Literature DB >> 9023278

Active transport of nitrofurantoin across a mouse mammary epithelial monolayer.

V S Toddywalla1, F W Kari, M C Neville.   

Abstract

The antibiotic nitrofurantoin is transported against an electrochemical gradient into milk. A monolayer of CIT3 cells, a subline of the Comma 1D normal mouse mammary epithelial cell line, transports [14C]-nitrofurantoin against a concentration gradient from the basal to the apical solution when grown on membrane filters. In a side-by-side diffusion chamber with well-stirred solutions on both sides, the transfer rate is 50% higher in the basal-to-apical than in the apical-to-basal direction. Nonlabeled nitrofurantoin (500 microM) in the basal chamber equalized the transport in both directions, suggesting that a specific transporter is responsible for the basal-to-apical increment in flux. From inhibition studies, the apparent affinity of this transporter for nitrofurantoin is 50 microM. Changes in pH between 6.4 and 7.8 had no effect on the active transport component of the flux but did affect the passive flux component. Passive flux of the nonionized molecule was 2.6 times faster than that of the ionized molecule, but the ionized molecule did appear to cross the membrane passively. Our findings show that nitrofurantoin is actively transported across a mammary epithelial cell monolayer by a transporter whose affinity for nitrofurantoin does not depend on the anionic charge on nitrofurantoin. The pH dependence of a parallel passive pathway suggests that both nonionized and ionized forms of nitrofurantoin cross the membranes of the mammary epithelial cell by passive diffusion.

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Year:  1997        PMID: 9023278

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


  10 in total

Review 1.  Transferrin and prolactin transcytosis in the lactating mammary epithelial cell.

Authors:  M Ollivier-Bousquet
Journal:  J Mammary Gland Biol Neoplasia       Date:  1998-07       Impact factor: 2.673

2.  N-(4-[2-(1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolinyl)ethyl]-phenyl)-9,10-dihydro-5-methoxy-9-oxo-4-acridine carboxamide (GF120918) as a chemical ATP-binding cassette transporter family G member 2 (Abcg2) knockout model to study nitrofurantoin transfer into milk.

Authors:  Lipeng Wang; Markos Leggas; Mamta Goswami; Philip E Empey; Patrick J McNamara
Journal:  Drug Metab Dispos       Date:  2008-09-17       Impact factor: 3.922

3.  Molecular and functional identification of organic anion transporter isoforms in cultured bovine mammary epithelial cells (BME-UV).

Authors:  M M Al-Bataineh; D Van Der Merwe; B D Schultz; R Gehring
Journal:  J Vet Pharmacol Ther       Date:  2011-05-30       Impact factor: 1.786

4.  Sodium dependence of nitrofurantoin active transport across mammary epithelia and effects of dipyridamole, nucleosides, and nucleobases.

Authors:  Phillip M Gerk; Linda Hanson; Margaret C Neville; Patrick J McNamara
Journal:  Pharm Res       Date:  2002-03       Impact factor: 4.200

5.  An in vitro human mammary epithelial cell permeability assay to assess drug secretion into breast milk.

Authors:  Tao Zhang; Zachary Applebee; Peng Zou; Zhen Wang; Erika Solano Diaz; Yanyan Li
Journal:  Int J Pharm X       Date:  2022-06-22

6.  The ABCG2 C421A polymorphism does not affect oral nitrofurantoin pharmacokinetics in healthy Chinese male subjects.

Authors:  Kimberly K Adkison; Soniya S Vaidya; Daniel Y Lee; Seok Hwee Koo; Linghui Li; Amar A Mehta; Annette S Gross; Joseph W Polli; Yu Lou; Edmund J D Lee
Journal:  Br J Clin Pharmacol       Date:  2008-04-22       Impact factor: 4.335

7.  Cultured mammary epithelial monolayers (BME-UV) express functional organic anion and cation transporters.

Authors:  M M Al-Bataineh; D van der Merwe; B D Schultz; R Gehring
Journal:  J Vet Pharmacol Ther       Date:  2009-10       Impact factor: 1.786

8.  Knocking down breast cancer resistance protein (Bcrp) by adenoviral vector-mediated RNA interference (RNAi) in sandwich-cultured rat hepatocytes: a novel tool to assess the contribution of Bcrp to drug biliary excretion.

Authors:  Wei Yue; Koji Abe; Kim L R Brouwer
Journal:  Mol Pharm       Date:  2009 Jan-Feb       Impact factor: 4.939

9.  Disruption of occludin function in polarized epithelial cells activates the extrinsic pathway of apoptosis leading to cell extrusion without loss of transepithelial resistance.

Authors:  Neal E Beeman; Heidi K Baumgartner; Patricia G Webb; Jerome B Schaack; Margaret C Neville
Journal:  BMC Cell Biol       Date:  2009-12-09       Impact factor: 4.241

10.  Prolactin-induced Subcellular Targeting of GLUT1 Glucose Transporter in Living Mammary Epithelial Cells.

Authors:  Arieh Riskin; Yehudit Mond
Journal:  Rambam Maimonides Med J       Date:  2015-10-26
  10 in total

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