79. Chronic schisandrin B treatment
improves mitochondrial antioxidant status and tissue heat shock protein
production in various tissues of young adult and middle-aged rats
Chiu, Po; Leung,
Hoi; Poon, Michel; Ko,
Kam
The effects of chronic schisandrin B (Sch B) treatment
(10 mg/kg/day×15) on mitochondrial antioxidant status and sensitivity to Ca2+-induced
permeability transition, as well as tissue heat shock protein (Hsp)25/70 production were examined in various tissues
(brain, heart, liver, skeletal muscle) of young adult and middle-aged female
rats. Age-dependent impairment in mitochondrial antioxidant status, as assessed
by levels/activities of antioxidant components (reduced glutathione, α-tocopherol, Se-glutathione peroxidase
and Mn-superoxide dismutase) and the extent of
reactive oxygen species generation in vitro, was
observed in brain, heart, liver and skeletal muscle tissues. While tissue Hsp25
levels remained relatively unchanged with aging, the Hsp70 level was increased
in both brain and heart tissues of middle-aged rats. Chronic Sch B treatment was able to enhance mitochondrial
antioxidant status and the resistance to Ca2+-induced mitochondrial
permeability transition in an age-independent manner in various tissues of
rats. However, Hsp25 and Hsp70 levels were only increased in young adult rats.
The Sch B-induced enhancement of mitochondrial
protective parameters in the heart was associated with the protection against
myocardial ischemia-reperfusion injury in both young adult and middle-aged
rats. The results suggest that chronic Sch B
treatment may be beneficial for reversing the mitochondrial changes with aging
and enhancing the heat shock response.
Keywords: Aging;
Glutathione;
Glutathione
peroxidase; Heat shock
protein; Mitochondria;
Mitochondrial
permeability transition; Myocardial
ischemia-reperfusion injury; Schisandrin B;
Superoxide
dismutase; α-Tocopherol