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Cholinesterase inhibitors including Razadyne, Exelon and Aricept, disrupt the degradation of acetylcholine thus extending the half-life and availability of this neurotransmitter acting at central cholinergic muscarinic and nicotinic receptors [19-21]

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BPC-157 and TB-500 are commonly studied in controlled laboratory settings involving peptide signalling, cellular migration models, extracellular matrix systems, angiogenesis-related research, cytoskeletal pathway models, and tissue-remodelling investigations

Our work resulted in one receptor agonist, Nle 1 -AngIV and two receptor antagonists, divalinal-AngIV and norleual-AngIV [66-69]