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Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo

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Abstract 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 [18F]-fluoro-L-thymidine ([18F]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 [18F]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.
Title: Aromatic-turmerone induces neural stem cell proliferation in vitro and in vivo
Description:
Abstract 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 [18F]-fluoro-L-thymidine ([18F]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 [18F]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.

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