The University of Southampton
University of Southampton Institutional Repository

Calcipotriol inhibits rectal epithelial cell proliferation in ulcerative proctocolitis

Calcipotriol inhibits rectal epithelial cell proliferation in ulcerative proctocolitis
Calcipotriol inhibits rectal epithelial cell proliferation in ulcerative proctocolitis

Vitamin D3 reduces human rectal crypt cell production rate (CCPR) and may thereby protect against colorectal cancer. Cell turnover is increased in ulcerative proctocolitis, which might therefore respond to vitamin D3 metabolites. This study investigated the effect of calcipotriol, a synthetic vitamin D3 analogue that avoids hypercalcaemia, on human rectal CCPR in ulcerative proctocolitis. Paired rectal biopsy specimens from seven patients with severe disease were established in organ culture with or without calcipotriol (1 x 10-6 M). After 15 hours, vincristine (0.6 μg/ml) was added to induce metaphase arrest, and CCPR was determined by linear regression analysis of accumulated metaphases. Compared with values in 17 controls with incidental anal conditions, median rectal CCPR was 28% higher in ulcerative proctocolitis: 5.90 (5.00-9.50) v 4.80 (2.85-7.07) cells/crypt/hour (p < 0.01). Calcipotriol reduced CCPR by 62% in patients with ulcerative proctocolitis, from 5.90 (5.00-9.50) to 2.21 (0.81-3.22) cells/crypt/hour (median with range) p < 0.01. Thus calcipotriol can dampen the hyperproliferative state in ulcerative proctocolitis and could have a therapeutic role in the control of this inflammatory condition.

0017-5749
1718-1720
Thomas, M. G.
53d1e88a-242b-4ab5-8d0d-f68c8d26064a
Nugent, K. P.
79fcb89d-6ff2-47b8-ac2c-2afb24954456
Forbes, A.
6b977d93-b977-4390-b37e-4d46e6e6edc0
Williamson, R. C.N.
2e8449c1-9898-4dcd-b346-ebc9d3b1b51b
Thomas, M. G.
53d1e88a-242b-4ab5-8d0d-f68c8d26064a
Nugent, K. P.
79fcb89d-6ff2-47b8-ac2c-2afb24954456
Forbes, A.
6b977d93-b977-4390-b37e-4d46e6e6edc0
Williamson, R. C.N.
2e8449c1-9898-4dcd-b346-ebc9d3b1b51b

Thomas, M. G., Nugent, K. P., Forbes, A. and Williamson, R. C.N. (1994) Calcipotriol inhibits rectal epithelial cell proliferation in ulcerative proctocolitis. Gut, 35 (12), 1718-1720. (doi:10.1136/gut.35.12.1718).

Record type: Article

Abstract

Vitamin D3 reduces human rectal crypt cell production rate (CCPR) and may thereby protect against colorectal cancer. Cell turnover is increased in ulcerative proctocolitis, which might therefore respond to vitamin D3 metabolites. This study investigated the effect of calcipotriol, a synthetic vitamin D3 analogue that avoids hypercalcaemia, on human rectal CCPR in ulcerative proctocolitis. Paired rectal biopsy specimens from seven patients with severe disease were established in organ culture with or without calcipotriol (1 x 10-6 M). After 15 hours, vincristine (0.6 μg/ml) was added to induce metaphase arrest, and CCPR was determined by linear regression analysis of accumulated metaphases. Compared with values in 17 controls with incidental anal conditions, median rectal CCPR was 28% higher in ulcerative proctocolitis: 5.90 (5.00-9.50) v 4.80 (2.85-7.07) cells/crypt/hour (p < 0.01). Calcipotriol reduced CCPR by 62% in patients with ulcerative proctocolitis, from 5.90 (5.00-9.50) to 2.21 (0.81-3.22) cells/crypt/hour (median with range) p < 0.01. Thus calcipotriol can dampen the hyperproliferative state in ulcerative proctocolitis and could have a therapeutic role in the control of this inflammatory condition.

This record has no associated files available for download.

More information

Published date: December 1994

Identifiers

Local EPrints ID: 445634
URI: http://eprints.soton.ac.uk/id/eprint/445634
ISSN: 0017-5749
PURE UUID: e57387b4-80e5-453c-b5e2-724a29f9c0fd

Catalogue record

Date deposited: 04 Jan 2021 17:35
Last modified: 16 Mar 2024 09:43

Export record

Altmetrics

Contributors

Author: M. G. Thomas
Author: K. P. Nugent
Author: A. Forbes
Author: R. C.N. Williamson

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×