VARIATIONS IN LIPID INTAKE AND THEIR INFLUENCE ON RESPIRATION AND TRICARBOXYLIC ACID CYCLE ACTIVITY

1965 ◽  
Vol 43 (9) ◽  
pp. 1575-1587 ◽  
Author(s):  
Hector F. DeLuca

The possible role of dietary lipids and lipid-soluble constituents in the tricarboxylic acid cycle, respiratory systems, and mitochondrial structure is discussed, with special emphasis on vitamin D, vitamin A, and essential fatty acids. Deficiency of any of these substances produces structural alterations in isolated kidney or liver mitochondria. In the case of vitamin D deficiency the structural alteration in kidney mitochondria is accompanied by an increased rate of citrate and isocitrate oxidation and a decreased transfer of calcium ions from inside to outside the mitochondria. Vitamin D added in vitro or given to the intact rat specifically decreases citrate oxidation and increases the translocation of calcium. Vitamin A deficiency increases the respiration of liver homogenates and mitochondria in the absence of phosphate acceptor, an effect which could readily be reversed within 48 hours after vitamin A administration. Increased ATPase and decreased respiratory control were also noted in liver mitochondria from vitamin A deficient rats. The structural change as well as the biochemical lesions could also be reversed within 48 hours after vitamin A administration. Similar experiments with essential fatty acid deficient mitochondria also revealed a high ATPase, low respiratory control, and marked structural damage. These changes could be reversed by the feeding of essential fatty acids to the deficient animals for 1–3 weeks. Despite many attempts, it was not possible to demonstrate structural changes in mitochondria in situ as a result of any of the deficiencies described. It is suggested that the respiratory and tricarboxylic acid cycle changes that have been attributed to the lipid constituents of the diet are secondary to alterations in subcellular membrane systems. The use of these membrane systems as tools or models in a study of the mechanism of action of the dietary lipid and lipid-soluble materials is discussed.

1996 ◽  
Vol 317 (3) ◽  
pp. 791-795 ◽  
Author(s):  
Lesley DRYNAN ◽  
Patti A. QUANT ◽  
Victor A. ZAMMIT

The Flux Control Coefficients of mitochondrial outer membrane carnitine palmitoyltransferase (CPT I) with respect to the overall rates of β-oxidation, ketogenesis and tricarboxylic acid cycle activity were measured in hepatocytes isolated from rats in different metabolic states (fed, 24 h-starved, starved–refed and starved/insulin-treated). These conditions were chosen because there is controversy as to whether, when significant control ceases to be exerted by CPT I over the rate of fatty oxidation [Moir and Zammit (1994) Trends Biochem. Sci. 19, 313–317], this is transferred to one or more steps proximal to acylcarnitine synthesis (e.g. decreased delivery of fatty acids to the liver) or to the reaction catalysed by mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase [Hegardt (1995) Biochem. Soc. Trans. 23, 486–490]. Therefore isolated hepatocytes were used in the present study to exclude the involvement of changes in the rate of delivery of non-esterified fatty acids (NEFA) to the liver, such as occur in vivo, and to ascertain whether, under conditions of constant supply of NEFA, CPT I retains control over the relevant fluxes of fatty acid oxidation to ketones and carbon dioxide, or whether control is transferred to another (intrahepatocytic) site. The results clearly show that the Flux Control Coefficients of CPT I with respect to overall β-oxidation and ketogenesis are very high under all conditions investigated, indicating that control is not lost to another intrahepatic site during the metabolic transitions studied. The control of CPT I over tricarboxylic acid cycle activity was always very low. The significance of these findings for the integration of fatty acid and carbohydrate metabolism in the liver is discussed.


Award of Medals 1961 The Copley Medal is awarded to Sir Hans Krebs, F.R.S. Sir Hans Krebs has made outstanding contributions to knowledge of the chemical pathways of metabolism. In 1932, with Henseleit, he used tissue slices to demonstrate the synthesis of urea and found that additions of ornithine stimulated the process. Ornithine was regarded as uniting with carbon dioxide and ammonia to give arginine, with citrulline as an intermediate. The enzyme arginase liberated urea and a molecule of ornithine, so that the process could begin again. Subsequent research has shown that the postulated cycle is essentially valid, although more detail has been introduced; carbamyl phosphate, argininosuccinate and adenosine triphosphate have been brought in and aspartic acid has replaced ammonia in the reaction with citrulline. The more complicated version owes much to the fundamental work initiated by Krebs in 1937 on the tricarboxylic acid cycle. This process is now seen as the main route for oxidizing the two-carbon fragment produced in the biological degradation of carbohydrates, fatty acids and arninoacids.


1986 ◽  
Vol 239 (1) ◽  
pp. 121-125 ◽  
Author(s):  
P Newsholme ◽  
R Curi ◽  
S Gordon ◽  
E A Newsholme

Maximum activities of some key enzymes of metabolism were studied in elicited (inflammatory) macrophages of the mouse and lymph-node lymphocytes of the rat. The activity of hexokinase in the macrophage is very high, as high as that in any other major tissue of the body, and higher than that of phosphorylase or 6-phosphofructokinase, suggesting that glucose is a more important fuel than glycogen and that the pentose phosphate pathway is also important in these cells. The latter suggestion is supported by the high activities of both glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase. However, the rate of glucose utilization by ‘resting’ macrophages incubated in vitro is less than the 10% of the activity of 6-phosphofructokinase: this suggests that the rate of glycolysis is increased dramatically during phagocytosis or increased secretory activity. The macrophages possess higher activities of citrate synthase and oxoglutarate dehydrogenase than do lymphocytes, suggesting that the tricarboxylic acid cycle may be important in energy generation in these cells. The activity of 3-oxoacid CoA-transferase is higher in the macrophage, but that of 3-hydroxybutyrate dehydrogenase is very much lower than those in the lymphocytes. The activity of carnitine palmitoyltransferase is higher in macrophages, suggesting that fatty acids as well as acetoacetate could provide acetyl-CoA as substrate for the tricarboxylic acid cycle. No detectable rate of acetoacetate or 3-hydroxybutyrate utilization was observed during incubation of resting macrophages, but that of oleate was 1.0 nmol/h per mg of protein or about 2.2% of the activity of palmitoyltransferase. The activity of glutaminase is about 4-fold higher in macrophages than in lymphocytes, which suggests that the rate of glutamine utilization could be very high. The rate of utilization of glutamine by resting incubated macrophages was similar to that reported for rat lymphocytes, but was considerably lower than the activity of glutaminase.


1976 ◽  
Vol 231 (2) ◽  
pp. 522-528 ◽  
Author(s):  
DK Kasbekar

Spontaneously secreting gastric mucosae of the bullfrog (Rana catesbeiana) were brought to resting states in the absence of both the exogenous secretagogue and energy-yielding substrate, either by treatment with burimamide or by the classical method of prolonged preincubation. Glucose, pyruvate, lactate, and tricarboxylic acid cycle intermediates were compared with short- and long-chain fatty acids as potential substrates on these resting mucosae to determine if the latter could initiate and sustain H+ secretion in the absence of added secretagogues. The experimental data indicate that fatty acids cannot stimulate acid secretion from the resting state by preempting the requirement for secretagogues. Although fatty acids may serve as preferred substrates in comparison with glucose, glycolytic intermediates, and tricarboxylic acid cycle intermediates, acid secretion is obligatorily dependent on the presence of endogenous or added secretagogues. The implications of this finding with respect to one of the recently proposed hypothesis for secretagogue regulation of gastric hydrochloric acid secretion are discussed.


1959 ◽  
Vol 10 (1) ◽  
pp. 81 ◽  
Author(s):  
RL Reid ◽  
JP Hogan

Relationships between blood levels of glucose, ketone bodies, volatile fatty acids (V.F.X.), and citrate have been studied in ewes fed on a submaintenance diet of wheaten chaff during the last 5 weeks of pregnancy. Pre-feeding levels, changes during S hr after feeding, and changes during fasting were studied. Pre-feeding hypoglycaemia was consistently more severe and the post'-prandial increase in blood glucose was less in ewes carrying twins than in ewes carrying single lambs. Blood citrate consistently increased after feeding, the magnitude of the increase depending on the extent of the increase in blood glucose. Mean citrate levels after feeding were highly correlated with mean glucose levels, which suggested that blood citrate reflected the activity of the tricarboxylic acid cycle in tissues. Pre-feeding ketone levels tended to vary inversely as blood glucose when hyperlietonaemia was moderate (less than 20 mg per cent. ketones) hut the correlation disappeared v-hen hyperketonaemia was severe (20-53 mg per cent.). When glucose increased appreciably after feeding, ketones usually declined and V.F.A. levels were normal, but when the increase in glucose was small and levels remained below 30 mg per cent. after feeding, ketone levels often did not change and V.F.A. levels were high. Mean values for ketones over a period of 8 hr after feeding were highly correlated with mean values for V.F.A. over a wide range. This can be explained on the basis of present knowledge of the metabolism of the acetyl-coenzyme A (acetyl- Co4) derived from absorbed acetate and from oxidation of higher fatty acids; it is suggested that the oxidation of acetyl-CoA is impaired as a result of depression of tricarboxylic acid cycle activity. During fasting, blood ketones varied inversely with glucose, but very high ketone levels (above 30 mg per cent.) were probably not due simply to the hypoglycaemia. The hypothesis is advanced that an excess of circulating hydrocortisone further depressed acetyl-CoA metabolism. The apparent correlations between blood glucose and ketones would then be due largely to the fact that the magnitude of the adrenal response, at any particular time in these experiments, was a function of the severity of hypoglycaemia and of the period during which it was previously maintained.


1959 ◽  
Vol 10 (6) ◽  
pp. 854 ◽  
Author(s):  
CH Gallagher

Enzymic activities in vitro of liver and brain tissue of sheep with pregnancy toxaemia were measured. Anaerobic glycolysis and oxidations of tricarboxylic acid cycle intermediates and related substrates were normal for both brain and liver enzyme preparations. Fatty acid oxidation by liver mitochondria was abnormal. Liver mitochondria from cases of pregnancy toxaemia were invariably incapable of oxidizing octanoate and palmitate, and frequently unable to oxidize propionate. The rate of propionate oxidation was low even when this substrate was oxidized. Butyrate oxidation was not much reduced by pregnancy toxaemia. Starvation of ewes in late pregnancy did not inactivate the fatty acid oxidation chains of liver mitochondria. Possible reasons for the failure of lipid metabolism are discussed. The dependence of sheep liver metabolism upon fatty acid oxidation is discussed. Insignificant amounts of glucose are absorbed from the alimentary canal in sheep and, even if absorbed, are not catabolized to supply acetyl coenzyme A for oxidation in the tricarboxylic acid cycle. Consequently sheep liver is prone to failure from interference with fatty acid oxidation. Pregnancy toxaemia is discussed in relevance to the disturbance of fatty acid metabolism which is thought to be of considerable significance in the disease.


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