Effects of age and caloric restriction on glutathione redox state in mice
The main purpose of this study was to determine whether the aging process in the mouse is associated with a pro-oxidizing shift in the redox state of glutathione and whether restriction of caloric intake, which results in the extension of life span, retards such a shift. Amounts of reduced and oxidi...
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Published in | Free radical biology & medicine Vol. 35; no. 6; pp. 626 - 635 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
15.09.2003
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Subjects | |
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Abstract | The main purpose of this study was to determine whether the aging process in the mouse is associated with a pro-oxidizing shift in the redox state of glutathione and whether restriction of caloric intake, which results in the extension of life span, retards such a shift. Amounts of reduced and oxidized forms of glutathione (GSH and GSSG, respectively) and protein-glutathione mixed disulfides (protein-SSG) were measured in homogenates and mitochondria of liver, kidney, heart, brain, eye, and testis of 4, 10, 22, and 26 month old ad libitum-fed (AL) mice and 22 month old mice fed a diet containing 40% fewer calories than the AL group from the age of 4 months. The concentrations of GSH, GSSG, and protein-SSG vary greatly (∼10-, 30-, and 9-fold, respectively) from one tissue to another. During aging, the ratios of GSH:GSSG in mitochondria and tissue homogenates decreased, primarily due to elevations in GSSG content, while the protein-SSG content increased significantly. Glutathione redox potential in mitochondria became less negative, i.e., more pro-oxidizing, as the animal aged. Caloric restriction (CR) lowered the GSSG and protein-SSG content. Results suggest that the aging process in the mouse is associated with a gradual pro-oxidizing shift in the glutathione redox state and that CR attenuates this shift. |
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AbstractList | The main purpose of this study was to determine whether the aging process in the mouse is associated with a pro-oxidizing shift in the redox state of glutathione and whether restriction of caloric intake, which results in the extension of life span, retards such a shift. Amounts of reduced and oxidized forms of glutathione (GSH and GSSG, respectively) and protein-glutathione mixed disulfides (protein-SSG) were measured in homogenates and mitochondria of liver, kidney, heart, brain, eye, and testis of 4, 10, 22, and 26 month old ad libitum-fed (AL) mice and 22 month old mice fed a diet containing 40% fewer calories than the AL group from the age of 4 months. The concentrations of GSH, GSSG, and protein-SSG vary greatly (∼10-, 30-, and 9-fold, respectively) from one tissue to another. During aging, the ratios of GSH:GSSG in mitochondria and tissue homogenates decreased, primarily due to elevations in GSSG content, while the protein-SSG content increased significantly. Glutathione redox potential in mitochondria became less negative, i.e., more pro-oxidizing, as the animal aged. Caloric restriction (CR) lowered the GSSG and protein-SSG content. Results suggest that the aging process in the mouse is associated with a gradual pro-oxidizing shift in the glutathione redox state and that CR attenuates this shift. The main purpose of this study was to determine whether the aging process in the mouse is associated with a pro-oxidizing shift in the redox state of glutathione and whether restriction of caloric intake, which results in the extension of life span, retards such a shift. Amounts of reduced and oxidized forms of glutathione (GSH and GSSG, respectively) and protein-glutathione mixed disulfides (protein-SSG) were measured in homogenates and mitochondria of liver, kidney, heart, brain, eye, and testis of 4, 10, 22, and 26 month old ad libitum-fed (AL) mice and 22 month old mice fed a diet containing 40% fewer calories than the AL group from the age of 4 months. The concentrations of GSH, GSSG, and protein-SSG vary greatly (approximately 10-, 30-, and 9-fold, respectively) from one tissue to another. During aging, the ratios of GSH:GSSG in mitochondria and tissue homogenates decreased, primarily due to elevations in GSSG content, while the protein-SSG content increased significantly. Glutathione redox potential in mitochondria became less negative, i.e., more pro-oxidizing, as the animal aged. Caloric restriction (CR) lowered the GSSG and protein-SSG content. Results suggest that the aging process in the mouse is associated with a gradual pro-oxidizing shift in the glutathione redox state and that CR attenuates this shift. |
Author | Sohal, Rajindar S Rebrin, Igor Kamzalov, Sergey |
Author_xml | – sequence: 1 givenname: Igor surname: Rebrin fullname: Rebrin, Igor organization: Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, CA, USA – sequence: 2 givenname: Sergey surname: Kamzalov fullname: Kamzalov, Sergey organization: Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, CA, USA – sequence: 3 givenname: Rajindar S surname: Sohal fullname: Sohal, Rajindar S email: sohal@usc.edu organization: Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, CA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/12957655$$D View this record in MEDLINE/PubMed |
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Keywords | Glutathiolation Oxidative stress Mitochondria Free radicals Protein-mixed disulfides S-thiolation Aging Redox potential Glutathione Caloric restriction |
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SubjectTerms | Aging Aging - physiology Animals Brain - metabolism Caloric Restriction Eye - metabolism Free radicals Glutathiolation Glutathione Glutathione - metabolism Glutathione Disulfide - metabolism Kidney - metabolism Liver - metabolism Male Mice Mitochondria Mitochondria - metabolism Myocardium - metabolism Oxidation-Reduction Oxidative stress Protein-mixed disulfides Redox potential S-thiolation Testis - metabolism |
Title | Effects of age and caloric restriction on glutathione redox state in mice |
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