Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.9.3.1 (cytochrome oxidase)
 8,822 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Effects of changes in dietary protein have been investigated on three mitochondrial enzymes, succinate dehydrogenase, isocitrate dehydrogenase and cytochrome oxidase. Weanling rats (21 days old) were fed for 30 days on (a) a commercially produced diet (CPD) containing 21.0% dietary protein and (b) a low protein-high carbohydrate diet (LPD) containing 3.47% dietary protein. Signs of protein-energy malnutrition developed in the animals having the low protein diet. The mitochondrial enzymes were assayed. Some of the experimental rats were repleted by feeding them on a protein-rich diet for 3 weeks, and the same mitochondrial enzymes were assayed. The activity of mitochondrial cytochrome oxidase, which fell to 24% of the control values during the period of deficiency, rose to 91% of the values for control rats during rehabilitation. The activities of succinate dehydrogenase and NAD+-isocitrate dehydrogenase fell to 75 and 73% of the control values, respectively, during depletion and rose to 83 and 88% during repletion in line with the general rate of recovery of the malnourished rats as reflected by the changes in the body weights during repletion. These results show that mitochondrial cytochrome oxidase is very sensitive to changes in dietary protein. Its activity drops sharply with reduction in dietary protein intake and rises rapidly, outstripping the rate of general recovery on reverting to a protein-rich diet.
 ...
PMID:Cytochrome oxidase status in protein-energy-deficient rats. 300 81

We studied energy metabolism after experimental subarachnoid hemorrhage in rats. Four different cerebral areas were tested: frontal cortex, occipital cortex, hippocampus, and brainstem. Vmax of the following enzymatic activities was evaluated: in the homogenate: hexokinase, phosphofructokinase, and lactate dehydrogenase for the glycolytic pathway, and glucose-6-phosphate dehydrogenase for the hexose monophosphate shunt; in the purified nonsynaptic mitochondria: NAD+-isocitrate dehydrogenase, citrate synthase, and succinate dehydrogenase for the Krebs cycle, and cytochrome oxidase for the electron transfer chain. We also evaluated some parameters related to the respiration of nonsynaptic mitochondria (State 3, State 4, uncoupled state, respiratory control ratio, and ADP:O ratio). Subarachnoid hemorrhage did not significantly affect Vmax of the enzymatic activities related to anaerobic and aerobic metabolism; however, mitochondrial respiration was affected, particularly in the presence of NADH-producing substrates (glutamate + malate).
 ...
PMID:Bioenergetics of different brain areas after experimental subarachnoid hemorrhage in rats. 335 25