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Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
4-oxo-4H-pyran-2.6-dicarboxylic acid (chelidonic acid, ChA) in the native state and in the complex with calcium [Ca(ChA)(H(2)O)(3)], named saucalchelin (CaChA), was isolated from the extract of Saussurea controversa leaves for the first time for the Asteraceae family. The structure of ChA was determ...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572306/ https://www.ncbi.nlm.nih.gov/pubmed/31100934 http://dx.doi.org/10.3390/biom9050189 |
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author | Avdeeva, Elena Shults, Elvira Rybalova, Tatyana Reshetov, Yaroslav Porokhova, Ekaterina Sukhodolo, Irina Litvinova, Larisa Shupletsova, Valeria Khaziakhmatova, Olga Khlusov, Igor Guryev, Artem Belousov, Mikhail |
author_facet | Avdeeva, Elena Shults, Elvira Rybalova, Tatyana Reshetov, Yaroslav Porokhova, Ekaterina Sukhodolo, Irina Litvinova, Larisa Shupletsova, Valeria Khaziakhmatova, Olga Khlusov, Igor Guryev, Artem Belousov, Mikhail |
author_sort | Avdeeva, Elena |
collection | PubMed |
description | 4-oxo-4H-pyran-2.6-dicarboxylic acid (chelidonic acid, ChA) in the native state and in the complex with calcium [Ca(ChA)(H(2)O)(3)], named saucalchelin (CaChA), was isolated from the extract of Saussurea controversa leaves for the first time for the Asteraceae family. The structure of ChA was determined by NMR, MS and confirmed by X-ray analysis of its monomethyl ester, and CaChA was described by IR, ICP-MS, CHN analysis. The yield of ChA and CaChA was 45 mg/g and 70 mg/g of extract, respectively. The osteogenic activity of ChA, n-monobutyl ester of chelidonic acid, and CaChA has been studied in vitro in a 21-day culture of human adipose-derived multipotent mesenchymal stromal cells (hAMMSCs) in a standard nutrient medium without osteogenic supplements. CaChA significantly stimulated the growth of cell mass and differentiation of hAMMSCs into osteoblasts with subsequent mineralization of the culture and it may be a promising substance for accelerating bone tissue regeneration and engineering. |
format | Online Article Text |
id | pubmed-6572306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65723062019-06-18 Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro Avdeeva, Elena Shults, Elvira Rybalova, Tatyana Reshetov, Yaroslav Porokhova, Ekaterina Sukhodolo, Irina Litvinova, Larisa Shupletsova, Valeria Khaziakhmatova, Olga Khlusov, Igor Guryev, Artem Belousov, Mikhail Biomolecules Article 4-oxo-4H-pyran-2.6-dicarboxylic acid (chelidonic acid, ChA) in the native state and in the complex with calcium [Ca(ChA)(H(2)O)(3)], named saucalchelin (CaChA), was isolated from the extract of Saussurea controversa leaves for the first time for the Asteraceae family. The structure of ChA was determined by NMR, MS and confirmed by X-ray analysis of its monomethyl ester, and CaChA was described by IR, ICP-MS, CHN analysis. The yield of ChA and CaChA was 45 mg/g and 70 mg/g of extract, respectively. The osteogenic activity of ChA, n-monobutyl ester of chelidonic acid, and CaChA has been studied in vitro in a 21-day culture of human adipose-derived multipotent mesenchymal stromal cells (hAMMSCs) in a standard nutrient medium without osteogenic supplements. CaChA significantly stimulated the growth of cell mass and differentiation of hAMMSCs into osteoblasts with subsequent mineralization of the culture and it may be a promising substance for accelerating bone tissue regeneration and engineering. MDPI 2019-05-16 /pmc/articles/PMC6572306/ /pubmed/31100934 http://dx.doi.org/10.3390/biom9050189 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Avdeeva, Elena Shults, Elvira Rybalova, Tatyana Reshetov, Yaroslav Porokhova, Ekaterina Sukhodolo, Irina Litvinova, Larisa Shupletsova, Valeria Khaziakhmatova, Olga Khlusov, Igor Guryev, Artem Belousov, Mikhail Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title | Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title_full | Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title_fullStr | Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title_full_unstemmed | Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title_short | Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro |
title_sort | chelidonic acid and its derivatives from saussurea controversa: isolation, structural elucidation and influence on the osteogenic differentiation of multipotent mesenchymal stromal cells in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572306/ https://www.ncbi.nlm.nih.gov/pubmed/31100934 http://dx.doi.org/10.3390/biom9050189 |
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