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Middle aged turn point in parameters of oxidative stress and glucose catabolism in mouse cerebellum during lifespan: minor effects of every-other-day fasting
The cerebellum is considered to develop aging markers more slowly than other parts of the brain. Intensification of free radical processes and compromised bioenergetics, critical hallmarks of normal brain aging, may be slowed down by caloric restriction. This study aimed to evaluate the intensity of...
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Published in: | Biogerontology (Dordrecht) 2021-06, Vol.22 (3), p.315-328 |
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creator | Bayliak, Maria M. Mosiichuk, Nadia M. Sorochynska, Oksana M. Kuzniak, Oksana V. Sishchuk, Lesia O. Hrushchenko, Anastasiia O. Semchuk, Alina O. Pryimak, Taras V. Vasylyk, Yulia V. Gospodaryov, Dmytro V. Storey, Kenneth B. Garaschuk, Olga Lushchak, Volodymyr I. |
description | The cerebellum is considered to develop aging markers more slowly than other parts of the brain. Intensification of free radical processes and compromised bioenergetics, critical hallmarks of normal brain aging, may be slowed down by caloric restriction. This study aimed to evaluate the intensity of oxidative stress and the enzymatic potential to utilize glucose via glycolysis or the pentose phosphate pathway (PPP) in the cerebellum of mice under
ad
libitum
versus every-other-day fasting (EODF) feeding regimens. Levels of lipid peroxides, activities of antioxidant and key glycolytic and PPP enzymes were measured in young (6-month), middle-aged (12-month) and old (18-month) C57BL/6J mice. The cerebellum showed the most dramatic increase in lipid peroxide levels, antioxidant capacity and PPP key enzyme activities and the sharpest decline in the activities of key glycolytic enzymes under transition from young to middle age but these changes slowed when transiting from middle to old age. A decrease in the activity of the key glycolytic enzyme phosphofructokinase was accompanied by a concomitant increase in the activities of hexokinase and glucose-6-phosphate dehydrogenase (G6PDH), which may suggest that during normal cerebellar aging glucose metabolism shifts from glycolysis to the pentose phosphate pathway. The data indicate that intensification of free radical processes in the cerebellum occurred by middle age and that activation of the PPP together with increased antioxidant capacity can help to resist these changes into old age. However, the EODF regime did not significantly modulate or alleviate any of the metabolic processes studied in this analysis of the aging cerebellum. |
doi_str_mv | 10.1007/s10522-021-09918-x |
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ad
libitum
versus every-other-day fasting (EODF) feeding regimens. Levels of lipid peroxides, activities of antioxidant and key glycolytic and PPP enzymes were measured in young (6-month), middle-aged (12-month) and old (18-month) C57BL/6J mice. The cerebellum showed the most dramatic increase in lipid peroxide levels, antioxidant capacity and PPP key enzyme activities and the sharpest decline in the activities of key glycolytic enzymes under transition from young to middle age but these changes slowed when transiting from middle to old age. A decrease in the activity of the key glycolytic enzyme phosphofructokinase was accompanied by a concomitant increase in the activities of hexokinase and glucose-6-phosphate dehydrogenase (G6PDH), which may suggest that during normal cerebellar aging glucose metabolism shifts from glycolysis to the pentose phosphate pathway. The data indicate that intensification of free radical processes in the cerebellum occurred by middle age and that activation of the PPP together with increased antioxidant capacity can help to resist these changes into old age. However, the EODF regime did not significantly modulate or alleviate any of the metabolic processes studied in this analysis of the aging cerebellum.</description><identifier>ISSN: 1389-5729</identifier><identifier>EISSN: 1573-6768</identifier><identifier>DOI: 10.1007/s10522-021-09918-x</identifier><identifier>PMID: 33786674</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Aging ; Antioxidants ; Bioenergetics ; Biomedical and Life Sciences ; Cell Biology ; Cerebellum ; Developmental Biology ; Dietary restrictions ; Enzymatic activity ; Enzymes ; Fasting ; Free radicals ; Geriatrics/Gerontology ; Glucose ; Glucose metabolism ; Glucosephosphate dehydrogenase ; Glycolysis ; Hexokinase ; Laboratory testing ; Life Sciences ; Life span ; Middle age ; Oxidative stress ; Pentose phosphate pathway ; Peroxide ; Phosphofructokinase ; Research Article</subject><ispartof>Biogerontology (Dordrecht), 2021-06, Vol.22 (3), p.315-328</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-a28d177f4718ddb7ffbdaa07b14d99ceadd24ddbe1e6a45ac1ae8c259b239de83</citedby><cites>FETCH-LOGICAL-c375t-a28d177f4718ddb7ffbdaa07b14d99ceadd24ddbe1e6a45ac1ae8c259b239de83</cites><orcidid>0000-0002-7363-1853 ; 0000-0001-5773-760X ; 0000-0001-7400-5654 ; 0000-0001-6268-8910 ; 0000-0001-8387-339X ; 0000-0001-5602-3330 ; 0000-0002-5362-1164</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2519561720/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2519561720?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,777,781,21375,27905,27906,33592,33593,43714,73970</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33786674$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bayliak, Maria M.</creatorcontrib><creatorcontrib>Mosiichuk, Nadia M.</creatorcontrib><creatorcontrib>Sorochynska, Oksana M.</creatorcontrib><creatorcontrib>Kuzniak, Oksana V.</creatorcontrib><creatorcontrib>Sishchuk, Lesia O.</creatorcontrib><creatorcontrib>Hrushchenko, Anastasiia O.</creatorcontrib><creatorcontrib>Semchuk, Alina O.</creatorcontrib><creatorcontrib>Pryimak, Taras V.</creatorcontrib><creatorcontrib>Vasylyk, Yulia V.</creatorcontrib><creatorcontrib>Gospodaryov, Dmytro V.</creatorcontrib><creatorcontrib>Storey, Kenneth B.</creatorcontrib><creatorcontrib>Garaschuk, Olga</creatorcontrib><creatorcontrib>Lushchak, Volodymyr I.</creatorcontrib><title>Middle aged turn point in parameters of oxidative stress and glucose catabolism in mouse cerebellum during lifespan: minor effects of every-other-day fasting</title><title>Biogerontology (Dordrecht)</title><addtitle>Biogerontology</addtitle><addtitle>Biogerontology</addtitle><description>The cerebellum is considered to develop aging markers more slowly than other parts of the brain. Intensification of free radical processes and compromised bioenergetics, critical hallmarks of normal brain aging, may be slowed down by caloric restriction. This study aimed to evaluate the intensity of oxidative stress and the enzymatic potential to utilize glucose via glycolysis or the pentose phosphate pathway (PPP) in the cerebellum of mice under
ad
libitum
versus every-other-day fasting (EODF) feeding regimens. Levels of lipid peroxides, activities of antioxidant and key glycolytic and PPP enzymes were measured in young (6-month), middle-aged (12-month) and old (18-month) C57BL/6J mice. The cerebellum showed the most dramatic increase in lipid peroxide levels, antioxidant capacity and PPP key enzyme activities and the sharpest decline in the activities of key glycolytic enzymes under transition from young to middle age but these changes slowed when transiting from middle to old age. A decrease in the activity of the key glycolytic enzyme phosphofructokinase was accompanied by a concomitant increase in the activities of hexokinase and glucose-6-phosphate dehydrogenase (G6PDH), which may suggest that during normal cerebellar aging glucose metabolism shifts from glycolysis to the pentose phosphate pathway. The data indicate that intensification of free radical processes in the cerebellum occurred by middle age and that activation of the PPP together with increased antioxidant capacity can help to resist these changes into old age. However, the EODF regime did not significantly modulate or alleviate any of the metabolic processes studied in this analysis of the aging cerebellum.</description><subject>Aging</subject><subject>Antioxidants</subject><subject>Bioenergetics</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Biology</subject><subject>Cerebellum</subject><subject>Developmental Biology</subject><subject>Dietary restrictions</subject><subject>Enzymatic activity</subject><subject>Enzymes</subject><subject>Fasting</subject><subject>Free radicals</subject><subject>Geriatrics/Gerontology</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Glucosephosphate dehydrogenase</subject><subject>Glycolysis</subject><subject>Hexokinase</subject><subject>Laboratory testing</subject><subject>Life Sciences</subject><subject>Life span</subject><subject>Middle age</subject><subject>Oxidative stress</subject><subject>Pentose phosphate 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aged turn point in parameters of oxidative stress and glucose catabolism in mouse cerebellum during lifespan: minor effects of every-other-day fasting</title><author>Bayliak, Maria M. ; Mosiichuk, Nadia M. ; Sorochynska, Oksana M. ; Kuzniak, Oksana V. ; Sishchuk, Lesia O. ; Hrushchenko, Anastasiia O. ; Semchuk, Alina O. ; Pryimak, Taras V. ; Vasylyk, Yulia V. ; Gospodaryov, Dmytro V. ; Storey, Kenneth B. ; Garaschuk, Olga ; Lushchak, Volodymyr I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-a28d177f4718ddb7ffbdaa07b14d99ceadd24ddbe1e6a45ac1ae8c259b239de83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aging</topic><topic>Antioxidants</topic><topic>Bioenergetics</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Biology</topic><topic>Cerebellum</topic><topic>Developmental Biology</topic><topic>Dietary restrictions</topic><topic>Enzymatic 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O.</au><au>Semchuk, Alina O.</au><au>Pryimak, Taras V.</au><au>Vasylyk, Yulia V.</au><au>Gospodaryov, Dmytro V.</au><au>Storey, Kenneth B.</au><au>Garaschuk, Olga</au><au>Lushchak, Volodymyr I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Middle aged turn point in parameters of oxidative stress and glucose catabolism in mouse cerebellum during lifespan: minor effects of every-other-day fasting</atitle><jtitle>Biogerontology (Dordrecht)</jtitle><stitle>Biogerontology</stitle><addtitle>Biogerontology</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>22</volume><issue>3</issue><spage>315</spage><epage>328</epage><pages>315-328</pages><issn>1389-5729</issn><eissn>1573-6768</eissn><abstract>The cerebellum is considered to develop aging markers more slowly than other parts of the brain. Intensification of free radical processes and compromised bioenergetics, critical hallmarks of normal brain aging, may be slowed down by caloric restriction. This study aimed to evaluate the intensity of oxidative stress and the enzymatic potential to utilize glucose via glycolysis or the pentose phosphate pathway (PPP) in the cerebellum of mice under
ad
libitum
versus every-other-day fasting (EODF) feeding regimens. Levels of lipid peroxides, activities of antioxidant and key glycolytic and PPP enzymes were measured in young (6-month), middle-aged (12-month) and old (18-month) C57BL/6J mice. The cerebellum showed the most dramatic increase in lipid peroxide levels, antioxidant capacity and PPP key enzyme activities and the sharpest decline in the activities of key glycolytic enzymes under transition from young to middle age but these changes slowed when transiting from middle to old age. A decrease in the activity of the key glycolytic enzyme phosphofructokinase was accompanied by a concomitant increase in the activities of hexokinase and glucose-6-phosphate dehydrogenase (G6PDH), which may suggest that during normal cerebellar aging glucose metabolism shifts from glycolysis to the pentose phosphate pathway. The data indicate that intensification of free radical processes in the cerebellum occurred by middle age and that activation of the PPP together with increased antioxidant capacity can help to resist these changes into old age. However, the EODF regime did not significantly modulate or alleviate any of the metabolic processes studied in this analysis of the aging cerebellum.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>33786674</pmid><doi>10.1007/s10522-021-09918-x</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-7363-1853</orcidid><orcidid>https://orcid.org/0000-0001-5773-760X</orcidid><orcidid>https://orcid.org/0000-0001-7400-5654</orcidid><orcidid>https://orcid.org/0000-0001-6268-8910</orcidid><orcidid>https://orcid.org/0000-0001-8387-339X</orcidid><orcidid>https://orcid.org/0000-0001-5602-3330</orcidid><orcidid>https://orcid.org/0000-0002-5362-1164</orcidid></addata></record> |
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subjects | Aging Antioxidants Bioenergetics Biomedical and Life Sciences Cell Biology Cerebellum Developmental Biology Dietary restrictions Enzymatic activity Enzymes Fasting Free radicals Geriatrics/Gerontology Glucose Glucose metabolism Glucosephosphate dehydrogenase Glycolysis Hexokinase Laboratory testing Life Sciences Life span Middle age Oxidative stress Pentose phosphate pathway Peroxide Phosphofructokinase Research Article |
title | Middle aged turn point in parameters of oxidative stress and glucose catabolism in mouse cerebellum during lifespan: minor effects of every-other-day fasting |
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