Metabolic Zonation of the Liver

The liver is the central service organ of the organism. First, the liver is the centre of metabolism: it is responsible, on the one hand, for the maintenance of the energy supply: 1. it functions as a glucostat supplying glucose when required and removing it when in excess, 2. it produces ketone bodies to feed a.o. the central nervous system, 3. it is the main site of amino acid catabolism, 4. it removes ammonia operating as a pH-stat, and 5. it processes nutrient triglycerides and fatty acids. On the other hand, the organ catalyses important biosynthetic and biodegradative processes: 1. it has a key position in the metabolism of phospholipids and cholesterol, i.e. of lipoproteins, 2. it synthesizes and probably degrades most plasma proteins, 3. it forms bile for the digestive process, and 4. it is the main organ of biochemical defense removing xenobiotics. Second, the liver is a control station of the hormonal system producing signal substances and degrading hormones during liver passage thus contributing to the maintenance of peripheral hormone levels. Third, the liver is a passive and active blood reservoir.

[1]  A. Novikoff,et al.  CELL HETEROGENEITY WITHIN THE HEPATIC LOBULE OF THE RAT (STAINING REACTIONS) , 1959, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[2]  K. Jungermann,et al.  Regulation of hepatic metabolism : intra- and intercellular compartmentation , 1986 .

[3]  K. Jungermann,et al.  Induction in primary culture of 'gluconeogenic' and 'glycolytic' hepatocytes resembling periportal and perivenous cells. , 2005, European journal of biochemistry.

[4]  K. Jungermann,et al.  Modulation of the glucagon-dependent induction of phosphoenolpyruvate carboxykinase and tyrosine aminotransferase by arterial and venous oxygen concentrations in hepatocyte cultures. , 1981, European journal of biochemistry.

[5]  K. Jungermann,et al.  The glucagon-insulin antagonism and glucagon-dexamethasone synergism in the induction of phosphoenolpyruvate carboxykinase in cultured rat hepatocytes. , 1983, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[6]  K. Jungermann,et al.  Functional heterogeneity of periportal and perivenous hepatocytes. , 1986, Enzyme.

[7]  J. McGarry,et al.  The glucose paradox. Is glucose a substrate for liver metabolism? , 1984, The Journal of clinical investigation.

[8]  K. Jungermann,et al.  Functional Hepatocellular Heterogeneity , 2007, Hepatology.

[9]  A. Cherrington,et al.  What the papers say: Role of hepatic glycolysis and gluconeogenesis in glycogen synthesis , 1985 .

[10]  J. McGarry,et al.  The glucose paradox: new perspectives on hepatic carbohydrate metabolism , 1986 .

[11]  J. Chayen,et al.  The distribution of glutathione in the rat liver lobule. , 1979, The Biochemical journal.

[12]  K. Jungermann,et al.  Autoregulatory shift from fructolysis to lactate gluconeogenisis in rat hepatocyte suspensions. The problem of metabolic zonation of liver parenchyma. , 1976, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[13]  K. Lindros,et al.  Digitonin-collagenase perfusion for efficient separation of periportal or perivenous hepatocytes. , 1985, The Biochemical journal.

[14]  S. Yoshimura,et al.  Purification and immunohistochemical localization of rat liver glutathione peroxidase. , 1980, Biochimica et biophysica acta.

[15]  B. Quistorff,et al.  Digitonin perfusion of rat liver. A new approach in the study of intra-acinar and intracellular compartmentation in the liver. , 1985, The Biochemical journal.