dc.creator | Figueiredo, J F | |
dc.creator | Bertels, I M V | |
dc.creator | Gontijo, J A R | |
dc.date | 2008-Dec | |
dc.date | 2015-11-27T13:13:24Z | |
dc.date | 2015-11-27T13:13:24Z | |
dc.date.accessioned | 2018-03-29T01:07:53Z | |
dc.date.available | 2018-03-29T01:07:53Z | |
dc.identifier | Transplantation Proceedings. v. 40, n. 10, p. 3311-5, 2008-Dec. | |
dc.identifier | 0041-1345 | |
dc.identifier | 10.1016/j.transproceed.2008.06.060 | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/19100379 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/198077 | |
dc.identifier | 19100379 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1298310 | |
dc.description | Proximal tubule cells have specialized apical membranes with microvilli that provide an extensive surface area for unidirectional transport of solute from lumen to blood. The major structural solute component is F-actin, which interacts with transmembrane proteins, including ion transport molecules related to normal absorptive and secretory functions. Our study was to evaluate F-actin and fluid absorption (Jv) in proximal tubules after exposure to preservation solutions. In vitro microperfusion technique and immunohistochemistry analysis. 1. Absorptions were similar in 1- and 24-hour-preserved tubules, as well as in fresh tubules. The exception was tubules for 24 hours in Euro-Collins solution, which did not show absorption, suggesting that it was affected. 2. Fluorescence intensity of actin tubules preserved for 1 hour in both solutions showed similar values to each other and to the control group; tubules preserved for 24 hours in both solutions were similar to each other, although statistically different than the control group and those preserved for 1 hour in Belzer (UW) solution. There were differences among groups in the distribution of F-actin; Jv values were different for 24-hour preservation in each solution, whereas fluorescence intensity was similar in both 24-hour solutions. Thus, actin cytoskeleton was not responsible for it, because 24-hour preservation in UW showed Jv results comparable to the control group. | |
dc.description | 40 | |
dc.description | 3311-5 | |
dc.language | eng | |
dc.relation | Transplantation Proceedings | |
dc.relation | Transplant. Proc. | |
dc.rights | fechado | |
dc.rights | | |
dc.source | PubMed | |
dc.subject | Absorption | |
dc.subject | Actin Cytoskeleton | |
dc.subject | Actins | |
dc.subject | Adenosine | |
dc.subject | Allopurinol | |
dc.subject | Animals | |
dc.subject | Cytoskeleton | |
dc.subject | Glutathione | |
dc.subject | Insulin | |
dc.subject | Kidney Tubules, Collecting | |
dc.subject | Kidney Tubules, Proximal | |
dc.subject | Male | |
dc.subject | Microscopy, Confocal | |
dc.subject | Microvilli | |
dc.subject | Models, Animal | |
dc.subject | Organ Preservation | |
dc.subject | Organ Preservation Solutions | |
dc.subject | Perfusion | |
dc.subject | Rabbits | |
dc.subject | Raffinose | |
dc.title | Actin Cytoskeletal And Functional Studies Of The Proximal Convoluted Tubules After Preservation. | |
dc.type | Artículos de revistas | |