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 inFree radical biology & medicine Vol. 35; no. 6; pp. 626 - 635
Main Authors Rebrin, Igor, Kamzalov, Sergey, Sohal, Rajindar S
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.09.2003
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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.
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
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Issue 6
Keywords Glutathiolation
Oxidative stress
Mitochondria
Free radicals
Protein-mixed disulfides
S-thiolation
Aging
Redox potential
Glutathione
Caloric restriction
Language English
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PublicationYear 2003
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet 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...
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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
URI https://dx.doi.org/10.1016/S0891-5849(03)00388-5
https://www.ncbi.nlm.nih.gov/pubmed/12957655
https://search.proquest.com/docview/73613081
https://pubmed.ncbi.nlm.nih.gov/PMC2837076
Volume 35
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