Literature DB >> 2019985

Transport of cyclosporin A in kidney epithelial cell line (LLC-PK1).

A Takayama1, Y Okazaki, K Fukuda, M Takano, K Inui, R Hori.   

Abstract

The characteristics of cyclosporin A transport have been studied in cultured kidney epithelial cell line LLC-PK1. The uptake of cyclosporin A by LLC-PK1 cells was time-dependent and reached a steady state at about 30 min. The initial uptake was saturable and was inhibited by cyclosporin A analogs, cyclosporin C and D and by verapamil, but not by metabolic inhibitors such as 2,4-dinitrophenol and rotenone. Cyclosporin A uptake as well as efflux was strongly dependent on temperature. The Arrhenius plot for cyclosporin A uptake was biphasic, whereas the Arrhenius plot for sulfanilamide uptake, which is transported by a simple diffusion, was linear. These results indicate that a specific mechanism is concerned in the transport of cyclosporin A in LLC-PK1, cells.

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Year:  1991        PMID: 2019985

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  3 in total

1.  Establishment and characterization of the transformants stably-expressing MDR1 derived from various animal species in LLC-PK1.

Authors:  Toshiyuki Takeuchi; Sumie Yoshitomi; Tomoaki Higuchi; Keiko Ikemoto; Shin-ichi Niwa; Takuya Ebihara; Miki Katoh; Tsuyoshi Yokoi; Satoru Asahi
Journal:  Pharm Res       Date:  2006-06-21       Impact factor: 4.200

2.  Characterization of cyclosporine A uptake in human erythrocytes.

Authors:  C Reichel; M von Falkenhausen; D Brockmeier; H J Dengler
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

3.  Contribution of ion-pair complexation with bile salts to the transport of organic cations across LLC-PK1 cell monolayers.

Authors:  Im-Sook Song; Yong-Hae Han; Suk-Jae Chung; Chang-Koo Shim
Journal:  Pharm Res       Date:  2003-04       Impact factor: 4.200

  3 in total

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