POSTNATAL-DEVELOPMENT OF PEROXISOMAL AND MITOCHONDRIAL-ENZYMES IN RAT-LIVER

Subcellular organelles from livers of rats three days prenatal to 50 weeks postnatal were separated on sucrose gradients. The peroxisomes had a constant density of 1.243 g/ml throughout the life of the animal. The density of the mitochondria changed from about 1.236 g/ml at birth to a constant value of 1.200 g/ml after two weeks. The peroxisomal and mitochondrial fatty acid β‐oxidation and the peroxisomal and supernatant activities of catalase and glycerol‐3‐phosphate dehydrogenase were measured at each age, as well as the peroxisomal core enzyme, urate oxidase, and the mitochondrial matrix enzyme, glutamate dehydrogenase. All of these activities were very low or undetectable before birth. Mitochondrial glutamate dehydrogenase and peroxisomal urate oxidase reached maximal activities per g of liver at two and five weeks of age, respectively. Fatty acid β‐oxidation in both peroxisomes and mitochondria and peroxisomal glycerol‐3‐phosphate dehydrogenase exhibited maximum activities per g of liver between one and two weeks of age before weaning and then decreased to steady state levels in the adult. Peroxisomal β‐oxidation accounted for at least 10% of the total β‐oxidation activity in the young rat liver, but became 30% of the total in the liver of the adult female and 20% in the adult male due to a decrease in mitochondrial β‐oxidation after two weeks of age. The greatest change in β‐oxidation was in the mitochondrial fraction rather than in the peroxisomes. At two weeks of age, four times as much β‐oxidation activity was in the mitochondria as in the peroxisomal fraction. Peroxisomal glycerol‐3‐phosphate dehydrogenase activity accounted for 5% to 7% of the total activity in animals younger than one week, but only 1% to 2% in animals older than one week. Up to three weeks of age, 85% to 90% of the liver catalase was recovered in the peroxisomes. The activity of peroxisomal catalase per g of rat liver remained constant after three weeks of age, but the total activity of catalase further increased 2.5‐ to 3‐fold, and all of the increased activity was in the supernatant fraction. Copyright © 1979 Wiley‐Liss, Inc.