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Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo
INTRODUCTION: Aromatic (ar-) turmerone is a major bioactive compound of the herb Curcuma longa. It has been suggested that ar-turmerone inhibits microglia activation, a property that may be useful in treating neurodegenerative disease. Furthermore, the effects of ar-turmerone on neural stem cells (N...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180255/ https://www.ncbi.nlm.nih.gov/pubmed/25928248 http://dx.doi.org/10.1186/scrt500 |
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author | Hucklenbroich, Joerg Klein, Rebecca Neumaier, Bernd Graf, Rudolf Fink, Gereon Rudolf Schroeter, Michael Rueger, Maria Adele |
author_facet | Hucklenbroich, Joerg Klein, Rebecca Neumaier, Bernd Graf, Rudolf Fink, Gereon Rudolf Schroeter, Michael Rueger, Maria Adele |
author_sort | Hucklenbroich, Joerg |
collection | PubMed |
description | INTRODUCTION: Aromatic (ar-) turmerone is a major bioactive compound of the herb Curcuma longa. It has been suggested that ar-turmerone inhibits microglia activation, a property that may be useful in treating neurodegenerative disease. Furthermore, the effects of ar-turmerone on neural stem cells (NSCs) remain to be investigated. METHODS: We exposed primary fetal rat NSCs to various concentrations of ar-turmerone. Thereafter, cell proliferation and differentiation potential were assessed. In vivo, naïve rats were treated with a single intracerebroventricular (i.c.v.) injection of ar-turmerone. Proliferative activity of endogenous NSCs was assessed in vivo, by using noninvasive positron emission tomography (PET) imaging and the tracer [(18)F]-fluoro-L-thymidine ([(18)F]FLT), as well as ex vivo. RESULTS: In vitro, ar-turmerone increased dose-dependently the number of cultured NSCs, because of an increase in NSC proliferation (P < 0.01). Proliferation data were supported by qPCR-data for Ki-67 mRNA. In vitro as well as in vivo, ar-turmerone promoted neuronal differentiation of NSCs. In vivo, after i.c.v. injection of ar-turmerone, proliferating NSCs were mobilized from the subventricular zone (SVZ) and the hippocampus of adult rats, as demonstrated by both [(18)F]FLT-PET and histology (P < 0.05). CONCLUSIONS: Both in vitro and in vivo data suggest that ar-turmerone induces NSC proliferation. Ar-turmerone thus constitutes a promising candidate to support regeneration in neurologic disease. |
format | Online Article Text |
id | pubmed-4180255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41802552014-10-03 Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo Hucklenbroich, Joerg Klein, Rebecca Neumaier, Bernd Graf, Rudolf Fink, Gereon Rudolf Schroeter, Michael Rueger, Maria Adele Stem Cell Res Ther Research INTRODUCTION: Aromatic (ar-) turmerone is a major bioactive compound of the herb Curcuma longa. It has been suggested that ar-turmerone inhibits microglia activation, a property that may be useful in treating neurodegenerative disease. Furthermore, the effects of ar-turmerone on neural stem cells (NSCs) remain to be investigated. METHODS: We exposed primary fetal rat NSCs to various concentrations of ar-turmerone. Thereafter, cell proliferation and differentiation potential were assessed. In vivo, naïve rats were treated with a single intracerebroventricular (i.c.v.) injection of ar-turmerone. Proliferative activity of endogenous NSCs was assessed in vivo, by using noninvasive positron emission tomography (PET) imaging and the tracer [(18)F]-fluoro-L-thymidine ([(18)F]FLT), as well as ex vivo. RESULTS: In vitro, ar-turmerone increased dose-dependently the number of cultured NSCs, because of an increase in NSC proliferation (P < 0.01). Proliferation data were supported by qPCR-data for Ki-67 mRNA. In vitro as well as in vivo, ar-turmerone promoted neuronal differentiation of NSCs. In vivo, after i.c.v. injection of ar-turmerone, proliferating NSCs were mobilized from the subventricular zone (SVZ) and the hippocampus of adult rats, as demonstrated by both [(18)F]FLT-PET and histology (P < 0.05). CONCLUSIONS: Both in vitro and in vivo data suggest that ar-turmerone induces NSC proliferation. Ar-turmerone thus constitutes a promising candidate to support regeneration in neurologic disease. BioMed Central 2014-09-26 /pmc/articles/PMC4180255/ /pubmed/25928248 http://dx.doi.org/10.1186/scrt500 Text en © Hucklenbroich et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hucklenbroich, Joerg Klein, Rebecca Neumaier, Bernd Graf, Rudolf Fink, Gereon Rudolf Schroeter, Michael Rueger, Maria Adele Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title | Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title_full | Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title_fullStr | Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title_full_unstemmed | Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title_short | Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
title_sort | aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4180255/ https://www.ncbi.nlm.nih.gov/pubmed/25928248 http://dx.doi.org/10.1186/scrt500 |
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