doi.org/10.1016/j.prostaglandins.2019.106351 The role of n-3 PUFA-derived fatty acid derivatives and their oxygenated metabolites in the modulation of inflammation Ian de Bus1,2, Renger Witkamp1, Han Zuilhof2,3,4, Bauke Albada2*, Michiel Balvers1* 1) Nutrition and Pharmacology Group, Division of Human Nutrition, Wageningen University & Research, Stippeneng 4, 6708 WE, Wageningen, The Netherlands 2) Laboratory of Organic Chemistry, Wageningen University & Research, Stippeneng 4, 6708 WE, Wageningen, The Netherlands 3) School of Pharmaceutical Sciences and Technology, Tianjin University, 92 Weijin Road, Tianjin, P.R. China. -
An Overview of Lipid Membrane Models for Biophysical Studies
biomimetics Review Mimicking the Mammalian Plasma Membrane: An Overview of Lipid Membrane Models for Biophysical Studies Alessandra Luchini 1 and Giuseppe Vitiello 2,3,* 1 Niels Bohr Institute, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark; [email protected] 2 Department of Chemical, Materials and Production Engineering, University of Naples Federico II, Piazzale Tecchio 80, 80125 Naples, Italy 3 CSGI-Center for Colloid and Surface Science, via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy * Correspondence: [email protected] Abstract: Cell membranes are very complex biological systems including a large variety of lipids and proteins. Therefore, they are difficult to extract and directly investigate with biophysical methods. For many decades, the characterization of simpler biomimetic lipid membranes, which contain only a few lipid species, provided important physico-chemical information on the most abundant lipid species in cell membranes. These studies described physical and chemical properties that are most likely similar to those of real cell membranes. Indeed, biomimetic lipid membranes can be easily prepared in the lab and are compatible with multiple biophysical techniques. Lipid phase transitions, the bilayer structure, the impact of cholesterol on the structure and dynamics of lipid bilayers, and the selective recognition of target lipids by proteins, peptides, and drugs are all examples of the detailed information about cell membranes obtained by the investigation of biomimetic lipid membranes. This review focuses specifically on the advances that were achieved during the last decade in the field of biomimetic lipid membranes mimicking the mammalian plasma membrane. In particular, we provide a description of the most common types of lipid membrane models used for biophysical characterization, i.e., lipid membranes in solution and on surfaces, as well as recent examples of their Citation: Luchini, A.; Vitiello, G. -
Membrane Proteins Are Associated with the Membrane of a Cell Or Particular Organelle and Are Generally More Problematic to Purify Than Water-Soluble Proteins
Strategies for the Purification of Membrane Proteins Sinéad Marian Smith Department of Clinical Medicine, School of Medicine, Trinity College Dublin, Ireland. Email: [email protected] Abstract Although membrane proteins account for approximately 30 % of the coding regions of all sequenced genomes and play crucial roles in many fundamental cell processes, there are relatively few membranes with known 3D structure. This is likely due to technical challenges associated with membrane protein extraction, solubilization and purification. Membrane proteins are classified based on the level of interaction with membrane lipid bilayers, with peripheral membrane proteins associating non- covalently with the membrane, and integral membrane proteins associating more strongly by means of hydrophobic interactions. Generally speaking, peripheral membrane proteins can be purified by milder techniques than integral membrane proteins, whose extraction require phospholipid bilayer disruption by detergents. Here, important criteria for strategies of membrane protein purification are addressed, with a focus on the initial stages of membrane protein solublilization, where problems are most frequently are encountered. Protocols are outlined for the successful extraction of peripheral membrane proteins, solubilization of integral membrane proteins, and detergent removal which is important not only for retaining native protein stability and biological functions, but also for the efficiency of downstream purification techniques. Key Words: peripheral membrane protein, integral membrane protein, detergent, protein purification, protein solubilization. 1. Introduction Membrane proteins are associated with the membrane of a cell or particular organelle and are generally more problematic to purify than water-soluble proteins. Membrane proteins represent approximately 30 % of the open-reading frames of an organism’s genome (1-4), and play crucial roles in basic cell functions including signal transduction, energy production, nutrient uptake and cell-cell communication. -
Download Product Insert (PDF)
PRODUCT INFORMATION 17(R)-Resolvin D1 Item No. 13060 CAS Registry No.: 528583-91-7 Formal Name: 7S,8R,17R-trihydroxy- 4Z,9E,11E,13Z,15E19Z- HO docosahexaenoic acid Synonyms: Aspirin-triggered Resolvin D1, AT-RvD1, 17-epi-Resolvin D1, 17(R)-RvD1 COOH OH MF: C22H32O5 FW: 376.5 Purity: ≥95% Stability: ≥1 year at -80°C Supplied as: A solution in ethanol OH Special Conditions: Light Sensitive UV/Vis.: λmax: 302 nm Laboratory Procedures For long term storage, we suggest that 17(R)-resolvin D1 (17(R)-RvD1) be stored as supplied at -80°C. It should be stable for at least one year. 17(R)-RvD1 is supplied as a solution in ethanol. To change the solvent, simply evaporate the ethanol under a gentle stream of nitrogen and immediately add the solvent of choice. It is recommended that this product be stored and handled in an ethanol solution. Resolvins can isomerize and degrade when put into freeze thaw conditions and/or in solvents such as DMF or DMSO. Further dilutions of the stock solution into aqueous buffers or isotonic saline should be made prior to performing biological experiments. Ensure that the residual amount of organic solvent is insignificant, since organic solvents may have physiological effects at low concentrations. If an organic solvent-free solution of 17(R)-RvD1 is needed, it can be prepared by evaporating the ethanol and directly dissolving the neat oil in aqueous buffers. The solubility of 17(R)-RvD1 in PBS, pH 7.2, is approximately 0.05 mg/ml. Aqueous solutions of 17(R)-RvD1 should be discarded immediately after use.