Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition

Background: Queen bee acid (QBA; 10-hydroxy-2-decenoic acid) is the predominant fatty acid in royal jelly (RJ) and has activity at estrogen receptors, which affect brain function and body composition. However, few, long-term studies have assessed QBA effects in brain health and body composition. Met...

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Main Authors: Michael J. Weiser, Vivian Grimshaw, Kelly M. Wynalda, M. Hasan Mohajeri, Christopher M. Butt
Format: Article
Language:English
Published: MDPI AG 2017-12-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/10/1/13
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spelling doaj-fbe869ca6d4f422a8cd81802afd44ac22020-11-24T21:12:13ZengMDPI AGNutrients2072-66432017-12-011011310.3390/nu10010013nu10010013Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body CompositionMichael J. Weiser0Vivian Grimshaw1Kelly M. Wynalda2M. Hasan Mohajeri3Christopher M. Butt4Translational Biology, DSM Nutritional Products, 4909 Nautilus Court North, Suite 230, Boulder, CO 80301, USATranslational Biology, DSM Nutritional Products, 4909 Nautilus Court North, Suite 230, Boulder, CO 80301, USATranslational Biology, DSM Nutritional Products, 4909 Nautilus Court North, Suite 230, Boulder, CO 80301, USABiological Models, DSM Nutritional Products, Wurmisweg 576, Bld. 205/216, CH 4303 Kaiseraugst, SwitzerlandTranslational Biology, DSM Nutritional Products, 4909 Nautilus Court North, Suite 230, Boulder, CO 80301, USABackground: Queen bee acid (QBA; 10-hydroxy-2-decenoic acid) is the predominant fatty acid in royal jelly (RJ) and has activity at estrogen receptors, which affect brain function and body composition. However, few, long-term studies have assessed QBA effects in brain health and body composition. Methods: Primary hippocampal neurons were treated with QBA (0–30 µM) and challenged with glutamate or hypoxia. QBA was fed to aged, male Sprague-Dawley rats (12–24 mg/kg/day) and to adult male and female Balb/C mice (30–60 mg/kg/day) for ≥3.5 months. Rats were evaluated in a behavioral test battery of brain function. Mice were measured for fat and muscle composition, as well as bone density. Results: QBA increased neuron growth and protected against glutamate challenge and hypoxia challenge. Rats receiving QBA had reduced anxiety-like behavior, increased body weight, and better maintenance of body weight with age. Mice receiving QBA exhibited increased body weight, muscle mass, and adiposity in males, and increased bone density, but decreased adiposity, in females. Conclusions: QBA is an active component of RJ that promotes the growth and protection of neurons, reduces anxiety-like phenotypes, and benefits bone, muscle and adipose tissues in a sex-dependent manner, which further implicates estrogen receptors in the effects of QBA.https://www.mdpi.com/2072-6643/10/1/13queen bee acidneuroprotectionbehaviormoodbody composition
collection DOAJ
language English
format Article
sources DOAJ
author Michael J. Weiser
Vivian Grimshaw
Kelly M. Wynalda
M. Hasan Mohajeri
Christopher M. Butt
spellingShingle Michael J. Weiser
Vivian Grimshaw
Kelly M. Wynalda
M. Hasan Mohajeri
Christopher M. Butt
Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
Nutrients
queen bee acid
neuroprotection
behavior
mood
body composition
author_facet Michael J. Weiser
Vivian Grimshaw
Kelly M. Wynalda
M. Hasan Mohajeri
Christopher M. Butt
author_sort Michael J. Weiser
title Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
title_short Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
title_full Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
title_fullStr Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
title_full_unstemmed Long-Term Administration of Queen Bee Acid (QBA) to Rodents Reduces Anxiety-Like Behavior, Promotes Neuronal Health and Improves Body Composition
title_sort long-term administration of queen bee acid (qba) to rodents reduces anxiety-like behavior, promotes neuronal health and improves body composition
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2017-12-01
description Background: Queen bee acid (QBA; 10-hydroxy-2-decenoic acid) is the predominant fatty acid in royal jelly (RJ) and has activity at estrogen receptors, which affect brain function and body composition. However, few, long-term studies have assessed QBA effects in brain health and body composition. Methods: Primary hippocampal neurons were treated with QBA (0–30 µM) and challenged with glutamate or hypoxia. QBA was fed to aged, male Sprague-Dawley rats (12–24 mg/kg/day) and to adult male and female Balb/C mice (30–60 mg/kg/day) for ≥3.5 months. Rats were evaluated in a behavioral test battery of brain function. Mice were measured for fat and muscle composition, as well as bone density. Results: QBA increased neuron growth and protected against glutamate challenge and hypoxia challenge. Rats receiving QBA had reduced anxiety-like behavior, increased body weight, and better maintenance of body weight with age. Mice receiving QBA exhibited increased body weight, muscle mass, and adiposity in males, and increased bone density, but decreased adiposity, in females. Conclusions: QBA is an active component of RJ that promotes the growth and protection of neurons, reduces anxiety-like phenotypes, and benefits bone, muscle and adipose tissues in a sex-dependent manner, which further implicates estrogen receptors in the effects of QBA.
topic queen bee acid
neuroprotection
behavior
mood
body composition
url https://www.mdpi.com/2072-6643/10/1/13
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