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