Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/93851
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Type: Journal article
Title: Oral nucleotides only minimally improve 5-fluorouracil-induced mucositis in rats
Author: Mashtoub, S.
Feo, B.
Whittaker, A.
Lymn, K.
Martinez-Puig, D.
Howarth, G.
Citation: Nutrition and Cancer, 2015; 67(6):994-1000
Publisher: Taylor & Francis Group
Issue Date: 2015
ISSN: 1532-7914
1532-7914
Statement of
Responsibility: 
Suzanne Mashtoub, Benjamin Feo and Alexandra L. Whittaker, Kerry A. Lymn, Daniel Martinez-Puig, Gordon S. Howarth
Abstract: Chemotherapy-induced mucositis is characterized by inflammation and ulceration of the intestinal mucosa, compromising intestinal function. Exogenous nucleotides have been reported to repair the mucosa. The nucleotide preparation, Nucleoforce F0328 (Nucleoforce), was investigated for its potential to ameliorate intestinal mucositis in rats. Female Dark Agouti rats (n = 8/group) were gavaged once daily with Nucleoforce (175 mg/kg) or water from Days 0 to 8 and injected (i.p.) with 5-fluorouracil (5-FU; 150 mg/kg) or saline on Day 5. Histological parameters (disease severity, crypt depth, and villus height measurements) and myeloperoxidase activity were quantified. P < 0.05 was considered significant. Jejunal and ileal histological disease severity scores were significantly increased by 5-FU, compared to normal controls (P < 0.05). Nucleoforce treatment in 5-FU-injected rats significantly reduced jejunal and ileal disease severity compared to 5-FU controls (P < 0.05). In 5-FU-injected rats, jejunal and ileal villus heights and crypt depths were significantly decreased compared to 5-FU controls, with no additional Nucleoforce effect (P > 0.05). Intestinal myeloperoxidase activity was significantly elevated by 5-FU (8.8-fold), compared to normal controls (P < 0.05), which was not normalized by Nucleoforce treatment (P > 0.05). Nucleoforce only partially improved parameters associated with experimentally-induced mucositis. Future studies could investigate increased concentrations, more frequent administration, or protective microencapsulation delivery methods, to increase bioavailability.
Keywords: Intestinal Mucosa; Intestine, Small; Animals; Rats; Fluorouracil; Nucleotides; Organ Size; Female; Mucositis
Rights: Copyright © 2015, Taylor & Francis Group, LLC
RMID: 0030033246
DOI: 10.1080/01635581.2015.1062118
Appears in Collections:Animal and Veterinary Sciences publications

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