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Inhibitory effects and actions of pentacyclic triterpenes upon glycation

Pentacyclic triterpenic compounds including asiatic, betulinic, maslinic, oleanolic and ursolic acid occur naturally in many herbs and plant foods. It is well known that these triterpenoids possess anti-oxidative and anti-inflammatory activities. Furthermore, recent in vitro and in vivo researches i...

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Autor principal: Yin, Mei-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: China Medical University 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530523/
https://www.ncbi.nlm.nih.gov/pubmed/26260291
http://dx.doi.org/10.7603/s40681-015-0013-x
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author Yin, Mei-Chin
author_facet Yin, Mei-Chin
author_sort Yin, Mei-Chin
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description Pentacyclic triterpenic compounds including asiatic, betulinic, maslinic, oleanolic and ursolic acid occur naturally in many herbs and plant foods. It is well known that these triterpenoids possess anti-oxidative and anti-inflammatory activities. Furthermore, recent in vitro and in vivo researches indicated that these compounds could inhibit the production of advanced glycation end-products (AGEs). The impact of these triterpenes upon the activity and protein expression of enzymes involved in polyol pathway including aldose reductase and sorbitol dehydrogenase has been examined, and positive results are reported. These studies suggest that certain triterpenes are potent anti-glycative agents, and may benefit the prevention and/or therapy of glycation-related diseases such as diabetes mellitus and Alzheimer’s disease. In this review article, the anti-glycative activity and action mode of certain triterpenes are highlighted. These information may promote the anti-glycative application of these natural compounds.
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spelling pubmed-45305232015-08-11 Inhibitory effects and actions of pentacyclic triterpenes upon glycation Yin, Mei-Chin Biomedicine (Taipei) Article Pentacyclic triterpenic compounds including asiatic, betulinic, maslinic, oleanolic and ursolic acid occur naturally in many herbs and plant foods. It is well known that these triterpenoids possess anti-oxidative and anti-inflammatory activities. Furthermore, recent in vitro and in vivo researches indicated that these compounds could inhibit the production of advanced glycation end-products (AGEs). The impact of these triterpenes upon the activity and protein expression of enzymes involved in polyol pathway including aldose reductase and sorbitol dehydrogenase has been examined, and positive results are reported. These studies suggest that certain triterpenes are potent anti-glycative agents, and may benefit the prevention and/or therapy of glycation-related diseases such as diabetes mellitus and Alzheimer’s disease. In this review article, the anti-glycative activity and action mode of certain triterpenes are highlighted. These information may promote the anti-glycative application of these natural compounds. China Medical University 2015-08-11 /pmc/articles/PMC4530523/ /pubmed/26260291 http://dx.doi.org/10.7603/s40681-015-0013-x Text en © China Medical University 2015 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided original author(s) and source are credited.
spellingShingle Article
Yin, Mei-Chin
Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title_full Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title_fullStr Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title_full_unstemmed Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title_short Inhibitory effects and actions of pentacyclic triterpenes upon glycation
title_sort inhibitory effects and actions of pentacyclic triterpenes upon glycation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530523/
https://www.ncbi.nlm.nih.gov/pubmed/26260291
http://dx.doi.org/10.7603/s40681-015-0013-x
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