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Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model

Altered skeletal development in Down syndrome (DS) results in a brachycephalic skull, flattened face, shorter mandibular ramus, shorter limbs, and reduced bone mineral density (BMD). Our previous study showed that low doses of green tea extract enriched in epigallocatechin-3-gallate (GTE-EGCG), admi...

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Autores principales: Llambrich, Sergi, González-Colom, Rubèn, Wouters, Jens, Roldán, Jorge, Salassa, Sara, Wouters, Kaat, Van Bulck, Vicky, Sharpe, James, Callaerts-Vegh, Zsuzsanna, Vande Velde, Greetje, Martínez-Abadías, Neus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9572077/
https://www.ncbi.nlm.nih.gov/pubmed/36235819
http://dx.doi.org/10.3390/nu14194167
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author Llambrich, Sergi
González-Colom, Rubèn
Wouters, Jens
Roldán, Jorge
Salassa, Sara
Wouters, Kaat
Van Bulck, Vicky
Sharpe, James
Callaerts-Vegh, Zsuzsanna
Vande Velde, Greetje
Martínez-Abadías, Neus
author_facet Llambrich, Sergi
González-Colom, Rubèn
Wouters, Jens
Roldán, Jorge
Salassa, Sara
Wouters, Kaat
Van Bulck, Vicky
Sharpe, James
Callaerts-Vegh, Zsuzsanna
Vande Velde, Greetje
Martínez-Abadías, Neus
author_sort Llambrich, Sergi
collection PubMed
description Altered skeletal development in Down syndrome (DS) results in a brachycephalic skull, flattened face, shorter mandibular ramus, shorter limbs, and reduced bone mineral density (BMD). Our previous study showed that low doses of green tea extract enriched in epigallocatechin-3-gallate (GTE-EGCG), administered continuously from embryonic day 9 to postnatal day 29, reduced facial dysmorphologies in the Ts65Dn (TS) mouse model of DS, but high doses could exacerbate them. Here, we extended the analyses to other skeletal structures and systematically evaluated the effects of high and low doses of GTE-EGCG treatment over postnatal development in wild-type (WT) and TS mice using in vivo µCT and geometric morphometrics. TS mice developed shorter and wider faces, skulls, and mandibles, together with shorter and narrower humerus and scapula, and reduced BMD dynamically over time. Besides facial morphology, GTE-EGCG did not rescue any other skeletal phenotype in TS treated mice. In WT mice, GTE-EGCG significantly altered the shape of the skull and mandible, reduced the length and width of the long bones, and lowered the BMD. The disparate effects of GTE-EGCG depended on the dose, developmental timepoint, and anatomical structure analyzed, emphasizing the complex nature of DS and the need to further investigate the simultaneous effects of GTE-EGCG supplementation.
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spelling pubmed-95720772022-10-17 Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model Llambrich, Sergi González-Colom, Rubèn Wouters, Jens Roldán, Jorge Salassa, Sara Wouters, Kaat Van Bulck, Vicky Sharpe, James Callaerts-Vegh, Zsuzsanna Vande Velde, Greetje Martínez-Abadías, Neus Nutrients Article Altered skeletal development in Down syndrome (DS) results in a brachycephalic skull, flattened face, shorter mandibular ramus, shorter limbs, and reduced bone mineral density (BMD). Our previous study showed that low doses of green tea extract enriched in epigallocatechin-3-gallate (GTE-EGCG), administered continuously from embryonic day 9 to postnatal day 29, reduced facial dysmorphologies in the Ts65Dn (TS) mouse model of DS, but high doses could exacerbate them. Here, we extended the analyses to other skeletal structures and systematically evaluated the effects of high and low doses of GTE-EGCG treatment over postnatal development in wild-type (WT) and TS mice using in vivo µCT and geometric morphometrics. TS mice developed shorter and wider faces, skulls, and mandibles, together with shorter and narrower humerus and scapula, and reduced BMD dynamically over time. Besides facial morphology, GTE-EGCG did not rescue any other skeletal phenotype in TS treated mice. In WT mice, GTE-EGCG significantly altered the shape of the skull and mandible, reduced the length and width of the long bones, and lowered the BMD. The disparate effects of GTE-EGCG depended on the dose, developmental timepoint, and anatomical structure analyzed, emphasizing the complex nature of DS and the need to further investigate the simultaneous effects of GTE-EGCG supplementation. MDPI 2022-10-07 /pmc/articles/PMC9572077/ /pubmed/36235819 http://dx.doi.org/10.3390/nu14194167 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Llambrich, Sergi
González-Colom, Rubèn
Wouters, Jens
Roldán, Jorge
Salassa, Sara
Wouters, Kaat
Van Bulck, Vicky
Sharpe, James
Callaerts-Vegh, Zsuzsanna
Vande Velde, Greetje
Martínez-Abadías, Neus
Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title_full Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title_fullStr Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title_full_unstemmed Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title_short Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model
title_sort green tea catechins modulate skeletal development with effects dependent on dose, time, and structure in a down syndrome mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9572077/
https://www.ncbi.nlm.nih.gov/pubmed/36235819
http://dx.doi.org/10.3390/nu14194167
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