<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fitzgerald AJ</submitter><funding>Wellcome Trust</funding><pagination>775-81</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1774533</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>A partially hydrolysed and dried product of pacific whiting fish is currently marketed as a health food supplement to support "intestinal health". However, there has been only limited scientific study regarding its true biological activity.&lt;h4>Aims&lt;/h4>We therefore tested its efficacy in a variety of models of epithelial injury and repair.&lt;h4>Methods&lt;/h4>Effects on proliferation were determined using [(3)H] thymidine incorporation into epithelial rat intestinal RIE-1 and human colonic HT29 cells. Effects on restitution (cell migration) were analysed using wounded HT29 monolayers and its ability to influence gastric injury analysed using a rat indomethacin restraint model. Partial characterisation of bioactive agents was performed using mass spectroscopy, high pressure liquid chromatography, and gas chromatography.&lt;h4>Results&lt;/h4>Both cell proliferation and cell migration were increased by about threefold when added at 1 mg/ml (p&lt;0.01). Gastric injury was reduced by 59% when gavaged at 25 mg/ml (p&lt;0.05), results similar to using the potent cytoprotective agent epidermal growth factor at 12.5 mug/ml. The vast majority of biological activity was soluble in ethanol, with glutamine in its single, di-, and tripeptide forms probably accounting for approximately 40% of the total bioactivity seen. Fatty acid constituents may also have contributed to cell migratory activity.&lt;h4>Conclusions&lt;/h4>Fish protein hydrolysate possesses biological activity when analysed in a variety of models of injury and repair and could provide a novel inexpensive approach for the prevention and treatment of the injurious effects of non-steroidal anti-inflammatory drugs and other ulcerative conditions of the bowel. Further studies appear justified.</pubmed_abstract><journal>Gut</journal><pubmed_title>Reparative properties of a commercial fish protein hydrolysate preparation.</pubmed_title><pmcid>PMC1774533</pmcid><funding_grant_id>054787/B/98/Z</funding_grant_id><pubmed_authors>Playford RJ</pubmed_authors><pubmed_authors>Ghosh S</pubmed_authors><pubmed_authors>Fitzgerald AJ</pubmed_authors><pubmed_authors>Taylor GW</pubmed_authors><pubmed_authors>Marchbank T</pubmed_authors><pubmed_authors>Rai PS</pubmed_authors><pubmed_authors>Ritz BW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reparative properties of a commercial fish protein hydrolysate preparation.</name><description>&lt;h4>Background&lt;/h4>A partially hydrolysed and dried product of pacific whiting fish is currently marketed as a health food supplement to support "intestinal health". However, there has been only limited scientific study regarding its true biological activity.&lt;h4>Aims&lt;/h4>We therefore tested its efficacy in a variety of models of epithelial injury and repair.&lt;h4>Methods&lt;/h4>Effects on proliferation were determined using [(3)H] thymidine incorporation into epithelial rat intestinal RIE-1 and human colonic HT29 cells. Effects on restitution (cell migration) were analysed using wounded HT29 monolayers and its ability to influence gastric injury analysed using a rat indomethacin restraint model. Partial characterisation of bioactive agents was performed using mass spectroscopy, high pressure liquid chromatography, and gas chromatography.&lt;h4>Results&lt;/h4>Both cell proliferation and cell migration were increased by about threefold when added at 1 mg/ml (p&lt;0.01). Gastric injury was reduced by 59% when gavaged at 25 mg/ml (p&lt;0.05), results similar to using the potent cytoprotective agent epidermal growth factor at 12.5 mug/ml. The vast majority of biological activity was soluble in ethanol, with glutamine in its single, di-, and tripeptide forms probably accounting for approximately 40% of the total bioactivity seen. Fatty acid constituents may also have contributed to cell migratory activity.&lt;h4>Conclusions&lt;/h4>Fish protein hydrolysate possesses biological activity when analysed in a variety of models of injury and repair and could provide a novel inexpensive approach for the prevention and treatment of the injurious effects of non-steroidal anti-inflammatory drugs and other ulcerative conditions of the bowel. Further studies appear justified.</description><dates><release>2005-01-01T00:00:00Z</release><publication>2005 Jun</publication><modification>2024-02-15T06:49:42.547Z</modification><creation>2019-03-27T02:03:14Z</creation></dates><accession>S-EPMC1774533</accession><cross_references><pubmed>15888784</pubmed><doi>10.1136/gut.2004.060608</doi></cross_references></HashMap>