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Poplar Propolis Ethanolic Extract Reduces Body Weight Gain and Glucose Metabolism Disruption in High-Fat Diet-Fed Mice.

Identifieur interne : 000199 ( Main/Exploration ); précédent : 000198; suivant : 000200

Poplar Propolis Ethanolic Extract Reduces Body Weight Gain and Glucose Metabolism Disruption in High-Fat Diet-Fed Mice.

Auteurs : Nicolas Cardinault [France] ; Franck Tourniaire [France] ; Julien Astier [France] ; Charlène Couturier [France] ; Estelle Perrin [France] ; Julie Dalifard [France] ; Eva Seipelt [France] ; Lourdes Mounien [France] ; Claire Letullier [France] ; Lauriane Bonnet [France] ; Esma Karkeni [France] ; Naïma Delbah [France] ; Stéphane Georgé [France] ; Jean-François Landrier [France]

Source :

RBID : pubmed:32729164

Abstract

SCOPE

Current evidence supports the beneficial effect of polyphenols on the management of obesity and associated comorbidities. This is the case for propolis, a polyphenol-rich substance produced by bees. The aim of the present study is to evaluate the effect of a poplar propolis ethanolic extract (PPEE) on obesity and glucose homeostasis, and to unveil its putative molecular mechanisms of action.

METHODS AND RESULTS

Male high-fat (HF) diet-fed mice are administered PPEE for 12 weeks. PPEE supplementation reduces the HF-mediated adiposity index, adipocyte hypertrophy, and body weight gain. It also improves HOMA-IR and fasting glucose levels. Gene expression profiling of adipose tissue (AT) shows an induction of mRNA related to lipid catabolism and mitochondrial biogenesis and inhibition of mRNA coding for inflammatory markers. Interestingly, several Nrf2-target genes are induced in AT following administration of PPEE. The ability of PPEE to induce the expression of Nrf2-target genes is studied in adipocytes. PPEE is found to transactivate the Nrf2 response element and the Nrf2 DNA-binding, suggesting that part of the effect of PPEE can be mediated by Nrf2.

CONCLUSION

PPEE supplementation may represent an interesting preventive strategy to tackle the onset of obesity and associated metabolic disorders.


DOI: 10.1002/mnfr.202000275
PubMed: 32729164


Affiliations:


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<title level="j">Molecular nutrition & food research</title>
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<p>
<b>SCOPE</b>
</p>
<p>Current evidence supports the beneficial effect of polyphenols on the management of obesity and associated comorbidities. This is the case for propolis, a polyphenol-rich substance produced by bees. The aim of the present study is to evaluate the effect of a poplar propolis ethanolic extract (PPEE) on obesity and glucose homeostasis, and to unveil its putative molecular mechanisms of action.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS AND RESULTS</b>
</p>
<p>Male high-fat (HF) diet-fed mice are administered PPEE for 12 weeks. PPEE supplementation reduces the HF-mediated adiposity index, adipocyte hypertrophy, and body weight gain. It also improves HOMA-IR and fasting glucose levels. Gene expression profiling of adipose tissue (AT) shows an induction of mRNA related to lipid catabolism and mitochondrial biogenesis and inhibition of mRNA coding for inflammatory markers. Interestingly, several Nrf2-target genes are induced in AT following administration of PPEE. The ability of PPEE to induce the expression of Nrf2-target genes is studied in adipocytes. PPEE is found to transactivate the Nrf2 response element and the Nrf2 DNA-binding, suggesting that part of the effect of PPEE can be mediated by Nrf2.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>PPEE supplementation may represent an interesting preventive strategy to tackle the onset of obesity and associated metabolic disorders.</p>
</div>
</front>
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<ArticleTitle>Poplar Propolis Ethanolic Extract Reduces Body Weight Gain and Glucose Metabolism Disruption in High-Fat Diet-Fed Mice.</ArticleTitle>
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<AbstractText Label="SCOPE">Current evidence supports the beneficial effect of polyphenols on the management of obesity and associated comorbidities. This is the case for propolis, a polyphenol-rich substance produced by bees. The aim of the present study is to evaluate the effect of a poplar propolis ethanolic extract (PPEE) on obesity and glucose homeostasis, and to unveil its putative molecular mechanisms of action.</AbstractText>
<AbstractText Label="METHODS AND RESULTS">Male high-fat (HF) diet-fed mice are administered PPEE for 12 weeks. PPEE supplementation reduces the HF-mediated adiposity index, adipocyte hypertrophy, and body weight gain. It also improves HOMA-IR and fasting glucose levels. Gene expression profiling of adipose tissue (AT) shows an induction of mRNA related to lipid catabolism and mitochondrial biogenesis and inhibition of mRNA coding for inflammatory markers. Interestingly, several Nrf2-target genes are induced in AT following administration of PPEE. The ability of PPEE to induce the expression of Nrf2-target genes is studied in adipocytes. PPEE is found to transactivate the Nrf2 response element and the Nrf2 DNA-binding, suggesting that part of the effect of PPEE can be mediated by Nrf2.</AbstractText>
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<li>France</li>
</country>
<region>
<li>Aquitaine</li>
<li>Nouvelle-Aquitaine</li>
<li>Provence-Alpes-Côte d'Azur</li>
</region>
<orgName>
<li>Université d'Aix-Marseille</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Nouvelle-Aquitaine">
<name sortKey="Cardinault, Nicolas" sort="Cardinault, Nicolas" uniqKey="Cardinault N" first="Nicolas" last="Cardinault">Nicolas Cardinault</name>
</region>
<name sortKey="Astier, Julien" sort="Astier, Julien" uniqKey="Astier J" first="Julien" last="Astier">Julien Astier</name>
<name sortKey="Bonnet, Lauriane" sort="Bonnet, Lauriane" uniqKey="Bonnet L" first="Lauriane" last="Bonnet">Lauriane Bonnet</name>
<name sortKey="Couturier, Charlene" sort="Couturier, Charlene" uniqKey="Couturier C" first="Charlène" last="Couturier">Charlène Couturier</name>
<name sortKey="Dalifard, Julie" sort="Dalifard, Julie" uniqKey="Dalifard J" first="Julie" last="Dalifard">Julie Dalifard</name>
<name sortKey="Delbah, Naima" sort="Delbah, Naima" uniqKey="Delbah N" first="Naïma" last="Delbah">Naïma Delbah</name>
<name sortKey="George, Stephane" sort="George, Stephane" uniqKey="George S" first="Stéphane" last="Georgé">Stéphane Georgé</name>
<name sortKey="Karkeni, Esma" sort="Karkeni, Esma" uniqKey="Karkeni E" first="Esma" last="Karkeni">Esma Karkeni</name>
<name sortKey="Landrier, Jean Francois" sort="Landrier, Jean Francois" uniqKey="Landrier J" first="Jean-François" last="Landrier">Jean-François Landrier</name>
<name sortKey="Landrier, Jean Francois" sort="Landrier, Jean Francois" uniqKey="Landrier J" first="Jean-François" last="Landrier">Jean-François Landrier</name>
<name sortKey="Letullier, Claire" sort="Letullier, Claire" uniqKey="Letullier C" first="Claire" last="Letullier">Claire Letullier</name>
<name sortKey="Mounien, Lourdes" sort="Mounien, Lourdes" uniqKey="Mounien L" first="Lourdes" last="Mounien">Lourdes Mounien</name>
<name sortKey="Perrin, Estelle" sort="Perrin, Estelle" uniqKey="Perrin E" first="Estelle" last="Perrin">Estelle Perrin</name>
<name sortKey="Seipelt, Eva" sort="Seipelt, Eva" uniqKey="Seipelt E" first="Eva" last="Seipelt">Eva Seipelt</name>
<name sortKey="Tourniaire, Franck" sort="Tourniaire, Franck" uniqKey="Tourniaire F" first="Franck" last="Tourniaire">Franck Tourniaire</name>
<name sortKey="Tourniaire, Franck" sort="Tourniaire, Franck" uniqKey="Tourniaire F" first="Franck" last="Tourniaire">Franck Tourniaire</name>
</country>
</tree>
</affiliations>
</record>

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