Upwind Interpolation of Ghost Cells for More Accurate Building-Cube Method Simulations

2019 ◽  
Vol 2019.32 (0) ◽  
pp. 119
Author(s):  
Srikanth SURENDRANATH ◽  
Akira OYAMA ◽  
Ryoji TAKAKI
Keyword(s):  
2020 ◽  
Vol 20 (3) ◽  
pp. 453-463
Author(s):  
Svetlana Yagubova ◽  
Aliy Zhanataev ◽  
Rita Ostrovskaya ◽  
Еlena Anisina ◽  
Тatiana Gudasheva ◽  
...  

Background: NGF deficiency is one of the reasons for reduced β-cells survival in diabetes. Our previous experiments revealed the ability of low-weight NGF mimetic, GK-2, to reduce hyperglycaemia in a model of advanced diabetes. The increase in DNA damage in advanced diabetes was repeatedly reported, while there were no data about DNA damage in the initial diabetes. Aim: The study aimed to establish whether DNA damage occurs in initial diabetes and whether GK-2 is able to overcome the damage. Methods: The early-stage diabetes was modelled in Balb/c mice by streptozotocin (STZ) (130 mg/kg, i.p.). GK-2 was administered at a dose of 0.5 mg/kg, i.p., subchronically. The evaluation of DNA damage was performed using the alkaline comet assay; the percentage of DNA in the tail (%TDNA) and the percentage of the atypical DNA comets (“ghost cells”) were determined. Results: STZ at this subthreshold dose produced a slight increase in glycemia and MDA. Meanwhile, pronounced DNA damage was observed, concerning mostly the percentage of “ghost cells” in the pancreas, the liver and kidneys. GK-2 attenuated the degree of hyperglycaemia and reduced the % of “ghost cells” and %TDNA in all the organs examined; this effect continued after discontinuation of the therapy. Conclusion: Early-stage diabetes is accompanied by DNA damage, manifested by the increase of “ghost cells” percentage. The severity of these changes significantly exceeds the degree of hyperglycaemia and MDA accumulation. GK-2 exerts an antihyperglycaemic effect and attenuates the degree of DNA damage. Our results indicate that the comet assay is a highly informative method for search of antidiabetic medicines.


1991 ◽  
Vol 10 (4) ◽  
pp. 339-350 ◽  
Author(s):  
W. Gerald Robinson ◽  
Michael L. McCaleb ◽  
Leonard G. Feld ◽  
Otho E. Michaelis ◽  
Nora Laver And ◽  
...  

1973 ◽  
Vol 36 (6) ◽  
pp. 851-855 ◽  
Author(s):  
Bernard A. Levy
Keyword(s):  

2014 ◽  
Vol 44 (4) ◽  
pp. 284-290 ◽  
Author(s):  
Alicia Rumayor ◽  
Román Carlos ◽  
Hernán Molina Kirsch ◽  
Bruno A. Benevenuto de Andrade ◽  
Mario J. Romañach ◽  
...  

2021 ◽  
pp. 76-78
Author(s):  
Reema Raina ◽  
Nikita Gulati ◽  
Saurabh Juneja ◽  
Devi Charan Shetty

Cellular identities in the past have been based on the structural and functional aspects. Proper delineation of cellular structure occasionally could be ambiguous because of their varied existence either structurally similar or functionally dissimilar or vice versa. “Ghost cells”- is an area which is entailed by controversies allocated to their functionality and appearance. In odontogenic lesions they are considered as the enlarged epithelial cells with central space consequential to lost nucleus. Many authors have documented on the histogenesis and formation of ghost cells yet nothing relevant till date. This article is an attempt to concise the literature in precise manner to elaborate the ghost cell origin in histopathologic arena.


1952 ◽  
Vol 35 (5) ◽  
pp. 669-701 ◽  
Author(s):  
Torsten Teorell

1. Erythrocyte ghosts from human blood were produced by gentle water hemolysis. The ghost-containing hemolysate (about 20 mN) was added to media of different composition (KCl, NaCl, glucose, sucrose, etc.) and varying concentration ranging from 8 to 840 mN. The volume changes of the ghost cells were followed by a light absorption method. The potassium and sodium concentrations were also analyzed in some representative cases. 2. The ghosts shrank, or swelled, in two stages. An initial phase with a momentary expulsion, or uptake, of water leading to an osmotic equilibrium, was followed by a second phase in which a slow swelling or shrinking proceeded toward a final constant volume. 3. The ghosts were semipermeable in the sense that water always passed rapidly in either direction so as to maintain isotonicity with the external medium. The relation between ghost cell volumes (V) and the total concentration (Ce) of the suspension medium can be expressed by a modified van't Hoff-Mariotte law: (Ce + a)(V – b) = constant. Here a is a term correcting for an internal pressure and b is the non-solvent volume of the ghost cells. This means that the ghosts behave as perfect osmometers. 4. On the other hand appreciable concentration differences of the K and Na ions could be maintained across the intact ghost cell membranes for long periods. Whether this phenomenon is due simply to very low cation permeability or to active transport processes cannot be decided, although the first assumption appears more probable. 5. When the ghosts were treated with small concentrations of a lytic substance like Na oleate, the alkali ion transfer was greatly increased. This seems to be a simple exchange diffusion process with simultaneous, continued maintenance of osmotic equilibrium (= the second phase). A simplified theory is also given for the kinetics of the volume variations and ion exchange during the second phase (cf. the Appendix). 6. Miscellaneous observations on the effects of pH, and of some other substances are discussed. Some shape transformations of the ghost cells are also described.


1967 ◽  
Vol 32 (1) ◽  
pp. 55-70 ◽  
Author(s):  
Philip Seeman

Ferritin and colloidal gold were found to permeate human erythrocytes during rapid or gradual hypotonic hemolysis. Only hemolysed cells contained these particles; adjacent intact cells did not contain the tracers. Ferritin or gold added 3 min after the onset of hypotonic hemolysis did not permeate the ghost cells which had, therefore, become transiently permeable. By adding ferritin at various times after the onset of hemolysis, it was determined that for the majority of the cells the permeable state (or interval between the time of development and closure of membrane holes) existed only from about 15 to 25 sec after the onset of hemolysis. It was possible to fix the transient "holes" in the open position by adding glutaraldehyde only between 10 and 20 sec after the onset of hemolysis. The existence of such fixed holes was shown by the cell entry of ferritin and gold which were added to these prefixed cells. Membrane defects or discontinuities (of the order of 200–500 A wide) were observed only in prefixed cells which were permeated by ferritin subsequently added. Adjacent prefixed cells which did not become permeated by added ferritin did not reveal any membrane discontinuities. Glutaraldehyde does not per se induce or create such membrane defects since cells which had been fixed by glutaraldehyde before the 10-sec time point or after the 180-sec time point were never permeable to added ferritin, and the cell membranes never contained any defects. It was also observed that early in hemolysis (7–12 sec) a small bulge in one zone of the membrane often occurred. Ghost cells produced by holothurin A (a saponin) and fixed by glutaraldehyde became permeated by ferritin subsequently added, but no membrane discontinuities were seen. Ghosts produced by lysolecithin and fixed by glutaraldehyde also became permeated by subsequently added ferritin, and many membrane defects were seen here (about 300 A wide).


1999 ◽  
Vol 5 (7) ◽  
pp. 446-448 ◽  
Author(s):  
Ismail H. Kara ◽  
Fuat Gürkan ◽  
Mehmet Boşnak ◽  
Bünyamin Dikici ◽  
Mehmet Kervancioğlu ◽  
...  
Keyword(s):  

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