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11 results on '"Garcia-Carrasco A"'

1. Plant-animal extracts and biocompatible polymers forming oil-in-water emulsions: Formulations for food and pharmaceutical industries

Author

Kenia G. Felix-Sagaste, Melissa Garcia-Carrasco, Lorenzo A. Picos-Corrales, Tania Gonzalez-Ruelas, and Josué A. Rodriguez-Mercado

Subjects
Plant-animal extracts, Biocompatible polymers, Oil-in-water emulsions, Encapsulation methods, Pickering emulsions, Technology
Abstract

The development of formulations from plant or animal extracts and polymeric platforms has been well established toward emulsion-based delivery systems, avoiding the use of conventional surfactants. This approach involves the stabilization of poorly water-soluble extracts by polymers, improving their dispersion into food and pharmaceutical products, avoiding premature degradation, and resulting in better bioavailability. According to the literature, extracts are obtained via conventional and novel methods, which exhibit advantages and disadvantages related to using organic solvent, temperature, time, pressure, and equipment cost. Similarly, for polymer-based emulsifiers, there are different methods to obtain them. Also, their chemical composition and morphology (linear, branched, and crosslinked) play relevant roles in their performance as stabilizing agents. On the other hand, oil-in-water emulsions from plant-animal extracts and biocompatible polymers have been prepared using different strategies focused on achieving high stability of the colloidal system. Hence, this review provides current information regarding some protocols used for the extraction/synthesis of materials and the development of promising formulations.

Published
2023
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2. Alterations of the Ca2+ clearing mechanisms by type 2 diabetes in aortic smooth muscle cells of Zucker diabetic fatty rat

Author

Adriana Moreno-Salgado, Nayeli Coyotl-Santiago, Roberto Moreno-Vazquez, Mayte Lopez-Teyssier, Mario Garcia-Carrasco, Francesco Moccia, and Roberto Berra-Romani

Subjects
type 2 diabetes mellitus, intracellular Ca2+, Fura-2, freshly isolated vascular smooth muscle cells, Zucker diabetic fatty, Physiology, QP1-981
Abstract

Type 2 Diabetes Mellitus (T2DM) is a rapidly rising disease with cardiovascular complications constituting the most common cause of death among diabetic patients. Chronic hyperglycemia can induce vascular dysfunction through damage of the components of the vascular wall, such as vascular smooth muscle cells (VSMCs), which regulate vascular tone and contribute to vascular repair and remodeling. These functions are dependent on intracellular Ca2+ changes. The mechanisms by which T2DM affects Ca2+ handling in VSMCs still remain poorly understood. Therefore, the objective of this study was to determine whether and how T2DM affects Ca2+ homeostasis in VSMCs. We evaluated intracellular Ca2+ signaling in VSMCs from Zucker Diabetic Fatty rats using Ca2+ imaging with Fura-2/AM. Our results indicate that T2DM decreases Ca2+ release from the sarcoplasmic reticulum (SR) and increases the activity of store-operated channels (SOCs). Moreover, we were able to identify an enhancement of the activity of the main Ca2+ extrusion mechanisms (SERCA, PMCA and NCX) during the early stage of the decay of the ATP-induced Ca2+ transient. In addition, we found an increase in Ca2+ entry through the reverse mode of NCX and a decrease in SERCA and PMCA activity during the late stage of the signal decay. These effects were appreciated as a shortening of ATP-induced Ca2+ transient during the early stage of the decay, as well as an increase in the amplitude of the following plateau. Enhanced cytosolic Ca2+ activity in VSMCs could contribute to vascular dysfunction associated with T2DM.

Published
2023
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3. Loading and Release of Phenolic Compounds Present in Mexican Oregano (Lippia graveolens) in Different Chitosan Bio-Polymeric Cationic Matrixes

Author

Melissa Garcia-Carrasco, Lorenzo A. Picos-Corrales, Erick P. Gutiérrez-Grijalva, Miguel A. Angulo-Escalante, Angel Licea-Claverie, and J. Basilio Heredia

Subjects
chitosan, polyethylene glycol methacrylate, oregano, phenolic compounds, nanoencapsulation, bioaccessibility, Organic chemistry, QD241-441
Abstract

Mexican oregano (Lippia graveolens) polyphenols have antioxidant and anti-inflammatory potential, but low bioaccessibility. Therefore, in the present work the micro/nano-encapsulation of these compounds in two different matrixes of chitosan (CS) and chitosan-b-poly(PEGMA2000) (CS-b-PPEGMA) is described and assessed. The particle sizes of matrixes of CS (~955 nm) and CS-b-PPEGMA (~190 nm) increased by 10% and 50%, respectively, when the phenolic compounds were encapsulated, yielding loading efficiencies (LE) between 90–99% and 50–60%, correspondingly. The release profiles in simulated fluids revealed a better control of host–guest interactions by using the CS-b-PPEGMA matrix, reaching phenolic compounds release of 80% after 24 h, while single CS retained the guest compounds. The total reducing capacity (TRC) and Trolox equivalent antioxidant capacity (TEAC) of the phenolic compounds (PPHs) are protected and increased (more than five times) when they are encapsulated. Thus, this investigation provides a standard encapsulation strategy and relevant results regarding nutraceuticals stabilization and their improved bioaccessibility.

Published
2022
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4. Elimination of Vitamin D Signaling Causes Increased Mortality in a Model of Overactivation of the Insulin Receptor: Role of Lipid Metabolism

Author

Maria Crespo-Masip, Aurora Perez-Gomez, Alicia Garcia-Carrasco, Ramiro Jover, Carla Guzmán, Xavier Dolcet, Mercé Ibarz, Cristina Martínez, Àuria Eritja, Juan Miguel Diaz-Tocados, and José Manuel Valdivielso

Subjects
hypoglycemia, diabetes, insulin overdose, fatty acids, lipolysis, Nutrition. Foods and food supply, TX341-641
Abstract

Vitamin D (VD) deficiency has been associated with cancer and diabetes. Insulin signaling through the insulin receptor (IR) stimulates cellular responses by activating the PI3K/AKT pathway. PTEN is a tumor suppressor and a negative regulator of the pathway. Its absence enhances insulin signaling leading to hypoglycemia, a dangerous complication found after insulin overdose. We analyzed the effect of VD signaling in a model of overactivation of the IR. We generated inducible double KO (DKO) mice for the VD receptor (VDR) and PTEN. DKO mice showed severe hypoglycemia, lower total cholesterol and increased mortality. No macroscopic tumors were detected. Analysis of the glucose metabolism did not show clear differences that would explain the increased mortality. Glucose supplementation, either systemically or directly into the brain, did not enhance DKO survival. Lipidic liver metabolism was altered as there was a delay in the activation of genes related to β-oxidation and a decrease in lipogenesis in DKO mice. High-fat diet administration in DKO significantly improved its life span. Lack of vitamin D signaling increases mortality in a model of overactivation of the IR by impairing lipid metabolism. Clinically, these results reveal the importance of adequate Vitamin D levels in T1D patients.

Published
2022
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5. Plasma impact on diagnostic mirrors in JET

Author

A. Garcia-Carrasco, P. Petersson, M. Rubel, A. Widdowson, E. Fortuna-Zalesna, S. Jachmich, M. Brix, and L. Marot

Subjects
Nuclear engineering. Atomic power, TK9001-9401
Abstract

Metallic mirrors will be essential components of all optical systems for plasma diagnosis in ITER. This contribution provides a comprehensive account on plasma impact on diagnostic mirrors in JET with the ITER-Like Wall. Specimens from the First Mirror Test and the lithium-beam diagnostic have been studied by spectrophotometry, ion beam analysis and electron microscopy. Test mirrors made of molybdenum were retrieved from the main chamber and the divertor after exposure to the 2013–2014 experimental campaign. In the main chamber, only mirrors located at the entrance of the carrier lost reflectivity (Be deposition), while those located deeper in the carrier were only slightly affected. The performance of mirrors in the JET divertor was strongly degraded by deposition of beryllium, tungsten and other species. Mirrors from the lithium-beam diagnostic have been studied for the first time. Gold coatings were severely damaged by intense arcing. As a consequence, material mixing of the gold layer with the stainless steel substrate occurred. Total reflectivity dropped from over 90% to less than 60%, i.e. to the level typical for stainless steel. Keywords: JET, First mirror test, Diagnostic mirrors, Erosion-deposition

Published
2017
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6. Overview of the JET ITER-like wall divertor

Author

A. Widdowson, E. Alves, A. Baron-Wiechec, N.P. Barradas, N. Catarino, J.P. Coad, V. Corregidor, A. Garcia-Carrasco, K. Heinola, S. Koivuranta, S. Krat, A. Lahtinen, J. Likonen, M. Mayer, P. Petersson, M. Rubel, and S. Van Boxel

Subjects
Nuclear engineering. Atomic power, TK9001-9401
Abstract

The work presented draws on new analysis of components removed following the second JET ITER-like wall campaign 2013–14 concentrating on the upper inner divertor, inner and outer divertor corners, lifetime issues relating to tungsten coatings on JET carbon fibre composite divertor tiles and dust/particulate generation. The results show that the upper inner divertor remains the region of highest deposition in the JET-ILW. Variations in plasma configurations between the first and second campaign have altered material migration to the corners of the inner and outer divertor. Net deposition is shown to be beneficial in the sense that it reduces W coating erosion, covers small areas of exposed carbon surfaces and even encapsulates particles. Keywords: Jet, Erosion, Deposition, Fuel retention, Dust, Tungsten coating

Published
2017
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7. Studies of dust from JET with the ITER-Like Wall: Composition and internal structure

Author

E. Fortuna-Zaleśna, J. Grzonka, M. Rubel, A. Garcia-Carrasco, A. Widdowson, A. Baron-Wiechec, L. Ciupiński, and JET Contributors

Subjects
Nuclear engineering. Atomic power, TK9001-9401
Abstract

Results are presented for the dust survey performed at JET after the second experimental campaign with the ITER-Like Wall: 2013–2014. Samples were collected on adhesive stickers from several different positions in the divertor both on the tiles and on the divertor carrier. Brittle dust-forming deposits on test mirrors from the inner divertor wall were also studied. Comprehensive characterization accomplished by a wide range of high-resolution microscopy techniques, including focused ion beam, has led to the identification of several classes of particles: (i) beryllium flakes originating either from the Be coatings from the inner wall cladding or Be-rich mixed co-deposits resulting from material migration; (ii) beryllium droplets and splashes; (iii) tungsten and nickel-rich (from Inconel) droplets; (iv) mixed material layers with a various content of small (8–200nm) W-Mo and Ni-based debris. A significant content of nitrogen from plasma edge cooling has been identified in all types of co-deposits. A comparison between particles collected after the first and second experimental campaign is also presented and discussed. Keywords: Dust, JET, ITER-Like Wall, Beryllium, Tungsten, Material mixing

Published
2017
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8. Investigation of probe surfaces after ion cyclotron wall conditioning in ASDEX upgrade

Author

A. Garcia-Carrasco, P. Petersson, T. Schwarz-Selinger, T. Wauters, D. Douai, V. Bobkov, R. Cavazzana, K. Krieger, A. Lyssoivan, S. Möller, M. Spolaore, V. Rohde, and M. Rubel

Subjects
Nuclear engineering. Atomic power, TK9001-9401
Abstract

For the first time, material analysis techniques have been applied to study the effect of ion cyclotron wall conditioning (ICWC) on probe surfaces in a metal-wall machine. ICWC is a technique envisaged to contribute to the removal of fuel and impurities from the first wall of ITER. The objective of this work was to assess impurity migration under ICWC operation. Tungsten probes were exposed in ASDEX Upgrade to discharges in helium. After wall conditioning, the probes were covered with a co-deposited layer containing D, B, C, N, O and relatively high amount of He. The concentration ratio He/C+B was 0.7. The formation of the co-deposited layer indicates that a fraction of the impurities desorbed from the wall under ICWC operation are transported by plasma and deposited away from their original location. Keywords: ICWC, Erosion-deposition, Fuel removal, Ion beam analysis, ASDEX Upgrade

Published
2017
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9. Global scaling of the heat transport in fusion plasmas

Author

Sara Moradi, Johan Anderson, Michele Romanelli, Hyun-Tae Kim, JET contributors, X. Litaudon, S. Abduallev, M. Abhangi, P. Abreu, M. Afzal, K. M. Aggarwal, T. Ahlgren, J. H. Ahn, L. Aho-Mantila, N. Aiba, M. Airila, R. Albanese, V. Aldred, D. Alegre, E. Alessi, P. Aleynikov, A. Alfier, A. Alkseev, M. Allinson, B. Alper, E. Alves, G. Ambrosino, R. Ambrosino, L. Amicucci, V. Amosov, E. Andersson Sundén, M. Angelone, M. Anghel, C. Angioni, L. Appel, C. Appelbee, P. Arena, M. Ariola, H. Arnichand, S. Arshad, A. Ash, N. Ashikawa, V. Aslanyan, O. Asunta, F. Auriemma, Y. Austin, L. Avotina, M. D. Axton, C. Ayres, M. Bacharis, A. Baciero, D. Baião, S. Bailey, A. Baker, I. Balboa, M. Balden, N. Balshaw, R. Bament, J. W. Banks, Y. F. Baranov, M. A. Barnard, D. Barnes, M. Barnes, R. Barnsley, A. Baron Wiechec, L. Barrera Orte, M. Baruzzo, V. Basiuk, M. Bassan, R. Bastow, A. Batista, P. Batistoni, R. Baughan, B. Bauvir, L. Baylor, B. Bazylev, J. Beal, P. S. Beaumont, M. Beckers, B. Beckett, A. Becoulet, N. Bekris, M. Beldishevski, K. Bell, F. Belli, M. Bellinger, É. Belonohy, N. Ben Ayed, N. A. Benterman, H. Bergsȧker, J. Bernardo, M. Bernert, M. Berry, L. Bertalot, C. Besliu, M. Beurskens, B. Bieg, J. Bielecki, T. Biewer, M. Bigi, P. Bìlkovà, F. Binda, A. Bisoffi, J. P. S. Bizarro, C. Björkas, J. Blackburn, K. Blackman, T. R. Blackman, P. Blanchard, P. Blatchford, V. Bobkov, A. Boboc, G. Bodnàr, O. Bogar, I. Bolshakova, T. Bolzonella, N. Bonanomi, F. Bonelli, J. Boom, J. Booth, D. Borba, D. Borodin, I. Borodkina, A. Botrugno, C. Bottereau, P. Boulting, C. Bourdelle, M. Bowden, C. Bower, C. Bowman, T. Boyce, C. Boyd, H. J. Boyer, J. M. A. Bradshaw, V. Braic, R. Bravanec, B. Breizman, S. Bremond, P. D. Brennan, S. Breton, A. Brett, S. Brezinsek, M. D. J. Bright, M. Brix, W. Broeckx, M. Brombin, A. Brosawski, D. P. D. Brown, M. Brown, E. Bruno, J. Bucalossi, J. Buch, J. Buchanan, M. A. Buckley, R. Budny, H. Bufferand, M. Bulman, N. Bulmer, P. Bunting, P. Buratti, A. Burckhart, A. Buscarino, A. Busse, N. K. Butler, I. Bykov, J. Byrne, P. Cahyna, G. Calabrò, I. Calvo, Y. Camenen, P. Camp, D. C. Campling, J. Cane, B. Cannas, A. J. Capel, P. J. Card, A. Cardinali, P. Carman, M. Carr, D. Carralero, L. Carraro, B. B. Carvalho, I. Carvalho, P. Carvalho, F. J. Casson, C. Castaldo, N. Catarino, J. Caumont, F. Causa, R. Cavazzana, K. Cave-Ayland, M. Cavinato, M. Cecconello, S. Ceccuzzi, E. Cecil, A. Cenedese, R. Cesario, C. D. Challis, M. Chandler, D. Chandra, C. S. Chang, A. Chankin, I. T. Chapman, S. C. Chapman, M. Chernyshova, G. Chitarin, G. Ciraolo, D. Ciric, J. Citrin, F. Clairet, E. Clark, M. Clark, R. Clarkson, D. Clatworthy, C. Clements, M. Cleverly, J. P. Coad, P. A. Coates, A. Cobalt, V. Coccorese, V. Cocilovo, S. Coda, R. Coelho, J. W. Coenen, I. Coffey, L. Colas, S. Collins, D. Conka, S. Conroy, N. Conway, D. Coombs, D. Cooper, S. R. Cooper, C. Corradino, Y. Corre, G. Corrigan, S. Cortes, D. Coster, A. S. Couchman, M. P. Cox, T. Craciunescu, S. Cramp, R. Craven, F. Crisanti, G. Croci, D. Croft, K. Crombé, R. Crowe, N. Cruz, G. Cseh, A. Cufar, A. Cullen, M. Curuia, A. Czarnecka, H. Dabirikhah, P. Dalgliesh, S. Dalley, J. Dankowski, D. Darrow, O. Davies, W. Davis, C. Day, I. E. Day, M. De Bock, A. de Castro, E. de la Cal, E. de la Luna, G. De Masi, J. L. de Pablos, G. De Temmerman, G. De Tommasi, P. de Vries, K. Deakin, J. Deane, F. Degli Agostini, R. Dejarnac, E. Delabie, N. den Harder, R. O. Dendy, J. Denis, P. Denner, S. Devaux, P. Devynck, F. Di Maio, A. Di Siena, C. Di Troia, P. Dinca, R. Dinca, B. Ding, T. Dittmar, H. Doerk, R. P. Doerner, T. Donné, S. E. Dorling, S. Dormido-Canto, S. Doswon, D. Douai, P. T. Doyle, A. Drenik, P. Drewelow, P. Drews, Ph. Duckworth, R. Dumont, P. Dumortier, D. Dunai, M. Dunne, I. Duran, F. Durodié, P. Dutta, B. P. Duval, R. Dux, K. Dylst, N. Dzysiuk, P. V. Edappala, J. Edmond, A. M. Edwards, J. Edwards, Th. Eich, A. Ekedahl, R. El-Jorf, C. G. Elsmore, M. Enachescu, G. Ericsson, F. Eriksson, J. Eriksson, L. G. Eriksson, B. Esposito, S. Esquembri, H. G. Esser, D. Esteve, B. Evans, G. E. Evans, G. Evison, G. D. Ewart, D. Fagan, M. Faitsch, D. Falie, A. Fanni, A. Fasoli, J. M. Faustin, N. Fawlk, L. Fazendeiro, N. Fedorczak, R. C. Felton, K. Fenton, A. Fernades, H. Fernandes, J. Ferreira, J. A. Fessey, O. Février, O. Ficker, A. Field, S. Fietz, A. Figueiredo, J. Figueiredo, A. Fil, P. Finburg, M. Firdaouss, U. Fischer, L. Fittill, M. Fitzgerald, D. Flammini, J. Flanagan, C. Fleming, K. Flinders, N. Fonnesu, J. M. Fontdecaba, A. Formisano, L. Forsythe, L. Fortuna, E. Fortuna-Zalesna, M. Fortune, S. Foster, T. Franke, T. Franklin, M. Frasca, L. Frassinetti, M. Freisinger, R. Fresa, D. Frigione, V. Fuchs, D. Fuller, S. Futatani, J. Fyvie, K. Gàl, D. Galassi, K. Galazka, J. Galdon-Quiroga, J. Gallagher, D. Gallart, R. Galvão, X. Gao, Y. Gao, J. Garcia, A. Garcia-Carrasco, M. Garca-Munoz, J.-L. Gardarein, L. Garzotti, P. Gaudio, E. Gauthier, D. F. Gear, S. J. Gee, B. Geiger, M. Gelfusa, S. Gerasimov, G. Gervasini, M. Gethins, Z. Ghani, M. Ghate, M. Gherendi, J. C. Giacalone, L. Giacomelli, C. S. Gibson, T. Giegerich, C. Gil, L. Gil, S. Gilligan, D. Gin, E. Giovannozzi, J. B. Girardo, C. Giroud, G. Giruzzi, S. Glöggler, J. Godwin, J. Goff, P. Gohil, V. Goloborod'ko, R. Gomes, B. Goncalves, M. Goniche, M. Goodliffe, A. Goodyear, G. Gorini, M. Gosk, R. Goulding, A. Goussarov, R. Gowland, B. Graham, M. E. Graham, J. P. Graves, N. Grazier, P. Grazier, N. R. Green, H. Greuner, B. Grierson, F. S. Griph, C. Grisolia, D. Grist, M. Groth, R. Grove, C. N. Grundy, J. Grzonka, D. Guard, C. Guérard, C. Guillemaut, R. Guirlet, C. Gurl, H. H. Utoh, L. J. Hackett, S. Hacquin, A. Hagar, R. Hager, A. Hakola, M. Halitovs, S. J. Hall, S. P. Hallworth Cook, C. Hamlyn-Harris, K. Hammond, C. Harrington, J. Harrison, D. Harting, F. Hasenbeck, Y. Hatano, D. R. Hatch, T. D. V. Haupt, J. Hawes, N. C. Hawkes, J. Hawkins, P. Hawkins, P. W. Haydon, N. Hayter, S. Hazel, P. J. L. Heesterman, K. Heinola, C. Hellesen, T. Hellsten, W. Helou, O. N. Hemming, T. C. Hender, M. Henderson, S. S. Henderson, R. Henriques, D. Hepple, G. Hermon, P. Hertout, C. Hidalgo, E. G. Highcock, M. Hill, J. Hillairet, J. Hillesheim, D. Hillis, K. Hizanidis, A. Hjalmarsson, J. Hobirk, E. Hodille, C. H. A. Hogben, G. M. D. Hogeweij, A. Hollingsworth, S. Hollis, D. A. Homfray, J. Horàcek, G. Hornung, A. R. Horton, L. D. Horton, L. Horvath, S. P. Hotchin, M. R. Hough, P. J. Howarth, A. Hubbard, A. Huber, V. Huber, T. M. Huddleston, M. Hughes, G. T. A. Huijsmans, C. L. Hunter, P. Huynh, A. M. Hynes, D. Iglesias, N. Imazawa, F. Imbeaux, M. Imrìŝek, M. Incelli, P. Innocente, M. Irishkin, I. Ivanova-Stanik, S. Jachmich, A. S. Jacobsen, P. Jacquet, J. Jansons, A. Jardin, A. Järvinen, F. Jaulmes, S. Jednoróq, I. Jenkins, C. Jeong, I. Jepu, E. Joffrin, R. Johnson, T. Johnson, Jane Johnston, L. Joita, G. Jones, T. T. C. Jones, K. K. Hoshino, A. Kallenbach, K. Kamiya, J. Kaniewski, A. Kantor, A. Kappatou, J. Karhunen, D. Karkinsky, I. Karnowska, M. Kaufman, G. Kaveney, Y. Kazakov, V. Kazantzidis, D. L. Keeling, T. Keenan, J. Keep, M. Kempenaars, C. Kennedy, D. Kenny, J. Kent, O. N. Kent, E. Khilkevich, H. T. Kim, H. S. Kim, A. Kinch, C. King, D. King, R. F. King, D. J. Kinna, V. Kiptily, A. Kirk, K. Kirov, A. Kirschner, G. Kizane, C. Klepper, A. Klix, P. Knight, S. J. Knipe, S. Knott, T. Kobuchi, F. Köchl, G. Kocsis, I. Kodeli, L. Kogan, D. Kogut, S. Koivuranta, Y. Kominis, M. Köppen, B. Kos, T. Koskela, H. R. Koslowski, M. Koubiti, M. Kovari, E. Kowalska-Strzeciwilk, A. Krasilnikov, V. Krasilnikov, N. Krawczyk, M. Kresina, K. Krieger, A. Krivska, U. Kruezi, I. Ksiazek, A. Kukushkin, A. Kundu, T. Kurki-Suonio, S. Kwak, R. Kwiatkowski, O. J. Kwon, L. Laguardia, A. Lahtinen, A. Laing, N. Lam, H. T. Lambertz, C. Lane, P. T. Lang, S. Lanthaler, J. Lapins, A. Lasa, J. R. Last, E. Laszynska, R. Lawless, A. Lawson, K. D. Lawson, A. Lazaros, E. Lazzaro, J. Leddy, S. Lee, X. Lefebvre, H. J. Leggate, J. Lehmann, M. Lehnen, D. Leichtle, P. Leichuer, F. Leipold, I. Lengar, M. Lennholm, E. Lerche, A. Lescinskis, S. Lesnoj, E. Letellier, M. Leyland, W. Leysen, L. Li, Y. Liang, J. Likonen, J. Linke, Ch. Linsmeier, B. Lipschultz, G. Liu, Y. Liu, V. P. Lo Schiavo, T. Loarer, A. Loarte, R. C. Lobel, B. Lomanowski, P. J. Lomas, J. Lönnroth, J. M. López, J. López-Razola, R. Lorenzini, U. Losada, J. J. Lovell, A. B. Loving, C. Lowry, T. Luce, R. M. A. Lucock, A. Lukin, C. Luna, M. Lungaroni, C. P. Lungu, M. Lungu, A. Lunniss, I. Lupelli, A. Lyssoivan, N. Macdonald, P. Macheta, K. Maczewa, B. Magesh, P. Maget, C. Maggi, H. Maier, J. Mailloux, T. Makkonen, R. Makwana, A. Malaquias, A. Malizia, P. Manas, A. Manning, M. E. Manso, P. Mantica, M. Mantsinen, A. Manzanares, Ph. Maquet, Y. Marandet, N. Marcenko, C. Marchetto, O. Marchuk, M. Marinelli, M. Marinucci, T. Markovic, D. Marocco, L. Marot, C. A. Marren, R. Marshal, A. Martin, Y. Martin, A. Martín de Aguilera, F. J. Martínez, J. R. Martín-Solís, Y. Martynova, S. Maruyama, A. Masiello, M. Maslov, S. Matejcik, M. Mattei, G. F. Matthews, F. Maviglia, M. Mayer, M. L. Mayoral, T. May-Smith, D. Mazon, C. Mazzotta, R. McAdams, P. J. McCarthy, K. G. McClements, O. McCormack, P. A. McCullen, D. McDonald, S. McIntosh, R. McKean, J. McKehon, R. C. Meadows, A. Meakins, F. Medina, M. Medland, S. Medley, S. Meigh, A. G. Meigs, G. Meisl, S. Meitner, L. Meneses, S. Menmuir, K. Mergia, I. R. Merrigan, Ph. Mertens, S. Meshchaninov, A. Messiaen, H. Meyer, S. Mianowski, R. Michling, D. Middleton-Gear, J. Miettunen, F. Militello, E. Militello-Asp, G. Miloshevsky, F. Mink, S. Minucci, Y. Miyoshi, J. Mlynàr, D. Molina, I. Monakhov, M. Moneti, R. Mooney, S. Moradi, S. Mordijck, L. Moreira, R. Moreno, F. Moro, A. W. Morris, J. Morris, L. Moser, S. Mosher, D. Moulton, A. Murari, A. Muraro, S. Murphy, N. N. Asakura, Y. S. Na, F. Nabais, R. Naish, T. Nakano, E. Nardon, V. Naulin, M. F. F. Nave, I. Nedzelski, G. Nemtsev, F. Nespoli, A. Neto, R. Neu, V. S. Neverov, M. Newman, K. J. Nicholls, T. Nicolas, A. H. Nielsen, P. Nielsen, E. Nilsson, D. Nishijima, C. Noble, M. Nocente, D. Nodwell, K. Nordlund, H. Nordman, R. Nouailletas, I. Nunes, M. Oberkofler, T. Odupitan, M. T. Ogawa, T. O'Gorman, M. Okabayashi, R. Olney, O. Omolayo, M. O'Mullane, J. Ongena, F. Orsitto, J. Orszagh, B. I. Oswuigwe, R. Otin, A. Owen, R. Paccagnella, N. Pace, D. Pacella, L. W. Packer, A. Page, E. Pajuste, S. Palazzo, S. Pamela, S. Panja, P. Papp, R. Paprok, V. Parail, M. Park, F. Parra Diaz, M. Parsons, R. Pasqualotto, A. Patel, S. Pathak, D. Paton, H. Patten, A. Pau, E. Pawelec, C. Paz Soldan, A. Peackoc, I. J. Pearson, S.-P. Pehkonen, E. Peluso, C. Penot, A. Pereira, R. Pereira, P. P. Pereira Puglia, C. Perez von Thun, S. Peruzzo, S. Peschanyi, M. Peterka, P. Petersson, G. Petravich, A. Petre, N. Petrella, V. Petrzilka, Y. Peysson, D. Pfefferlé, V. Philipps, M. Pillon, G. Pintsuk, P. Piovesan, A. Pires dos Reis, L. Piron, A. Pironti, F. Pisano, R. Pitts, F. Pizzo, V. Plyusnin, N. Pomaro, O. G. Pompilian, P. J. Pool, S. Popovichev, M. T. Porfiri, C. Porosnicu, M. Porton, G. Possnert, S. Potzel, T. Powell, J. Pozzi, V. Prajapati, R. Prakash, G. Prestopino, D. Price, M. Price, R. Price, P. Prior, R. Proudfoot, G. Pucella, P. Puglia, M. E. Puiatti, D. Pulley, K. Purahoo, Th. Pütterich, E. Rachlew, M. Rack, R. Ragona, M. S. J. Rainford, A. Rakha, G. Ramogida, S. Ranjan, C. J. Rapson, J. J. Rasmussen, K. Rathod, G. Rattà, S. Ratynskaia, G. Ravera, C. Rayner, M. Rebai, D. Reece, A. Reed, D. Réfy, B. Regan, J. Regana, M. Reich, N. Reid, F. Reimold, M. Reinhart, M. Reinke, D. Reiser, D. Rendell, C. Reux, S. D. A. Reyes Cortes, S. Reynolds, V. Riccardo, N. Richardson, K. Riddle, D. Rigamonti, F. G. Rimini, J. Risner, M. Riva, C. Roach, R. J. Robins, S. A. Robinson, T. Robinson, D. W. Robson, R. Roccella, R. Rodionov, P. Rodrigues, J. Rodriguez, V. Rohde, F. Romanelli, M. Romanelli, S. Romanelli, J. Romazanov, S. Rowe, M. Rubel, G. Rubinacci, G. Rubino, L. Ruchko, M. Ruiz, C. Ruset, J. Rzadkiewicz, S. Saarelma, R. Sabot, E. Safi, P. Sagar, G. Saibene, F. Saint-Laurent, M. Salewski, A. Salmi, R. Salmon, F. Salzedas, D. Samaddar, U. Samm, D. Sandiford, P. Santa, M. I. K. Santala, B. Santos, A. Santucci, F. Sartori, R. Sartori, O. Sauter, R. Scannell, T. Schlummer, K. Schmid, V. Schmidt, S. Schmuck, M. Schneider, K. Schöpf, D. Schwörer, S. D. Scott, G. Sergienko, M. Sertoli, A. Shabbir, S. E. Sharapov, A. Shaw, R. Shaw, H. Sheikh, A. Shepherd, A. Shevelev, A. Shumack, G. Sias, M. Sibbald, B. Sieglin, S. Silburn, A. Silva, C. Silva, P. A. Simmons, J. Simpson, J. Simpson-Hutchinson, A. Sinha, S. K. Sipilä, A. C. C. Sips, P. Sirén, A. Sirinelli, H. Sjöstrand, M. Skiba, R. Skilton, K. Slabkowska, B. Slade, N. Smith, P. G. Smith, R. Smith, T. J. Smith, M. Smithies, L. Snoj, S. Soare, E. R. Solano, A. Somers, C. Sommariva, P. Sonato, A. Sopplesa, J. Sousa, C. Sozzi, S. Spagnolo, T. Spelzini, F. Spineanu, G. Stables, I. Stamatelatos, M. F. Stamp, P. Staniec, G. Stankunas, C. Stan-Sion, M. J. Stead, E. Stefanikova, I. Stepanov, A. V. Stephen, M. Stephen, A. Stevens, B. D. Stevens, J. Strachan, P. Strand, H. R. Strauss, P. Ström, G. Stubbs, W. Studholme, F. Subba, H. P. Summers, J. Svensson, L. Swiderski, T. Szabolics, M. Szawlowski, G. Szepesi, T. T. Suzuki, B. Tàl, T. Tala, A. R. Talbot, S. Talebzadeh, C. Taliercio, P. Tamain, C. Tame, W. Tang, M. Tardocchi, L. Taroni, D. Taylor, K. A. Taylor, D. Tegnered, G. Telesca, N. Teplova, D. Terranova, D. Testa, E. Tholerus, J. Thomas, J. D. Thomas, P. Thomas, A. Thompson, C.-A. Thompson, V. K. Thompson, L. Thorne, A. Thornton, A. S. Thrysoe, P. A. Tigwell, N. Tipton, I. Tiseanu, H. Tojo, M. Tokitani, P. Tolias, M. Tomes, P. Tonner, M. Towndrow, P. Trimble, M. Tripsky, M. Tsalas, P. Tsavalas, D. Tskhakaya jun, I. Turner, M. M. Turner, M. Turnyanskiy, G. Tvalashvili, S. G. J. Tyrrell, A. Uccello, Z. Ul-Abidin, J. Uljanovs, D. Ulyatt, H. Urano, I. Uytdenhouwen, A. P. Vadgama, D. Valcarcel, M. Valentinuzzi, M. Valisa, P. Vallejos Olivares, M. Valovic, M. Van De Mortel, D. Van Eester, W. Van Renterghem, G. J. van Rooij, J. Varje, S. Varoutis, S. Vartanian, K. Vasava, T. Vasilopoulou, J. Vega, G. Verdoolaege, R. Verhoeven, C. Verona, G. Verona Rinati, E. Veshchev, N. Vianello, J. Vicente, E. Viezzer, S. Villari, F. Villone, P. Vincenzi, I. Vinyar, B. Viola, A. Vitins, Z. Vizvary, M. Vlad, I. Voitsekhovitch, P. Vondràcek, N. Vora, T. Vu, W. W. Pires de Sa, B. Wakeling, C. W. F. Waldon, N. Walkden, M. Walker, R. Walker, M. Walsh, E. Wang, N. Wang, S. Warder, R. J. Warren, J. Waterhouse, N. W. Watkins, C. Watts, T. Wauters, A. Weckmann, J. Weiland, H. Weisen, M. Weiszflog, C. Wellstood, A. T. West, M. R. Wheatley, S. Whetham, A. M. Whitehead, B. D. Whitehead, A. M. Widdowson, S. Wiesen, J. Wilkinson, J. Williams, M. Williams, A. R. Wilson, D. J. Wilson, H. R. Wilson, J. Wilson, M. Wischmeier, G. Withenshaw, A. Withycombe, D. M. Witts, D. Wood, R. Wood, C. Woodley, S. Wray, J. Wright, J. C. Wright, J. Wu, S. Wukitch, A. Wynn, T. Xu, D. Yadikin, W. Yanling, L. Yao, V. Yavorskij, M. G. Yoo, C. Young, D. Young, I. D. Young, R. Young, J. Zacks, R. Zagorski, F. S. Zaitsev, R. Zanino, A. Zarins, K. D. Zastrow, M. Zerbini, W. Zhang, Y. Zhou, E. Zilli, V. Zoita, S. Zoletnik, and I. Zychor

Subjects
Physics, QC1-999
Abstract

A global heat flux model based on a fractional derivative of plasma pressure is proposed for the heat transport in fusion plasmas. The degree of the fractional derivative of the heat flux, α, is defined through the power balance analysis of the steady state. The model was used to obtain the experimental values of α for a large database of the Joint European Torus (JET) carbon-wall as well as ITER like-wall plasmas. The fractional degrees of the electron heat flux are found to be α

Published
2020
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10. The impact of glucocorticoids and anti-cd20 therapy on cervical human papillomavirus infection risk in women with systemic lupus erythematosus

Author

Claudia Mendoza-Pinto, Mario Garcia-Carrasco, Veronica Vallejo-Ruiz, Alejandro Taboada-Cole, Margarita Munoz-Guarneros, Juan Carlos Solis-Poblano, Elias Pezzat-Said, Adriana Aguilar-Lemarroy, Luis Felipe Jave-Suarez, Luis Vazquez de Lara, Gloria Ramos-Alvarez, Julio Reyes-Leyva, and Aurelio Lopez-Colombo

Subjects
Cervical Human Papillomavirus Infection, Systemic Lupus Erythematosus, Risk Factors, Rituximab, Medicine (General), R5-920
Abstract

OBJECTIVE: To identify the prevalence and factors associated with cervical human papillomavirus infection in women with systemic lupus erythematosus METHODS: This cross-sectional study collected traditional and systemic lupus erythematosus-related disease risk factors, including conventional and biologic therapies. A gynecological evaluation and cervical cytology screen were performed. Human papillomavirus detection and genotyping were undertaken by PCR and linear array assay. RESULTS: A total of 148 patients were included, with a mean age and disease duration of 42.5±11.8 years and 9.7±5.3 years, respectively. The prevalence of squamous intraepithelial lesions was 6.8%. The prevalence of human papillomavirus infection was 29%, with human papillomavirus subtype 59 being the most frequent. Patients with human papillomavirus were younger than those without the infection (38.2±11.2 vs. 44.2±11.5 years, respectively; p = 0.05), and patients with the virus had higher daily prednisone doses (12.8±6.8 vs. 9.7±6.7 mg, respectively; p = 0.01) and cumulative glucocorticoid doses (14.2±9.8 vs. 9.7±7.3 g, respectively; p = 0.005) compared with patients without. Patients with human papillomavirus infection more frequently received rituximab than those without (20.9% vs. 8.5%, respectively; p = 0.03). In the multivariate analysis, only the cumulative glucocorticoid dose was associated with human papillomavirus infection. CONCLUSIONS: The cumulative glucocorticoid dose may increase the risk of human papillomavirus infection. Although rituximab administration was more frequent in patients with human papillomavirus infection, no association was found. Screening for human papillomavirus infection is recommended in women with systemic lupus erythematosus.

Published
2013
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11. Phosphatidylethanolamine Induces an Antifibrotic Phenotype in Normal Human Lung Fibroblasts and Ameliorates Bleomycin-Induced Lung Fibrosis in Mice

Author

Luis G. Vazquez-de-Lara, Beatriz Tlatelpa-Romero, Yair Romero, Nora Fernández-Tamayo, Fernando Vazquez-de-Lara, Jaime M. Justo-Janeiro, Mario Garcia-Carrasco, René de-la-Rosa Paredes, José G. Cisneros-Lira, Criselda Mendoza-Milla, Francesco Moccia, and Roberto Berra-Romani

Subjects
pulmonary surfactant, phosphatidylethanolamine, lung fibrosis, bleomycin model, lung fibroblasts, Ca2+ signaling, Biology (General), QH301-705.5, Chemistry, QD1-999
Abstract

Lung surfactant is a complex mixture of phospholipids and specific proteins but its role in the pathogenesis of interstitial lung diseases is not established. Herein, we analyzed the effects of three representative phospholipid components, that is, dipalmitoilphosphatidylcoline (DPPC), phosphatidylglycerol (PG) and phosphatidylethanolamine (PE), on collagen expression, apoptosis and Ca2+ signaling in normal human lung fibroblasts (NHLF) and probed their effect in an experimental model of lung fibrosis. Collagen expression was measured with RT-PCR, apoptosis was measured by using either the APOPercentage assay kit (Biocolor Ltd., Northern Ireland, UK) or the Caspase-Glo 3/7 assay (Promega, Madison, WI, USA) and Ca2+ signaling by conventional epifluorescence imaging. The effect in vivo was tested in bleomycin-induced lung fibrosis in mice. DPPC and PG did not affect collagen expression, which was downregulated by PE. Furthermore, PE promoted apoptosis and induced a dose-dependent Ca2+ signal. PE-induced Ca2+ signal and apoptosis were both blocked by phospholipase C, endoplasmic reticulum pump and store-operated Ca2+ entry inhibition. PE-induced decrease in collagen expression was attenuated by blocking phospholipase C. Finally, surfactant enriched with PE and PE itself attenuated bleomycin-induced lung fibrosis and decreased the soluble collagen concentration in mice lungs. This study demonstrates that PE strongly contributes to the surfactant-induced inhibition of collagen expression in NHLF through a Ca2+ signal and that early administration of Beractant enriched with PE diminishes lung fibrosis in vivo.

Published
2018
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