Literature DB >> 3485062

Oral administration of synthetic human urogastrone promotes healing of chronic duodenal ulcers in rats.

P Skov Olsen, S S Poulsen, K Therkelsen, E Nexø.   

Abstract

The effect of oral administration of synthetic human epidermal growth factor/urogastrone (EGF/URO) on healing of chronic duodenal ulcers induced by cysteamine in rats was investigated and compared with that of cimetidine, a H2-receptor antagonist. After 25 and 50 days of treatment, synthetic human EGF/URO significantly increased healing of chronic duodenal ulcers to the same extent as cimetidine. Combined treatment with synthetic human EGF/URO and cimetidine for 25 days was more effective than synthetic human EGF/URO given alone, whereas combined treatment for 50 days was significantly more effective than cimetidine alone. These results show that a combination of an agent inhibiting gastric acid secretion and the cytoprotective and growth-stimulating peptide EGF/URO seems to be more effective with regard to duodenal ulcer healing than individual administration of the two substances. Synthetic human EGF/URO is a potent inhibitor of gastric acid secretion when administered intravenously, but had no effect on acid secretion when given intraduodenally, which suggests that the effect of synthetic human EGF/URO is a direct action on the duodenal mucosa. In conclusion, this study showed that oral synthetic human EGF/URO has a significant effect on healing of duodenal ulcers in rats. The amount of synthetic human EGF/URO administered is comparable to that found in saliva during stimulation of the salivary glands. Our results, therefore, suggest that EGF/URO is one of the endogenous factors participating in healing of duodenal ulcers.

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Year:  1986        PMID: 3485062     DOI: 10.1016/0016-5085(86)90867-x

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  18 in total

1.  Characterization of epidermal growth factor receptors on plasma membranes isolated from rat gastric mucosa.

Authors:  R Hori; H Nomura; S Iwakawa; K Okumura
Journal:  Pharm Res       Date:  1990-06       Impact factor: 4.200

2.  Growth factor mRNA expression in normal colorectal mucosa and in uninvolved mucosa from ulcerative colitis patients.

Authors:  A Chowdhury; R Fukuda; S Fukumoto
Journal:  J Gastroenterol       Date:  1996-06       Impact factor: 7.527

3.  Effect of repeated colloidal bismuth subcitrate treatment on the response of the rat gastric mucosa to the presence of luminal ethanol.

Authors:  S M Hinsull; D Bellamy
Journal:  Gut       Date:  1990-04       Impact factor: 23.059

4.  Role of capsaicin sensitive nerves in epidermal growth factor effects on gastric mucosal injury and blood flow.

Authors:  J Y Kang; C H Teng; F C Chen; A Wee
Journal:  Gut       Date:  1998-03       Impact factor: 23.059

5.  Healing of chronic gastroduodenal ulcerations by antacids. Role of prostaglandins and epidermal growth factor.

Authors:  S J Konturek; T Brzozowski; D Drozdowicz; A Dembinski; C Nauert
Journal:  Dig Dis Sci       Date:  1990-09       Impact factor: 3.199

6.  Epidermal growth factor (EGF) in the gastroprotective and ulcer healing actions of colloidal bismuth subcitrate (De-Nol) in rats.

Authors:  S J Konturek; A Dembinski; Z Warzecha; W Bielanski; T Brzozowski; D Drozdowicz
Journal:  Gut       Date:  1988-07       Impact factor: 23.059

7.  Epidermal growth factor in saliva and gastric juice: response to histamine.

Authors:  A M Tunio; M Hobsley
Journal:  Gut       Date:  1995-09       Impact factor: 23.059

8.  Increased gastric juice epidermal growth factor after non-steroidal anti-inflammatory drug ingestion.

Authors:  S M Kelly; J R Jenner; R J Dickinson; J O Hunter
Journal:  Gut       Date:  1994-05       Impact factor: 23.059

9.  Effect of oral epidermal growth factor on mucosal healing in rats with duodenal ulcer.

Authors:  Jane C J Chao; Kuo-Yu Liu; Sheng-Hsuan Chen; Chia-Lang Fang; Chih-Wei Tsao
Journal:  World J Gastroenterol       Date:  2003-10       Impact factor: 5.742

10.  Systemic treatment with recombinant human epidermal growth factor accelerates healing of sclerotherapy-induced esophageal ulcers and prevents esophageal stricture formations in pigs.

Authors:  C O Juhl; L Vinter-Jensen; L S Jensen; E Nexø; J C Djurhuus; E Z Dajani
Journal:  Dig Dis Sci       Date:  1994-12       Impact factor: 3.199

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