Regional Difference of ROS Generation, lipid Peroxidation, and Antioxidant Enzyme Activity In Rat Brain and Their Dietary Modulation

  • Baek, Bong-Sook (College of Pharmacy, Research Institute of Drug Development, Pusan National University) ;
  • Kwon, Hyun-Joo (College of Pharmacy, Research Institute of Drug Development, Pusan National University) ;
  • Lee, Kyoung-Hee (College of Pharmacy, Research Institute of Drug Development, Pusan National University) ;
  • Yoo, Mi-Ae (Molecular Biology and Research Institute of Drug Development, Pusan National University) ;
  • Kim, Kyu-Won (Molecular Biology and Research Institute of Drug Development, Pusan National University) ;
  • Yuji-Ikeno (The University of Texas Health Science Center at San Antonio) ;
  • Yu, Byung-Pal (The University of Texas Health Science Center at San Antonio) ;
  • Chung, Hae-Young (College of Pharmacy, Research Institute of Drug Development, Pusan National University)
  • 발행 : 1999.08.01

초록

One of the potential causes of age-related neuronal damage can be reactive oxygen species (ROS), as the brain is particularly sensitive to oxidative damage. In the present study, we investigated the effects of aging and dietary restriction (DR) on ROS generation, lipid peroxidation, and antioxidant enzymes in cerebrum, hippocampus, and cerebellum of 6-, 12-, 18-, and 24-month-old rats. ROS generation significantly increased with age in cerebrum of ad libitum (AL) rats. However, no significant age-difference was observed in hippocampus and cerebellum. DR significantly decreased ROS generation in cerebrum and cerebellum at 24-months. On the other hand, the increased lipid peroxidation of AL rats during aging was significantly reduced by DR in all regions. Our results further showed that catalase activity decreased with age in cerebellum of AL rats, which was reversed by DR, although SOD activity had little change by aging and DR in all regions. In a similar way, glutathione (GSH) peroxidase activity increased with age in cerebrum of AL rats, while DR suppressed it at 24-months. These data further support the evidence that the vulnerability to oxidative stress in the brain is region-specific.

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