Novel Cytoprotective Mediator, Stable Gastric Pentadecapeptide BPC 157. Vascular Recruitment and Gastrointestinal Tract Healing

Author:

Sikiric Predrag1,Rucman Rudolf1,Turkovic Branko1,Sever Marko1,Klicek Robert1,Radic Bozo1,Drmic Domagoj1,Stupnisek Mirjana1,Misic Marija1,Vuletic Lovorka Batelja1,Pavlov Katarina Horvat1,Barisic Ivan1,Kokot Antonio1,Peklic Marina1,Strbe Sanja1,Blagaic Alenka Boban1,Tvrdeic Ante1,Rokotov Dinko Stancic1,Vrcic Hrvoje1,Staresinic Mario1,Seiwerth Sven1

Affiliation:

1. Department of Pharmacology, Medical Faculty, University of Zagreb, Zagreb, Croatia

Abstract

Years ago, we revealed a novel cytoprotective mediator, stable gastric pentadecapeptide BPC 157, particular anti-ulcer peptide that heals different organs lesions when given as a therapy, native in human gastric juice while maintaining GI-tract mucosal integrity, already tested in trials (ulcerative colitis and now multiple sclerosis). The stomach cytoprotection is the most fundamental concept, stomach cell protection and endothelium protection are largely elaborated, but so far cell, protection and endothelium protection outside of the stomach were not implemented in the therapy. However, having managed these two points, stomach cell protection and endothelium protection, either one or together, even much more than standard cytoprotective agents do, BPC 157 employed large scale of its beneficial effects seen in various organs. Providing endothelium protection, BPC 157 was shown to prevent formation and reverse established thrombosis in anastomosed abdominal aorta as well as venous thrombosis after inferior caval vein occlusion, and attenuate bleeding prolongation and thrombocytopenia after amputation, without or with anticoagulants, or venous occlusion, and finally counteract effect of L-NAME and/or L- arginine. Now, with BPC 157 application, we reveal the third most important part of the cytoprotection concept: with the stomach cell and endothelium protection to recover mucosal integrity, BPC 157 as prototype cytoprotective agent should also control blood vessel function, depending upon injury, perforated defect or vessel obstruction. After a perforated injury (i.e., stomach), BPC 157 therapy activates blood vessels “running” towards defect. After obstruction (i.e., inferior caval vein), BPC 157 activates vessels “running” towards bypassing defect, collaterals functioning. Reestablished blood flow, and largely reversed injurious course may practically implement the cytoprotection concept.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology

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