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Metabolic Control Patterns in Acute Phase and Regenerating Human Liver Determined in Vivo by 31-phosphorus Magnetic Resonance Spectroscopy

Overview
Journal Ann Surg
Specialty General Surgery
Date 2002 Mar 8
PMID 11882763
Citations 7
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Abstract

Objective: To elucidate the metabolic changes occurring within hepatocytes during acute phase reaction and liver regeneration.

Summary Background Data: The metabolic events occurring within the liver during the hepatic stress response are poorly understood. The authors used in vivo 31-phosphorus magnetic resonance spectroscopy to study hepatic metabolism after surgical trauma with and without loss of liver cell mass.

Methods: Three groups were studied: five patients undergoing partial hepatectomy; five patients in whom laparotomy and colonic resection was performed; and five patients treated by thyroidectomy. Hepatic metabolism was evaluated by 31-phosphorus magnetic resonance spectroscopy before surgery and serially thereafter on postoperative days 2, 4, 6, 14, and 28. Estimation of liver volume by magnetic resonance imaging and blood sampling for biochemistry were performed at the same time points.

Results: The authors found that alterations in hepatocyte phospholipid metabolism occurred after surgery that were correlated with changes in circulating acute phase proteins. Liver regeneration after hepatectomy was also associated with a derangement in energy metabolism, measured by a decrease in the ratio of ATP to its hydrolysis product inorganic phosphate. The depleted energy status was mirrored in biochemical indices of liver function, and restitution paralleled the course of restoration of hepatic cell mass.

Conclusions: These findings indicate that changes in liver metabolism after surgery reflect the magnitude of tissue injury and the quantity of functioning liver cells. Acute phase responses dominate the initial recovery period at the expense of less important endergonic functions. When liver parenchyma is lost, the acute phase reaction is maintained and further supported by a rapid replenishment of hepatocytes, which can even be considered a continuation of acute phase physiology. Modulation of liver function within the framework of overall hepatic energy economy is one mechanism for matching energy supply with increased demands during these processes.

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References
1.
Campbell K, Wu Y, Chacko V, Sitzmann J . In vivo 31P NMR spectroscopic changes during liver regeneration. J Surg Res. 1990; 49(3):244-7. DOI: 10.1016/0022-4804(90)90127-n. View

2.
Sobczak J, Tournier M, Lotti A, Duguet M . Gene expression in regenerating liver in relation to cell proliferation and stress. Eur J Biochem. 1989; 180(1):49-53. DOI: 10.1111/j.1432-1033.1989.tb14613.x. View

3.
Terrier F, Vock P, Cotting J, Ladebeck R, Reichen J, Hentschel D . Effect of intravenous fructose on the P-31 MR spectrum of the liver: dose response in healthy volunteers. Radiology. 1989; 171(2):557-63. DOI: 10.1148/radiology.171.2.2704824. View

4.
Atkinson D . The energy charge of the adenylate pool as a regulatory parameter. Interaction with feedback modifiers. Biochemistry. 1968; 7(11):4030-4. DOI: 10.1021/bi00851a033. View

5.
Dallenbach A, Marti U, Renner E . Hepatocellular Na+/H+ exchange is activated early, transiently and at a posttranscriptional level during rat liver regeneration. Hepatology. 1994; 19(5):1290-301. DOI: 10.1002/hep.1840190530. View