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The perceptions of natural compounds against dipeptidyl peptidase 4 in diabetes: from in silico to in vivo
Dipeptidyl peptidase IV (DPP-4), an incretin glucagon-like peptide-1 (GLP-1) degrading enzyme, contains two forms and it can exert various physiological functions particular in controlling blood glucose through the action of GLP-1. In diabetic use, the DPP-4 inhibitor can block the DDP-4 to attenuat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753520/ https://www.ncbi.nlm.nih.gov/pubmed/31555430 http://dx.doi.org/10.1177/2040622319875305 |
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author | Lin, Shian-Ren Chang, Chia-Hsiang Tsai, May-Jwan Cheng, Henrich Chen, Jian-Chyi Leong, Max K. Weng, Ching-Feng |
author_facet | Lin, Shian-Ren Chang, Chia-Hsiang Tsai, May-Jwan Cheng, Henrich Chen, Jian-Chyi Leong, Max K. Weng, Ching-Feng |
author_sort | Lin, Shian-Ren |
collection | PubMed |
description | Dipeptidyl peptidase IV (DPP-4), an incretin glucagon-like peptide-1 (GLP-1) degrading enzyme, contains two forms and it can exert various physiological functions particular in controlling blood glucose through the action of GLP-1. In diabetic use, the DPP-4 inhibitor can block the DDP-4 to attenuate GLP-1 degradation and prolong GLP-1 its action and sensitize insulin activity for the purpose of lowering blood glucose. Nonetheless the adverse effects of DPP-4 inhibitors severely hinder their clinical applications, and notably there is a clinical demand for novel DPP-4 inhibitors from various sources including chemical synthesis, herbs, and plants with fewer side effects. In this review, we highlight various strategies, namely computational biology (in silico), in vitro enzymatic and cell assays, and in vivo animal tests, for seeking natural DPP-4 inhibitors from botanic sources including herbs and plants. The pros and cons of all approaches for new inhibitor candidates or hits will be under discussion. |
format | Online Article Text |
id | pubmed-6753520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67535202019-09-25 The perceptions of natural compounds against dipeptidyl peptidase 4 in diabetes: from in silico to in vivo Lin, Shian-Ren Chang, Chia-Hsiang Tsai, May-Jwan Cheng, Henrich Chen, Jian-Chyi Leong, Max K. Weng, Ching-Feng Ther Adv Chronic Dis Review Dipeptidyl peptidase IV (DPP-4), an incretin glucagon-like peptide-1 (GLP-1) degrading enzyme, contains two forms and it can exert various physiological functions particular in controlling blood glucose through the action of GLP-1. In diabetic use, the DPP-4 inhibitor can block the DDP-4 to attenuate GLP-1 degradation and prolong GLP-1 its action and sensitize insulin activity for the purpose of lowering blood glucose. Nonetheless the adverse effects of DPP-4 inhibitors severely hinder their clinical applications, and notably there is a clinical demand for novel DPP-4 inhibitors from various sources including chemical synthesis, herbs, and plants with fewer side effects. In this review, we highlight various strategies, namely computational biology (in silico), in vitro enzymatic and cell assays, and in vivo animal tests, for seeking natural DPP-4 inhibitors from botanic sources including herbs and plants. The pros and cons of all approaches for new inhibitor candidates or hits will be under discussion. SAGE Publications 2019-09-19 /pmc/articles/PMC6753520/ /pubmed/31555430 http://dx.doi.org/10.1177/2040622319875305 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Lin, Shian-Ren Chang, Chia-Hsiang Tsai, May-Jwan Cheng, Henrich Chen, Jian-Chyi Leong, Max K. Weng, Ching-Feng The perceptions of natural compounds against dipeptidyl peptidase 4 in diabetes: from in silico to in vivo |
title | The perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
title_full | The perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
title_fullStr | The perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
title_full_unstemmed | The perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
title_short | The perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
title_sort | perceptions of natural compounds against dipeptidyl peptidase 4
in diabetes: from in silico to in
vivo |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753520/ https://www.ncbi.nlm.nih.gov/pubmed/31555430 http://dx.doi.org/10.1177/2040622319875305 |
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