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From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase

It was reported three decades ago that intracerebroventricular injection of angiotensin IV (Ang IV, Val-Tyr-Ile-His-Pro-Phe) improved memory and learning in the rat. There are several explanations for these positive effects of the hexapeptide and related analogues on cognition available in the liter...

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Autores principales: Hallberg, Mathias, Larhed, Mats
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593869/
https://www.ncbi.nlm.nih.gov/pubmed/33178027
http://dx.doi.org/10.3389/fphar.2020.590855
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author Hallberg, Mathias
Larhed, Mats
author_facet Hallberg, Mathias
Larhed, Mats
author_sort Hallberg, Mathias
collection PubMed
description It was reported three decades ago that intracerebroventricular injection of angiotensin IV (Ang IV, Val-Tyr-Ile-His-Pro-Phe) improved memory and learning in the rat. There are several explanations for these positive effects of the hexapeptide and related analogues on cognition available in the literature. In 2001, it was proposed that the insulin-regulated aminopeptidase (IRAP) is a main target for Ang IV and that Ang IV serves as an inhibitor of the enzyme. The focus of this review is the efforts to stepwise transform the hexapeptide into more drug-like Ang IV peptidemimetics serving as IRAP inhibitors. Moreover, the discovery of IRAP inhibitors by virtual and substance library screening and direct design applying knowledge of the structure of IRAP and of related enzymes is briefly presented.
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spelling pubmed-75938692020-11-10 From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase Hallberg, Mathias Larhed, Mats Front Pharmacol Pharmacology It was reported three decades ago that intracerebroventricular injection of angiotensin IV (Ang IV, Val-Tyr-Ile-His-Pro-Phe) improved memory and learning in the rat. There are several explanations for these positive effects of the hexapeptide and related analogues on cognition available in the literature. In 2001, it was proposed that the insulin-regulated aminopeptidase (IRAP) is a main target for Ang IV and that Ang IV serves as an inhibitor of the enzyme. The focus of this review is the efforts to stepwise transform the hexapeptide into more drug-like Ang IV peptidemimetics serving as IRAP inhibitors. Moreover, the discovery of IRAP inhibitors by virtual and substance library screening and direct design applying knowledge of the structure of IRAP and of related enzymes is briefly presented. Frontiers Media S.A. 2020-10-15 /pmc/articles/PMC7593869/ /pubmed/33178027 http://dx.doi.org/10.3389/fphar.2020.590855 Text en Copyright © 2020 Hallberg and Larhed http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Hallberg, Mathias
Larhed, Mats
From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title_full From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title_fullStr From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title_full_unstemmed From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title_short From Angiotensin IV to Small Peptidemimetics Inhibiting Insulin-Regulated Aminopeptidase
title_sort from angiotensin iv to small peptidemimetics inhibiting insulin-regulated aminopeptidase
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593869/
https://www.ncbi.nlm.nih.gov/pubmed/33178027
http://dx.doi.org/10.3389/fphar.2020.590855
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