Undernutrition during hyperoxic exposure induces CYP2E1 in rat liver

• Published in: Archives of toxicology Vol. 71; no. 11; pp. 684 - 689
• Main Authors: KHATSENKO, O. G, SINDHU, R. K, KIKKAWA, Y
• Format: Journal Article
• Language: English
• Published: Berlin Springer 1997
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Blotting, Northern; Blotting, Western; Body Weight - drug effects; Cytochrome P-450 CYP1A1 - metabolism; Cytochrome P-450 CYP2E1 - biosynthesis; Enzymes and enzyme inhibitors; Fundamental and applied biological sciences. Psychology; Hyperoxia - enzymology; Liver - enzymology; Male; Microsomes, Liver - enzymology; Nutrition Disorders - enzymology; Oxidoreductases; Protein Biosynthesis; Proteins - isolation & purification; Rats; Rats, Sprague-Dawley; RNA, Messenger - biosynthesis; Enzyme inducer; Starvation; Oxygen; Rat; Isozyme; Cytochrome P450; Liver; Rodentia; Nutrition disorder; Gene expression; Vertebrata; Mammalia; Messenger RNA; Animal; Hyperoxia; Malnutrition
• ISSN: 0340-5761; 1432-0738
• DOI: 10.1007/s002040050445

Induction of cytochrome P450 2E1 (CYP2E1) has been shown to occur through two distinct mechanisms. The first is seen by treatment of rats with acetone, pyrazole, and 4-methyl-pyrazole, which induces CYP2E1 protein without affecting the mRNA level. The second is observed in starvation, diabetes, and obesity, in which an increase of CYP2E1 protein is associated with an increase of the CYP2E1 mRNA. It has been reported by (Tindberg and Ingelman-Sundberg 1989) that hyperoxic exposure (95% O2) induced a several-fold increase of CYP2E1 protein in both the liver and lung of exposed rats without affecting the level of CYP2E1 mRNA. During the course of our previous study which demonstrated hyperoxia-induced specific pretranslational induction of CYP1A1/2 in the liver and CYP1A1 in the lung, we observed a progressive increase of hepatic CYP2E1 mRNA in animals of the hyperoxia group. Hyperoxia is accompanied by some degree of starvation and our earlier experiments were conducted with rats of significantly greater body weight than those used by Tindberg and Ingelman-Sundberg (260 vs 150 g). Thus we reevaluated the changes of CYP2E1 in the current study with the use of food-restricted control, and by utilizing rats of comparable weight (approximately 150 g) to that utilized by Tindberg and Ingelman-Sundberg. The results obtained in the present study showed that there was a significant increase in the levels of hepatic CYP2E1 mRNA, protein, and p-nitrophenol hydroxylase activity in the food-restricted control group compared to the untreated controls. Rats from the hyperoxia group also demonstrated a similar increase of these three parameters in their livers but showed no significant difference compared with the results of the food-restricted control group. Rats weighing approximately 260 g were also examined with similar food restriction and hyperoxia, and the results were essentially similar to those obtained with the younger rats. The lungs of rats from food-restricted control and hyperoxia groups showed no increase of any of the CYP2E1 parameters. The results obtained in the current study, therefore, indicate that hyperoxia has no effect on CYP2E1 expression in both the liver and lung. Increased CYP2E1 mRNA, protein, and p-nitrophenol hydroxylase activity seen in the liver of rats, but not in the lungs, are consistent with the notion that undernutrition during hyperoxia is the underlying mechanism for this induction.