Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:2.3.3.1 (citrate synthase)
 4,488 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Thyroxine and cortisone acetate administration of rats of 4--7 days of age is not only accompanied by the induction of the muscle-specific enzyme, creatine kinase, but the hormones also induce morphological changes in the gastrocnemius during this period. Administration of thyroxine to these rats causes a splitting of myofibrils as shown by stereological measurements on electron micrographs. This splitting of myofibrils was not observed upon cortisone acetate administration and when both hormones were given simultaneously. It is suggested that cortisone acetate counteracts the effect of thyroxine. Both thyroxine and cortisone acetate increase the volume percentage taken by the mitochondria at 7 days of age. The effect of the simultaneous injection of both hormones is equal to the sum of the separate effects of these hormones. These changes in volume percentage of the mitochondria were compared with changes in a mitochondrial marker enzyme, i.e. citrate synthase. The difference between the morphological measurements and citrate synthase activity is due to a change in the specific activity of citrate synthase in the mitochondria.
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PMID:Quantitative analysis of morphological changes in skeletal muscle of the rat after hormone administration. 42 Aug 82

This study investigates the effects of exogenous thyroxine (T4) on running endurance, tissue masses, and the activities of citrate synthase (CS), pyruvate kinase (PK), cytosolic alpha-glycerophosphate dehydrogenase (alpha-GPDH), and beta-hydroxyacyl Coenzyme A dehydrogenase (HOAD) in Sceloporus undulatus (eastern fence lizard). The enzymes were assayed to indicate maximal catabolic activities that support exercise. Parallel experiments were done on captive and field-active groups to determine whether responses in captive studies adequately predict responses in nature. Exogenous T4 was administered via intraperitoneal pellets. The effect of T4 on running endurance was dependent on the location of the experiment (P = 0.040) such that stamina was increased by T4 only in field-active lizards. At lower levels of biological organization, interactivity between T4 and experimental location was evident but less prevalent than at the level of the whole animal, and some location effects occurred independent of T4 treatment. Heart and kidney masses were significantly greater and total hind leg muscle mass was less in captive than in field-active lizards. Thyroxine reduced liver mass in both locations and kidney mass only in captive lizards. Mass-specific CS and alpha-GPDH in gastrocnemius muscle (mixed fiber type) and HOAD in heart were lower in captive than in field-active lizards; PK in heart and liver and alpha-GPDH in heart were higher in captive lizards. Thyroxine increased CS in liver and HOAD in heart, decreased alpha-GPDH in liver in both locations, and decreased alpha-GPDH in gastrocnemius only in captive lizards. The effects of T4 differed significantly between experimental locations in gastrocnemius muscle (T4 decreased PK only in captive lizards) and in liver (T4 increased PK in field-active lizards and decreased PK in captive lizards). The mechanistic basis of differences in stamina between captive and field-active and between placebo and T4-treated lizards is largely unexplained by the factors measured here, thus illustrating the uncertainty of predicting organismal performance from lower level measurements. Nonetheless, T4 has now been shown to have greater physiological activity in field-active than in captive Sceloporus with regard to resting and total daily metabolic rates and running endurance. The results of this study further confirm that endocrine experiments on captive animals may not predict responses in nature. Further efforts to clarify the physiological significance of seasonal variations in levels of thyroid hormones will have to involve, at least in part, invasive studies on field-active lizards.
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PMID:Interactive effects of thyroxine and experimental location on running endurance, tissue masses, and enzyme activities in captive versus field-active lizards (Sceloporus undulatus). 202 10

Experimental hyperthyroidism induced in rats by daily injections of 3,3',5,5'-tetraiode-L-thyroxine (0.5 mg/kg i.p.) for 14 days resulted in a significant increase in heart weight and heart weight/body weight ratio. Hemodynamic and morphological studies were performed in one group. Thyroxine-treated rats showed a characteristic cardiovascular hyperdynamic state, such as tachycardia and augmented rate of contraction, but no evidence of heart failure such as elevated end-diastolic pressures. The cardiac cells in hyperthyroid rats had a significantly larger diameter and more mitochondria than did those of the control rats. In another group the activities of cardiac enzymes involved in energy utilization and liberation were measured biochemically and compared with those of normal controls. Hyperthyroidism resulted in increased specific activity of cytochrome C oxidase and actomyosin ATPase in the myocardium. The specific activity of long-chain acyl-CoA synthetase, carnitine palmityl-transferase, carnitine acetyltransferase, malate dehydrogenase and citrate synthase showed a moderate to marked increment, whereas the specific activity of lactate dehydrogenase and pyruvate kinase remained at the control values. These results suggest that in hyperthyroid rat hearts the functions of both energy liberation and utilization systems are enhanced to meet the added workload. Moreover, the increased activity of the enzymes participating in fatty acid metabolism suggest that in thyroxine-induced hypertrophic and hyperdynamic rat hearts, fatty acids contribute more to the energy supply than do carbohydrates.
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PMID:Biochemical and morphological study of cardiac hypertrophy. Effects of thyroxine on enzyme activities in the rat myocardium. 315 81