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alpha-Tocopherol transfer protein expression in rat liver exposed to hyperoxia
Ryoichi Ban1, Kimitaka Takitani, Han-Suk Kim
1Department of Pediatrics, Osaka Medical College, Daigaku-machi 2-7, Takatsuki, Osaka 569-8686, Japan.
Free Radical Research
|November 27, 2002
Summary
Exposure to hyperoxia decreases hepatic alpha-tocopherol transfer protein (alpha TTP) mRNA levels in rats. This suggests alpha TTP mRNA is highly responsive to oxidative stress, unlike antioxidant enzymes.
Area of Science:
- Biochemistry
- Molecular Biology
- Physiology
Background:
- Alpha-tocopherol transfer protein (alpha TTP) is crucial for alpha-tocopherol transport in the liver.
- Factors regulating hepatic alpha TTP expression remain largely unknown.
- Oxidative stress is implicated in various cellular dysfunctions.
Purpose of the Study:
- To investigate the effect of hyperoxia on hepatic alpha TTP expression.
- To examine the relationship between alpha TTP and antioxidant enzymes (GPX, Mn-SOD) under oxidative stress.
- To determine the responsiveness of alpha TTP mRNA to oxidative stress.
Main Methods:
- Rats were exposed to hyperoxia (>95% O2) for 48 hours.
- Thiobarbituric acid-reactive substances (TBARS) measured to assess oxidative stress.
- Northern blotting used to analyze mRNA expression levels of alpha TTP, Mn-SOD, and GPX.
- Protein levels of Mn-SOD and alpha TTP were also assessed.
Main Results:
- Hyperoxia significantly increased TBARS levels in plasma and liver, indicating oxidative stress.
- Hepatic alpha TTP mRNA levels significantly decreased following hyperoxia exposure.
- Alpha TTP protein levels remained unchanged despite decreased mRNA.
- Expression of Mn-SOD mRNA and protein, and GPX mRNA, remained stable under hyperoxia.
Conclusions:
- Hepatic alpha TTP mRNA is highly sensitive to oxidative stress induced by hyperoxia.
- Unlike Mn-SOD and GPX, alpha TTP mRNA levels are significantly altered by hyperoxia.
- These findings highlight a specific regulatory response of alpha TTP to oxidative conditions.

