Effect of aging on the metabolism of pyruvate and 3-hydroxybutyrate in nonsynaptic and synaptic mitochondria from rat brain.

Abstract

Abstract: Age‐dependent changes in the oxidative metabolism in nonsynaptic and synaptic mitochondria from brains of 3, 12, and 24‐month‐old rats were investigated. When pyruvate and malate were used in conjunction as substrates, a significant reduction in State 3 respiration was observed in both mitochondrial populations from 12‐and 24‐month‐old rats compared with 3‐month‐old animals. A similar age‐dependent reduction in the oxidation of [1‐11C]pyruvate was also observed in nonsynaptic and synaptic mitochondria from senescent rats. Pyruvate dehydrogenase complex activity (both active and total) was, however, not decreased in the two mitochondrial populations from brains of 3, 12, and 24‐month‐old rats. When DL‐3‐hydroxybutyrate plus malate were used as substrates, a decrease in State 3 respiration was observed only in synaptic mitochondria from 24‐month‐old rats compared with 3‐ month‐old animals. Similarly, an age‐dependent reduction in the oxidation of 3‐hydroxy[3‐11C]butyrate was also observed only in synaptic mitochondria from 12‐and 24‐month‐old rats. However, a significant reduction in the activities of ketone body‐metabolizing enzymes, namely, 3‐hydroxybutyrate dehydrogenase, 3‐ketoacid CoA transferase, and acetoacetyl‐CoA thiolase was observed in both mitochondrlal populations from 12‐ and 24‐month‐old rats compared with 3 month‐old animals. These findings show that specific alterations in oxidative metabolism occur in nonsynaptic and synaptic mitochondria from aging rats. The data also suggest that in addition to alterations in enzyme activities, permeability of anions (e.g. pyruvate) across the inner mitochondrial membrane may be altered in nonsynaptic and synaptic mitochondria from senescent animals.