Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 1, 2004; 10(7): 1032-1036
Published online Apr 1, 2004. doi: 10.3748/wjg.v10.i7.1032
Protective effects of pentadecapeptide BPC 157 on gastric ulcer in rats
Xiao-Chang Xue, Yong-Jie Wu, Ming-Tang Gao, Wen-Guang Li, Ning Zhao, Zeng-Lu Wang, Chun-Jie Bao, Zhen Yan, Ying-Qi Zhang
Xiao-Chang Xue, Ning Zhao, Zeng-Lu Wang, Chun-Jie Bao, Zhen Yan, Ying-Qi Zhang, Biotechnology Centre, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China
Yong-Jie Wu, Ming-Tang Gao, Wen-Guang Li, Department of Pharmacology, Lanzhou Medical College, Lanzhou 730000, Gansu Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Ying-Qi Zhang, Biotechnology Centre, Fourth Military Medical University, 169 West Changle Road, Xi’an 710032, Shaanxi Province, China. xue_xiaochang@yahoo.com Telephone: +86-29-3247213 Fax: +86-29-3224537
Received: July 12, 2003
Revised: July 17, 2003
Accepted: July 30, 2003
Published online: April 1, 2004
Abstract

AIM: To investigate the protective effects of gastric pentadecapeptide BPC 157 on acute and chronic gastric ulcers in rats and to compare the results in therapy of human gastric ulcers by different administration methods.

METHODS: Gastric pentadecapeptide BPC 157 was administered (initial single or continuous administration) into rats either intragastrically or intramuscularly before (induced acute gastric ulcer) or after (induced chronic gastric ulcer) the applications of inducing agents, and each animal was sacrificed to observe the protective effects of BPC 157 on gastric ulcers.

RESULTS: Both intramuscular (im) and intragastric (ig) administration of BPC 157 could apparently reduce the ulcer area and accelerate the healing of induced ulcer in different models and the effect of im administered BPC 157 was better than that of ig. The rats treated with higher dosages (400 ng/kg, 800 ng/kg) of BPC 157 (im and ig) showed significantly less lesion (P < 0.01 vs excipient or saline control), the inhibition ratio of ulcer formation varied between 45.7% and 65.6%, from all measurements except 400 ng/kg BPC 157 in pylorus ligation induced model (P < 0.05), in which the inhibition rate was 54.2%. When im administered (800 ng/kg BPC 157) in three models, the inhibition ratio of ulcer formation was 65.5%, 65.6% and 59.9%, respectively, which was better than that of famotidine (its inhibition rate was 60.8%, 57.2% and 34.3%, respectively). Continuous application of BPC 157 (in chronic acetate induced gastric ulcer) could accelerate rebuilding of glandular epithelium and formation of granulation tissue (P < 0.05 at 200 ng/kg and P < 0.01 at 400 ng/kg and 800 ng/kg vs excipient or saline control).

CONCLUSION: Both im and ig administered gastric pentadecapeptide BPC 157 can apparently ameliorate acute gastric ulcer in rats and antagonize the protracted effect of acetate challenge on chronic ulcer. The effect of im administration of BPC 157 is better than that of ig, and the effective dosage of the former is lower than that of the latter.

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