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Brain region-specific effects of long-term caloric restriction on redox balance of the aging rat.

Identifieur interne : 000192 ( Main/Exploration ); précédent : 000191; suivant : 000193

Brain region-specific effects of long-term caloric restriction on redox balance of the aging rat.

Auteurs : Emmanuel Moyse [France] ; Madeleine Arsenault [Canada] ; Pierrette Gaudreau [Canada] ; Guylaine Ferland [Canada] ; Charles Ramassamy [Canada]

Source :

RBID : pubmed:30659860

Descripteurs français

English descriptors

Abstract

Caloric restriction (CR) is the most effective intervention to improve health span and extend lifespan in preclinical models. This anti-aging effect of CR is related to attenuation of oxidative damage in various tissues, with divergent results in the brain. We addressed how brain oxidoreductive balance would be modulated in male Sprague-Dawley (SD) rats submitted to a 40% CR from 8 to 19 months of age, by reference to ad libitum-fed (AL) rats at 2 and 19 months of age. Four brain structures were compared: hippocampus, striatum, parietal cortex, cerebellum. Our CR diet elicits significant prevention of oxidative damages with the upregulation of antioxidant defenses (levels of glutathione [GSH], mRNAs of clusterin and of three key antioxidant enzymes) as compared to age-matched AL controls, in a strikingly region-specific pattern. CR also prevented a drastic rise of the glial fibrillary acidic protein in the hippocampus of old AL rats. Besides, the CR effects at age 19 months mainly consist in improving endogenous defenses before the onset of age-related redox alterations. These effects are more prominent in the hippocampus.

DOI: 10.1016/j.mad.2019.01.002
PubMed: 30659860


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Caloric restriction (CR) is the most effective intervention to improve health span and extend lifespan in preclinical models. This anti-aging effect of CR is related to attenuation of oxidative damage in various tissues, with divergent results in the brain. We addressed how brain oxidoreductive balance would be modulated in male Sprague-Dawley (SD) rats submitted to a 40% CR from 8 to 19 months of age, by reference to ad libitum-fed (AL) rats at 2 and 19 months of age. Four brain structures were compared: hippocampus, striatum, parietal cortex, cerebellum. Our CR diet elicits significant prevention of oxidative damages with the upregulation of antioxidant defenses (levels of glutathione [GSH], mRNAs of clusterin and of three key antioxidant enzymes) as compared to age-matched AL controls, in a strikingly region-specific pattern. CR also prevented a drastic rise of the glial fibrillary acidic protein in the hippocampus of old AL rats. Besides, the CR effects at age 19 months mainly consist in improving endogenous defenses before the onset of age-related redox alterations. These effects are more prominent in the hippocampus.</div>
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<DescriptorName UI="D051152" MajorTopicYN="N">Clusterin</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005247" MajorTopicYN="N">Feeding Behavior</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005904" MajorTopicYN="N">Glial Fibrillary Acidic Protein</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D054477" MajorTopicYN="N">Glutaredoxins</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D005978" MajorTopicYN="N">Glutathione</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006624" MajorTopicYN="N">Hippocampus</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008136" MajorTopicYN="N">Longevity</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010084" MajorTopicYN="Y">Oxidation-Reduction</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018384" MajorTopicYN="Y">Oxidative Stress</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D051381" MajorTopicYN="N">Rats</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017207" MajorTopicYN="N">Rats, Sprague-Dawley</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000072105" MajorTopicYN="N">Superoxide Dismutase-1</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013879" MajorTopicYN="N">Thioredoxins</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">Clusterin</Keyword>
<Keyword MajorTopicYN="Y">Glial fibrillary acidic protein</Keyword>
<Keyword MajorTopicYN="Y">Glutaredoxine-1</Keyword>
<Keyword MajorTopicYN="Y">Glutathione</Keyword>
<Keyword MajorTopicYN="Y">Superoxide dismutase-1</Keyword>
<Keyword MajorTopicYN="Y">Thioredoxine-1</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2018</Year>
<Month>09</Month>
<Day>01</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2018</Year>
<Month>12</Month>
<Day>01</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2019</Year>
<Month>01</Month>
<Day>03</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2019</Year>
<Month>1</Month>
<Day>20</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2019</Year>
<Month>8</Month>
<Day>6</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2019</Year>
<Month>1</Month>
<Day>20</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">30659860</ArticleId>
<ArticleId IdType="pii">S0047-6374(18)30176-3</ArticleId>
<ArticleId IdType="doi">10.1016/j.mad.2019.01.002</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>Canada</li>
<li>France</li>
</country>
<region>
<li>Centre-Val de Loire</li>
<li>Québec</li>
<li>Région Centre</li>
</region>
<settlement>
<li>Nouzilly</li>
<li>Québec (ville)</li>
</settlement>
<orgName>
<li>Université Laval</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Centre-Val de Loire">
<name sortKey="Moyse, Emmanuel" sort="Moyse, Emmanuel" uniqKey="Moyse E" first="Emmanuel" last="Moyse">Emmanuel Moyse</name>
</region>
</country>
<country name="Canada">
<noRegion>
<name sortKey="Arsenault, Madeleine" sort="Arsenault, Madeleine" uniqKey="Arsenault M" first="Madeleine" last="Arsenault">Madeleine Arsenault</name>
</noRegion>
<name sortKey="Ferland, Guylaine" sort="Ferland, Guylaine" uniqKey="Ferland G" first="Guylaine" last="Ferland">Guylaine Ferland</name>
<name sortKey="Gaudreau, Pierrette" sort="Gaudreau, Pierrette" uniqKey="Gaudreau P" first="Pierrette" last="Gaudreau">Pierrette Gaudreau</name>
<name sortKey="Ramassamy, Charles" sort="Ramassamy, Charles" uniqKey="Ramassamy C" first="Charles" last="Ramassamy">Charles Ramassamy</name>
</country>
</tree>
</affiliations>
</record>

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