Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents. / Kjellev, S.; Nexo, E.; Thim, L.; Poulsen, S.S.

In: British Journal of Pharmacology, Vol. 149, No. 1, 2006, p. 92-99.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Kjellev, S, Nexo, E, Thim, L & Poulsen, SS 2006, 'Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents', British Journal of Pharmacology, vol. 149, no. 1, pp. 92-99. https://doi.org/10.1038/sj.bjp.0706840

APA

Kjellev, S., Nexo, E., Thim, L., & Poulsen, S. S. (2006). Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents. British Journal of Pharmacology, 149(1), 92-99. https://doi.org/10.1038/sj.bjp.0706840

Vancouver

Kjellev S, Nexo E, Thim L, Poulsen SS. Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents. British Journal of Pharmacology. 2006;149(1):92-99. https://doi.org/10.1038/sj.bjp.0706840

Author

Kjellev, S. ; Nexo, E. ; Thim, L. ; Poulsen, S.S. / Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents. In: British Journal of Pharmacology. 2006 ; Vol. 149, No. 1. pp. 92-99.

Bibtex

@article{f473af8070eb11dcbee902004c4f4f50,
title = "Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents",
abstract = "Trefoil factors (TFFs) secreted by mucus-producing cells are essential for the defence of the gastrointestinal mucosa. TFFs probably influence the viscoelastic properties of mucus, but this has not been demonstrated in vivo. We therefore studied the gastric secretion of systemically administered TFF2 and TFF3, and their influence on the viscosity of the secretions.",
keywords = "Animals, Autoradiography, Enzyme-Linked Immunosorbent Assay, Female, Gastrointestinal Contents, Immunohistochemistry, In Situ Hybridization, Injections, Intravenous, Mice, Mice, Inbred C57BL, Peptides, Rats, Rats, Wistar, Stomach, Tissue Distribution, Viscosity",
author = "S. Kjellev and E. Nexo and L. Thim and S.S. Poulsen",
year = "2006",
doi = "10.1038/sj.bjp.0706840",
language = "English",
volume = "149",
pages = "92--99",
journal = "British Journal of Pharmacology",
issn = "0007-1188",
publisher = "Wiley",
number = "1",

}

RIS

TY - JOUR

T1 - Systemically administered trefoil factors are secreted into the gastric lumen and increase the viscosity of gastric contents

AU - Kjellev, S.

AU - Nexo, E.

AU - Thim, L.

AU - Poulsen, S.S.

PY - 2006

Y1 - 2006

N2 - Trefoil factors (TFFs) secreted by mucus-producing cells are essential for the defence of the gastrointestinal mucosa. TFFs probably influence the viscoelastic properties of mucus, but this has not been demonstrated in vivo. We therefore studied the gastric secretion of systemically administered TFF2 and TFF3, and their influence on the viscosity of the secretions.

AB - Trefoil factors (TFFs) secreted by mucus-producing cells are essential for the defence of the gastrointestinal mucosa. TFFs probably influence the viscoelastic properties of mucus, but this has not been demonstrated in vivo. We therefore studied the gastric secretion of systemically administered TFF2 and TFF3, and their influence on the viscosity of the secretions.

KW - Animals

KW - Autoradiography

KW - Enzyme-Linked Immunosorbent Assay

KW - Female

KW - Gastrointestinal Contents

KW - Immunohistochemistry

KW - In Situ Hybridization

KW - Injections, Intravenous

KW - Mice

KW - Mice, Inbred C57BL

KW - Peptides

KW - Rats

KW - Rats, Wistar

KW - Stomach

KW - Tissue Distribution

KW - Viscosity

U2 - 10.1038/sj.bjp.0706840

DO - 10.1038/sj.bjp.0706840

M3 - Journal article

C2 - 16880764

VL - 149

SP - 92

EP - 99

JO - British Journal of Pharmacology

JF - British Journal of Pharmacology

SN - 0007-1188

IS - 1

ER -

ID: 1203034