Literature DB >> 10205196

Characterisation of penicillin G uptake in human small intestinal brush border membrane vesicles.

J F Poschet1, S M Hammond, P D Fairclough.   

Abstract

BACKGROUND: Many beta lactams are well absorbed by the small intestine, although the reasons for this are poorly understood. AIMS: To characterise the uptake of penicillin G into human small intestinal brush border membrane vesicles (BBMV) and to compare the uptake characteristics to those of rabbit BBMV. METHODS AND
RESULTS: Uptake of penicillin G was studied in human BBMV. Penicillin G was actively transported into the lumen of BBMV via an H+ dependent, Na+ independent uptake system. The carrier mediated process was saturable and adhered to Michaelis-Menten kinetics (Vmax 52 nmol penicillin G per mg protein per 30 seconds, Km 13.9 mM). These results are similar to those previously reported in rabbit BBMV.
CONCLUSIONS: It is suggested that penicillin G can be used as a model molecule for peptide and beta lactam transport studies as it is cheap and readily available in isotopically labelled form. Furthermore, rabbit BBMV may be used as an acceptable substitute for human BBMV for the study of penicillin transport.

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Year:  1999        PMID: 10205196      PMCID: PMC1727494          DOI: 10.1136/gut.44.5.620

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  49 in total

1.  Characteristics of tripeptide transport in human jejunal brush-border membrane vesicles.

Authors:  D Wilson; J A Barry; K Ramaswamy
Journal:  Biochim Biophys Acta       Date:  1989-11-17

2.  Preparation and properties of brush-border membrane vesicles from human small intestine.

Authors:  S P Shirazi-Beechey; A G Davies; K Tebbutt; J Dyer; A Ellis; C J Taylor; P Fairclough; R B Beechey
Journal:  Gastroenterology       Date:  1990-03       Impact factor: 22.682

3.  Intestinal uptake of dipeptides and beta-lactam antibiotics. I. The intestinal uptake system for dipeptides and beta-lactam antibiotics is not part of a brush border membrane peptidase.

Authors:  W Kramer; C Dechent; F Girbig; U Gutjahr; H Neubauer
Journal:  Biochim Biophys Acta       Date:  1990-11-30

4.  Uptake of cephalosporins by human intestinal brush-border membrane vesicles.

Authors:  J Lowther; S M Hammond; K Russell; P D Fairclough
Journal:  J Antimicrob Chemother       Date:  1990-01       Impact factor: 5.790

5.  Comparison of transport characteristics of amino beta-lactam antibiotics and dipeptides across rat intestinal brush border membrane.

Authors:  K Iseki; M Sugawara; H Saitoh; K Miyazaki; T Arita
Journal:  J Pharm Pharmacol       Date:  1989-09       Impact factor: 3.765

Review 6.  Pharmacokinetic properties of the cephalosporins.

Authors:  T Bergan
Journal:  Drugs       Date:  1987       Impact factor: 9.546

7.  A common mechanism for transport of di- and tri-peptides by hamster jejunum in vitro.

Authors:  J M Addison; D Burston; J A Dalrymple; D M Matthews; J W Payne; M H Sleisenger; S Wilkinson
Journal:  Clin Sci Mol Med       Date:  1975-10

8.  Transport characteristics of ceftibuten (7432-S), a new oral cephem, in rat intestinal brush-border membrane vesicles: proton-coupled and stereoselective transport of ceftibuten.

Authors:  T Yoshikawa; N Muranushi; M Yoshida; T Oguma; K Hirano; H Yamada
Journal:  Pharm Res       Date:  1989-04       Impact factor: 4.200

9.  H+ coupled transport of p.o. cephalosporins via dipeptide carriers in rabbit intestinal brush-border membranes: difference of transport characteristics between cefixime and cephradine.

Authors:  K Inui; T Okano; H Maegawa; M Kato; M Takano; R Hori
Journal:  J Pharmacol Exp Ther       Date:  1988-10       Impact factor: 4.030

10.  Transport characteristics of ceftibuten, a new oral cephem, in rat intestinal brush-border membrane vesicles: relationship to oligopeptide and amino beta-lactam transport.

Authors:  N Muranushi; T Yoshikawa; M Yoshida; T Oguma; K Hirano; H Yamada
Journal:  Pharm Res       Date:  1989-04       Impact factor: 4.200

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3.  Ethanol inhibits functional activity of the human intestinal dipeptide transporter hPepT1 expressed in Xenopus oocytes.

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